In recent years, concerns have arisen regarding the poorer outcomes of patients undergoing abdominoperineal excision (APE), compared with those having total mesorectal excision (TME). This was attributed to higher rates of involved circumferential resection margins (CRMs) and tumour perforations after APE, and was thought to have occurred due to adherence of the TME plane to the puborectalis sling. This apparent disparity was addressed by the re-introduction of a more radical approach to APE surgery, which closely mirrored the operation described by Miles [1]. The procedure, extra-levator abdominoperineal excision (ELAPE), entails a more extensive, wider perineal dissection down to the origin of the levators. Several retrospective studies have reported a reduction in rates of CRM positivity and intraoperative perforation with ELAPE, compared with standard APE (SAPE). Each of these histopathological findings is deemed a crucial marker in determining prognosis for low rectal cancer. Thus, pathological assessment of the resected specimen, as a surrogate marker of oncological superiority, can also be used as a surrogate marker for long-term outcome. Although the loco-regional clearance obtained by ELAPE may be superior to SAPE, the substantial perineal defect, which is often too large for primary closure, can result in delayed wound healing and perineal herniation. Asplund [2] compared outcomes for 158 patients with low rectal cancer, half of whom underwent SAPE and half ELAPE. No advantage for ELAPE was shown, in terms of local recurrence, intraoperative perforation and CRM positivity, but higher rates of perineal wound complications were reported. This is in contradiction to other studies demonstrating higher rates of CRM positivity and intraoperative perforations with SAPE. Having adopted the ELAPE technique (performed with the patient in the prone position), we sought to ascertain whether the wider cylindrical dissection offers any oncological advantage over SAPE, through comparing the pathological findings of our resected specimens. We studied 34 consecutive patients who underwent APE: 17 underwent SAPE and 17 ELAPE. The results are outlined in Table 1. There was no difference in patient demographics or tumour T stage between the two groups. Similar proportions of patients in each group had received preoperative radiotherapy, ELAPE: 71 % (12) and SAPE: 88 % (15) (p = 0.40). The mean distance to the CRM did not differ between groups, ELAPE: 6.5 mm and SAPE: 5.8 mm (p = 0.80), nor did the R0 resection rate, ELAPE: 82 % (14) SAPE: 71 % (12) (p = 0.69). There was 1 intraoperative tumour perforation in the ELAPE group (6 %), and 2 (12 %) of the SAPE specimens were perforated (p = 1.00). Comparable mean numbers of lymph nodes were harvested (ELAPE: 8.9 and SAPE: 8.6) (p = 0.90). Throughout the period, that ELAPE was performed tumour perforation, and R1 or 2 resections occurred sporadically and did not correlate with a perceived learning curve. We have not detected any difference in short-term surrogate markers for oncological outcome between ELAPE and SAPE. Our numbers are small; however, the results mirror those of Asplund et al. [2] who reported a specimen perforation rate of 13 % (ELAPE) versus 10 % (SAPE), and CRM positivity of 17 and 20 %, respectively. The Asplund study failed to find any oncological advantage of K. J. Gash (&) L. Cooper N. Smart R. Longman M. Thomas University Hospitals Bristol NHS Foundation Trust, Bristol BS2 8HW, UK e-mail: kat_jg@hotmail.com
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