Abdominoperineal excision or extralevator abdominoperineal excision: which is the best oncological treatment?
Introduction
In tumors of the lower third of the rectum, surgical technique is particularly difficult due to the complex anatomy of the pelvis where the mesorectum tapers at the origin of the levators and can lead to an incomplete radical resection (1). There is a maximum area of surgical narrowing at 3–4 cm above the anal verge where the perineal and abdominal phases of the abdominoperineal excision (APE) usually meet. APE can increase rates of circumferential resection margin infiltration and iatrogenic tumor perforation. When compared with low anterior resection of the rectum, APE has been related with a worse quality of the mesorectum probably due to the conicity induced during surgery while dissection between both distal mesorectum and levatorani planes is performed (2-4). APE is performed in 25–30% of patients with rectal cancer, with a significant morbidity that reaches 40% (5).
In 2007, Holm described a new technique for patients with low rectal cancer when abdominal perineal excision was indicated. This modified approach consisted of a broader resection of the pelvic floor muscles, called extralevator abdominoperineal excision (ELAPE) (6). In theory, a specimen cylindrically shaped obtained with an ELAPE would reduce the risk of infiltration of the circumferential resection margin (CRM) and tumor perforation incidence improving oncological results, including local recurrence (2,7).
The present review focuses on the analysis of the published scientific evidence on which of the two techniques, APE or ELAPE, is the best oncological treatment. Overall survival and progression-free survival, local recurrence and quality of mesorectal excision have been analyzed, as well as postoperative complications and quality of life. Other aspects considered were the position of the patient for the operation and open vs. laparoscopic approach.
PubMed database were searched for publications comparing APE vs. ELAPE for rectal cancer of the last 5 years (between 2012 and 2018). In addition, relevant articles involved in the description of both techniques have been also included.
Indications and surgical technique
A proper definition of rectal cancer is important to plan the best oncological treatment, including neoadjuvant therapy and surgical strategy. “Low” rectal cancer is currently defined as an MRI-based anatomical definition of an adenocarcinoma with its lower edge, at or below the origin of the levators at the pelvic side-wall, which is commonly located within 6 cm of the anal verge (8). The origin of the definition has been adopted from the Low Rectal Cancer Development Program (LOREC) and accepted by the most recent Guidelines (2,8,9).
In order to achieve a total mesorectal excision (TME), the operative strategy should be tailored to individual patients (10). For low rectal cancer lying above the level of the anal sphincter more than one millimeter of the levator muscle or mesorectal fascia, a TME and coloanal anastomosis may be feasible. In the presence of contraindications, an APE (conventional or intersphincteric) should be performed (8). Likewise, if the tumour is lying at the level of the sphincter involving the submucosa only or the inner layer of the muscularis propria, the mesorectal plane can be dissected, continuing inferiorly into the intersphincteric plane as an APE (conventional or intersphincteric). On the other hand, a low rectal cancer situated over the anal sphincter, which is less than one millimeter from the levator muscle or mesorectal fascia or invading the levator, or lying at the level of the sphincter involving the entire broadness of the muscularis propria or extending into or beyond the intersphincteric plane to involve the external sphincter, an APE should be performed (8,11).
APE technique comprises a dissection on TME plane to the prostate in men or below the cervix in women and the resection of the anus and distal rectum performing a perineal procedure (2). The circular external sphincter is closed primarily with suture, with resulting superior healing rates in most patients, even in those who have had preoperative therapy (8). ELAPE is initially performed via an abdominal approach. Limits of the TME are under the vesicles in men and cervix in women anteriorly, the uppermost part of the coccyx posteriorly, and under the autonomic nerves laterally. Thereafter, for the perineal phase the patient might remain in supine position or turned to a prone position. Depending on the tumor infiltration, the perianal incision can be made at the lateral margin of the external anal sphincter or wider and continue the dissection in the ischioanal fossa to the insertion of the pelvic floor muscles. The disarticulation of the coccyx might be necessary for a total excision. As a result of a wider excision, it results in a larger perineal defect and reconstructions of this defect haven been proposed such as surgical flap (biological graft, rectus abdominis or gluteus maximus myocutaneous flap) or biological mesh (2,8). A tailored ELAPE approach consisting of unilateral or bilateral excision based on clinical examination and MRI imaging has been proposed in order to reduce morbidity (8).
ELAPE technique can be performed both prone and supine position. It is discussed which one is best for optimal dissection during the perineal phase. Comparing prone ELAPE to supine ELAPE, the prone position provides greatly pelvic exposure allowing a top-down dissection under excellent visualization of the plane between the rectum and the prostate or vagina, and direct vision which is more comfortable for the operating surgeons and so facilitates training, but requires turning the patient during the operation (12). Nevertheless, there is no evidence of better oncologic results or less morbidity and mortality in prone position (3). For this reason, it may also be adequate to complete the surgery in the supine Lloyd-Davis position (8). A recent survey to the membership of the Association of Coloproctology of Great Britain and Ireland (ACPGBI) showed that most of the surgeons (67%) perform perineal phase in the supine position (13).
