Page 13 - Read Online
P. 13

Thomas et al. Mini-invasive Surg 2018;2:17  I  http://dx.doi.org/10.20517/2574-1225.2018.25                                      Page 5 of 7

               of using an evidence-based strategy that is tailored to the individual patient. In patients in whom we
               can confidently predict favourable T1 disease we would offer local excision, either by TEM or standard
               transanal excision as appropriate, or radical resection. In patients who opt for local excision and have
               pT1 disease with unfavourable histology, then we would offer adjuvant LCCRT in addition to standard
               radical resection. For pT2 disease and above, oncological options are compromised, and we would strongly
               recommend completion radical surgery. In patients with cT1/T2 disease that appears amenable to local
               excision, we offer the options of neoadjuvant therapy prior to LE or conventional resection. If patients elect
               to undergo neoadjuvant therapy and local excision, then we undertake a detailed assessment of treatment
               response using endoscopy, colonoscopic EUS and MRI prior to surgery. If a cCR is demonstrated, then
               we will operate a watchful waiting policy in selected cases. Where a significant partial response or near-
               cCR has been obtained, then we would proceed to local excision. This also gives us the option to offer
               completion radical surgery if there has been minimal tumour regression or the disease has progressed
               despite neoadjuvant treatment.

               While the STAR-TREC trial aims to compare differing neoadjuvant regimens with radical surgery in early
                                  [38]
               rectal cancer (T1-T3a) , a direct comparison of neoadjuvant and local excision versus local excision and
               adjuvant therapy has never been compared in a prospective study. It is possible that this debate may never
               been resolved with randomized controlled trials owing to the complexity in study design. It is likely that
               the neoadjuvant vs. adjuvant debate may only be answered with the use of large scale prospective registries.
               The management of early rectal cancer that combines local excision techniques with neoajuvant/adjuvant
               therapy is an evolving area of practice and we await the results of future studies with interest.


               In patients with pT2 disease with unfavourable histology or pT3 disease not breaching the mesorectal
               resection margin (based on MRI) we offer conventional laparoscopic or open anterior resection with or
               without short course radiotherapy. In patients with more advanced disease our preference is to routinely
               offer pre-operative CRT followed by surgery in 3-6 months. Indeed, we are moving towards at least 3
               months following CRT after post-operative re staging. In patients with low disease not suitable for anterior
               resection or local excision we favour extralevator abdominoperineal excision with immediate biologic
               mesh reconstruction of the pelvic inlet augmented by the use of myocutaneous flaps where indicated [39,40] .
               Our use of myocutaneous flaps has evolved over the last 10 years and we have recently found that bilateral
               gluteal advancement flaps provide excellent healing and quality of life (unpublished data, Thomas, Warr,
               Longman, Messenger).


               DECLARATIONS
               Authors’ contributions
               Clinical and scientific data: Thomas MG, Messenger DE, Gash K
               Systematic review data: Thomas MG, Messenger DE
               Manuscript preparation: Thomas MG, Messenger DE, Gash K

               Availability of data and materials
               Not applicable.

               Financial support and sponsorship
               The study was supported by Fulbright Scholarship, Above and Beyond Research Trust, David Telling
               Trust, RCS research Scholership, Bristol Cancer Research UK 5 year programme grant, and John James
               Foundation Bristol.


               Conflicts of interest
               All authors declare that there are no conflicts of interest.
   8   9   10   11   12   13   14   15   16   17   18