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Cameron
Platell, Daniel Lim, Nazreen Tajudeen, Ji-Li Tan, Karen Wong, Department
of Surgery, University of Western Australia, Fremantle Hospital, Australia
Correspondence to: Cameron Platell, Associate Professor, University
Department of Surgery, Fremantle Hospital, PO Box 480, Fremantle, 6160,
Australia. cplatell@cyllene.uwa.edu.au
Telephone: +61-8-94312500
Fax: +61-8-94312623
Received: 2003-01-04 Accepted:
2003-01-17
Abstract
AIM: To perform a review of patients with colorectal cancer to a community
hospital and to compare the risk-adjusted survival between patients
managed in general surgical units versus a colorectal unit.
METHODS:
The study evaluated all patients with colorectal cancer referred to either
general surgical units or a colorectal unit from 1/1996 to 6/2001. These
results were compared to a historical control group treated within general
surgical units at the same hospital from 1/1989 to 12/1994. A Kaplan-Meier
survival analysis compared the overall survivals (all-cause mortality)
between the groups. A Cox proportional hazards model was used to determine
the influence of a number of independent variables on survival. These
variables included age, ASA score, disease stage, emergency surgery,
adjuvant chemotherapy and/or radiotherapy, disease location, and surgical
unit.
RESULTS:
There were 974 patients involved in this study. There were no significant
differences in the demographic details for the three groups. Patients in
the colorectal group were more likely to have rectal cancer and Stage I
cancers, and less likely to have Stage II cancers. Patients treated in the
colorectal group had a significantly higher overall 5-year survival when
compared with the general surgical group and the historical control group
(56 % versus 45 % and 40 % respectively, P<0.01). Survival regression
analysis identified age, ASA score, disease stage, adjuvant chemotherapy,
and treatment in a colorectal unit (Hazards ratio: 0.67; 95 % CI: 0.53 to
0.84, P =0.0005), as significant independent predictors of survival.
CONCLUSION:
The results suggest that there may be a survival advantage for patients
with colon and rectal cancers being treated within a specialist colorectal
surgical unit.
Platell
C, Lim D, Tajudeen N, Tan JL, Wong K. Dose surgical sub-specialization
influence survival in patients with colorectal cancer? World J
Gastroenterol 2003; 9(5):
961-964
http://www.wjgnet.com/1007-9327/9/961.asp
INTRODUCTION
The question of who should be performing surgery on patients with
colorectal cancer has important implications for both specialist
colorectal surgeons and general surgeons. This is because it impacts on
not only patient management, but also surgical training and the provision
of surgical services in regional areas.
A significant volume of literature has been
devoted to try and define if sub-specialization benefits patients with
colorectal cancer[1-3]. However, there is currently little
convincing evidence that specialist colorectal surgeons can achieve
superior results when compared to general surgeons. The Australian NHMRC
guidelines for the management of colorectal cancer[4] address
only the issue of who should perform elective rectal cancer surgery. It
states rather enigmatically that "such surgery should be performed by
surgeons who have undergone a period of special exposure to this form of
surgery and who have satisfactory experience in the surgical management of
rectal cancer".
The aim of this study was to determine if
there was a risk-adjusted survival advantage for patients with colorectal
cancer being treated within a specialist colorectal surgical unit when
compared to general surgical units.
MATERIALS
AND METHODS
The
colorectal service was established at Fremantle Hospital in 1996 with the
appointment of a single surgeon who had received accredited training in
colorectal surgery. The management of these patients was standardized
through the use of treatment pathways, and protocols for the use of
adjuvant chemo and/or radiotherapy. All patients referred to the service
with a histologically proven colorectal cancer were prospectively entered
into a designated colorectal computer database (Filemaker Pro 3.0 and 5.0,
Claris) managed by the service. The three general surgical units at the
hospital comprised of 10 different general surgeons who were employed by
the hospital over the study period. All patients referred to these units
with a histologically proven colorectal cancer were prospectively entered
into the general surgical database managed through the Department of
Surgery. A medical student group crosschecked these database entries with
the patients' medical records and pathological records to accurately
determine tumour stage, use of adjuvant therapy, and whether the operation
was an emergency. These data were validated by the author. The study
period was from 1/1/1996 to 1/6/2001. Patients presenting with recurrent
colorectal cancers for management were included in the analysis.
