Skip to main content

SYSTEMATIC REVIEW article

Front. Oncol., 29 September 2022
Sec. Cancer Epidemiology and Prevention

The worldwide impact of COVID-19 on cancer care: A meta-analysis of surveys published after the first wave of the pandemic

  • 1Platform of Integrated Biology Unit, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy
  • 2School of Medicine: Interdisciplinary of Medicine, Aldo Moro University of Bari, Bari, Italy
  • 3Scientific Directorate, Fondazione IRCCS Istituto Nazionale Tumori, Milan, Italy
  • 4Medical Oncology Unit, Department of Human Pathology “G. Barresi”, University of Messina, Messina, Italy

Background: The rapid and global spread of COVID-19 posed a massive challenge to healthcare systems, which came across the need to provide high-intensity assistance to thousands of patients suffering from SARS-CoV-2 infection while assuring continuous care for all other diseases. This has been of particular importance in the oncology field. This study explores how oncology centers responded to the pandemic at a single center level by assessing surveys addressing different aspects of cancer care after the pandemic outbreak.

Methods: We performed a systematic review and meta-analysis of the cancer care surveys published until December 11th, 2020. Data were analyzed according to three main areas of interest, namely health care organization, including cancellation/delay and/or modification of scheduled treatments, cancellation/delay of outpatient visits, and reduction of overall cancer care activities; routine use of preventive measures, such as personal protective equipment (PPE) by both patients and health care workers, and systematic SARS-CoV-2 screening by nasopharyngeal swabs; and implementation of telemedicine through remote consultations.

Findings: Fifty surveys reporting data on 9150 providers from 121 countries on 5 continents were included. Cancellation/delay of treatment occurred in 58% of centers; delay of outpatient visits in 75%; changes in treatment plans in 65%; and a general reduction in clinical activity in 58%. Routine use of PPE by patients and healthcare personnel was reported by 81% and 80% of centers, respectively; systematic SARS-CoV-2 screening by nasopharyngeal swabs was reported by only 41% of centers. Virtual visits were implemented by the majority (72%) of centers.

Interpretation: These results describe the negative impact of COVID-19 on cancer care, the rapid response of cancer centers in terms of preventive measures and alternative treatment approaches such as telemedicine, and confirm that surveys can provide the valuable, low-cost and immediate information that critical situations require.

Introduction

COVID-19 has posed unprecedented challenges to both individuals and society (1, 2). Responding to the pandemic requires decisions based on accurate real-time information. In order to understand and anticipate the demand on health care services, there is the urgent need to know not only the spread of the virus but especially the response to its spread (3, 4). Once in a lifetime, the need to rapidly collect and evaluate data has never been more apparent, allowing decision-makers the ability to move quickly and effectively in a crisis. Real-time data can be managed with the survey tools cheaply (5). In health epidemiology, the most prevalent sort of survey is represented by online survey. Even sophisticated surveys can be cost-effective because of the availability of specialized and easy-to-use software for survey development and distribution (6). The absence of involved interviewer(s) increases the availability of respondent sharing. There is no universally agreement upon minimum response for surveys, and response rates for online surveys range from 20% to 30% (7).

Surveys have recently become quite popular, especially among oncologists, to gather data on behavioral, policy, and healthcare system responses to the pandemic. Individual or aggregate information, mostly focused on patient management and protection of health workers, was collected with the ultimate goal of descriptive analyses (8, 9). Given the possible volume and timeliness of the data generated, it is worthwhile to explore how the survey design and conduct may have influenced their generalizability. For example, in terms of study design, sampling challenges may develop due to accessibility or the low involvement of less motivated groups (i.e., selection bias) [reviewed in Andrade (10)]. In addition, external factors such as geographic area may have influenced survey results even with the same study design and implementation. Herein, we report a systemic review and meta-analysis of primary data from surveys on COVID-19 and its impact on oncological practice, specifically health care organization, promotion of patients and health workers preventive measures, and implementation of telemedicine.

Methods

Search strategy, selection criteria, and data extraction

The current systematic review and meta-analysis was conducted according to the PRISMA guidelines. A literature search on PubMed, Scopus and Web Of Science was performed from databases inception to December 11, 2020. An example search string is provided in the Supplementary material. Titles and abstracts for potentially relevant articles were screened by two authors (V.R. and N.Su.). The conflict was resolved with a consensus between the two authors. All English-language articles reporting results of surveys on the SARS-CoV-2 pandemic impact on oncological clinical practice or on the use of countermeasures to limit this impact were considered relevant for inclusion. The articles were screened by Rayyan software. The following data were extracted for each study: first author name, month and year of publication, week of survey beginning and end, country of survey dissemination, the specialty of respondents, type of cancer, a center/operator categorization variable, number of recipients, and respondents, survey dissemination modality, number of questions, country income according to the World Bank Group and the mean Government Response Stringency Index (GRSI) developed by the Blavatnik School of Government at the University of Oxford during the study period. The outcomes of interest were expressed as proportions of respondents over recipients and included: cancellation/delay of treatments, modification of treatments, cancellation/delay of clinic visits, reduction of activity, routine personal protective equipment (PPE) use by patients and workers, use of remote consultations, and systematic execution of screening SARS-CoV-2 nasopharyngeal swab. These domains were chosen a priori to analyze the response of health care system to two different and complementary needs posed by the pandemic, specifically the continuity of cancer care and the containment of infection of both patients and health care workers. Only studies reporting the specialty of interest (oncology, or surgery, or radiotherapy) were included. The results were analyzed according to the volume and typology of the surveys reported and geographical area.

Data analysis

A random-effects meta-analysis was performed using the DerSimonian-Laird estimator for variance. The I2 (the proportion of the variance in observed effects reflecting variance in true effects rather than sampling error) and p-value (the probability value describing how likely it is that data would have occurred under the null hypothesis of statistical test) for the Q-test (based on a chi-square distribution to generate a probability, that, when large, indicates larger variation across studies rather than within subjects within a study) were chosen as measures of heterogeneity. Proportions were transformed with double-arcsine transformation to approximate a normal distribution and then back-transformed to facilitate data interpretation. Since a high level of heterogeneity was found for all outcomes of interest, a thorough moderator analysis was performed to account for this heterogeneity with subgroup analysis and meta-regression. The following covariates were used as moderator variables: specialty, geographical area of survey dissemination, week of study beginning, week of study end, study sample size, and the center/operator categorization variable. Regarding geographical area subgroup analysis and meta-regression, studies conducted worldwide were excluded because it was impossible to assign them to a specific geographical area. The survey by Balakrishnan et. al (11). was excluded from this analysis for the same reason.

Publication bias was assessed by visual inspection of funnel plots and by the test of Egger. A p-value ≤0.05 was considered statistically significant for all analyses.

A qualitative evaluation of the risk of bias of the studies was performed using the “Risk of bias instrument for cross-sectional surveys of attitudes and practices” from the CLARITY Group at McMaster University (12). All the analyses were performed using R software (R version 3.6.2, release date: 2019–12-12; R Foundation for Statistical Computing, Vienna, Austria).

Role of the funding source

There was no funding source.

Results

Literature search

The literature search initially provided 9660 results, which, after duplicates removal, yielded 6026 publications. These were screened through title and abstract reading, providing 216 papers for full-text analysis. 56 articles (11, 1367) were deemed eligible for the systematic review, and among these 50 reported quantitative data of at least one outcome of interest and were included in the meta-analysis (11, 1866) (Figure 1).

FIGURE 1
www.frontiersin.org

Figure 1 PRISMA flow-chart.

Studies characteristics

Table 1 shows the characteristics of the studies included in the systematic review. Answers from 1391 centers (1378 included in the quantitative synthesis) and 8386 operators (7772 included in the quantitative synthesis) from 121 countries were considered (Figure 2). Notably, the geographical distribution of the analyzed surveys roughly reflects that of COVID-19 spreading over the same study period. Italy was included in most surveys, twice as much as the second most commonly included country represented by Brazil. This parallels the spreading of COVID-19, as Italy was the most affected country during the first outbreak, followed by Brazil a few weeks later. China, where the pandemic originated, was not included among the top countries producing COVID-19 surveys. The lack of surveys from Africa may partly reflect a relative lack of dedicated oncology facilities and COVID-19 data collection compared to higher-income countries.

TABLE 1
www.frontiersin.org

Table 1 Characteristics of the studies included in the systematic review.

FIGURE 2
www.frontiersin.org

Figure 2 Worldwide distribution of the included studies.

The period of the included surveys ranged from the 11th to the 27th week of 2020, as there was no other eligible study according to the pre-specified selection criteria afterwards.

Twenty-four surveys (42.9%) were conducted in more than one country, 28 (50%) were national, 3 (5.4%) were regional, and 1 (1.8%) was conducted at the single-hospital level. A wide range of cancer types was represented: brain, head and neck, gynecological, breast, hepato-bilio-pancreatic, hematological, colorectal, skin, pediatric, urinary tract, esophagogastric, neuroendocrine, lung and soft tissues cancers. 54 surveys (96.4%) dealt with the clinical impact of COVID-19 on oncology practice, 38 surveys (67.9%) with the countermeasures taken to limit SARS-CoV-2 spreading, 9 surveys (16.1%) with the impact it had on the workers personal well-being, and 7 surveys (12.5%) with the impact on the oncological research. None of the surveys considered the role of the pandemic on the outcome of oncological treatments. Table 2 shows the summary of findings of the single studies included in the quantitative synthesis and Figure 3 shows the meta-analysis results stratified according to the specialty (either oncology, surgery or radiotherapy) of each center/operator.

TABLE 2
www.frontiersin.org

Table 2 Summary of the findings of the studies included in the meta-analysis. Rt, radiotherapy; sur, surgery; onc, oncology.

FIGURE 3
www.frontiersin.org

Figure 3 Forest plots of the meta-analysis results for the 8 outcomes. (A) Treatment delay/cancellation; (B) Reduction of activity; (C) Modification of treatment; (D) Delay of visits; (E) Routine use of PPE (patients); (F) Routine use of PPE (workers); (G) Use of remote consultations; (H) Routine screening SARS-CoV-2 swab.

Effect of COVID-19 and cancer treatment schedules

Taken together, 58% (confidence interval, c.i. 48%-67%, I2 98%, number of studies: 28 [11, 22, 2427, 3133, 36, 39, 41, 4650, 52, 55, 56, 66)] reported cancellation or delay of treatments. Apparently, the stratification according to specialty did not modify this result, nor did any other of the moderator variables. Meta-regression considering the geographical area in which the survey was conducted and the week of survey beginning (n=17) seemed to explain a small amount of heterogeneity (R2 15.9%, indicating the relative amount of heterogeneity explained by this variable, I2 95.7%, indicating the residual heterogeneity), with the test of moderators in the meta-regression not being statistically significant (p=0.43).

Overall, 75% [c.i. 49%-95%, I2 99%, number of studies: 10 (22, 25, 26, 32, 36, 40, 44, 45, 51, 52)] of studies reported delay of clinic visits. Stratification according to specialty seemed to show a lower proportion of visits delay in the surgery subgroup, but with only one study belonging to this subgroup. In the meta-regression analysis, the stratification of surgery vs oncology and radiotherapy yielded a tiny value of R2 (1.2%), with a p-value nearly reaching statistical significance (p=0.09). In contrast, the geographical area in which the study was conducted explains a higher amount of heterogeneity (n=9, R2 87.3%, I2 58%), with a p-value<0.0001 at the moderators’ test and a p-value for the Q-test for residual heterogeneity (which indicates whether the residual heterogeneity, or I2, is significantly different from 0) of 0.05 in the meta-regression. The analysis of geographical area with the study sample size explains all the heterogeneity, with no residual heterogeneity (n=9, R2 100%, I2 0%, p-value for the test of moderators <0.0001, p-value for the Q-test for heterogeneity=0.4).

Overall, 65% [c.i. 53%-75%, I2 98%, number of studies: 14 (2729, 3638, 4244)] of studies reported some modification of the treatment regimens or surgical interventions. The moderator variable which alone explained the most heterogeneity was the geographical area in which the study was conducted (n=9, R2 31%, I2 96.9%, p-value for the test of moderators in meta-regression=0.02). A model including geographical area and week of survey end accounted for a great part of heterogeneity (n=9, R2 85.2%, I2 87%, p-value for the test of moderators <0.0001, the p-value for the Q-test for residual heterogeneity <0.0001). Adding specialty to the model yielded an R2 of 100%, with no residual heterogeneity (n=9, the p-value for the test of moderators<0.0001, p-value for the Q statistic of residual heterogeneity=0.59).

Taken together, 58% [c.i. 47%-68%, I2 93%, number of studies: 14 (11, 1821, 25, 34, 35, 48, 51, 54, 57, 58, 60)] of the studies reported reduction in activity. None of the moderator variables taken alone seemed to explain the between-studies variance. A meta-regression model considering specialty and geographical area accounted for some of this heterogeneity (n=12, R2 40.5%, I2 88.3%, p-value for the test of moderators=0.2, Q-test for residual heterogeneity<0.0001). Adding the week of survey beginning to this model yielded similar results (n=10, R2 43.2%, I2 89.4%, p-value for the test of moderators=0.1, p-value for the Q-test for residual heterogeneity <0.0001).

Countermeasures to limit infection spread

Seven studies (18, 32, 34, 35, 40, 52, 53) reported information on the routine use of PPE by patients. No studies belonged to the surgery subgroup. Overall, routine PPE use by the patients was reported in 81% (c.i. 59%-96%, I2 96%, number of studies: 7) of centers/operators. The moderator analysis showed that the geographical area alone was able to explain a minimal part of the true heterogeneity observed, but with significant residual heterogeneity (n=6, R2 15.8%, I2 90.2%, p-value for the test of moderators=0.5, p-value for the Q-test of residual heterogeneity<0.0001). Adding the sample size to this meta-regression model resulted in a significant explanation of true heterogeneity (n=6, R2 77.4%, I2 60.6%, p-value for the test of moderators=0.003, p-value for the Q-test for residual heterogeneity=0.08). GRSI alone explained a great part of the observed heterogeneity (n=5, R2 74.2%, I2 79.6%, p-value for the test of moderators=0.03, p-value for the Q-test of residual heterogeneity=0.002). Adding sample size to GRSI in the model further improved heterogeneity explanation (n=5, R2 92.9%, I2 43.8%, p-value for the test of moderators<0.0001, p-value for the Q-test of residual heterogeneity=0.17).

PPE were routinely used by workers in 80% [c.i. 61%-94%, I2 99%, number of studies: 16 (18, 26, 31, 3335, 3739, 44, 52, 53, 59, 61, 63, 65)] of cases. No moderator was alone able to explain the true heterogeneity. A meta-regression model including geographical area, week of survey end and sample size accounted for a substantial part of this heterogeneity (n=10, R2 78.9%, I2 80.7%, p-value for test of moderators <0.0001, p-value for the Q-test for residual heterogeneity=0.006). Adding GRSI resulted in a better explanation of heterogeneity (n=8, R2 98.7%, I2 17.1%, p-value for test of moderators <0.0001, p-value for the Q-test for residual heterogeneity=0.27)

72% [c.i. 59%-84%, I2 99%, number of studies (18, 2126, 3335, 38, 40, 44, 45, 47, 51, 53, 55, 56, 5860, 62, 64, 65)] of the surveyed centers/operators reported use of remote consultations. None of the moderators accounted for a substantial part of this heterogeneity. A meta-regression model including geographical area, specialty, sample size and the center/operator categorization seemed to explain a part of the true heterogeneity, but without statistical significance (n=20, R2 29.7%, I2 92.3%, p-value for the test of moderators=0.39, p-value for the Q-test for residual heterogeneity<0.0001).

18 studies (11, 19, 28, 30, 31, 33, 37, 43, 45, 48, 53, 54, 56, 60, 61, 63) reported information on the systematic screening SARS-CoV-2 PCR on naso-pharingeal swab execution on patients. Systematic swab execution was reported in 41% (c.i. 30%-53%, I2 96%, number of studies: 18) of studies. None of the moderators was able alone to account for the true heterogeneity. A meta-regression model including specialty, sample size and center/operator categorization explained part of the heterogeneity (n=17, R2 24.6%, I2 95.6%, p-value for the test of moderators=0.13, p-value for the Q-test for residual heterogeneity <0.0001).

Publication bias

Publication bias was detected only for the modification of treatments outcome (Egger test p-value=0.03).

Discussion

This systematic review and meta-analysis attempt to sketch the worldwide response to the COVID-19 pandemic in the oncology field. We chose to investigate the first months of the pandemic because it appeared more fascinating to us to analyze the first moves of an unprepared globe. At the point when this meta-analysis was conducted, most studies did not specifically report the prevalence of COVID-19 among cancer patients. None of the included studies reported outcomes of COVID-19 patients based on their underlying oncological disease (68). In this context, our work offers several insights for the implementation of surveys in the oncology field. Firstly, it is possible to evaluate the qualitative and quantitative information of surveys in a rigorous manner; secondly, surveys can provide prompt information on what is happening in the real-world; finally, this information is certainly heterogeneous, although it can be generalized according to specific domains, as in our specific case to meet the needs of cancer patients, their protection from infection and those of their care providers.

Our findings are consistent with current literature data that COVID-19 constrained cancer care (6976). Overall, it seems that the effects of the pandemic on clinical practice were comparable across the three considered subspecialties, with more than half of centers reporting cancellation and delay in the delivery of treatments. More broadly, a decline in activity was seen particularly affecting medical treatment in lower-income geographical area (7779). These data are consistent with healthcare authorities policy to advise hospitals and healthcare facilities to delay medical care for non-acute or not life-threatening conditions and to postpone cancer screenings while tackling the pandemic. According to a report by the World Health Organization, healthcare services for non-communicable diseases have been severely disrupted since the COVID-19 pandemic began (80).

Indeed, an increasing body of institutional but also nationwide and international evidence points towards major detrimental effects of the COVID-19 pandemic on several areas of healthcare including the provision of cancer care.

On the other hand, we examined the countermeasures taken to limit the intra-hospital infection spread. The routine use of PPE among patients and workers has been consistent, with about 80% of centers/operators reporting implementing this practice. Early precautionary measures were taken heterogeneously depending on country income level, consistently to already reported analyses (81). The proportions of respondents having noted an establishment of a remote consultation plan parallel that of the respondents reporting a delay in visits to the clinic. Thus, we can argue that the delay in visits has created the need for an alternative system to in-person consultation, and telemedicine has been the first response in many centers (82, 83).

Conversely, major efforts have been made not to defer active treatments. Finally, execution of a routine screening nasopharyngeal swab for asymptomatic patients has not been a widespread practice. Many centers reported using procedures like phone or in-person triage for suggestive COVID-19 symptoms instead. We chose not to quantify this response because it was expected to be largely implemented worldwide.

There are several strengths in our meta-analysis. To the best of our knowledge, this is the most comprehensive description of how cancer centers react to a rapidly evolving setting, in which researchers and medical professionals are continuously learning and contributing to dynamic adjustments in government policy. In this meta-analysis, we conducted a systematic search of the literature using a pre-defined inclusion and exclusion criteria; including a large number of studies to allow assessment of publication bias and subgroup analysis, detailed extraction of data on study outcomes; and the use of various statistical methods to evaluate the validity of our findings. This approach is crucial to manage the infodemic and promote the timely dissemination of accurate information, based on science and evidence, to all communities, particularly high-risk groups (84, 85).

Our work suffers the major issue of high level of heterogeneity among studies. We attempted to mitigate this limitation by performing subgroup analysis based on the characteristics of each study. Most of the included studies were limited by their small sample size. In addition, we considered data from countries with very different health systems response capacities and the surveys looked at them at different periods. This includes a variation in the temporary COVID-19 prevalence and incidence, as well as a difference in pandemic preparedness. Despite this, it seems that high heterogeneity is an issue intrinsic to meta-analyses of proportions. A systematic review of meta-analyses of proportion reports that about three-quarters of included studies had an I2 value of at least 90% (86).

Notwithstanding this limitation, we think that this systematic review and meta-analysis gives a particular piece of information on how oncology systems responded to the pandemic at a single-center level. The evaluation of local government guidelines, in fact, may be poorly informative of their actual implementation and efficacy at the individual center level. In this point of view, this represents a real-life study on which has oncology centers’ situation was at the beginning of the pandemic. Surveys seem an excellent tool to perform such analyses because of their quickness and ease of delivery. However, they are so highly heterogeneous: the portrait of the real situation they give is not a masterpiece to hang up on the wall of a museum, but they are a well-done sketch that suffices to understand the picture. Recently, some concerns were raised about the qualitative research of survey questionnaires. In particular, possible limitations include small sample sizes, potential response bias, self-selection bias and potentially inappropriate respondent questions (87). However, qualitative research has the potential to capture individual reactions and feelings without constraints, which is important in extraordinary circumstances such as a health emergency. Furthermore, recent studies such as that of Sneiderman et al. show that comprehensive analyses using qualitative/mixed methods are feasible as well as informative during the pandemic (88).

In conclusion, this study revealed that COVID-19 had a negative impact on cancer care, with deleterious effects felt in all medical, surgical and radiotherapy areas, leading to a reduction in care activities in more than half of cancer centres worldwide. The impact has not been uniform, but has affected all countries regardless of income, reflecting the truly global nature of the pandemic consequences. The individual and rapid response of cancer centres that emerged from this meta-analysis would suggest that the oncology community has already pre-existing strengths in collaboration, advocacy, respect for multidisciplinary teams, and a strong sense of its mission. However, it is imperative that health organisations around the world put measures in place to support professionals, both during the evolution of the current pandemic and in planning for future catastrophic events.

Data availability statement

The original contributions presented in the study are included in the article/ Supplementary Material. Further inquiries can be directed to the corresponding author.

Author contributions

SDC, NSi, GA, and VR designed the study. VR and NSu did the literature search. NSu did the statistical analyses. All authors wrote the manuscript. All authors had full access to all the data in the study and had final responsibility for the decision to submit for publication. VR and NSu have accessed and verified the data. All authors contributed to the article and approved the submitted version.

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.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2022.961380/full#supplementary-material

References

1. Lal A, Lim C, Almeida G, Fitzgerald J. Minimizing COVID-19 disruption: Ensuring the supply of essential health products for health emergencies and routine health services. Lancet Reg Health Am (2022) 6:100129. doi: 10.1016/j.lana.2021.100129

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Lal A, Erondu NA, Heymann DL, Gitahi G, Yates R. Fragmented health systems in COVID-19: rectifying the misalignment between global health security and universal health coverage. Lancet (2021) 397(10268):61–7. doi: 10.1016/S0140-6736(20)32228-5

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Ratzan SC, Sommariva S, Rauh L. Enhancing global health communication during a crisis: lessons from the COVID-19 pandemic. Public Health Res Pract (2020) 30(2):3022010. doi: 10.17061/phrp3022010

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Sacco PL, Gallotti R, Pilati F, Castaldo N, De Domenico M. Emergence of knowledge communities and information centralization during the COVID-19 pandemic. Soc Sci Med (2021) 285:114215. doi: 10.1016/j.socscimed.2021.114215

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Houston JD, Fiore DC. Online medical surveys: using the Internet as a research tool. MD Comput (1998) 15(2):116–20.

PubMed Abstract | Google Scholar

6. Lane TS, Armin J, Gordon JS. Online recruitment methods for web-based and mobile health studies: A review of the literature. J Med Internet Res (2015) 17(7):e183. doi: 10.2196/jmir.4359

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Silvestris N, Moschetta A, Paradiso A, Delvino A. COVID-19 pandemic and the crisis of health systems: The experience of the apulia cancer network and of the comprehensive cancer center istituto tumori ‘Giovanni Paolo II’ of bari. Int J Environ Res Public Health (2020) 17(8):E2763. doi: 10.3390/ijerph17082763

PubMed Abstract | CrossRef Full Text | Google Scholar

9. van de Haar J, Hoes LR, Coles CE, Seamon K, Fröhling S, Jäger D, et al. Caring for patients with cancer in the COVID-19 era. Nat Med (2020) 26(5):665–71. doi: 10.1038/s41591-020-0874-8

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Andrade C. The limitations of online surveys. Indian J Psychol Med (2020) 42(6):575–6. doi: 10.1177/0253717620957496