If we compare laparoscopic vs. open approach for the abdominal phase of ELAPE, laparoscopy seems to be the best surgical approach, although it has not been demonstrated by large prospective studies so far (3,14,15).
Postoperative complications
Different studies have described and compared the postoperative complications of APE and ELAPE. It is also believed that ELAPE might cause higher morbidity rates due to the final larger perineal defect (12). The most recent meta-analysis published in 2017 by Chen et al. (16) included high quality clinical studies (11 observational studies and one randomized controlled trial) comparing the APE and ELAPE between 2007 and 2016 and analyzed intraoperative perforation rate, CRM involvement, local recurrence rate and perineal wound complications. Regarding perineal wound complications, there were no significant differences between both groups [risk ratio (RR) =0.94, P=0.8)].
A different meta-analysis published in 2016 by Negoi et al. included one randomized controlled trial and 10 nonrandomized studies that compared ELAPE with conventional APE (7). As for the postoperative complications, the results showed less blood loss in ELAPE patients. A propensity case-matched analysis performed by Ortiz et al. (2) comparing APE and ELAPE postoperative overall morbidity incidence (including surgical-site infection, perineal wound problems, urinary infections, respiratory and heart complications) did not find differences between both techniques in term of postoperative complication rates (52.3% vs. 48.1%; P=0.209), need for reoperation (7.7% vs. 7.0%; P=0.703), perineal wound problems (26.0% vs. 21.9%; P=0.141) and postoperative mortality rate (2.0% vs. 2.0%; P=1.000). Similarly, Han et al., in a randomized clinical trial, did not find differences between APE and ELAPE approaches in terms of sexual dysfunction, urinary retention, peristomal hernia, and perineal wound complications (17). Another prospective controlled study published in 2015 by Shen et al. comparing the safety and oncological outcomes of conventional APE vs. ELAPE, showed lower rates of blood loss (P=0.021) and perineal wound complication (P=0.039) in ELAPE (18). In relation to urinary function, sexual function and quality of life there were no statistical difference between both groups in this last study.
Wang et al. (19) have reported high rate of sexual dysfunction, perineal complications and urinary retention among patients that underwent ELAPE for primary locally advanced low rectal cancer (40.5%, 23.5% and 18.6% respectively). In addition, 13.7% of the included patients presented chronic perineal pain. Reconstruction of pelvic floor with biologic mesh was associated with lower rate of perineal dehiscence and overall perineal wound complications compared with primary closure.
In summary, according to the current evidence, relevant differences have been not observed between APE and ELAPE in terms of postoperative complications including perineal wound complications, surgical-site infection, urinary infections, respiratory and heart complications, need for reoperation and postoperative mortality rate. It seems to be less blood loss in ELAPE patients (7,20).
Quality of mesorectum
According to the latest recommendations and in order to describe if it is involved by the tumor, after an APE, it is mandatory for the pathologist to analyse the margin of the circumferential resection of the not peritonealized rectum (8). It can be scored in three grades: mesorectal (complete), intramesorectal (nearly complete) and muscular (incomplete). The mesorectal plane implies no affectation of the fascial covering, with no cones in the distal margin and no defects more than 5 mm deep. Intramesorectal grade admits a moderate degree of coning towards the distal margin, but no visible muscle except in the area of insertion of the levator muscles. In the muscularis propria grade, it might be substantial areas where the mesorectal tissue is missing with deep cuts and tear the muscularis propria (8).
Likewise, an excision plane of the sphincter is recorded after APE in three grades: extractor, sphincter and intrasphincteric-submucosa-perforation. In the extractor grade the surgical plane is located outside the levatorani muscles, which are removed in bloc with the mesorectum and the anal canal, creating a more cylindrical sample. In the sphincter grade either there is no levator muscles attached to the sample or just a very small cuff with the CRM formed by the surface of the sphincter muscles. Moreover, the specimen shows conicity at the puborectal muscle level that results in the classic surgical waist. Other dissections entering the sphincter muscle or into the submucosa or perforations should be classified separately (8).
The number of lymph nodes recovered should be a median of at least 12 per specimen. The involvement of CRM ≤1 mm is associated with a bad prognosis and should be recorded routinely (8).
Oncological results
ELAPE technique involves a wider tissue removal and, as some studies have showed, also a reduction in CRM involvement or intraoperative perforation (12). Chen et al. describe lower intraoperative perforation rate of ELAPE than APE (RR =0.52, P=0.002), without significant differences of CRM involvement (RR =0.72, P=0.10) and local recurrence rate [(odds ratio (OR) =0.55, P=0.17)] (16). Negoi et al. describe similar results concluding that ELAPE significantly lessens the intraoperative perforation incidence, with no benefits in regard to CRM infiltration and local recurrence rate (7). The Spanish study did not find either differences between APE and ELAPE in terms of CRM involvement (13.1% vs. 13.6%; P=0.846), intraoperative tumor perforation (7.9% vs. 7.7%; P=0.902) and local recurrence rate at 2 years (2.7% vs. 5.6%; P=0.664) (2). Similarly, Zhou et al. published a meta-analysis in 2015 and did not find differences in those criteria either (20).
