Skip to main content

REVIEW article

Front. Oncol., 12 January 2023
Sec. Surgical Oncology
This article is part of the Research Topic Oncoplastic Surgery for Breast Cancer View all 13 articles

Does breast oncoplastic surgery improve quality of life?

Ren Aloisio da Costa Vieira,,,*René Aloisio da Costa Vieira1,2,3,4*Antnio Bailo-Junior,Antônio Bailão-Junior1,5Idam de Oliveira-Junior,,Idam de Oliveira-Junior1,2,5
  • 1Programa de Pós-Graduação em Tocoginecologia, Faculdade de Medicina de Botucatu, Botucatu/SP, Brazil
  • 2Programa de Pós-Graduação em Oncologia, Hospital de Câncer de Barretos, Barretos/SP, Brazil
  • 3Departamento de Cirurgia Oncológica, Divisão de Mastologia, Hospital de Câncer de Muriaé, Muriaé/MG, Brazil
  • 4Active Member of European Organisation for Research and Treatment (EORTC) Quality of life Group, Brussels, Belgium
  • 5Departamento de Mastologia e Reconstrução Mamária, Hospital de Câncer de Barretos, Barretos/SP, Brazil

Breast Oncoplastic Surgery (OS) has established itself as a safe procedure associated with the treatment of breast cancer, but the term is broad, encompassing procedures associated with breast-conserving surgeries (BCS), conservative mastectomies and fat grafting. Surgeons believe that OS is associated with an increase in quality of life (QOL), but the diversity of QOL questionnaires and therapeutic modalities makes it difficult to assess from the patient’s perspective. To answer this question, we performed a search for systematic reviews on QOL associated with different COM procedures, and in their absence, we selected case-control studies, discussing the main results. We observed that: (1) Patients undergoing BCS or breast reconstruction have improved QoL compared to those undergoing mastectomy; (2) In patients undergoing BCS, OS has not yet shown an improvement in QOL, a fact possibly influenced by patient selection bias; (3) In patients undergoing mastectomy with reconstruction, the QoL results are superior when the reconstruction is performed with autologous flaps and when the areola is preserved; (4) Prepectoral implants improves QOL in relation to subpectoral implant-based breast reconstruction; (5) ADM do not improves QOL; (6) In patients undergoing prophylactic mastectomy, satisfaction is high with the indication, but the patient must be informed about the potential complications associated with the procedure; (7) Satisfaction is high after performing fat grafting. It is observed that, in general, OS increases QOL, and when evaluating the procedures, any preservation or repair, or the use of autologous tissues, increases QOL, justifying OS.

Introduction

The World Health Organization (WHO) (1) defines quality of life (QOL) as “the individual’s perception of their position in life, in the context of culture, value systems in which they live in relation to their goals, expectations, standards and concerns”. In patients treated for breast cancer, many of the acute symptoms disappear. However, emotional deficits in social relationships and cognitive functions, associated with specific symptoms and concerns arising from cancer, impair QOL (2).

In the past, the only surgical treatment for breast cancer was mastectomy, with the possibility of late reconstruction with a myocutaneous flap (3). Subsequently, breast-conserving surgery (BCS) was established when combined with radiotherapy (4, 5). However, it is not always associated with good cosmetic results, as up to 30% of patients undergoing quadrantectomy require delayed repair due to unsatisfactory aesthetic results (6).

Thus, the concept of oncoplastic surgery (OS) is born, which is defined as the use of plastic surgery techniques to improve the aesthetic result of oncological surgery (7, 8). The surgery can be performed after mastectomy or BCS (9), with increasing indications in clinical practice. From an oncological point of view, greater ease of wide resection is observed, with the possibility of wider margins (10), a lower index of compromised margins (11) and a greater amount of resected tissue, without aesthetic damage (12).

Many patients who are not initially candidates for BCS (13) can undergo this procedure with the help of OS (14, 15), especially in the presence of tumours larger than 5 centimetres and with localized skin infiltration and multifocal and multicentric tumours, provided that it is possible to obtain neoplasia-free margins and that the residual breast volume allows an aesthetically satisfactory result. In this sense, the concept of extreme oncoplasty (EO) emerges (16).

Likewise, radical mastectomies have become more conservative, through skin preservation, with skin-sparing mastectomy (SSM) and nipple-sparing mastectomy (NSM) (17, 18). Immediate breast reconstruction, initially performed with myocutaneous flaps, was mostly replaced by the use of prostheses, and was considered a safe procedure, given the low cancer recurrence rates (1922) and the high degree of patient satisfaction (23).

However, OS is generally used to describe a broad group of surgeries associated with BCS, including mastectomy with immediate reconstruction and late reconstruction surgeries (7, 8). Thus, when evaluating OS, we must consider the type of surgery, the conditions associated with its indication, the cosmetic quality and the QOL of the patient (24, 25). OS seems to be associated with the improvement of QOL (8). The articles usually assess specific situations and little studies evaluate all situations associated with OS and QOL (2628). In this study, we sought to identify the main circumstances leading to OS, QOL questionnaires, systematic reviews and case−control studies.

Quality-of-life questionnaires

Several questionnaires can be found in the literature, but they need to be validated through a specific methodology (29, 30). The patient-reported outcome measures (PROMs) are organized in domains and questions. Domains correspond to the grouping of questions that evaluate the same subject. Grouping similar situations allows us to consider the subject and compare groups of patients in similar situations.

QOL associated with breast reconstruction were validated (26, 31, 32). To better understand and value the QOL questionnaires, we must understand how they are created (33, 34), the importance of the domains, the validation studies (35) and the steps associated with linguistic translation (36, 37).

The construction of a QOL questionnaire involves four main phases (34). The first phase is the question generation phase. Patients at different stages of the disease and health professionals are interviewed to determine the main questions to be asked. In the second phase, a list of questions is created, measurement scales are evaluated, health professionals are consulted, and an initial version of the questionnaire is drafted. A smaller group of patients evaluates questions for redundancy and low response rates, decreasing the number of questions, organizing the potential domains and drafts a potential questionnaire. In the third phase, the questionnaire is administered to a group of patients, and a validation test is performed. The acceptability, the structure of the questionnaire and the variability are evaluated, and changes are suggested. In the fourth phase, the module is completed, and validation tests are performed, aiming at a final review, regarding the number of questions and domains, and reaching a final version (33, 34).

There are several steps associated with the validation of a QOL questionnaire (38, 39). To validate a QOL questionnaire, in general, construct validity and reliability can be evaluated. Validity is the ability of a test to measure what it is proposed to measure. Factor analysis group questions organizing the domains. The internal consistency is assessed, which evaluates the degree of uniformity or coherence between the responses of the subjects to each of the domains that make up the instrument. In addition, the test-retest is performed, which evaluates the reliability at two different times, when no changes in the disease are observed. Construct validity evaluates the construction of the questionnaire through known, convergent or divergent (discriminant) groups and factor analysis. In the convergent validation of the scale, the correlations between the questionnaires and the conceptually related measures are evaluated, and they are expected to be substantially related to each other. For this purpose, domains of different QOL questionnaires are compared. This method allows the separation of the domains of the original questionnaire and tests whether the relationship of the original scale will be confirmed between other QOL and the variables observed in another language. Reliability evaluates whether the instrument is reliable and measures a construct over time between different individuals and situations. Confirmatory factor analysis is used to test the hypothetical scale structure and cross-cultural equivalence of the measurement properties.

A questionnaire is valid in the language in which it was created. To be used in another language, it must be translated, and the questions must have the same meaning in the translated language. There are different methods of translation and cultural adaptation (36, 37). Briefly, considering an example of translation into Portuguese/Brazil (36, 40), we have the following: translation from English to Portuguese/Brazil, by native Brazilians with English skills; synthesis of the translation by an expert committee; reverse translation into English; evaluating the versions by a committee of experts, comparing the versions and arriving at the initial version for the Portuguese language; pretest with 10 patients, aiming to evaluate understanding, eliminate embarrassing items, respond to semantic questions, adapt the questions, and test them with a small number of patients, reaching the final Portuguese/Brazil version (40).

Quality-of-life questionnaires associated with breast cancer

There are several QOL questionnaires related to cancer. In the literature, we found questionnaires used to evaluate cancer in general, questionnaires associated with specific situations (such as anxiety and depression), specific questionnaires for breast cancer and questionnaires developed to evaluate surgical results. In addition, there were questionnaires used for other pathologies, which can be used in breast cancer given the sequelae associated with treatment. In the context of cancer, there are reviews on the subject (29, 32), and the most used in breast cancer studies are those presented in Table 1. Of these, the EORTC QLQ-BR45 (41) (update of EORTC QLQ-BR23) is in Phase 4 of validation.

TABLE 1
www.frontiersin.org

Table 1 Main questionnaires associated with breast cancer treatment.

Quality-of-life questionnaires associated with breast surgery

Despite the existence of general questionnaires for breast cancer, questionnaires were created to evaluate the relationship between the type of surgery and QOL (32).

For patients undergoing BCS, we have the BCTOS (Breast Cancer Treatment Outcome Scale) (35, 40) and the Breast-Q module for BCS (42). The BCTOS, when formulated, used another methodology for the construction of questionnaires, and for a long time it was the only questionnaire associated with BCS. The 22-item survey subjectively evaluates the aesthetic and functional outcomes after breast cancer treatment through questions about functional status, cosmetic status, specific breast pain and oedema (43). In patients undergoing BCS combined with radiotherapy, BCTOS was effective (44). It was observed, through the BCTOS, that the specific breast pain related to the treatment exceeds the importance of the cosmetic result in relation to QOL. Nevertheless, the appearance of the breast after conservation surgery is significantly associated with psychosocial outcomes, and women with large breast asymmetry are more likely to have a worse psychosocial state than those with minimal asymmetry (43). Regarding the Breast-Q, the initial questionnaire for plastic surgery was used, and recently a version of the BCS was created (42).

For patients who have undergone mastectomy and breast reconstruction, historically, the MBROS (32), followed by the Breast-Q reconstruction module (45) and EORTC QLQ BRECON23 (46) have been used. Using MBROS, delayed reconstruction increases emotional well-being and body image. Immediate and delayed breast reconstruction provide substantial psychosocial benefits for mastectomy patients, but the type of reconstruction did not impact in QOL (47). BRECON23 was published in 2018 and uses new methodology for QOL development. It is divided in scales are related to surgical side-effects, sexuality, satisfaction (breast cosmesis, nipple cosmesis, surgery), donor-site symptoms and single items (46). The number of publications using MBROS and BRECON are low.

New methodologies and validation studies were used for Breast-Q and BRECON questionnaires (31). The Breast-Q, initially developed for the evaluation of plastic and reconstructive breast surgery (48), is divided into six domains: satisfaction with the breasts, overall outcome, care processes, psychosocial, physical and sexual. In the first version, questionnaires related to augmentation mammoplasty, reduction mammoplasty and reconstruction were created (48). Currently, the Breast-Q is in its the second edition and is the most popular questionnaire for breast reconstruction (49, 50). Regarding the Breast-Q, the main domains related to cancer modules are summarized in Table 2.

TABLE 2
www.frontiersin.org

Table 2 Summary of domains and number of questions in BREAST-Q version 2.0 for breast cancer.

Quality of life and oncoplastic surgery

To evaluate QOL in OS setting, we performed a literature review in PubMed database. We choose the terms: Breast Neoplasms [Mesh] and (“Surgery, Plastic”[Mesh] or “oncoplastic surgery” or “oncoplasty” or “oncoplastic” or “Reconstructive Surgical Procedures”[Mesh] or “Mammaplasty”[Mesh] or “Mastectomy, Segmental”[Mesh]) and “Quality of Life”[Mesh]. The terms were evaluated (09/12/2022) without (n=926) or with filters (Meta-analysis, Review and Systematic Review; n=127). Based on title and resume, 25 articles were selected. In the absence of review articles, case-control studies or observational studies were evaluated.

OS has become a generic term. With regard to BCS, the concept goes beyond reduction mastoplasty techniques, with different techniques aimed at the readjustment of breast tissue to contralateral symmetrisation. Char et al (26) performed a systematic review of QL in level 2 volume displacement or volume replacement OS, including NSM, SSM with autologous or IBBR. The studies used Breast-Q or other validated PROMs. Of the 702 initial articles, 43 were included, representing 14,994 patients, and the main questionnaire used was the Breast-Q (n = 11,176). Using Breast-Q, 1,400 patients who underwent BCS and OS, 2,970 who had reconstruction with autologous flap and 6,806 who received implants were selected. Superior results were observed in the BCS in relation to mastectomy with implant, in autologous reconstruction in relation to the implant, in nipple preservation in relation to the absence of nipple preservation, and in the use of the prepectoral implant in relation to the retro-pectoral (26).

Many studies have compared specific surgical situations of OS and its relationship with QOL. We then sought, through systematic reviews, to choose more representative studies that evaluated OS in different surgical situations related to the treatment of breast cancer. In the absence of systematic reviews case-control studies or case series were selected for discussion.