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Balakrishnan A, Lesurtel M, Siriwardena AK, Heinrich S, Serrablo A, Besselink MGH, et al. Delivery of hepato-pancreato-biliary surgery during the COVID-19 pandemic: an European-African hepato-Pancreato-Biliary association (E-AHPBA) cross-sectional survey. HPB (Oxford) (2020) 22(8):1128–34. doi: 10.1016/j.hpb.2020.05.012

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Poggio F, Tagliamento M, Di Maio M, Martelli V, De Maria A, Barisione E, et al. Assessing the impact of the COVID-19 outbreak on the attitudes and practice of Italian oncologists toward breast cancer care and related research activities. JCO Oncol Practice (2020) 16(11):e1304–14. doi: 10.1200/OP.20.00297

CrossRef Full Text | Google Scholar

14. Folkard SS, Sturch P, Mahesan T, Garnett S. Effect of coronavirus disease 2019 on urological surgery services and training up to the peak of the pandemic in south East England. J Clin Urol (2021) 14(1):47–54. doi: 10.1177/2051415820970396

CrossRef Full Text | Google Scholar

15. Subbian A, Kaur S, Patel V, Rajanbabu A. COVID-19 and its impact on gynaecologic oncology practice in India-results of a nationwide survey. Ecancermedicalscience (2020) 14:1067. doi: 10.3332/ecancer.2020.1067

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Bhandoria G, Shylasree TS, Bhandarkar P, Ahuja V, Maheshwari A, Sekhon R, et al. Impact of COVID-19 pandemic on gynecological oncology care: Glimpse into association of gynecological oncologists of India (AGOI) perspective. Indian J Gynecol Oncol (2020) 18(3):71. doi: 10.1007/s40944-020-00421-8

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Koffman B, Mato A, Byrd JC, Danilov A, Hedrick B, Ujjani C, et al. Management of CLL patients early in the COVID-19 pandemic: An international survey of CLL experts. Am J Hematol (2020) 95(8):E199–203. doi: 10.1002/ajh.25851

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Achard V, Aebersold DM, Allal AS, Andratschke N, Baumert BG, Beer KT, et al. A national survey on radiation oncology patterns of practice in Switzerland during the COVID-19 pandemic: Present changes and future perspectives. Radiother Oncol (2020) 150:1–3. doi: 10.1016/j.radonc.2020.05.047

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Torzilli G, Viganò L, Galvanin J, Castoro C, Quagliuolo V, Spinelli A, et al. A snapshot of elective oncological surgery in Italy during COVID-19 emergency: Pearls, pitfalls, and perspectives. Ann Surg (2020) 272(2):e112–7. doi: 10.1097/SLA.0000000000004081

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Mathiesen T, Arraez M, Asser T, Balak N, Barazi S, Bernucci C, et al. A snapshot of European neurosurgery December 2019 vs. march 2020: just before and during the covid-19 pandemic. Acta Neurochir (Wien) (2020) 162(9):2221–33. doi: 10.1007/s00701-020-04482-8

PubMed Abstract | CrossRef Full Text | Google Scholar

21. De Felice F, D’Angelo E, Ingargiola R, Iacovelli NA, Alterio D, Franco P, et al. A snapshot on radiotherapy for head and neck cancer patients during the COVID-19 pandemic: a survey of the Italian association of radiotherapy and clinical oncology (AIRO) head and neck working group. Radiol Med (2021) 126(2):343–7. doi: 10.1007/s11547-020-01296-7

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Nakayama J, El-Nashar SA, Waggoner S, Traughber B, Kesterson J. Adjusting to the new reality: Evaluation of early practice pattern adaptations to the COVID-19 pandemic. Gynecol Oncol (2020) 158(2):256–61. doi: 10.1016/j.ygyno.2020.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Rodriguez J, Fletcher A, Heredia F, Fernandez R, Ramírez Salazar H, Sanabria D, et al. Alternative management for gynecological cancer care during the COVID-2019 pandemic: A Latin American survey. Int J Gynecol Obstet (2020) 150(3):368–78. doi: 10.1002/ijgo.13272

CrossRef Full Text | Google Scholar

24. Aghemo A, Masarone M, Montagnese S, Petta S, Ponziani FR, Russo FP, et al. Assessing the impact of COVID-19 on the management of patients with liver diseases: A national survey by the Italian association for the study of the liver. Dig Liver Dis (2020) 52(9):937–41. doi: 10.1016/j.dld.2020.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Jereczek-Fossa BA, Pepa M, Marvaso G, Isaksson JL, Soatti CP, Cazzaniga LF, et al. Back to (new) normality-a CODRAL/AIRO-l survey on cancer radiotherapy in Lombardy during Italian COVID-19 phase 2. Med Oncol (2020) 37(11):108. doi: 10.1007/s12032-020-01434-1

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Gautam P, Gandhi V, Naik S, Mane A, Kanitkar G, Hegde S, et al. Cancer care in a Western Indian tertiary center during the pandemic: Surgeon’s perspective. J Surg Oncol (2020) 122(8):1525–33. doi: 10.1002/jso.26217

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Hui JYC, Yuan J, Teoh D, Thomaier L, Jewett P, Beckwith H, et al. Cancer management during the COVID-19 pandemic in the united states: Results from a national physician cross-sectional survey. Am J Clin Oncol (2020) 43(10):679–84. doi: 10.1097/COC.0000000000000757

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Martinelli F, Garbi A. Change in practice in gynecologic oncology during the COVID-19 pandemic: a social media survey. Int J Gynecol Cancer (2020) 30(8):1101–7. doi: 10.1136/ijgc-2020-001585

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Gasparri ML, Gentilini OD, Lueftner D, Kuehn T, Kaidar-Person O, Poortmans P. Changes in breast cancer management during the corona virus disease 19 pandemic: An international survey of the European breast cancer research association of surgical trialists (EUBREAST). Breast (2020) 52:110–5. doi: 10.1016/j.breast.2020.05.006

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Breccia M, Abruzzese E, Bocchia M, Bonifacio M, Castagnetti F, Fava C, et al. Chronic myeloid leukemia management at the time of the COVID-19 pandemic in Italy. A campus CML survey Leukemia (2020) 34(8):2260–1. doi: 10.1038/s41375-020-0904-z

CrossRef Full Text | Google Scholar

31. Caricato M, Baiocchi GL, Crafa F, Scabini S, Brisinda G, Clementi M, et al. Colorectal surgery in Italy during the Covid19 outbreak: a survey from the iCral study group. Updates Surg (2020) 72(2):249–57. doi: 10.1007/s13304-020-00760-3

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Nardin C, Puzenat E, Dalac S, Maubec E, Aubin F, , GCC. COVID-19 and skin cancer management: French nation-wide questionnaire survey from real-life practice. J Dermatolog Treat (2022) 33(2):1200–1. doi: 10.1080/09546634.2020.1801972

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Nunoo-Mensah JW, Rizk M, Caushaj PF, Giordano P, Fortunato R, Dulskas A, et al. COVID-19 and the global impact on colorectal practice and surgery. Clin Colorectal Cancer (2020) 19(3):178–190.e1. doi: 10.1016/j.clcc.2020.07.008

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Jereczek-Fossa BA, Pepa M, Marvaso G, Bruni A, Buglione di Monale E Bastia M, Catalano G, et al. COVID-19 outbreak and cancer radiotherapy disruption in Italy: Survey endorsed by the Italian association of radiotherapy and clinical oncology (AIRO). Radiother Oncol (2020) 149:89–93. doi: 10.1016/j.radonc.2020.04.061

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Martinez D, Sarria GJ, Wakefield D, Flores C, Malhotra S, Li B, et al. COVID’s impact on radiation oncology: A Latin American survey study. Int J Radiat Oncol Biol Phys (2020) 108(2):374–8. doi: 10.1016/j.ijrobp.2020.06.058

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Vasquez L, Sampor C, Villanueva G, Maradiegue E, Garcia-Lombardi M, Gomez-García W, et al. Early impact of the COVID-19 pandemic on paediatric cancer care in Latin America. Lancet Oncol (2020) 21(6):753–5. doi: 10.1016/S1470-2045(20)30280-1

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Champagne P-O, McDowell MM, Wang EW, Snyderman CH, Zenonos GA, Gardner PA. Early practices in endonasal skull base surgery during the COVID-19 pandemic: a global survey. Neurosurg Focus (2020) 49(6):E12. doi: 10.3171/2020.9.FOCUS20569

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Gill S, Colwell B, Hirte H, Stephen W, Campbell A, Hao D. Abstract PO-016: Evaluating the impact of COVID-19 on medical oncology workforce and cancer care in Canada: A serial survey study. In: Poster presentations - proffered abstracts. Philadelphia, PA, USA: American Association for Cancer Research (2020). p. PO–016-PO-016. doi: 10.1158/1557-3265.COVID-19-PO-016

CrossRef Full Text | Google Scholar

39. Autrán-Gómez AM, Tobia I, Molina RC, Covarrubias FR, Benzing F, Maruccia S, et al. Exploring urological experience in the COVID-19 outbreak: American confederation of urology (CAU) survey. Int Braz J Urol (2020) 46(suppl.1):156–64. doi: 10.1590/s1677-5538.ibju.2020.s119

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Brandes AA, Ardizzoni A, Artioli F, Cappuzzo F, Cavanna L, Frassineti GL, et al. Fighting cancer in coronavirus disease era: organization of work in medical oncology departments in Emilia romagna region of Italy. Future Oncol (2020) 16(20):1433–9. doi: 10.2217/fon-2020-0358

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Dotzauer R, Böhm K, Brandt MP, Sparwasser P, Haack M, Frees SK, et al. Global change of surgical and oncological clinical practice in urology during early COVID-19 pandemic. World J Urol (2021) 39(9):3139–45. doi: 10.1007/s00345-020-03333-6

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Kumari S. Gynaecologic cancer care during COVID-19 pandemic in India: a social media survey. Cancer Rep (Hoboken) (2020) 3(5):e1280. doi: 10.1002/cnr2.1280

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Bogani G, Apolone G, Ditto A, Scambia G, Panici PB, Angioli R, et al. Impact of COVID-19 in gynecologic oncology: a nationwide Italian survey of the SIGO and MITO groups. J Gynecol Oncol (2020) 31(6):e92. doi: 10.3802/jgo.2020.31.e92

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Gill S, Hao D, Hirte H, Campbell A, Colwell B. Impact of COVID-19 on Canadian medical oncologists and cancer care: Canadian association of medical oncologists survey report. Curr Oncol (2020) 27(2):71–4. doi: 10.3747/co.27.6643

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Rouger-Gaudichon J, Gariazzo L, Thébault E, Brethon B, Fenwarth L, Gambart M, et al. Impact of COVID-19 on cancer care: A survey from the French society of pediatric oncology (SFCE). Pediatr Blood Cancer (2021) 68(1):e28554. doi: 10.1002/pbc.28554

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Chazan G, Franchini F, Alexander M, Banerjee S, Mileshkin L, Blinman P, et al. Impact of COVID-19 on cancer service delivery: a follow-up international survey of oncology clinicians. ESMO Open (2021) 6(5):100224. doi: 10.1016/j.esmoop.2021.100224

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Ottaviano M, Curvietto M, Rescigno P, Tortora M, Palmieri G, Giannarelli D, et al. Impact of COVID-19 outbreak on cancer immunotherapy in Italy: a survey of young oncologists. J Immunother Cancer (2020) 8(2):e001154. doi: 10.1136/jitc-2020-001154

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Rebecchi F, Arolfo S, Ugliono E, Morino M, Asti E, Bonavina L, et al. Impact of COVID-19 outbreak on esophageal cancer surgery in northern Italy: lessons learned from a multicentric snapshot. Dis Esophagus (2021) 34(6):doaa124. doi: 10.1093/dote/doaa124

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Saab R, Obeid A, Gachi F, Boudiaf H, Sargsyan L, Al-Saad K, et al. Impact of the coronavirus disease 2019 (COVID-19) pandemic on pediatric oncology care in the middle East, north Africa, and West Asia region: A report from the pediatric oncology East and Mediterranean (POEM) group. Cancer (2020) 126(18):4235–45. doi: 10.1002/cncr.33075

