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Overall survival after resection for colon cancer in a national cohort study was adversely affected by TNM stage, lymph node ratio, gender, and old age.
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MedLine Citation:
PMID:  21562744     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
BACKGROUND: A national surveillance program of colon cancer treatment was introduced in 2007. We examined prognostic factors for colon cancer operated in 2000 with an aim of improving survival in the new program and a special focus on the merit of lymph node yield.
METHODS: A cohort of 269 patients, 152 women (56.5%), with a mean age of 71 years, was operated for colon cancer in 2000 at three teaching hospitals and followed up for 7 years.
RESULTS: Overall 5-year survival was 58.0%, and overall hospital mortality was 5.2%, with 4.5% in elective cases and 12.5% after urgent surgery. In only 41.1% of the specimens were 12 or more lymph nodes retrieved, but this did not affect survival in the combined cohort, although one of the hospitals achieved a significantly better result with a harvest of 12 or more lymph nodes. In a multivariate analysis, old age, gender, a high lymph node ratio (LNR) at stage III, and tumor-node-metastasis stage were adverse factors for survival.
CONCLUSIONS: The operative mortality was high and should be reassessed. The lymph node count did not have a significant impact on outcome overall, whereas the LNR proved significant for stage III. A prospective protocol using overall lymph node yield as a surrogate measure for more radical surgery, nevertheless, seems warranted to improve the lymph node harvest according to international recommendations.
Authors:
Kristian E Storli; Karl Søndenaa; Ida R K Bukholm; Idunn Nesvik; Tore Bru; Bjørg Furnes; Bjarte Hjelmeland; Knut B Iversen; