Part 1 - Surgical management
by Katie Armstrong, Dianne O'Connell, David Leong, Allan Spigelman, Bruce Armstrong
The Cancer Council NSW, The University Of Newcastle
April 2004
Contents
Summary 
Summary, Background, Coverage, Aim, Scope of this report, Data Quality
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Results [
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Characteristics of patients studied
Characteristics of patients' cancer
Caseloads of surveyed surgeons
Characteristics of treating institutions
Clinical presentation
Pre-treatment investigations for diagnosis and staging
Preparation for surgery
Initial surgical management
Surgery for primary colon cancer
Surgery for rectal cancer
Emergency surgery
Surgical complications
Use of chemotherapy and radiotherapy for colon cancer
Use of chemotherapy and radiotherapy for rectal cancer
Management of locally advanced rectal cancer
Surgery for metastatic colorectal cancer
Participation in clinical trials
Follow-up intentions
Further analyses proposed [
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Appendices
Appendix 1 Surgical Questionnaire [
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Appendices 2 - 5 [
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- Membership of the Expert Advisory Group
- Cancer stage assignment using questionnaire responses
- Classification of hospitals
- References
Summary
The primary aim of the New South Wales (NSW) Colorectal Cancer Care Survey was to determine the proportion of colorectal cancer cases in NSW managed according to recommendations in the National Health and Medical Research Council guidelines (http://www.health.gov.au/nhmrc/publications/pdf/cp62.pdf). These guidelines were released and widely disseminated to practitioners involved in the management of patients with colorectal cancer including surgeons and radiation and medical oncologists in Australia just before the Survey began.
Information was sought from primary treating practitioners regarding their management of patients newly diagnosed with colorectal cancer who were notified to the New South Wales (NSW) Central Cancer Registry between 1 February 2000 and 31 January 2001; 94% of eligible patients ascertained were diagnosed in 2000, 2% in 1999 and 4% in 2001. This report covers initial surgical treatment and referral for chemotherapy and radiotherapy.
Data on surgical treatment were obtained on 3,095 (93%) of 3,314 eligible patients. Assessment of surgical management with reference to the guidelines was limited to 2,914 patients who had only one primary cancer diagnosed and generally also to the 2,810 patients who had some surgical treatment.
Thirty-two of the NHMRC guidelines deal with primary surgical management. Concordance of management with guidelines is summarised below for 18 of the recommendations.
|
NHMRC Guideline |
Management |
Preoperative assessment |
Colonoscopy is the investigation of choice, but air contrast barium enema and sigmoidoscopy is an alternative to colonoscopy. If colonoscopy is incomplete, barium enema must be included. (Level III evidence) |
79% of patients had colonoscopy, 3% had sigmoidoscopy and barium enema and 81% had either or both (Table 17). |
Endorectal ultrasound is more accurate than either CT or MRI for assessing the depth of invasion and lymph node status. It is the preferred initial method of locally staging a rectal cancer preoperatively. While endorectal ultrasound is the most accurate method to preoperatively stage rectal cancer locally, it is not necessarily indicated for all rectal cancers. Its main role will be:
for advanced (T3–4) rectal cancers where neoadjuvant therapy is being considered;
for small cancers in the distal rectum where a local transanal excision may be an alternative to abdomino-perineal excision of the rectum with a permanent colostomy, so accurate assessment of the depth of local tumour invasion and state of the lymph nodes is essential; and
if neoadjuvant chemoradiotherapy or a transanal local excision is planned. (No guideline given; quoted from page 64 of the NHMRC guidelines)
|