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Jazieh AR, Akbulut H, Curigliano G, Rogado A, Alsharm AA, Razis ED, et al. Impact of the COVID-19 pandemic on cancer care: A global collaborative study. JCO Glob Oncol (2020) 6:1428–38. doi: 10.1200/GO.20.00351

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Panzuto F, Maccauro M, Campana D, Faggiano A, Massironi S, Pusceddu S, et al. Impact of the SARS-CoV2 pandemic dissemination on the management of neuroendocrine neoplasia in Italy: a report from the Italian association for neuroendocrine tumors (Itanet). J Endocrinol Invest (2021) 44(5):989–94. doi: 10.1007/s40618-020-01393-4

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Tamari K, Nagata Y, Nishiki S, Nakamura S, Ogawa K, Uno T. Nationwide survey of COVID-19 prevention measures in Japanese radiotherapy departments via online questionnaire for radiation oncologists. Radiother Oncol (2020) 149:219–21. doi: 10.1016/j.radonc.2020.05.042

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Onesti CE, Rugo HS, Generali D, Peeters M, Zaman K, Wildiers H, et al. Oncological care organisation during COVID-19 outbreak. ESMO Open (2020) 5(4):e000853. doi: 10.1136/esmoopen-2020-000853

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Brunner M, Krautz C, Kersting S, Weber GF, Stinner B, Benz SR, et al. Oncological colorectal surgery during the COVID-19pandemic-a national survey. Int J Colorectal Dis (2020) 35(12):2219–25. doi: 10.1007/s00384-020-03697-6

PubMed Abstract | CrossRef Full Text | Google Scholar

55. on behalf of the Cardio-Oncology International Collaborative Network, Sadler D, DeCara JM, Herrmann J, Arnold A, Ghosh AK, et al. Perspectives on the COVID-19 pandemic impact on cardio-oncology: results from the COVID-19 international collaborative network survey. Cardio-Oncology (2020) 6(1):28. doi: 10.1186/s40959-020-00085-5

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Singh HK, Patil V, Chaitanya G, Nair D. Preparedness of the cancer hospitals and changes in oncosurgical practices during COVID-19 pandemic in India: A cross-sectional study. J Surg Oncol (2020) 122(7):1276–87. doi: 10.1002/jso.26174

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Rimmer M, Al Wattar B, UKARCOG Members, Barlow C, Black N, Carpenter C, et al. Provision of obstetrics and gynaecology services during the COVID-19 pandemic: a survey of junior doctors in the UK national health service. BJOG: Int J Obstet Gy (2020) 127(9):1123–8. doi: 10.1111/1471-0528.16313

CrossRef Full Text | Google Scholar

58. Indini A, Aschele C, Cavanna L, Clerico M, Daniele B, Fiorentini G, et al. Reorganisation of medical oncology departments during the novel coronavirus disease-19 pandemic: a nationwide Italian survey. Eur J Cancer (2020) 132:17–23. doi: 10.1016/j.ejca.2020.03.024

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Hasford F, Ige TA, Trauernicht C. Safety measures in selected radiotherapy centres within Africa in the face of covid-19. Health Technol (Berl) (2020) 10(6):1391–6. doi: 10.1007/s12553-020-00472-z

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Depypere LP, Daddi N, Gooseman MR, Batirel HF, Brunelli A. The impact of coronavirus disease 2019 on the practice of thoracic oncology surgery: a survey of members of the European society of thoracic surgeons (ESTS). Eur J Cardio-Thoracic Surgery (2020) 58(4):752–62. doi: 10.1093/ejcts/ezaa284

CrossRef Full Text | Google Scholar

61. Kamarajah SK, Markar SR, Singh P, Griffiths EA, Oesophagogastric Anastomosis Audit Group. The influence of the SARS-CoV-2 pandemic on esophagogastric cancer services: an international survey of esophagogastric surgeons. Dis Esophagus (2020) 33(7):doaa054. doi: 10.1093/dote/doaa054

CrossRef Full Text | Google Scholar

62. Marandino L, Di Maio M, Procopio G, Cinieri S, Beretta GD, Necchi A. The shifting landscape of genitourinary oncology during the COVID-19 pandemic and how Italian oncologists reacted: Results from a national survey. Eur Urol (2020) 78(1):e27–35. doi: 10.1016/j.eururo.2020.04.004

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Harke NN, Radtke JP, Hadaschik BA, Bach C, Berger FP, Blana A, et al. To defer or not to defer? a German longitudinal multicentric assessment of clinical practice in urology during the COVID-19 pandemic. PloS One (2020) 15(9):e0239027. doi: 10.1371/journal.pone.0239027

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Tashkandi E, Zeeneldin A, AlAbdulwahab A, Elemam O, Elsamany S, Jastaniah W, et al. Virtual management of patients with cancer during the COVID-19 pandemic: Web-based questionnaire study. J Med Internet Res (2020) 22(6):e19691. doi: 10.2196/19691

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Boufkhed S, Harding R, Kutluk T, Husseini A, Pourghazian N, Shamieh O. What is the preparedness and capacity of palliative care services in middle-Eastern and north African countries to respond to COVID-19? a rapid survey. J Pain Symptom Manage (2021) 61(2):e13–50. doi: 10.1016/j.jpainsymman.2020.10.025

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Gulia A, Tiwari A, Arora RS, Gupta S, Raja A. Sarcoma care practice in India during COVID pandemic: A nationwide survey. JOIO (2020) 54(S2):350–7. doi: 10.1007/s43465-020-00206-3

CrossRef Full Text | Google Scholar

67. Thaler M, Khosravi I, Leithner A, Papagelopoulos PJ, Ruggieri P. Impact of the COVID-19 pandemic on patients suffering from musculoskeletal tumours. Int Orthop (2020) 44(8):1503–9. doi: 10.1007/s00264-020-04636-4

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Chavez-MacGregor M, Lei X, Zhao H, Scheet P, Giordano SH. Evaluation of COVID-19 mortality and adverse outcomes in US patients with or without cancer. JAMA Oncol (2022) 8(1):69–78. doi: 10.1001/jamaoncol.2021.5148