The historical control group consisted of a
cohort of patients with colorectal cancer who had been managed at
Fremantle Hospital from 1/1989 to 12/1994 by a group of 8 general
surgeons. This group of 475 patients had previously been part of a
retrospective analysis performed in 1996 by the author, and the results
published in 1997[5]. In view of the retrospective nature of the data
collection, some areas of information were not collected as accurately as
in the present prospective trial. In particular, the information required
to calculate cancer free survivals was not available. This control group
was chosen because it predated the widespread acceptance and use of
adjuvant chemotherapy and radiotherapy at Fremantle Hospital.All
the endpoints were defined prior to the collection of data. The surgical
procedure was termed curative if there was macroscopic removal of all the
tumour and histological assessment showed there to be clear margins. A
palliative procedure was where the surgeon had left tumour remaining
following surgery, or where no attempt had been made to remove the tumour.
Histological assessment of the resected specimen was required to
adequately determine this. A positive surgical margin was defined as the
presence of tumour within 1 mm of the resection line.
Primary was defined as the first presentation
with a colorectal neoplasia, or if a second presentation, where the tumour
occurred in a metachronous location. The rectum was defined as commencing
in the area where the taenia coli of the sigmoid colon coalesce into a
uniform outer longitudinal muscular wall. At colonoscopy, it included the
area up to 18 cm from the anal verge. An emergency procedure was where a
patient underwent urgent surgery (i.e. within 24 hours of admission)
without recourse to the normal pre-operative work up which includes
colonoscopy and bowel preparation (including presentations with acute
obstruction, perforation, and massive bleeding). The American Society of
Anaesthesia score (ASA score) was used as a general measure of patient
well-being. The TNM staging system was used in this study. For those
patients who received pre-operative radiotherapy to their rectal cancers,
and where there had been complete resolution of the primary tumour, the
staging was based upon the pre-treatment endoanal ultrasound and CT scan.
In the colorectal group, adjuvant
chemotherapy was offered to all patients with Stage III colon cancers and
a selected group of Stage II colon cancers if there was evidence of poor
prognostic markers (i.e. poorly differentiated, lymphovascular invasion)
or if they were of young age (<50 years). Adjuvant preoperative
radiotherapy was offered to patients with rectal cancers if the lesion was
- (1) less than or equal to 12 cm from the anal verge, (2) fixed in
position, (3) mobile lesions if found on endorectal ultrasound to be T3 or
T4 in staging, (4) no associated metastatic disease found on abdominal CT
scan. The general surgeons did not maintain guidelines for the use of
adjuvant chemo/radio therapy. There was minimal use of adjuvant therapy in
the historical control group.
The three data sets (a. colorectal group, b.
general surgeon group, c. historical group) were then linked to the
Mortality Registry of the Health Department of Western Australia. This
enabled cross checking of the date of death of patients, and the survival
curves were calculated from this information.
Statistical
analysis
The
mean, standard deviation, and range were used as descriptive statistics.
Survival was calculated using the Kaplan-Meier product-limit estimate of
survival. The survival time was calculated from the time of initial
surgery (or if no surgery was performed, from initial consultation) to
either death or 1-12-2002. The survival analysis was an overall analysis
and included patients dying - (1) in the 30 day postoperative period, (2)
from colorectal cancer, or (3) from unrelated causes (e.g. myocardial
infarct). Patients presenting with recurrent cancer were included in the
survival analysis. Comparisons of the overall (all-cause mortality)
survival data were made between the study groups using the log rank test
and the Breslow-Gehan-Wilcoxen test. The latter test was chosen because it
could give greater weight to times with more observations in the risk set,
and was therefore less sensitive than the log rank test to late events
when few subjects remained in the study. The Chi-square test was used in
comparisons of nominal data.
A Cox proportional hazards model (Statview
5.0, SAS Institute Inc.) was then applied to identify those factors
associated with the improved survival of patients with colorectal cancer.