Conservative breast treatment and oncoplastic surgery

The relationship between BCS and OS involves several criteria, ranging from indication (tumour, patient, safety), type of surgery (technique, oncological safety, laterality, symmetrisation, follow-up time), and cosmetic quality, influencing QOL (24). QOL, in turn, is influenced by conditions associated with treatment, reflected in the sequelae, return to usual activities, whether in relation to work, family or sexuality.

A systematic review that evaluated the topic compared BCS associated or not with OS. Of the 688 initial articles, 6 were selected, which included 832 patients with controversial results; OS was not associated with QOL improvement in 5 studies, and an association with improvement was observed in only one study (51). The nature of the studies, usually retrospective, the patient selection bias, the time since the performance of the primary procedure and the absence of systematic use of symmetrisation in all patients negatively influenced the results of patients undergoing OS-BCS (25, 52).

With regard to BCS associated with EO (16), there is only one study in the literature (53), which analysed 204 patients, only 33 of whom had undergone EO. The results were superior when performing EO in the face of psychological well-being and satisfaction with the breast, outcome and nipple-areola complex (53).

Mastectomy and oncoplastic mastectomy

The history of breast reconstruction begins with late reconstructions using myocutaneous flaps (autologous) and changed over time to immediate reconstructions in which the flaps were replaced by breast prostheses. We proceeded to skin-preserving mastectomies, followed by nipple-preserving mastectomies and then prophylactic mastectomies. All of these surgeries have pros and cons. Over time, asymmetries and adverse effects became more pronounced, especially in the presence of radiotherapy. Recently, to refine the results, we resorted to fat grafting.

Breast loss, without shape replacement, implies a decrease in QOL. Meta-analysis evaluated the QOL of patients undergoing mastectomy without reconstruction compared to patients undergoing BCS (54). Initially, 892 articles were evaluated, and 6 including a total of 1,931 patients were selected. It was found that patients undergoing BCS have better body image and future prospects, with a decrease in the effects associated with local effects.

BCS or reconstruction is always better than mastectomy without reconstruction. The role of the presence of breast reconstruction in relation to mastectomy was evaluated. A review of 277 studies, 9 were identified and 1.734 analysed, observing that the absence of reconstruction was associate with increased risk of depression (55). A study conducted with 400 patients using Breast-Q evaluated four groups (control, BCS, mastectomy with and without reconstruction), observing better satisfaction with breast appearance and sexual wellbeing in patients undergoing reconstructive mastectomy, followed by BCS and mastectomy without reconstruction. When evaluating the BCS in relation to the control group, the results were similar in relation to breast satisfaction, but the sexual wellbeing was superior in the control group (56). Another study evaluated 618 patients divided into BCS, mastectomy, and mastectomy with reconstruction groups using the EORTC QLQ-C30 and QLQ-BR23 questionnaires. Similar results were observed for role functioning and social functioning in patients undergoing BCS and mastectomy with reconstruction. However, when evaluating body image, the results were higher in patients undergoing BCS, followed by patients undergoing mastectomy with reconstruction compared to patients undergoing mastectomy without reconstruction (57). A meta-analysis comparing BCS versus mastectomy evaluated 9 studies identify 2.301 patient, observing better QV associated to BCS in relation to body image, emotional function and social function (58).

A systematic review and meta-analysis evaluated the impact of breast reconstruction in relation to BCS. From 12,192 initial articles, there were 16 articles, with the analysis of 5,544 patients (1,458 mastectomies, 2,612 undergoing BCS and 1,474 undergoing mastectomy with reconstruction). The results showed great heterogeneity among the studies, with similar results in relation to BCS and mastectomy with reconstruction. In turn, the patients who underwent mastectomy without reconstruction exhibited poorer physical health and body image (27).

The role of the presence of breast reconstruction in relation to mastectomy was evaluated. From 277 studies, 9 were identified and 1.734 analysed, observing that the absence of reconstruction was associate with increased risk of depression (55).

Platt et al (59), performed a review of different conditions related to mastectomy with breast reconstruction and QV, reporting: (1) Immediate and delayed breast reconstruction increases satisfaction and quality of life; (2) Autologous reconstruction demonstrates superior PROMs over long-term when compared with implant-based breast reconstruction (IBBR); (3) NSM was associated with increased satisfaction than SSM.

Saldanha et al (28) performed a systematic review of breast reconstruction after mastectomy, selecting 83 nonrandomized studies, 8 randomized controlled trials and 69 single group studies. They observed that: (1) autologous reconstruction were associated with clinically better patient satisfaction with breast and sexual well-being than IBBR; (2) There is insufficient evidence about IBBR versus radiotherapy and QV; (3) Silicone and saline implants result in clinically similar patient satisfaction; (3) The evidence related to acellular dermal matrix (ADM) and QV is insufficient; (4) The type of Autologous reconstruction did not influence QV.

Also, in the comparison between the different breast reconstruction modalities (autologous tissue or implant), a meta-analysis performed on 219 initial studies yielded 9 studies suitable for analysis, encompassing 2,954 patients (2,129 with implants and 825 with autologous tissue). High overall satisfaction was observed among patients who had undergone breast reconstruction, and overall satisfaction and satisfaction with the breast was higher with the use of autologous tissue. On the other hand, psychosocial, psychic and sexual well-being was higher in patients with breast implants (60). Another meta-analysis evaluated the same item, selecting from 280 articles, 10 full-texts, including a total of 4,957 patients, of which 3,836 were evaluated using the Breast-Q questionnaire. It was found that satisfaction with the results, the breasts and sexual well-being was higher with the use of autologous tissue (61).

The use of prepectoral or subpectoral IBBR was evaluated. A meta-analysis evaluates 3.789 studies, 7 publications and 548 patients, observing that patients with prepectoral implants reported higher Breast-Q scores and lower postoperative pain (62), suggesting the use of acellular dermal matrix (ADM). Although, the use of acellular dermal matrix (ADM) do not improve the QOL (63), and one or two-stage IBBR with ADM, also do not chance QOL (64).