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Patt D, Gordan L, Diaz M, Okon T, Grady L, Harmison M, et al. Impact of COVID-19 on cancer care: How the pandemic is delaying cancer diagnosis and treatment for American seniors. JCO Clin Cancer Informatics (2020) 4):1059–71. doi: 10.1200/CCI.20.00134

CrossRef Full Text | Google Scholar

70. Graetz D, Agulnik A, Ranadive R, Vedaraju Y, Chen Y, Chantada G, et al. Global effect of the COVID-19 pandemic on paediatric cancer care: a cross-sectional study. Lancet Child Adolesc Health (2021) 5(5):332–40. doi: 10.1016/S2352-4642(21)00031-6

PubMed Abstract | CrossRef Full Text | Google Scholar

71. Skovlund CW, Friis S, Dehlendorff C, Nilbert MC, Mørch LS. Hidden morbidities: drop in cancer diagnoses during the COVID-19 pandemic in Denmark. Acta Oncol (2021) 60(1):20–3. doi: 10.1080/0284186X.2020.1858235

PubMed Abstract | CrossRef Full Text | Google Scholar

72. Maringe C, Spicer J, Morris M, Purushotham A, Nolte E, Sullivan R, et al. The impact of the COVID-19 pandemic on cancer deaths due to delays in diagnosis in England, UK: a national, population-based, modelling study. Lancet Oncol (2020) 21(8):1023–34. doi: 10.1016/S1470-2045(20)30388-0

PubMed Abstract | CrossRef Full Text | Google Scholar

73. Dinmohamed AG, Visser O, Verhoeven RHA, Louwman MWJ, van Nederveen FH, Willems SM, et al. Fewer cancer diagnoses during the COVID-19 epidemic in the Netherlands. Lancet Oncol (2020) 21(6):750–1. doi: 10.1016/S1470-2045(20)30265-5

PubMed Abstract | CrossRef Full Text | Google Scholar

74. Kaufman HW, Chen Z, Niles J, Fesko Y. Changes in the number of US patients with newly identified cancer before and during the coronavirus disease 2019 (COVID-19) pandemic. JAMA Netw Open (2020) 3(8):e2017267. doi: 10.1001/jamanetworkopen.2020.17267

PubMed Abstract | CrossRef Full Text | Google Scholar

76. Maluchnik M, Podwójcic K, Więckowska B. Decreasing access to cancer diagnosis and treatment during the COVID-19 pandemic in Poland. Acta Oncol (2021) 60(1):28–31. doi: 10.1080/0284186X.2020.1837392

PubMed Abstract | CrossRef Full Text | Google Scholar

77. Ranganathan P, Sengar M, Chinnaswamy G, Agrawal G, Arumugham R, Bhatt R, et al. Impact of COVID-19 on cancer care in India: a cohort study. Lancet Oncol (2021) 22(7):970–6. doi: 10.1016/S1470-2045(21)00240-0

PubMed Abstract | CrossRef Full Text | Google Scholar

78. Pramesh CS, Chinnaswamy G, Sengar M, Ranganathan P, Badwe R. COVID-19 and cancer care in India. Nat Cancer (2021) 2(12):1257–9. doi: 10.1038/s43018-021-00290-w

PubMed Abstract | CrossRef Full Text | Google Scholar

79. Villain P, Carvalho AL, Lucas E, Mosquera I, Zhang L, Muwonge R, et al. Cross-sectional survey of the impact of the COVID-19 pandemic on cancer screening programs in selected low- and middle-income countries: Study from the IARC COVID-19 impact study group. Int J Cancer (2021) 149(1):97–107. doi: 10.1002/ijc.33500

PubMed Abstract | CrossRef Full Text | Google Scholar

81. Chowdhury AZ, Jomo KS. Responding to the COVID-19 pandemic in developing countries: Lessons from selected countries of the global south. Development (2020) 63(2-4):162–71. doi: 10.1057/s41301-020-00256-y

PubMed Abstract | CrossRef Full Text | Google Scholar

82. Shirke MM, Shaikh SA, Harky A. Implications of telemedicine in oncology during the COVID-19 pandemic. Acta Biomed (2020) 91(3):e2020022. doi: 10.23750/abm.v91i3.9849

PubMed Abstract | CrossRef Full Text | Google Scholar

83. Yadav K, Ginsburg O, Basu P, Mehrotra R. Telemedicine and cancer care in low- and middle-income countries during the SARS-CoV-2 pandemic. JCO Glob Oncol (2021) 7:1633–8. doi: 10.1200/GO.21.00249

PubMed Abstract | CrossRef Full Text | Google Scholar

84. The Lancet Infectious Diseases. The COVID-19 infodemic. Lancet Infect Dis (2020) 20(8):875. doi: 10.1016/S1473-3099(20)30565-X

PubMed Abstract | CrossRef Full Text | Google Scholar

85. Galvão J. COVID-19: the deadly threat of misinformation. Lancet Infect Dis (2021) 21(5):e114. doi: 10.1016/S1473-3099(20)30721-0

PubMed Abstract | CrossRef Full Text | Google Scholar

88. Sniderman ER, Graetz DE, Agulnik A, Ranadive R, Vedaraju Y, Chen Y, et al. Impact of the COVID-19 pandemic on pediatric oncology providers globally: A mixed-methods study. Cancer (2022) 128(7):1493–502. doi: 10.1002/cncr.34090

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: oncology, COVID-19, survey, healthcare, meta-analysis

Citation: Di Cosimo S, Susca N, Apolone G, Silvestris N and Racanelli V (2022) The worldwide impact of COVID-19 on cancer care: A meta-analysis of surveys published after the first wave of the pandemic. Front. Oncol. 12:961380. doi: 10.3389/fonc.2022.961380

Received: 04 June 2022; Accepted: 12 September 2022;
Published: 29 September 2022.

Edited by:

Maria Paula Curado, A.C.Camargo Cancer Center, Brazil

Reviewed by:

Daniel Moreira, St. Jude Children’s Research Hospital, United States
Errol Philip, University of California, San Francisco, United States
Zee Wan Wong, Peninsula Health, Australia

Copyright © 2022 Di Cosimo, Susca, Apolone, Silvestris and Racanelli. 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: Vito Racanelli, vito.racanelli1@uniba.it

†These authors share first authorship

‡These authors share last authorship

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.