61% of patients who underwent surgery for rectal cancer had either CT scanning (59%) or endorectal ultrasound preoperatively (9%). This included: 66% of patients with T3 or T4 rectal cancers (8% had endorectal ultrasound);
89% of patients who had pre-operative radiotherapy (25% had endorectal ultrasound); and 48% of patients who had transanal local excision (18% had endorectal ultrasound) (Table 20). |
Preparation for surgery |
All patients [having elective surgery for rectal cancer] who have a reasonable chance of a postoperative stoma should be informed about this possibility. This includes a visit, where possible, by the stomal therapy nurse. (Expert opinion) |
90% of patients who presented electively and had a stoma created, had been seen by a stomal therapist preoperatively (Table 22). |
Randomised trials do not demonstrate a benefit from routine bowel preparation (Level II evidence). If bowel preparation is to be used, then both polyethylene glycol preparation and sodium phosphate preparations are effective, but polyethylene glycol is more acceptable and has lower postoperative complication rates. (Level II evidence) |
90% of all patients and 96% of patients treated electively had bowel preparation. An oral preparation alone was used in 86% of all patients (Table 23). |
All patients undergoing surgery for colorectal cancer should receive prophylaxis for thromboembolic disease. Unfractionated heparin, low molecular weight heparin, and intermittent calf compression are effective in reducing the incidence of thromboembolism. (Level I evidence) |
98% of patients who had surgery for bowel cancer received heparin (fractionated or unfractionated), intermittent calf compression, or both (Table 24). |
All patients undergoing colorectal cancer surgery require prophylactic antibiotics. (Level I evidence)
A single preoperative dose of intravenous second or third generation cephalosporin and metronidazole is an effective regime. (Level II evidence) |
94% of patients who had surgery for bowel cancer received antibiotics pre-operatively.
A cephalosporin plus imidazole was given to only 28% of patients undergoing surgery (Table 25). 37% of patients who received antibiotic prophylaxis continued this treatment post-operatively (Table 26). |
Elective surgery for colon and rectal cancers |
For fixed tumours, en bloc resection of primary colonic cancer, together with the attached organ or the abdominal wall, should be performed in an attempt to obtain a curative resection. No attempt should be made to assess if the attachment is benign or malignant at the time of surgery. (Expert opinion) |
72% of patients who had a tumour that was adherent to adjacent structures, had this removed en bloc (Table 31). |
Bilateral oophorectomy should be performed if there is obvious malignant disease of one or both ovaries. Prophylactic bilateral oophorectomy for colon cancer cannot be supported by the available evidence. (Expert opinion) |
5% of women who had surgery for colon cancer had an oophorectomy performed as part of the primary surgical procedure. This procedure was performed with prophylactic intent for 2% (Table 33). |
Elective surgery for rectal cancer only |
Total excision of distal mesorectum beyond the transection of the rectal wall is not recommended as a routine procedure when resecting rectal cancer until more evidence is available to establish its efficacy. (Expert opinion) |
23% of patients who underwent surgery for rectal cancer (excluding the rectosigmoid) did not have the mesorectum completely excised (Table 37). |
Local excision of T1 rectal cancer is effective. (Level III evidence) |
2.9% of rectal cancer patients underwent local excision, of whom 69% had a T1 tumour (Table 39). 10% of T1 rectal cancers were locally excised. |
Sphincter-saving operations should be preferred to abdomino-perineal resection except in the presence of:
low-level infiltrating tumours with unfavourable histological grade;
tumours such that adequate distal clearance (>2 cm) cannot be achieved (often an operative decision);
the sphincter mechanism is not adequate for continence;
access to the pelvis makes restoration technically impossible (rare).