Nipple-areolar preservation improves QOL, although the number of studies and casuistry are limited, positive results were observed (59). Char et al (26) performed a systematic review of QL including NSM and SSM with autologous or IBBR, observing superior results related do NSM. A non-randomized, cross-sectional study used evaluated the impact of areolar preservation with Breast-Q questionnaire. It evaluated 137 patients (83 SSM x 53 NSM), observing that body image and sexual functioning associated to SSM (65). Wei et al, prospective evaluate patients submitted to NSM (n=52) and patients submitted do SSM and areolar reconstruction (202). NSM patients reported higher scores in psychosocial and sexual well-being (66). Two studies performed matched comparison, all using Breast-Q. The first (n = 62), matched by reconstruction type and operative period, compared NSM (n = 32) and SSM (n = 32), observing better satisfaction of results and the breasts in NSM (67). The second, with smaller number of patients (n = 52; 26x26), matched by age, race and body index, observed a significant improvement only in sexual well-being, associated with NSM (68).

Prophylactic mastectomy has risen in popularity, a fact associated with the dissemination of genetic tests, facilitating the selection of patients. It is observed that the patients are satisfied with the indication, but have complaints related to the prosthesis (69, 70). The first systematic review found 1,082 studies and selected 22 studies with a total of 2,046 patients. Satisfaction with the indication, high psychosocial well-being and body image were observed, with social well-being and somatosensory function being the most affected items (69). The second review, based on 7,272 articles, selected 7 articles that included 730 women and used different questionnaires. Overall satisfaction and cosmetic results were high, but surgery was associated with complaints related to breast hardness, numbness and sex, suggesting the importance of informing patients about the complications associated with the procedure (70).

Contralateral prophylactic mastectomy for unilateral breast cancer was evaluated in a systematic review of 19 articles, representing 6.088 patients. High levels of satisfaction were observed with the decision for surgery, with high satisfaction with cosmesis and reconstruction (71).

Evaluating robotic mastectomy, one study (n=80), using Breast Q, evaluated the impact in QOL, observing that Breast-Q scores in satisfaction with breasts, psychosocial, physical and sexual well-being were significantly higher after robotic mastectomy in relation to conventional mastectomy (72).

To improve the cosmetic results, we have fat grafting. A systematic review evaluating the technique found 2,915 articles and selected 6 that reported on Breast-Q, representing 1,437 patients. Although fat grafting improves breast satisfaction, the difference was not significant (73).

Discussion

When evaluating studies that selected patients for OS, it is necessary to consider that most of them are retrospective, and even in prospective patients, there may be a selection bias. Commonly, patients subjected to OS have a large tumour size, are younger, undergo neoadjuvant chemotherapy, have higher education, or are potentially more demanding, not accepting major defects or mastectomy without reconstruction, a fact that may influence the results (24, 74).

Breast symmetry, the timing of the procedure and the individual who evaluates outcomes are also considerations. OS is not always synonymous with the performance of symmetrisation, which improves the cosmetic effects, and time is an important risk factor for the appearance of asymmetries. In patients undergoing BCS, the irradiated breast undergoes little volume change, even with the increase in weight, which is contrary to the contralateral breast, which may present a volume increase and accentuation of ptosis, without alteration of the consistency (24). In patients undergoing mastectomy with prostheses, capsular contracture, the emergence of rippling, elevation of the breast furrow height and, when associated with increased weight, increased asymmetry in the contralateral breast are observed. Such outcomes may influence QOL and breast satisfaction. Regarding the cosmetic result, it is observed that in general, patients are less demanding than health professionals, with disagreement between them regarding the quality of the results, which makes it difficult to compare cosmetic results and QOL (75).

For a long time, the number of QOL questionnaires directed at breast cancer were few and evaluated specific situations, and the breast shape and outcomes were poorly evaluated. For cosmetic breast evaluation we used the BCTOS (43) and MBROS (32). The Breast-Q initially used in plastic surgery has been improved, and new questionnaires specific to the different conditions associated with breast cancer have emerged, allowing better evaluation of the impact of OS in different situations (29, 48, 76). Recently, we started to have the Breast-Q associated with BCS (42), and all questionnaires associated with the Breast-Q are in their second edition (77). The EORTC questionnaires have also evolved in this direction, and the BRECON23 was recently created (46). Updated EORTC QLQ-BR45 (41) aspects associated with breast shape were included, allowing a better evaluation of this aspect as it relates to QOL, but these questionnaires are recent, and the number of publications is limited. The Breast-Q is a questionnaire that has the greatest number of associated publications (49).

Quality of life involves multiple aspects. In breast cancer, there are many sequelae resulted from the treatment (78), many of which are poorly contextualized, since evaluating objective measurements and QOL questionnaires (35). In this context, sequelae associated with shoulder mobility after reconstruction (79), alterations associated with the use of IBBR, or alterations associated with the use of myocutaneous flaps, mainly the rectus abdominis muscle, are observed. Although the degree of satisfaction is high associated with OS, the look under the functional part is little discussed, and me must take care evaluating sequelae and functional functioning. Also, the impact of rehabilitation (80) and exercise (81) in OS is under reported. Future reviews evaluating these conditions are necessary.

The limitation of this study was to group literature results and not evaluate the quality of the studies. Although this situation it was possible to report multiple conclusions. Many studies are needed to accumulate evidence, especially in different populations (39), as the systematic reviews note the presence of heterogeneity in the literature (27, 6062), a fact possibly associated with the patient selection criteria, techniques used, differences in time since OS, presence of symmetrization and nonuniformity in relation to the questionnaires. Despite these limitations, due to the aforementioned limitations, OS improves QOL. Based on articles presented, we can conclude the following from these studies: (1) Patients undergoing BCS or breast reconstruction have improved QOL compared to those undergoing mastectomy; (2) Patients undergoing BCS or OS have not yet shown improvement in QOL, a fact possibly influenced by patient selection bias; (3) Patients undergoing mastectomy with reconstruction demonstrate better QOL results when reconstruction is performed compared to BCS using autologous flaps and when preserving the nipple-areola complex; (4) Prepectoral implants improves QOL in relation to subpectoral IIBR; (5) ADM do not improves QOL; (6) Patients undergoing prophylactic mastectomy indicate high satisfaction, but patients should be informed about the potential complications associated with the procedure; (7) Satisfaction is high after fat grafting.

Oncoplasty has become a routine procedure. As the literature increases, more publication will occur and new meta-analysis will appear increasing the number of patients for evaluation. The impact of surgery (mastectomy versus mastectomy with fasciocutaneous or myocutaneos flaps for skin closure) in QOL for locally advanced breast cancer was never studied in case-control study, although we believe that this surgery improves QOL (82). Also, new techniques, new indications of EO and robotic surgery are becoming popular, making space for new studies related to QOL. While there is usually a selection bias in studies and the studies are heterogeneous, some results possibly will not change: the preservation of the breast or the nipple-areola complex and the use of autologous flaps are associated with better QOL results. OS already has a defined role in improving QOL.

Author contributions

RV and AB-J conceived the manuscript. RV, AB-J, IO-J wrote the manuscript. RV, IO-J supervised and edited the manuscript. RV and AB-J share the same authorship. All authors contributed to the article and approved the submitted version.

Funding

Fundação Pio XII, Hospital de Câncer de Barretos; Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Heil J, Dahlkamp J, Golatta M, Rom J, Domschke C, Rauch G, et al. Aesthetics in breast conserving therapy: do objectively measured results match patients' evaluations? Ann Surg Oncol (2011) 18(1):134–8. doi: 10.1245/s10434-010-1252-4

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Arndt V, Merx H, Stegmaier C, Ziegler H, Brenner H. Persistence of restrictions in quality of life from the first to the third year after diagnosis in women with breast cancer. J Clin Oncol Off J Am Soc Clin Oncol (2005) 23(22):4945–53. doi: 10.1200/JCO.2005.03.475

CrossRef Full Text | Google Scholar

3. Kaya B, Serel S. Breast reconstruction. Exp Oncol (2013) 35(4):280–6.

PubMed Abstract | Google Scholar

4. Fisher B, Anderson S, Bryant J, Margolese RG, Deutsch M, Fisher ER, et al. Twenty-year follow-up of a randomized trial comparing total mastectomy, lumpectomy, and lumpectomy plus irradiation for the treatment of invasive breast cancer. New Engl J Med (2002) 347(16):1233–41. doi: 10.1056/NEJMoa022152

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Veronesi U, Cascinelli N, Mariani L, Greco M, Saccozzi R, Luini A, et al. Twenty-year follow-up of a randomized study comparing breast-conserving surgery with radical mastectomy for early breast cancer. New Engl J Med (2002) 347(16):1227–32. doi: 10.1056/NEJMoa020989

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Clough KB, Cuminet J, Fitoussi A, Nos C, Mosseri V. Cosmetic sequelae after conservative treatment for breast cancer: classification and results of surgical correction. Ann Plast surgery. (1998) 41(5):471–81. doi: 10.1097/00000637-199811000-00004

CrossRef Full Text | Google Scholar

7. Bertozzi N, Pesce M, Santi PL, Raposio E. Oncoplastic breast surgery: comprehensive review. Eur Rev Med Pharmacol Sci (2017) 21(11):2572–85.

PubMed Abstract | Google Scholar

8. Scomacao I, AlHilli Z, Schwarz G. The role of oncoplastic surgery for breast cancer. Curr Treat Options Oncol (2020) 21(12):94. doi: 10.1007/s11864-020-00793-1

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Audretsch W, Andree C. Is mastectomy still justified – And if, in which patients?. Onkologie (2006) 29:243–5. doi: 10.1159/000093477

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Losken A, Hart AM, Chatterjee A. Updated evidence on the oncoplastic approach to breast conservation therapy. Plast Reconstr Surg (2017) 140(5S Advances in Breast Reconstruction):14S–22S. doi: 10.1097/PRS.0000000000003951

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kaur N, Petit JY, Rietjens M, Maffini F, Luini A, Gatti G, et al. Comparative study of surgical margins in oncoplastic surgery and quadrantectomy in breast cancer. Ann Surg Oncol (2005) 12(7):539–45. doi: 10.1245/ASO.2005.12.046

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Clough KB, Lewis JS, Couturaud B, Fitoussi A, Nos C, Falcou MC. Oncoplastic techniques allow extensive resections for breast-conserving therapy of breast carcinomas. Ann Surg (2003) 237(1):26–34. doi: 10.1097/00000658-200301000-00005

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Carrara GF, Scapulatempo-Neto C, Abrahao-Machado LF, Brentani MM, Nunes JS, Folgueira MA, et al. Breast-conserving surgery in locally advanced breast cancer submitted to neoadjuvant chemotherapy. safety and effectiveness based on ipsilateral breast tumor recurrence and long-term follow-up]. Clinics (Sao Paulo). (2017) 72(3):134–42. doi: 10.6061/clinics/2017(03)02

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Vieira RA, Carrara GF, Scapulatempo Neto C, Morini MA, Brentani MM, Folgueira MA. The role of oncoplastic breast conserving treatment for locally advanced breast tumors. a matching case-control study. Ann Med Surg (Lond). (2016) 10:61–8. doi: 10.1016/j.amsu.2016.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Zucca Matthes AG, Uemura G, Kerr L, Matthes AC, Michelli RA, Folgueira MA, et al. Feasibility of oncoplastic techniques in the surgical management of locally advanced breast cancer. Int J Surg (2012) 10(9):500–5. doi: 10.1016/j.ijsu.2012.07.009

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Silverstein MJ, Savalia N, Khan S, Ryan J. Extreme oncoplasty: breast conservation for patients who need mastectomy. Breast J (2015) 21(1):52–9. doi: 10.1111/tbj.12356

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Foster RD, Esserman LJ, Anthony JP, Hwang ES, Do H. Skin-sparing mastectomy and immediate breast reconstruction: A prospective cohort study for the treatment of advanced stages of breast carcinoma. Ann Surg Oncol (2002) 9(5):462–6. doi: 10.1007/BF02557269

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Patani N, Mokbel K. Oncological and aesthetic considerations of skin-sparing mastectomy. Breast Cancer Res Treat (2008) 111(3):391–403. doi: 10.1007/s10549-007-9801-7

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Gieni M, Avram R, Dickson L, Farrokhyar F, Lovrics P, Faidi S, et al. Local breast cancer recurrence after mastectomy and immediate breast reconstruction for invasive cancer: a meta-analysis. Breast (2012) 21(3):230–6. doi: 10.1016/j.breast.2011.12.013

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Yang X, Zhu C, Gu Y. The prognosis of breast cancer patients after mastectomy and immediate breast reconstruction: a meta-analysis. PloS One (2015) 10(5):e0125655. doi: 10.1371/journal.pone.0125655

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Mota BS, Riera R, Ricci MD, Barrett J, de Castria TB, Atallah AN, et al. Nipple- and areola-sparing mastectomy for the treatment of breast cancer. Cochrane Database Syst Rev (2016) 11:CD008932. doi: 10.1002/14651858.CD008932.pub3

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Lanitis S, Tekkis PP, Sgourakis G, Dimopoulos N, Al Mufti R, Hadjiminas DJ. Comparison of skin-sparing mastectomy versus non-skin-sparing mastectomy for breast cancer: a meta-analysis of observational studies. Ann Surg (2010) 251(4):632–9. doi: 10.1097/SLA.0b013e3181d35bf8

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Galimberti V, Vicini E, Corso G, Morigi C, Fontana S, Sacchini V, et al. Nipple-sparing and skin-sparing mastectomy: Review of aims, oncological safety and contraindications. Breast (2017) 34 Suppl 1:S82–S4. doi: 10.1016/j.breast.2017.06.034

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Oliveira-Junior I, Silva IA, Silva FCB, Silva JJ, Sarri AJ, Paiva CE, et al. Oncoplastic surgery in breast-conserving treatment: Patient profile and impact on quality of life. Breast Care (Basel) (2020) 15):1–11. doi: 10.1159/000507240

CrossRef Full Text | Google Scholar

25. Oliveira-Junior I, Haikel RL, Vieira RAC. Breast-conserving treatment in oncoplastic times: indications, cosmesis, and quality of life. Mastology (2021) 31:e20200040. doi: 10.29289/2594539420200040

CrossRef Full Text | Google Scholar

26. Char S, Bloom JA, Erlichman Z, Jonczyk MM, Chatterjee A. A comprehensive literature review of patient-reported outcome measures (PROMs) among common breast reconstruction options: What types of breast reconstruction score well? Breast J (2021) 27(4):322–9. doi: 10.1111/tbj.14186

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Zehra S, Doyle F, Barry M, Walsh S, Kell MR. Health-related quality of life following breast reconstruction compared to total mastectomy and breast-conserving surgery among breast cancer survivors: a systematic review and meta-analysis. Breast Cancer. (2020) 27(4):534–66. doi: 10.1007/s12282-020-01076-1

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Saldanha IJ, Cao W, Broyles JM, Adam GP, Bhuma MR, Mehta S, et al. Breast reconstruction after mastectomy: A systematic review and meta-analysis. AHRQ Comp Effectiveness Rev (2021). doi: 10.23970/AHRQEPCCER245

CrossRef Full Text | Google Scholar

29. Pusic AL, Chen CM, Cano S, Klassen A, McCarthy C, Collins ED, et al. Measuring quality of life in cosmetic and reconstructive breast surgery: a systematic review of patient-reported outcomes instruments. Plast Reconstr Surg (2007) 120(4):823–37. doi: 10.1097/01.prs.0000278162.82906.81

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Oliveira IS, da Cunha Menezes Costa L, Fagundes FR, Cabral CM. Evaluation of cross-cultural adaptation and measurement properties of breast cancer-specific quality-of-life questionnaires: a systematic review. Qual Life Res (2015) 24(5):1179–95. doi: 10.1007/s11136-014-0840-3

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Davies CF, Macefield R, Avery K, Blazeby JM, Potter S. Patient-reported outcome measures for post-mastectomy breast reconstruction: A systematic review of development and measurement properties. Ann Surg Oncol (2021) 28(1):386–404. doi: 10.1245/s10434-020-08736-8

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Chen CM, Cano SJ, Klassen AF, King T, McCarthy C, Cordeiro PG, et al. Measuring quality of life in oncologic breast surgery: a systematic review of patient-reported outcome measures. Breast J (2010) 16(6):587–97. doi: 10.1111/j.1524-4741.2010.00983.x

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Wheelwright S, Bjordal K, Bottomley A, Gilbert A, Martinelli F, Pe M, et al. EORTC quality of life group guidelines for developing questionnaire modules Belgium: EORTC - European organization for research and treatment of cancer (2021). Available at: https://www.eortc.org/app/uploads/sites/2/2022/07/Module-Guidelines-Version-5-FINAL.pdf.

Google Scholar

34. Johnson C, Aeronson N, Blazeby JM, Bottomley A, Fayers P, Koller M, et al. EORTC quality of life group. guidelines for developing questionnaire modules. 4th ed. Brussels, Belgium: EORTC Quality of Life Group (2011).

Google Scholar

35. Brandini da Silva FC, Jose da Silva J, Sarri AJ, Paiva CE, Aloisio da Costa Vieira R. Comprehensive validation study of quality-of-Life questionnaire using objective clinical measures: Breast cancer treatment outcome scale (BCTOS), Brazilian Portuguese version. Clin Breast Cancer. (2019) 19(1):e85–e100. doi: 10.1016/j.clbc.2018.10.004

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Beaton DE, Bombardier C, Guillemin F, Ferlay MB. Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (2000) 25(24):3186–91. doi: 10.1097/00007632-200012150-00014

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Kulis D, Bottomley A, Velikova G, Greimel E, Koller M. EORTC quality of life group translation procedure Brussels: EORTC - European organization for research and treatment of cancer (2017). Available at: https://www.eortc.org/app/uploads/sites/2/2018/02/translation_manual_2017.pdf.

Google Scholar

38. Fayers PM, Machin D. Quality of life. 2nd ed. England: Wiley (2007). 544 p.

Google Scholar

39. Voineskos SH, Nelson JA, Klassen AF, Pusic AL. Measuring patient-reported outcomes: Key metrics in reconstructive surgery. Annu Rev Med (2018) 69:467–79. doi: 10.1146/annurev-med-060116-022831

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Vieira R, Silva F, Silva MES, Silva JJD, Sarri AJ, Paiva CE. Translation and cultural adaptation of the breast cancer treatment outcome scale (BCTOS) into Brazilian Portuguese. Rev Assoc Med Bras (1992). (2018) 64(7):627–34. doi: 10.1590/1806-9282.64.07.627

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Bjelic-Radisic V, Cardoso F, Cameron D, Brain E, Kuljanic K, da Costa RA, et al. An international update of the EORTC questionnaire for assessing quality of life in breast cancer patients: EORTC QLQ-BR45. Ann Oncol (2020) 31(2):283–8. doi: 10.1016/j.annonc.2019.10.027

PubMed Abstract | CrossRef Full Text | Google Scholar

42. O'Connell RL, DiMicco R, Khabra K, O'Flynn EA, deSouza N, Roche N, et al. Initial experience of the BREAST-q breast-conserving therapy module. Breast Cancer Res Treat (2016) 160(1):79–89. doi: 10.1007/s10549-016-3966-x

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Stanton AL, Krishnan L, Collins CA. Form or function? part 1. subjective cosmetic and functional correlates of quality of life in women treated with breast-conserving surgical procedures and radiotherapy. Cancer (2001) 91(12):2273–81.

PubMed Abstract | Google Scholar

44. Krishnan L, Stanton AL, Collins CA, Liston VE, Jewell WR. Form or function? part 2. objective cosmetic and functional correlates of quality of life in women treated with breast-conserving surgical procedures and radiotherapy. Cancer (2001) 91(12):2282–7.