Nevertheless, other authors showed lower intraoperative perforation rate and local recurrence in ELAPE compared to conventional APE, with greater CRM involvement in the conventional APE group without statistical significance (18). Moreover, overall survival and progression-free survival were similar between groups, even after that survival was analyzed according to TNM stage, T stage, N stage, and with or without neoadjuvant chemoradiotherapy.
Other authors found that ELAPE for low rectal cancer, performed in the prone position, is associated with a reduction in CRM infiltration, intraoperative perforations, and local recurrence (19). Similarly, Han et al. showed improvement in terms of local recurrence with a median follow-up time of 29 months in the ELAPE group and 22 months in the APE group (17). However, no significant differences in overall survival and disease-free survival were observed.
According to our findings and even though there are some publications recording a possible benefit in terms of reduction in CRM infiltration, iatrogenic perforations or local recurrence (Table 1), there is not enough evidence to affirm that the ELAPE leads to better oncological results when compared to conventional APE (21-24).
Table 1
Author | Year | Study type | Surgery (ELAPE/APE) | Intraoperative perforation rate | CRM infiltration | Local recurrence | Overall complications |
---|---|---|---|---|---|---|---|
Chen et al. (16) | 2017 | Meta-analysis | 2,141/1,647 | 0.52 (0.34–0.79); 0.002* | 0.72 (0.49–1.07); 0.10* | 0.55 (0.24–1.29); 0.17* | 0.94 (0.58–1.53); 0.8*‡ |
Wang et al. (21) | 2017 | Meta-analysis | 1,802/1,376 | 0.54 (0.31–0.93); 0.03* | 0.55 (0.28–1.06); 0.07* | 0.30 (0.21–0.42); <0.00001* | – |
Negoi et al. (7) | 2016 | Meta-analysis | 1,736/1,320 | 0.39 (0.22–0.68); <0.01# | 0.58 (0.31–1.09); 0.09# | 0.43 (0.13–1.42); 0.17# | 1.01 (0.85–1.21); 0.89+ |
Zhou et al. (20) | 2015 | Meta-analysis | 1,531/1,141 | 0.79 (0.40–1.57); 0.5* | 0.61 (0.37–1.00); 0.05* | – | 0.91 (0.71–1.16); 0.44* |
Shen et al. (18) | 2015 | Observational | 36/33 | 5.6 vs. 21.2; 0.028† | 4 vs. 12; 0.297† | 0 vs. 15.1; 0.034† | 33.3 vs. 33.3; 1.00† |
Ortiz et al. (4) | 2014 | Observational | 457/457 | 7.7 vs. 7.9; 0.902† | 13.6 vs. 13.1; 0.846† | 5.6 vs. 2.7; 0.664† | 48.1 vs. 52.3; 0.209† |
Prytz et al. (22) | 2016 | Observational | 518/209 | 8 vs. 11; 0.19† | 6 vs. 10; 0.12† | 4.91 (1.53–15.74); 0.007* | 45.9 vs. 41.6; 0.32† |
Klein et al. (23) | 2015 | Observational | 301/253 | 2 vs. 3, 0.28† | 2.59 (1.31–5.12); 0.006* | – | 11 vs. 10; 0.51† |
Han et al. (17) | 2012 | RCT | 35/32 | 5.7 vs. 15.6, 0.246† | 5.7 vs. 28.1; 0.013† | 2.8 vs. 18.8; 0.048† | 51 vs. 59; 0.515† |
West et al. (12) | 2010 | Observational | 176/124 | 4.21 (1.69, 10.50); <0.001# | 4.66 (1.89–11.47); <0.001# | – | 38 vs. 20; 0.019†‡ |
*, RR, 95% CI, P values; #, OR, 95% CI, P values; †, percentage, P values; ‡, only perineal wound complications. ELAPE, extralevator abdominoperineal excision; APE, abdominoperineal excision; RCT, randomized controlled trial; CRM, circumferential resection margin. Risk Ratio Odds Ratio
Conclusions
Several studies comparing APE and ELAPE approaches in patients with distal rectal cancer have been published. Nevertheless, when high-level quality studies are considered, differences between both techniques in terms of oncological results and postoperative complications are not evident. Further prospective, controlled and randomized studies are needed to conclude which of the two techniques is the most appropriate oncological treatment.
Acknowledgments
Funding: None.
Footnote
Provenance and Peer Review: This article was commissioned by the Guest Editors (Eduardo Ma Targarona and Andrea Balla) for the series “Rectal Cancer” published in Annals of Laparoscopic and Endoscopic Surgery. The article has undergone external peer review.
Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/ales.2018.04.03). The series “Rectal Cancer” was commissioned by the editorial office without any funding or sponsorship. The authors have no other conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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Cite this article as: Serrano M, Biondo S. Abdominoperineal excision or extralevator abdominoperineal excision: which is the best oncological treatment? Ann Laparosc Endosc Surg 2018;3:33.