Skip to main content

ORIGINAL RESEARCH article

Front. Surg., 25 October 2021
Sec. Surgical Oncology
This article is part of the Research Topic Advanced Approaches on Multidisciplinary Management of Rectal Cancer View all 21 articles

Risk Factors for Anorectal Dysfunction After Interspincteric Resection in Patients With Low Rectal Cancer

\nLi Min&#x;Li Min1Zhang Fan&#x;Zhang Fan1Wang ZhiWang Zhi1Li PingangLi Pingang1Xie LijuanXie Lijuan2Deng MinDeng Min2Wen YanWen Yan1Wang Xiaosong
Wang Xiaosong1*Tang Bo
Tang Bo1*
  • 1Department of General Surgery, Southwest Hospital Affiliated to Army Medical University, Chongqing, China
  • 2Department of Rehabilitation, Southwest Hospital Affiliated to Army Medical University, Chongqing, China

Purpose: The objective of this study was to explore the risk factors for anorectal dysfunction after intersphincteric resection in patients with low rectal cancer.

Methods: A total of 251 patients who underwent intersphincteric resection from July 2014 to June 2020 were included in this study, for which the Kirwan's grade, Wexner score, and anorectal manometric index were used to evaluate the anorectal function and other parameters including demographics, surgical features, and clinical and pathological characteristics. These parameters were analysed to explore the potential risk factors for anorectal function after intersphincteric resection.

Results: In the 251 included patients, 98 patients underwent partial intersphincteric resection, 87 patients underwent subtotal intersphincteric resection, and 66 patients underwent total intersphincteric resection. There were 53 (21.1%) patients who had postoperative complications, while no significant difference was observed between the three groups. Furthermore, 30 patients (45.5%) in the total intersphincteric resection group were classified as having anorectal dysfunction (Kirwan's grade 3–5), which was significantly higher than that in the partial intersphincteric resection group (27.6%) and subtotal intersphincteric resection group (29.9%). The mean Wexner score of patients that underwent total intersphincteric resection was 7.9, which was higher than that of patients that had partial intersphincteric resection (5.9, p = 0.002) and subtotal intersphincteric resection (6.4, p = 0.027). The initial perceived volume was lower in the total intersphincteric resection group than in the partial and subtotal intersphincteric resection groups at 1, 3, and 6 months after intersphincteric resection. In addition, the resting pressure, maximum squeeze pressure, and maximum tolerated volume in the total intersphincteric resection group were worse than those in the partial and subtotal groups at 3 and 6 months after intersphincteric resection. Univariate and multivariate analyses suggested that an age ≥65, total intersphincteric resection, and preoperative chemoradiotherapy were independent risk factors for anorectal dysfunction (P = 0.023, P = 0.003, and P = 0.008, respectively). Among the 66 patients who underwent total intersphincteric resection, 17 patients received preoperative chemoradiotherapy, of which 12 patients (70.6%) were classified as having anorectal dysfunction.

Conclusion: The current study concluded that age ≥65, total intersphincteric resection, and preoperative chemoradiotherapy were risk factors for anorectal dysfunction after intersphincteric resection. The morbidity of anorectal dysfunction after total intersphincteric resection for patients who received preoperative chemoradiotherapy was relatively high, and the indication should be carefully evaluated.