The variables which were evaluated were: (1) patients age, (2) stage of
disease, (3) location - colon versus rectum, (4) surgical timing -
elective versus emergency, (5) surgical management group - colorectal
group and the general surgical group versus the historical control group,
(6) use of adjuvant chemotherapy, (7) use of adjuvant radiotherapy (8) ASA
score. Those factors identified on univariate analysis as significant
predictors of survival were then included in a forward multiple linear
regression analysis (Statview 5.0, SAS Institute Inc.). Significance was
defined as the probability of a type I error of less than 5 %.
RESULTS
There
were 974 patients involved in this study. The basic demographic data for
the study groups was detailed in Table 1. The only significant differences
noted were that patients in the colorectal group were more likely to have
a rectal cancer, and those patients in the colorectal group and general
surgical groups were more likely to have an ASA score of 3 or 4 when
compared with the controls. The mean follow up time in the colorectal
group was shorter than that in the general surgical group. This was
because the rate of referrals was increasing in the former and declining
in the latter. For example, the general surgical group managed only 11
colorectal cancers during 2000.
Table
1 Basic demographic data for
the study groups of patients with colorectal cancer
|
Colorectal group
|
General
surgical group
|
Historical
group
|
| Number
|
362
|
137
|
475
|
| Mean
age-years
|
69 (±12)
|
70 (±11)
|
69 (±13)
|
| Age
range-years
|
29
to 93
|
38 to 93
|
32 to 95
|
| Sex
ration M:F
|
1.3:1
|
1.4:1
|
1.4:1
|
| ASA
score of 3 or 4
|
40 %
|
39 %
|
22 %
|
| Elective
vs emergency
|
319 vs 43
|
112 vs 25
|
394 vs 81 |
| procedures
|
(88% vs 12%)
|
(78%
vs 18%)
|
(79% vs 17%)
|
| Curative
vs palliative
|
264 vs 80
|
101 vs 23
|
366 vs 85
|
| pesections
|
(73 % vs 22%)
|
(74
% vs 17%)
|
(77 % vs 18%)
|
| No
surgery
|
18 (5%)
|
13 (9%)
|
24 (5%)
|
| Colon
cancer
|
170
(47%)a
|
90 (66%)
|
314 (66%)
|
| Rectal
cancer
|
192
(53%)b
|
47 (34%)
|
161 (34%)
|
| Adjuvant
chemotherapy
|
116
(32%)c
|
19 (14%)
|
17 (4%)
|
| Adjuvant
radiotherapy
|
65
(18%)d
|
9 (7%)
|
14 (4%)
|
| Mean
follow-up-years
|
2.75 (±1.2)e
|
4.5 (±1.4)
|
5.1 (±4.5)
|
| Max follow-up-years
|
6.8
|
6.9
|
13.9
|
a,b,c,d,e,fP<0.05
vs the other two group.
The information for staging for both colon
and rectal cancers for the three groups was presented in Table 2. Patients
in the colorectal group were significantly more likely to have a stage I
cancer, and had significantly fewer stage II cancers, when compared with
the other two groups. There was also a significant difference between the
two groups in the use of adjuvant chemotherapy for patients who were less
than 75 years of age and who had stage III colorectal cancers. For this
group of patients, the percentage receiving adjuvant therapy was 89 % in
the colorectal group, versus 41 % in the general surgery group, and 5.8 %
in the historical group. For patients with stage II colorectal cancer,
adjuvant chemotherapy was administered to 11 % of patients in the
colorectal group, and no patients in the general surgery or historical
groups. No patients with stage I cancer received adjuvant chemotherapy in
either group.
Table
2 Staging information for
colorectal cancers for the study groups
| Stage
|
Colorectal
group number (%)
|
General
surgical group number (%)
|
Historical
group number (%)
|
| Stage
I
|
81 (22
%)a
|
9 (7 %)
|
57 (12 %)
|
| Stage
II
|
95 (26
%)b
|
53 (39 %)
|
159 (33 %)
|
| Stage
III
|
91 (25 %)
|
41 (30 %)
|
146 (31 %)
|
| Stage
IV
|
91 (25 %)
|
29 (21 %)
|
106 (22 %)
|
| Stage
unknown
|
4 (1 %)
|
4 (3 %)
|
7 (2 %)
|
a,bP<0.05
vs the other two group with the Chi-square test.