PubMed Abstract | Google Scholar

45. Cordanto-Nopoulos FR, Sbalchiero JC, Silva CHD, Caiado-Neto BR, Derchain S. Tradução do questionário BREAST-q para a língua portuguesa e sua aplicação em mulheres com câncer de mama. Rev Bras Cir Plast (2013) 28(S1):79.

Google Scholar

46. Winters ZE, Afzal M, Rutherford C, Holzner B, Rumpold G, da Costa Vieira RA, et al. International validation of the European organisation for research and treatment of cancer QLQ-BRECON23 quality-of-life questionnaire for women undergoing breast reconstruction. Br J Surg (2018) 105(3):209–22. doi: 10.1002/bjs.10656

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Wilkins EG, Cederna PS, Lowery JC, Davis JA, Kim HM, Roth RS, et al. Prospective analysis of psychosocial outcomes in breast reconstruction: One-year postoperative results from the Michigan breast reconstruction outcome study. Plast Reconstr Surg (2000) 106(5):1014–25. doi: 10.1097/00006534-200010000-00010

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Pusic AL, Klassen AF, Scott AM, Klok JA, Cordeiro PG, Cano SJ. Development of a new patient-reported outcome measure for breast surgery: the BREAST-q. Plast Reconstr Surg (2009) 124(2):345–53. doi: 10.1097/PRS.0b013e3181aee807

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Cohen WA, Mundy LR, Ballard TN, Klassen A, Cano SJ, Browne J, et al. The BREAST-q in surgical research: A review of the literature 2009-2015. J Plast Reconstr Aesthet Surg (2016) 69(2):149–62. doi: 10.1016/j.bjps.2015.11.013

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Seth I, Seth N, Bulloch G, Rozen WM, Hunter-Smith DJ. Systematic review of breast-q: A tool to evaluate post-mastectomy breast reconstruction. Breast Cancer (Dove Med Press). (2021) 13:711–24. doi: 10.2147/BCTT.S256393

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Aristokleous I, Saddiq M. Quality of life after oncoplastic breast-conserving surgery: a systematic review. ANZ J Surg (2019) 89(6):639–46. doi: 10.1111/ans.15097

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Ojala K, Meretoja TJ, Leidenius MH. Aesthetic and functional outcome after breast conserving surgery - comparison between conventional and oncoplastic resection. Eur J Surg Oncol (2017) 43(4):658–64. doi: 10.1016/j.ejso.2016.11.019

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Acea Nebril B, Garcia Novoa A, Polidorio N, Cereijo Garea C, Bouzon Alejandro A, Mosquera Oses J. Extreme oncoplasty: The last opportunity for breast conservation-analysis of its impact on survival and quality of life. Breast J (2019) 25(3):535–6. doi: 10.1111/tbj.13267

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Ng ET, Ang RZ, Tran BX, Ho CS, Zhang Z, Tan W, et al. Comparing quality of life in breast cancer patients who underwent mastectomy versus breast-conserving surgery: A meta-analysis. Int J Environ Res Public Health (2019) 16(24). doi: 10.3390/ijerph16244970

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Padmalatha S, Tsai YT, Ku HC, Wu YL, Yu T, Fang SY, et al. Higher risk of depression after total mastectomy versus breast reconstruction among adult women with breast cancer: A systematic review and metaregression. Clin Breast Cancer. (2021) 21(5):e526–e38. doi: 10.1016/j.clbc.2021.01.003

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Howes BH, Watson DI, Xu C, Fosh B, Canepa M, Dean NR. Quality of life following total mastectomy with and without reconstruction versus breast-conserving surgery for breast cancer: A case-controlled cohort study. J Plast Reconstr Aesthet Surg (2016) 69(9):1184–91. doi: 10.1016/j.bjps.2016.06.004

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Kim MK, Kim T, Moon HG, Jin US, Kim K, Kim J, et al. Effect of cosmetic outcome on quality of life after breast cancer surgery. Eur J Surg Oncol (2015) 41(3):426–32. doi: 10.1016/j.ejso.2014.12.002

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Li Y, Guo J, Sui Y, Chen B, Li D, Jiang J. Quality of life in patients with breast cancer following breast conservation surgery: A systematic review and meta-analysis. J Healthc Eng. (2022) 2022:3877984. doi: 10.1155/2022/3877984

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Platt J, Zhong T. Patient-centered breast reconstruction based on health-related quality-of-Life evidence. Clin Plast Surg (2018) 45(1):137–43. doi: 10.1016/j.cps.2017.08.011

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Toyserkani NM, Jorgensen MG, Tabatabaeifar S, Damsgaard T, Sorensen JA. Autologous versus implant-based breast reconstruction: A systematic review and meta-analysis of breast-q patient-reported outcomes. J Plast Reconstr Aesthet Surg (2020) 73(2):278–85. doi: 10.1016/j.bjps.2019.09.040

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Eltahir Y, Krabbe-Timmerman IS, Sadok N, Werker PMN, de Bock GH. Outcome of quality of life for women undergoing autologous versus alloplastic breast reconstruction following mastectomy: A systematic review and meta-analysis. Plast Reconstr Surg (2020) 145(5):1109–23. doi: 10.1097/PRS.0000000000006720

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Ching AH, Lim K, Sze PW, Ooi A. Quality of life, pain of prepectoral and subpectoral implant-based breast reconstruction with a discussion on cost: A systematic review and meta-analysis. J Plast Reconstr Aesthet Surg (2022) 75(8):2550–60. doi: 10.1016/j.bjps.2022.02.019

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Lohmander F, Lagergren J, Johansson H, Roy PG, Brandberg Y, Frisell J. Effect of immediate implant-based breast reconstruction after mastectomy with and without acellular dermal matrix among women with breast cancer: A randomized clinical trial. JAMA Netw Open (2021) 4(10):e2127806. doi: 10.1001/jamanetworkopen.2021.27806

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Negenborn VL, Young-Afat DA, Dikmans REG, Smit JM, Winters HAH, Don Griot JPW, et al. Quality of life and patient satisfaction after one-stage implant-based breast reconstruction with an acellular dermal matrix versus two-stage breast reconstruction (BRIOS): primary outcome of a randomised, controlled trial. Lancet Oncol (2018) 19(9):1205–14. doi: 10.1016/S1470-2045(18)30378-4

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Metcalfe KA, Cil TD, Semple JL, Li LD, Bagher S, Zhong T, et al. Long-term psychosocial functioning in women with bilateral prophylactic mastectomy: Does preservation of the nipple-areolar complex make a difference? Ann Surg Oncol (2015) 22(10):3324–30. doi: 10.1245/s10434-015-4761-3