Introduction

Abdominoperineal resection is regarded as a standard procedure for curative surgical treatment in patients with low rectal cancer. In recent years, anus-preserving surgeries, including intersphincteric resection (ISR) and transanal total mesorectal excision (Ta_TME), have been widely performed for low rectal cancer and can significantly avoid a permanent stoma (13). With the development and application of laparoscopic and robotic systems for the resection of low rectal cancer, the ISR has become one of the most popular anus-preserving procedures. Previous evidence has indicated that its clinical and oncological outcomes are similar to abdominoperineal resection (APR), and the anal functional outcome is suggested to be acceptable (1, 4, 5). However, many patients suffer from anorectal dysfunction after ISR, especially total ISR, resulting in a conversion to a permanent colostomy and a reduction in the quality of daily life (6). Previous studies have shown that ~42% of patients experience major bowel dysfunction after ISR, indicating that the functional outcomes may be the main risk of undergoing ISR rather than oncological outcomes (7). Furthermore, ISR can be classified as partial ISR, subtotal ISR, and total ISR according to the resected grade of the internal sphincter. Partial ISR is defined as the distal resection line of the internal sphincter at the dentate line, subtotal ISR is located between the intersphincteric groove and dentate line, and total ISR is located at the intersphincteric groove (8). The internal anal sphincter should be partially or totally removed in different ISRs, wherein this sphincter was reported to contribute ~55% of anal pressure, and its removal resulted in varying degrees of anorectal dysfunction (9). To explore the potential factors that might influence anorectal function after ISR, we retrospectively analysed clinicopathological characteristics, surgical features, postoperative complications, and functional indicators in this study.

Methods

Patients

The present study included consecutive patients with low rectal cancer who underwent laparoscopic or robotic-assisted ISR from July 2014 to June 2020 at the Southwest Hospital affiliated with Army Medical University (<city>Chongqing</city>, China). Inclusion criteria were (1) an age of 18–70 years, (2) a distance between the lower edge of the tumour and Hilton line of 1–5 cm, (3) preoperatively evaluated well-differentiated adenocarcinoma, (4) estimated TNM stage (8th edition) p/ypT1−3N0−2M0, and (5) an Eastern Cooperative Oncology Group (ECOG) performance status of 0–2. The exclusion criteria were (1) synchronous cancer or metachronous cancer during follow-up, (2) rectal cancer associated with inflammatory bowel disease or hereditary rectal cancer, and (3) local tumour recurrence in 2 years. Patients with preoperatively estimated T4 or stage III disease received a long course of preoperative chemotherapy or chemoradiotherapy (CRT). After this, the estimated T stage was below T3, and non-external sphincter infiltration was determined according to preoperative enhanced rectal MRI and endoscopic ultrasonography evaluation.

Demographics and perioperative clinicopathological characteristics were investigated and compared in order to explore the risk factors for anorectal dysfunction after ISR.

Surgical Procedure

The ISR was performed by laparoscopic or robotic surgical systems according to previously reported methods (10). First, dissection was performed by the abdominal route, then the levator ani muscle hiatus was entered, and a division was created between the loose internal and external sphincter spaces to the level of the dentate line via the anal or abdominal route. Patients enrolled in this study who went through partial and subtotal ISR underwent transabdominal procedures, and total ISR was performed through transanal transabdominal procedures. The transanal dissection contains a circumferential incision of the mucosa at the Hilton line. Through a careful circumferential dissection and the protection of the external anal sphincter and levator ani muscle, confluence at the level of the abdominal dissection and total ISR were completed. After the removal of the specimen, bowel reconstruction was performed using an end-to-end procedure via a stapled anastomosis in the partial and subtotal ISR groups, a handsewn coloanal anastomosis with absorbable interrupted sutures in the total ISR group, and a diverting ileostomy.

Postoperative Follow-Up and Evaluation

Postoperative complications were recorded and classified as Clavien–Dindo grades. Anastomotic complications, including anastomotic leakage, anastomotic bleeding, and anastomotic stricture, were analysed to evaluate the risk factors for anorectal dysfunction. The manometric measurements were evaluated before a surgery and every 3 months after surgery. The clinical, pathological, and functional outcomes were evaluated every 3 months in 2 years after surgery via an outpatient service. Anorectal manometry was performed by High-resolution manometry (XDJ-S8G) (KAILIGUANGDIAN LLC, Hefei, Anhui, China), of which the resting pressure (RP), maximum squeeze pressure (MSP), initial perceived volume (IPV), and maximum tolerated volume (MTV) values were assessed to evaluate sphincteric and faecal function (11). Wexner scores (12) and Kirwan classification (13) were recorded before ISR and every 3 months after stoma closure.

Statistical Analysis

Categorical data are presented as the number of cases evaluated, and quantitative data are reported as the mean ± SD. A chi-square test was used to evaluate categorical variables, and a Fisher's exact test or Student's t-test was used for continuous variables. The factors related to potential risk factors were analysed by binary logistic regression analysis, and odds ratios (ORs) with 95% CIs were calculated. The Cox proportional hazards model was used to define prognostic factors related to anorectal dysfunction. Covariates with p < 0.05 were selected for the multivariate model. All statistical analyses were performed using SPSS 22 (SPSS Inc., Chicago, IL, USA). p < 0.05 were regarded as statistically significant.

Ethics

The institutional review board of the Southwest Hospital Affiliated to the Army Medical University approved the study protocol (KY2019138). All methods in this study were performed in accordance with relevant guidelines and regulations. Written informed consent was obtained from all included patients.

Results

Patient Enrollment

As the flow diagram of patient selection shows (Figure 1), a total of 266 patients were included according to the inclusion criteria, while 11 patients were excluded according to the exclusion criteria, and four patients were lost to follow-up. Thus, a total of 251 patients were enrolled in this study, of which 98 patients underwent partial ISR, 87 patients underwent subtotal ISR, and 66 patients underwent total ISR. The median follow-up was 26 (6–72) months.

FIGURE 1
www.frontiersin.org

Figure 1. Flow diagram of patient selection.

Operative and Clinicopathological Characteristics of Patients

For the enrolled patients in this study, the demographics and clinical characteristics, including sex, age, body mass index (BMI), American Society of Anesthesiologists (ASA) classification, haemoglobin level, albumin level, and preoperative CRT, were compared according to different surgical procedures. The results showed that there was no significant difference in any parameter between these three groups (Table 1). Preoperative CRT was recommended for patients with T3–4 or stage III rectal cancer or suspected anal sphincter invasion according to preoperative MRI. Tumour regression after preoperative CRT was assessed by the tumour regression grade provided by the American Joint Committee on Cancer (AJCC) and the College of American Pathologists (14).

TABLE 1
www.frontiersin.org

Table 1. Demographics and clinical characteristics of patients.

Operative and Pathological Characteristics of Patients Who Underwent ISR

The operative and pathological outcomes are presented in Table 2. We pathologically evaluated the resection of the external anal sphincter (EAS) for every patient after ISR and found that the EAS was reserved for all patients who underwent partial ISR. The EAS was partially resected for 9 out of 87 patients who underwent subtotal ISR and 19 out of 66 patients who underwent total ISR. In the partial ISR group, 45 patients received robotic ISR and 53 patients received laparoscopic ISR. In the subtotal ISR group, 49 patients received robotic ISR and 38 patients received laparoscopic ISR. In the total ISR group, 58 patients received robotic ISR and 8 patients received laparoscopic ISR. The proportion of robotic surgeries was significantly higher (p < 0.001) in the total ISR group. No significant difference was found in the anastomosis level from the anal verge, operation time, estimated blood loss, tumour differentiation, T or N stage according to the 8th edition of AJCC cancer staging criteria (15), the number of lymph nodes (LNs) harvested, and distal resection margin according to our results. The circumference margin of all the patients was pathologically proven as oncologically negative. A total of 92 patients were pathologically diagnosed with low differentiation after surgery, and 57 patients were stage III-IV, which were also included in the analysis for the evaluation of the risk factors for anorectal dysfunction.

TABLE 2
www.frontiersin.org

Table 2. Operative features and pathological characteristics in patients.

Postoperative Complications

Data on postoperative complications are shown in Table 3. No grade IV or V complications were observed in these 251 patients. There were 21 (21.4%) patients in the partial ISR group, 18 (20.7%) patients in the subtotal ISR group, and 14 (21.2%) patients in the total ISR group who had postoperative complications. Anastomotic complications, including anastomotic leakage, anastomotic bleeding, and anastomotic stricture, were compared, and no significant difference was observed between these groups.

TABLE 3
www.frontiersin.org

Table 3. Postoperative complications in patients.

Anorectal Function Evaluation After Stoma Closure

All patients enrolled in this study simultaneously underwent temporary ileostomy and ISR, and all of these patients underwent stoma closure 3–6 months after the first operation. To evaluate defecatory function after ISR, we assessed Kirwan's grade and Wexner score for every patient 3 months after stoma closure. As shown in Table 4, the daily bowel frequency in the partial ISR group was 4.2 ± 2.3, that in the subtotal ISR group was 4.3 ± 2.7, and that in the total ISR group was 5.5 ± 3. The bowel frequency in the total ISR group was slightly higher than that in the partial and subtotal groups, but no statistical significance was found. The faecal continent was classified as Kirwan's grade 1–2, while the faecal incontinent was classified as Kirwan's grade 3–5. As shown in Table 4, 27 patients in the partial ISR group (27.6%), 26 patients in the subtotal ISR group (29.9%), and 30 patients in the total ISR group (45.5%) suffered from anorectal dysfunction (Kirwan's grade 3–5). Compared with the partial and subtotal ISR groups, the total ISR group had a significantly higher faecal incontinence rate (p = 0.018 and 0.048, respectively). A similar result was observed for the Wexner score, and the mean score in the total ISR group (7.9 ± 5.2) was significantly higher (p = 0.002 and 0.027, respectively) than that of the partial ISR group (4.2 ± 2.3) and subtotal ISR group (4.3 ± 2.7).

TABLE 4
www.frontiersin.org

Table 4. The anorectal function was evaluated 3 months after stoma closure.

Anorectal Manometric Measurements in Patients Who Underwent ISR

To objectively assess the anorectal sensitivity and contractility, we measured the RP, MSP, IPV, and MTV for every patient before ISR and 1, 3, and 6 months after ISR. The results in Table 5 show no difference in every parameter before surgery. At 1 month after ISR, the IPV for the total ISR group was significantly lower than that of the partial and subtotal groups. At 3 and 6 months after ISR, almost all parameters for total ISR were lower than those of the other two groups, indicating that the total resection of the internal anal sphincter could strongly affect anorectal function. We also found that the manometric measurements could recover slowly, not only in the partial and subtotal ISR groups but also in the total group.

TABLE 5
www.frontiersin.org

Table 5. Anorectal manometric measurements after ISR.

Factors Influencing Defecatory Function After ISR

To define the risk factors for anorectal dysfunction after ISR, we analysed the potential factors mentioned in Tables 1, 2 by univariate and multivariate analyses. The univariate analysis indicated that an age >65, T (3–4) stage, total ISR procedure, preoperative CRT, and distal resection margin were potential risk factors. All these statistically significant parameters were included in a multivariate analysis, and the results showed that age (p = 0.023), total ISR (p = 0.003), and preoperative CRT (p = 0.008) were independent risk factors for anorectal dysfunction after ISR (Table 6).

TABLE 6
www.frontiersin.org

Table 6. Univariate and multivariate analyses for the risk of anorectal dysfunction.

The Safety of Total ISR for Patients Who Received Neoadjuvant CRT

The above results suggested that total ISR and preoperative CRT were both independent risk factors for anorectal dysfunction after ISR, which reminded us to explore the safety of total ISR for patients who received preoperative CRT. In this study, 66 patients underwent total ISR, of which 17 patients received preoperative CRT. Among these 17 patients, 12 patients (70.6%) were classified as having anorectal dysfunction (Kirwan's grade 3–5), indicating that preoperative CRT may be a crucial risk factor for anorectal dysfunction after total ISR (Table 7).

TABLE 7
www.frontiersin.org

Table 7. Anorectal function for patients who underwent total ISR.

Discussion

The ISR or Ta_TME have suggested procedures for the surgical treatment of patients with low or extremely low rectal cancer. In particular, ISR is very hard to perform in conventional open surgeries, but the application of laparoscopic, or especially robotic systems, makes this procedure become easier and more familiar to surgeons (16, 17). In this study, the robotic system was more commonly used for the treatment of total ISR, indicating that the robotic system could operate better in small spaces. The clinical outcomes were evaluated and reported to be safe in many studies, while anorectal complications, including oedematous haemorrhoids, anal stenosis, and neorectal mucosal prolapse, were more common after ISR (18). Regarding the oncological outcome, ISR showed comparable overall survival with APR for patients with low rectal cancer, especially for patients at stage I–II (4). It was reported that patients who underwent ISR also showed a relatively higher local recurrence rate, while a deeper analysis found that these local recurrences were mostly observed in T3 or T4 patients. Additionally, the local recurrence rate was comparable in T1 or T2 patients, indicating that the ISR should be carefully evaluated and chosen for these patients (1, 19). For cT3 or cT4 patients, radiotherapy and CRT followed by ISR is an option that has been proven to be oncologically safe (20). In this study, a total of 57 patients were postoperatively diagnosed as being in the T3–4 stage, of which 20 patients received folinic acid, fluorouracil, and oxaliplatin (FOLFOX) chemotherapy, and the other 37 patients received Xeloda (capecitabine) and oxaliplatin (XELOX) chemotherapy. None of the patients enrolled in this study received postoperative first-line radiotherapy, because the functional safety of postoperative radiotherapy is not well-proven for patients who received ISR.

In addition to the clinical and oncological outcomes, the anorectal functional outcome was another essential indicator for the safety evaluation of ISR. The present studies showed that the excision of the internal anal sphincter had negative effects on short- and long-term anorectal function, and some patients even suffered from complete incontinence resulting in a conversion to a permanent colostomy (6, 21). Kirwan's grade and Wexner score were applied to evaluate the defecatory function after ISR. Patients with liquid or solid incontinence (Kirwan's grade 3–5) were classified as having anorectal dysfunction. Given that the patients included in this study simultaneously underwent ISR and ileostomy, the defecatory function was assessed at 3 months after stoma closure. The results in Table 4 show that the anorectal dysfunction morbidity in patients who underwent total ISR was relatively higher than that in the partial ISR group (30/66 vs. 27/98, p = 0.048) and subtotal group (30/66 vs. 26/87, p = 0.018). Similar results were observed in postoperative bowel frequency and Wexner scores. Patients who underwent total ISR had a higher bowel frequency and higher mean Wexner score than the other two groups, indicating that the excision extension of the internal anal sphincter may correlate to anorectal function after ISR. In addition, the pathological results showed that nine patients (10.3%) who underwent subtotal ISR and 19 patients (28.8%) who underwent total ISR had all underwent partial external anal sphincter excision during the surgery, which may be another risk factor for anorectal dysfunction. From the functional results, we found that the defecatory function was comparable between the partial and subtotal groups, suggesting that, for postoperative anorectal function, the excision extension may be the main risk factor. Postoperative complications, especially anastomotic complications, might influence anorectal function (22). To explore the relationship between anastomotic complications and anorectal function, we analysed anastomotic leakage, anastomotic bleeding, and anastomotic stricture. The result showed that there was no significant difference in postoperative complications between different ISRs. Univariate analysis showed that the anastomotic complications were not risk factors for anorectal dysfunction.

In addition to the subjective evaluation parameters, anal manometry was applied to objectively evaluate the anorectal contractility and sensitivity in this study. Manometric parameters including RP, MSP, IPV, and MTV are widely used to assess anorectal function after ISR, which can objectively reflect defecatory function (4, 8, 23). In this study, the preoperative manometry was measured as the baseline and showed no difference between the different ISR groups. The measurements after ISR, especially 3 and 6 months after ISR, showed that almost every parameter was weaker in the total ISR group than in the other groups, which suggested similar results as the Kirwan's grade and Wexner score indicated. The present studies showed that the manometric values were reduced after ISR, while they could mostly recover to a continental level in 12–24 months (4, 5). In addition, from the results of postoperative manometric measurements, we found that postoperative IPV was lower than preoperative IPV. The IPV value is related to rectal sensitivity and defecation-control ability, and ISR would decrease such rectal sensitivity and defecation-control ability. The IPV results indicated that the defecation-control ability of a patient was severely damaged after ISR, which may play a more important than the anal sensitivity of the impact on IPV. The IPV increased with the time after surgery, indicating that the defecation-control ability of the patient recovered with time. The manometric results in this study also showed that anorectal function recovered after surgery, and the values at 6 months were better than those at 1 and 3 months after ISR. Compared to the baseline, the reduction was still apparent, especially in patients who underwent total ISR. Both the Wexner scores and the manometric measurements showed that the anorectal function recovery was time-dependent, and anorectal function would be recovered to a similar and acceptable level approximately 12–24 months after ISR (4, 5, 24). The manometric results also suggested that the values after ISR in the partial ISR and subtotal ISR groups were comparable and significantly better than those in the total ISR group, indicating that even the partial reservation of the internal anal sphincter could contribute to anorectal function after ISR.

Apart from the excision of the internal anal sphincter, other potential risk factors were explored. Denost et al. reported that the distance of the tumour from the anal ring being >1 cm and the anastomoses being higher than 2 cm above the anal verge were independent predictors of good faecal continence for patients who received ISR (25), according to a cohort of 101 patients. Other studies reported that age, tumour stage, preoperative CRT, operative approach, level of ISR, and the reconstruction of the rectum might influence faecal incontinence after ISR (1, 26). In this study, we analysed the clinicopathological characteristics, surgical features, postoperative complications, and functional indicators to systemically evaluate the risk factors for anorectal dysfunction. The univariate and multivariate analyses suggested that an age ≥65 (p = 0.023), total ISR (p = 0.003), and preoperative CRT (p = 0.008) were risk factors for anorectal dysfunction. We evaluated the safety of total ISR for patients who received preoperative CRT and found that 70.6% of patients in this subgroup suffered from anorectal dysfunction, which was relatively high morbidity.

In conclusion, the anal functional outcome after partial ISR and subtotal ISR is acceptable for patients with low rectal cancer, which could increase the anus-preserving rate. The indication of total ISR, especially for patients who receive preoperative CRT, should be strictly and carefully evaluated and defined. The safety of total ISR for patients who receive preoperative CRT should be further explored. There are some limitations to this study. First, this study is not a randomised clinical trial, and bias may exist. Second, this study is a retrospective study, and a prospective controlled trial should be carried out for further exploration.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics Statement

The studies involving human participants were reviewed and approved by the institutional review board of the Southwest Hospital Affiliated to Army Medical University approved the study protocol (KY2019138). The patients/participants provided their written informed consent to participate in this study.

Author Contributions

LM and ZF: data collection, management, analysis, and manuscript writing. WZ and LP: data management and analysis. XL, DM, and WY: data collection. WX: project development, data analysis, manuscript writing, and editing. TB: project development, data analysis, and manuscript editing. All authors contributed to the article and approved the submitted version.

Funding

This work was supported by Chongqing Postdoctoral Science Special Foundation (4142Z2374).

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. Yamada K, Saiki Y, Takano S, Iwamoto K, Tanaka M, Fukunaga M, et al. Long-term results of intersphincteric resection for low rectal cancer in Japan. Surg Today. (2019) 49:275–85. doi: 10.1007/s00595-018-1754-4

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Ito M. ISR for T1-2 low rectal cancer: a japanese approach. Clin Colon Rectal Surg. (2020) 33:361–5. doi: 10.1055/s-0040-1714240

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Vignali A, Elmore U, Milone M, Rosati R. Transanal total mesorectal excision (TaTME): current status and future perspectives. Updates Surg. (2019) 71:29–37. doi: 10.1007/s13304-019-00630-7

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Kim JC, Lee JL, Bong JW, Seo JH, Kim CW, Park SH, et al. Oncological and anorectal functional outcomes of robot-assisted intersphincteric resection in lower rectal cancer, particularly the extent of sphincter resection and sphincter saving. Surg Endosc. (2020) 34:2082–94. doi: 10.1007/s00464-019-06989-3

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Xiaosong W, Hongchang L, Min D, Lijuan X, Chuan L, Peiwu Y, et al. Postoperative functional management contributes to anal functional recovery in patients with low rectal cancer after robotic total intersphincteric resection. Front Oncol. (2020) 10:1373. doi: 10.3389/fonc.2020.01373

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Ito M, Saito N, Sugito M, Kobayashi A, Nishizawa Y, Tsunoda Y. Analysis of clinical factors associated with anal function after intersphincteric resection for very low rectal cancer. Dis Colon Rectum. (2009) 52:64–70. doi: 10.1007/DCR.0b013e31819739a0

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Denost Q, Moreau JB, Vendrely V, Celerier B, Rullier A, Assenat V, et al. Intersphincteric resection for low rectal cancer: the risk is functional rather than oncological. A 25-year experience from Bordeaux. Colorectal Dis. (2020) 22:1603–13. doi: 10.1111/codi.15258

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Yamada K, Ogata S, Saiki Y, Fukunaga M, Tsuji Y, Takano M. Functional results of intersphincteric resection for low rectal cancer. Br J Surg. (2007) 94:1272–7. doi: 10.1002/bjs.5534

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Kitaguchi D, Nishizawa Y, Sasaki T, Tsukada Y, Ito M. Clinical benefit of high resolution anorectal manometry for the evaluation of anal function after intersphincteric resection. Colorectal Dis. (2019) 21:335–41. doi: 10.1111/codi.14528

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Kim JC, Yu CS, Lim SB, Kim CW, Park IJ, Yoon YS. Outcomes of ultra-low anterior resection combined with or without intersphincteric resection in lower rectal cancer patients. Int J Colorectal Dis. (2015) 30:1311–21. doi: 10.1007/s00384-015-2303-x

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Ciriza de Los Ríos C, Mínguez M, Remes-Troche JM, Lacima G. High-resolution and high-definition anorectal manometry: rediscovering anorectal function. Rev Esp Enferm Dig. (2018) 110:794–805. doi: 10.17235/reed.2018.5705/2018

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Jorge JM, Wexner SD. Etiology and management of fecal incontinence. Dis Colon Rectum. (1993) 36:77–97. doi: 10.1007/BF02050307

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kirwan WO, Turnbull RB Jr, Fazio VW, Weakley FL. Pullthrough operation with delayed anastomosis for rectal cancer. Br J Surg. (1978) 65:695–8. doi: 10.1002/bjs.1800651008

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Mace AG, Pai RK, Stocchi L, Kalady MF. American joint committee on cancer and college of American pathologists regression grade: a new prognostic factor in rectal cancer. Dis Colon Rectum. (2015) 58:32–44. doi: 10.1097/DCR.0000000000000266

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Fleming ID, Cooper JS, Henson DE, Hunter RV, Kennedy BJ, Murphy GP, et al. American joint committee on cancer. Colon and rectum. AJCC Cancer Staging Manual. New York, NY: Springer (2017). p. 251-274.