A comparison of the survival between the
study groups found that patients in the colorectal group had a
significantly higher overall 5 year survival when compared with the
general surgical group and historical groups (56 % versus 45 % and 40 %
respectively, P<0.0001). The survivals for the various study groups
based on the tumour stage were presented in Table 3. Patients in the
colorectal group who had either Stage I or Stage III cancers were noted to
have significantly higher survivals when compared to the other two groups.
Table
3 A comparison of the overall
5 year survival based on stage for the study groups
| Stage
|
Colorectal
group
|
General
surgical group
|
Historical
group
|
| I
|
90
%a
|
67 %
|
72 %
|
| II
|
62 %
|
57 %
|
58
%
|
| III
|
60
%b
|
46 %
|
34 %
|
| IV
(2 year survivals)
|
22 %
|
21 %
|
19 %
|
a,bP<0.05
vs the other two group.
In the uni-variate analysis, those factors
that were found to be significant predictors of overall survival were:
age, ASA score, emergency surgery, and stage of disease, adjuvant
chemotherapy, adjuvant radiotherapy, and the surgical unit the patients
were managed in. These independent variables were then entered into a
multiple logistic regression analysis (Table 4) that identified: age, ASA
score, stage of disease, the use of adjuvant chemotherapy, and management
in the colorectal surgical group as significant independent predictors of
survival. The comparisons for the surgical groups were made against the
historical control group, with the general surgical group showing no
improvement in survival when compared with the controls.
Table
4 Cox survival regression
analysis of independent predictors of the overall survival in the 974
patients with colorectal cancer
| Independent
variables
|
P
|
Hazard
ratio
|
95%
Confidence interval
|
| Age
|
0.15
|
1.011
|
1.002-1.020
|
| ASA
score
|
<0.0001
|
1.477
|
1.29-1.69
|
| Adjuvant
chemotherapy
|
0.047
|
0.634
|
0.405-0.993
|
| Stage
I
|
<0.0001
|
0.211
|
0.107-0.418
|
| Stage
II
|
0.003
|
0.397
|
0.214-0.738
|
| Stage III
|
0.19
|
0.665
|
0.358-1.237
|
| Stage
IV
|
0.009
|
2.27
|
1.229-4.186
|
| Colorectal
surgical unit
vs control
|
0.0005
|
0.667
|
0.531-0.837
|
DISCUSSION
The
results of this study suggest that there was a survival advantage for
patients with colorectal cancer being managed within a specialist
colorectal surgical unit at a community based teaching hospital. These
improvements in survival appear to be independent of other known
predictors of survival that include stage of disease at presentation,
emergency procedures, and the use of adjuvant chemotherapy. It remains to
be determined as to why these differences exist. Do they simply reflect a
higher surgical case load, or are they a result of improved surgical
technique, better utilization of adjuvant therapy, or even standardized
care through the use of treatment pathways?
There are a number of difficulties in
designing a study to determine if there is a survival advantage in
patients with colorectal cancer being managed by different groups of
surgeons. A review of the surgical literature will show that rarely have
clinical trials been conducted which compared the performance of different
groups of surgeons. The logistics of trying to randomize patients into
such a trial are very difficult. In this study, we have attempted to
compare the risk adjusted survival of patients managed in general surgical
units with those in a colorectal unit, and have compared these results
with a well studied control group to see if there have been any
improvements. Evaluating risk-adjusted survival in large cohorts of
patients using historical controls is one recognized technique for
addressing this issue. Clearly there were significant differences between
the groups, with those patients in the colorectal group more likely to
have Stage I disease and rectal cancers and with a trend towards fewer
emergency procedures. However, the multivariate analysis is designed to
account for these differences, and to include those factors that have been
identified as independent predictors of survival. The individual surgeon
was not included as an independent risk factor in this study because the
majority of the general surgeons performed less than 20 cases during the
study period. Such a small number makes it difficult to assess an
individual surgeon's performance.
