Rectal Cancer Clinical Trial
Official title:
Treatment of AnastomotiC Leakage After Rectal Cancer Resection. TENTACLE Rectum Study
The TENTACLE: Rectum study is a multinational retrospective cohort study that includes
patients with anastomotic leakage after rectal cancer resection.
The study aims to develop an anastomotic leakage severity score and to evaluate the efficacy
of different treatments of anastomotic leakage.
Rationale:
Anastomotic leakage occurs in up to 20% after low anterior resection for rectal cancer. It is
a severe complication with high associated morbidity, ICU admission, prolonged hospital stay
and need for reinterventions and readmissions. Anastomotic leakage is independently
associated with the risk of local recurrence and reduced long term survival. Most literature
focusses on incidence and predictive factors. Remarkably, there is almost no data on the
efficiency of different treatments of anastomotic leakage after low anterior resection.
Anastomotic leakage after rectal cancer resection is generally underreported, mainly due to
subclinical leaks below a diverting stoma. However, up to 50% of the leaks do not heal with
fecal diversion alone, especially not in an irradiated field, related to a competent
sphincter which hampers adequate drainage of the presacral abscess. Late diagnosis of
'reactivated' leaks after stoma reversal is not an infrequent phenomenon. Chronic sinus,
gluteal abscess, and fistula formation have been reported in up to 10%, and permanent stoma
rates around 20%, both having significant impact on quality of life.
Examples of factors that may influence the severity and chance of healing of the anastomotic
leakage are: timing of diagnosis, degree of systemic inflammatory response, etiology (e.g.
ischemia of the afferent loop), degree of dehiscence and retraction, location of the leak
(e.g. circular staple line, blind loop), whether or not a diverting stoma is in place, and
extent of abdominal contamination. However, little is known about to what extent these and
other factors contribute to anastomotic leakage severity and chance of healing. In addition,
it is not known which anastomoses are likely to be preserved by which type of treatment, and
which anastomotic failures require redo surgery at a certain time frame.
Primary study objectives
1. To investigate which factors contribute to anastomotic leakage severity and to compose
an evidence based anastomotic leakage severity score, in which clinically relevant
subgroups will be explored (e.g. diversion or not), as well as different clinical
settings (e.g. leak diagnosis within or beyond 90 days postoperatively).
2. To evaluate the effects of different treatment approaches on all different pre-specified
outcome parameters, stratified for severity score, anatomical characteristics of
leakages and timing of diagnosis of leakage.
Study design:
International multicenter retrospective cohort study.
Study population:
Adult patients with anastomotic leakage after low anterior resection for rectal cancer.
Primary outcome parameter:
1-year stoma-free survival.
Secondary outcome parameters:
ICU length of stay, mortality, comprehensive complications index, total number of
reinterventions (surgical, radiological, endoscopic) within one year, total number of
unplanned readmissions within one year, total hospital stay during one year, total time of
having a stoma until one year, stoma present at one year, type of stoma present at one year
(diverting, permanent), secondary leakage related complications (extrapelvic abscess,
cutaneous fistula, vaginal fistula, bladder fistula, small bowel, ureteric fibrosis with
hydronephrosis), hospital related costs.
Sample size calculation:
Inclusion of 980 patients will be sufficient to analyze primary study objective 1 and this is
1246 patients for primary study objective 2. Therefore, the aim is to include at least 1246
patients.
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