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Colonic stents in the palliation of colorectal
cancer
Peter Carne, Greg Robertson and Frank Frizelle
Traditional surgical palliation of a patient with
non-resectable metastatic (stage 4) colorectal adenocarcinoma utilises major
surgery and its associated morbidity and mortality in order to provide
symptomatic relief and attempt to increase life expectancy. Patients with
widespread peritoneal carcinomatosis may not be amenable to any form of
palliative surgery due to the extensive nature of their disease and undergo an
‘open-and-close’ laparotomy. Such major surgery in a group of
patients with widespread malignancy, who may also be nutritionally deplete and
elderly, is associated with significant morbidity (5–50%) and mortality
(5–25%). These may be even greater in the setting of ascites or jaundice
that may accompany large-volume liver metastases. Whether or not resection of
the primary tumour improves survival is not entirely clear from the literature,
though intuitively one would suspect that the systemic disease is the limiting
factor in survival rather than the resection itself. The introduction of
self-expanding, metallic endoluminal colonic stents has broadened the palliative
armamentarium available to the physician treating this group of
patients.
A recent review article has shown that stents can be placed
with a morbidity and mortality less than those of traditional open
surgery.1 Re-obstruction due to tumour ingrowth
occurred in only 6% of patients. Stent migration rates were also low at 10%.
Repeat stenting can be performed should either of these complications occur. The
procedure is well tolerated, can be performed under sedation, and usually
requires little more than an overnight hospital stay. The avoidance of a stoma
is another benefit for the patient. Modern algorithms for palliation of
non-resectable metastatic colorectal cancer include the use of
stents;2,3 however, other than case reports and
small case series, objective data on their use for this indication are still
evolving.
A recent study from the Royal Marsden Hospital has also
suggested that the overall incidence of intestinal complications (haemorrhage,
obstruction, peritonitis and fistula formation) related to the primary
colorectal tumour in the setting of non-resectable metastatic disease is no
different when patients are treated with chemotherapy alone compared with
surgery followed by chemotherapy.4 This study
questions further the role of surgery in this group of patients with incurable
disease.
The median survival in a patient with incurable colorectal
cancer is 8 months.5 On average, palliative
chemotherapy adds a median of 3.7 months of life to the patient’s
survival.5 Furthermore, as the
treatment-related toxicity and quality-of-life benefits from chemotherapy in
this group of patients are poorly studied,5 the
decision to have chemotherapy is one that can be made only by the individual
patient, and it can not be recommended universally.
So when should a palliative stent be placed? The most
important factor in determining whether or not a stent should be placed as a
definitive procedure is ensuring that the patient does not have potentially
resectable metastatic disease. Appropriate staging investigations need to be
performed and specialist surgical consultation should be sought according to the
site of metastases. Should both the primary and metastatic disease be
resectable, and the patient a suitable candidate, curative surgery should be
considered. A stent should not normally be placed in this instance as a
definitive measure. The role of stents as a bridge to single-stage surgery in
obstructing tumours is another evolving area.
We recommend the placement of stents in patients with
non-resectable metastatic disease and symptomatic tumours; either acutely
obstructing or if the patient has obstructive symptoms. Generally, we have found
that if the passage of the colonoscope is not possible through the tumour a
stent should be placed. If the lumen is greater than this, obstructive symptoms
are unlikely and the stent is also unlikely to maintain its position. The
presence of low rectal tumours, where a deployed stent will impinge on the anal
canal, also contraindicates their use. Clearly, the risks and benefits of, and
alternatives to, both endoluminal stenting and open surgery need to be fully
discussed with the patient and a mutually acceptable management plan
formulated.
At this time there has been no prospective, randomized
controlled trial published that compares stents to traditional surgery for this
group of patients. What little information has been published is limited and
uses retrospective controls.6 We have found
that the procedure has low morbidity and mortality, the hospital stay is short,
the potential need for a stoma is almost eliminated, and that there also appears
to be no difference in survival when compared with traditional surgical
palliation.6 A prospective randomized trial is
needed though unlikely to be performed. We find that almost all patients, when
presented with the options available, will choose the placement of a
stent.
Palliative intervention in patients with non-resectable
metastatic colorectal adenocarcinoma should provide the greatest symptomatic
relief with minimal morbidity and mortality. Endoluminal stenting provides
another means of achieving this goal in a group of patients whose life
expectancy is short and need for quality of life high.
Author information:
Peter WG Carne, Colorectal Fellow; Greg Robertson, Colorectal Surgeon; Frank A
Frizelle, Professor of Colorectal Surgery, Colorectal Unit, Department of
Surgery, Christchurch Hospital, Christchurch
Correspondence:
Professor Frank A Frizelle, Colorectal Unit, Department of Surgery, Christchurch
Hospital, Private Bag 4710, Christchurch. Fax: (03) 364 0352; email: frank.frizelle@chmeds.ac.nz
References:
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