There have been a number of reports in the
literature detailing wide variations in outcomes between surgeons managing
patients with malignant disease[1-3]. An important aspect to this
variation appears to be case loads[6-8]. In both patients with breast
cancer[6], oesophageal cancer[7] and rectal cancer[1], surgeons managing
higher numbers of patients seem to gain improved results. A comprehensive
review of the relationship between volume of surgical procedures and
outcome has recently been published[9,10]. This review assessed
88 studies and found that 77 % of the trials demonstrated a
positive relationship between volume of work and reduced mortality, with
the other 23 % of studies showing no relationship. None of the studies
demonstrated a negative relationship.
The question of whether a surgeon who is
sub-specialized in colorectal surgery can achieve improved results remains
an unresolved issue. Porter et al.[1], in their study on factors which
influenced survival and local recurrence rates in patients treated for
rectal cancer, found that surgeons who were trained in colorectal cancer
had significantly improved survivals and reduced local recurrence rates
when compared to general surgeons performing less than 21 procedures over
the eight year study period. Nonetheless, there results were not
significantly better than when compared to general surgeons performing
greater than 21 procedures in the study period. Yet again this study
focuses on rectal cancer and ignores colonic cancers. It remains to be
determined whether these improvements relate to factors such as accuracy
of tumour excision, minimizing tissue trauma, reduced incidence of septic
complications (which may influence cancer survival)[11], and even possible
to reduced blood loss and transfusion requirements.
In conclusion, there appears to be a survival
advantage for patients with colorectal cancer being managed within a
specialized colorectal unit. However, it remains to be determined which
aspects of the management in such a unit are the most important
determinates in this improvement in out-come.
ACKNOWLEDGEMENTS
I
would like to thank Dr Di Rosman at the Health Department of Western
Australia for her assistance in linking information with the Deaths
Registry of Western Australia. I would also like to thank Dr James Semmens
of the Department of Public Health at the University of Western Australia
for acting as a consultant for the statistical analysis used in this
paper.
REFERENCES
1
Porter GA, Soskolne CL, Yakimets WW, Newman SC. Surgeon related
factors and outcome in rectal cancer. Ann Surg
1998; 227: 157-167
2
Khuri SF, Daley J, Henderson W, Hur K, Hossain M, Saybel D, Kizer
KW, Aust JB, Bell RH, Chang V, Demakis J, Faleri PJ,
Gibbs JO, Graver F,
Hammermeister K, McDonald G, Passaro E, Phillips L, Scamman F, Spencer J,
Stremple JF. Relation
of surgical volume to outcome in eight common
operations. Results from the VA national surgical quality improvement
program. Ann Surg 1999; 230: 414-432
3
Singh KK, Barry MK, Ralston P, Henderson MA, McCormick JS, Walls
AD, Auld CD. Audit of colorectal cancer surgery
by non-specialist
surgeons. Br J Surg 1997; 84: 343-347
4 NHMRC. Guidelines for the prevention, early detection and
management of colorectal cancer. 1999
5
Platell C. A community-based hospital experience with colorectal
cancer. Aust NZ J Surg 1997; 67: 420-423
6
Sainsbury R, Haward B, Rider L, Johnston C, Round C. Influence of
clinician workload and patterns of treatment on survival
from breast
cancer. Lancet 1995; 345: 1265-1270
7
Matthews HR, Powell DJ, McConkey CC. Effects of the result of
surgical experience on the results of resection for
oesophageal carcinoma.
Br J Surg 1986; 73: 621-623
8
McArdle CS, Hole D. Impact of variability among surgeons on
postoperative morbidity and mortality and ultimate survival. Br
Med J
1991; 302: 1501-1505
9 Committee on Quality of Health Care in America and the National
Cancer Policy Board. Interpreting the volume-
outcome relationship in the
context of health care quality. Washington: Institute of Medicine 2000
10
Birkmeyer JD, Finlayson EV, Birkmeyer BS. Volume standards for
high-risk surgical procedures: Potential benefits of the
Leapfrog
initiative. Surgery 2001; 130: 415-422
11 Fujita S, Teramoto T, Watanabe M, Kodaira S, Kitajima M.
Anastomotic leakage after colorectal cancer surgery: a risk
factor for
recurrence and poor prognosis. Jap J Clin Oncol 1993; 23: 299-302
Edited
by Xu XQ
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