PubMed Abstract

16. Lee SH, Kim DH, Lim SW. Robotic versus laparoscopic intersphincteric resection for low rectal cancer: a systematic review and meta-analysis. Int J Colorectal Dis. (2018) 33:1741–53. doi: 10.1007/s00384-018-3145-0

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Matsuhashi N, Takahashi T, Tanahashi T, Matsui S, Imai H, Tanaka Y, et al. Safety and feasibility of laparoscopic intersphincteric resection for a lower rectal tumor. Oncol Lett. (2017) 14:4142–50. doi: 10.3892/ol.2017.6664

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Kuo LJ, Ngu JC, Huang YJ, Lin YK, Chen CC, Tong YS, et al. Anorectal complications after robotic intersphincteric resection for low rectal cancer. Surg Endosc. (2017) 31:4466–71. doi: 10.1007/s00464-017-5499-8

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Abdel-Gawad W, Zaghloul A, Fakhr I, Sakr M, Shabana A, Lotayef M, et al. Evaluation of the frequency and pattern of local recurrence following intersphincteric resection for ultra-low rectal cancer. J Egypt Natl Canc Inst. (2014) 26:87–92. doi: 10.1016/j.jnci.2014.02.001

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Beppu N, Kimura F, Aihara T, Doi H, Tomita N, Yanagi H, et al. Patterns of local recurrence and oncologic outcomes in T3 low rectal cancer (≤5 cm from the Anal Verge) treated with short-course radiotherapy with delayed surgery : outcomes in T3 low rectal cancer treated with short-course radiotherapy with delayed surgery. Ann Surg Oncol. (2017) 24:219–26.

PubMed Abstract | Google Scholar

21. Shiokawa H, Funahashi K, Kaneko H, Teramoto T. Long-term assessment of anorectal function after extensive resection of the internal anal sphincter for treatment of low-lying rectal cancer near the anus. J Anus Rectum Colon. (2018) 1:29–34. doi: 10.23922/jarc.2016-002

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Yokota M, Ito M, Nishizawa Y, Kobayashi A, Saito N. The impact of anastomotic leakage on anal function following intersphincteric resection. World J Surg. (2017) 41:2168–77. doi: 10.1007/s00268-017-3960-4

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Yu S, Deng J, Luo T, Zhen Z, Ji Y. Study of anorectal dynamics in patients undergoing laparoscopic ultra-low resection and transanal intersphincteric resection for rectal cancer. ANZ J Surg. (2020) 90:2478–83. doi: 10.1111/ans.16077

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Kawada K, Hida K, Hasegawa S, Sakai Y. A comparison of the long-term anorectal function between laparoscopic intersphincteric resection and low anterior resection for low rectal cancer. Surg Today. (2018) 48:921–7. doi: 10.1007/s00595-018-1669-0

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Denost Q, Laurent C, Capdepont M, Zerbib F, Rullier E. Risk factors for fecal incontinence after intersphincteric resection for rectal cancer. Dis Colon Rectum. (2011) 54:963–8. doi: 10.1097/DCR.0b013e31821d3677

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Chamlou R, Parc Y, Simon T, Bennis M, Dehni N, Parc R, et al. Long-term results of intersphincteric resection for low rectal cancer. Ann Surg. (2007) 246:916–21; discussion 921–2. doi: 10.1097/SLA.0b013e31815c29ff

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: anorectal dysfunction, intersphincteric resection, risk factors, preoperative chemoradiation, low rectal cancer

Citation: Min L, Fan Z, Zhi W, Pingang L, Lijuan X, Min D, Yan W, Xiaosong W and Bo T (2021) Risk Factors for Anorectal Dysfunction After Interspincteric Resection in Patients With Low Rectal Cancer. Front. Surg. 8:727694. doi: 10.3389/fsurg.2021.727694

Received: 19 June 2021; Accepted: 17 September 2021;
Published: 25 October 2021.

Edited by:

Niccolo Petrucciani, Sapienza University of Rome, Italy

Reviewed by:

Jianhua Ding, The Characteristic Medical Center of PLA Rocket Force, China
Gaetano Luglio, University of Naples Federico II, Italy

Copyright © 2021 Min, Fan, Zhi, Pingang, Lijuan, Min, Yan, Xiaosong and Bo. 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: Wang Xiaosong, wxs1515@163.com; Tang Bo, tangtbo@sina.cn

These authors have contributed equally to this work

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.