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Wei CH, Scott AM, Price AN, Miller HC, Klassen AF, Jhanwar SM, et al. Psychosocial and sexual well-being following nipple-sparing mastectomy and reconstruction. Breast J (2016) 22(1):10–7. doi: 10.1111/tbj.12542

PubMed Abstract | CrossRef Full Text | Google Scholar

67. Bailey CR, Ogbuagu O, Baltodano PA, Simjee UF, Manahan MA, Cooney DS, et al. Quality-of-Life outcomes improve with nipple-sparing mastectomy and breast reconstruction. Plast Reconstr Surg (2017) 140(2):219–26. doi: 10.1097/PRS.0000000000003505

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Yoon-Flannery K, DeStefano LM, de la Cruz LM, Fisher CS, Lin LY, Coffua LS, et al. Quality of life and sexual well-being after nipple sparing mastectomy: A matched comparison of patients using the breast q. J Surg Oncol (2018) 118(1):238–42. doi: 10.1002/jso.25107

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Razdan SN, Patel V, Jewell S, McCarthy CM. Quality of life among patients after bilateral prophylactic mastectomy: a systematic review of patient-reported outcomes. Qual Life Res (2016) 25(6):1409–21. doi: 10.1007/s11136-015-1181-6

PubMed Abstract | CrossRef Full Text | Google Scholar

70. Aygin D, Cengiz H. Life quality of patients who underwent breast reconstruction after prophylactic mastectomy: systematic review. Breast Cancer. (2018) 25(5):497–505. doi: 10.1007/s12282-018-0862-8

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Srethbhakdi A, Brennan ME, Hamid G, Flitcroft K. Contralateral prophylactic mastectomy for unilateral breast cancer in women at average risk: Systematic review of patient reported outcomes. Psychooncology (2020) 29(6):960–73. doi: 10.1002/pon.5379

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Toesca A, Sangalli C, Maisonneuve P, Massari G, Girardi A, Baker JL, et al. A randomized trial of robotic mastectomy versus open surgery in women with breast cancer or BrCA mutation. Ann Surg (2022) 276(1):11–9. doi: 10.1097/SLA.0000000000004969

PubMed Abstract | CrossRef Full Text | Google Scholar

73. Schop SJ, Joosen MEM, Wolswijk T, Heuts EM, van der Hulst R, Piatkowski de Grzymala AA. Quality of life after autologous fat transfer additional to prosthetic breast reconstruction in women after breast surgery: A systematic review. Eur J Surg Oncol (2021) 47(4):772–7. doi: 10.1016/j.ejso.2020.10.021

PubMed Abstract | CrossRef Full Text | Google Scholar

74. Almeida NR, Brenelli FP, Dos Santos CC, Torresan RZ, Shinzato JY, Cardoso-Filho C, et al. Comparative study of surgical and oncological outcomes in oncoplastic versus non oncoplastic breast-conserving surgery for breast cancer treatment. JPRAS Open (2021) 29:184–94. doi: 10.1016/j.jpra.2021.05.010

PubMed Abstract | CrossRef Full Text | Google Scholar

75. de Oliveira-Junior I, Brandini da Silva FC, Nazima F, Ribeiro JC Jr., Castellani L, Zucca-Matthes G, et al. Oncoplastic surgery: Does patient and medical specialty influences the evaluation of cosmetic results? Clin Breast Cancer (2021) 21(3):247–55.e3. doi: 10.1016/j.clbc.2020.09.012

PubMed Abstract | CrossRef Full Text | Google Scholar

76. Oliveira IGE. Breast-q - breast reconstruciton expectations module (Pre operative). In: Tradução e adaptação cultural para o brasil. São Paulo: Unidade Federal de São Paulo (2018).

Google Scholar

77. Pusic AL, Klassen A, Cano S. Qportfolio - setting the bar in patient reported outcome measurement (2022). Available at: https://qportfolio.org/breast-q/breast-cancer/.

Google Scholar

78. Vieira RAC, Silva FCB, Biller G, Silva JJ, Paiva CE, Sarri AJ. Instruments of quantitative and qualitative evaluation of breast cancer treatment sequels. Rev Bras Mastol. (2016) 26(3):126–32. doi: 10.5327/Z201600030008RBM

CrossRef Full Text | Google Scholar

79. Vidt ME, Potochny J, Dodge D, Green M, Sturgeon K, Kass R, et al. The influence of mastectomy and reconstruction on residual upper limb function in breast cancer survivors. Breast Cancer Res Treat (2020) 182(3):531–41. doi: 10.1007/s10549-020-05717-z

PubMed Abstract | CrossRef Full Text | Google Scholar

80. Invernizzi M, de Sire A, Lippi L, Venetis K, Sajjadi E, Gimigliano F, et al. Impact of rehabilitation on breast cancer related fatigue: A pilot study. Front Oncol (2020) 10:556718. doi: 10.3389/fonc.2020.556718

PubMed Abstract | CrossRef Full Text | Google Scholar

81. Abbasi F, Pourjalali H, do Nascimento IJB, Zargarzadeh N, Mousavi SM, Eslami R, et al. The effects of exercise training on inflammatory biomarkers in patients with breast cancer: A systematic review and meta-analysis. Cytokine (2022) 149:155712. doi: 10.1016/j.cyto.2021.155712

PubMed Abstract | CrossRef Full Text | Google Scholar

82. Rini IS, Krisna MA, Kamayana J, Djarot KR, Gunardi AJ. Keystone perforator island flap for postmastectomy defect resurfacing in late-stage breast cancer patients. Plast Reconstr Surg Glob Open (2019) 7(11):e2457. doi: 10.1097/GOX.0000000000002457

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: quality of life, systematic review, meta-analysis (MA), breast cancer, oncoplastic surgery, patient-reported outcome measures

Citation: Vieira RAdC, Bailão-Junior A and de Oliveira-Junior I (2023) Does breast oncoplastic surgery improve quality of life? Front. Oncol. 12:1099125. doi: 10.3389/fonc.2022.1099125

Received: 15 November 2022; Accepted: 28 December 2022;
Published: 12 January 2023.

Edited by:

Marco Invernizzi, University of Eastern Piedmont, Italy

Reviewed by:

Arianna Folli, Università degli Studi del Piemonte Orientale, Italy
Vincenzo Vindigni, University of Padua, Italy

Copyright © 2023 Vieira, Bailão-Junior and de Oliveira-Junior. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: René Aloisio da Costa Vieira, cmVuZWFjdkBnbWFpbC5jb20=

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.