(Level III evidence) |
Sphincter-conserving surgery was achieved for 70% of patients who had surgery for rectal cancer. This figure was 90% for patients with tumours of the upper and middle thirds of the rectum, and 45% for patients with tumours of the lower third (Table 40). |
Where technically feasible, the colonic pouch may be the preferred form of reconstruction after low anterior resection of tumours of the lower half of the rectum to improve short-term postoperative neorectal function. The ideal length of the pouch lies between 5 cm and 8 cm. (Level II evidence) |
57% of patients who had sphincter preserving surgery for rectal cancer (excluding the rectosigmoid) had a colonic pouch constructed. For patients who had a pouch constructed, the length was between 5cm and 8cm for 83% (Table 41). |
Referral for chemotherapy and radiotherapy |
People with resected node-positive colon cancer should be offered adjuvant therapy. (Level I evidence) |
59% of patients who had resection for a node-positive bowel cancer received adjuvant chemotherapy; another 16% were considered for the treatment, but did not receive it (Table 46). |
Postoperative 5-FU based chemotherapy and radiotherapy (combined modality therapy) is recommended for patients with high-risk rectal cancer. (Level II evidence) |
13% of patients with tumours that had penetrated beyond the full thickness of the bowel wall, or involved regional nodes received post-operative combined modality therapy. However, another 12% of these patients received combined modality therapy based on pre-operative radiotherapy (Table 54). |
Management of locally advanced rectal cancer |
Preoperative radiation therapy, possibly with chemotherapy, is recommended in rectal cancers fixed or tethered within the pelvis if it is felt down-staging will enable successful resection. (Level II evidence) |
6% of patients having surgery for locally advanced (Stage T4) tumours underwent preoperative radiotherapy. Another 20% of patients in the same group had preoperative chemotherapy and radiotherapy (Table 56). |
Surgery for metastatic colorectal cancer |
Patients with up to four lesions that can be safely removed with an adequate margin and have no evidence of extrahepatic disease should be considered for resection. (Level III evidence) |
3% of patients presenting with liver metastases at the time of diagnosis of bowel cancer underwent liver resection concurrent with bowel resection (Table 57). |
Participation in clinical trials |
Doctors should encourage patients with colorectal cancer to consider participating in appropriate clinical trials for which they are eligible. (Expert opinion) |
Between 54% and 77% of patients who were eligible for a trial were offered the opportunity to participate. However only 4%-8% of all patients in this survey participated in a trial (Figure 1). |
Follow-up intentions |
All patients who have undergone surgery for colorectal cancer should have specialist follow up in conjunction with the patient's general practitioner. (Expert opinion) |
For 73% to 94% of patients who had had curative surgery, their surgeon intended to be involved in their follow-up (Table 59). |
There was high concordance between surgical practice for colorectal cancer in NSW in 2000 and major elements of the NHMRC guidelines – preoperative colonoscopic investigation, preoperative referral for stomal therapy when a stoma is likely, prophylaxis against thromboembolic disease, antibiotic prophylaxis, avoidance of prophylactic oophorectomy, and sphincter saving surgery for rectal cancer.
On the other hand, most patients had preoperative bowel preparation despite Level II evidence that it is not beneficial and a significant minority of patients (35%) continued on prophylactic antibiotics into the postoperative period despite Level II evidence that a single preoperative dose is sufficient.
There was evidence too of poorer concordance between practice and the guidelines in areas where recommended practice has changed in recent times. Few patients with T1 rectal cancer had local excision; although there is only Level III evidence in support of this practice. Only seventy five percent of patients with resected node positive colon cancer were offered adjuvant chemotherapy, which is supported by Level I evidence, and only 25% of patients with high risk rectal cancer had combined treatment with chemotherapy and radiotherapy, for which there is Level II evidence.
Taken as a whole, these findings suggest there is generally a high degree of conformity between the surgical treatment of colorectal cancer and well established, evidence-based practice; whereas conformity is less, sometimes much less, with recommended practices for which the evidence is more recent, particularly if the evidence is not deemed to be Level I.
More effective and rapid uptake of evidence into colorectal surgical practice might be achieved by regular review and updating of the NHMRC guidelines. This should be supported by more organised and active steps of professional organisations, health services and the new NSW Cancer Institute to ensure that guidelines are communicated to surgeons in ways that have been shown to influence practice.
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To obtain a copy of this report contact Cancer Epidemiology Research Unit,
The Cancer Council NSW email: crrd@nswcc.org.au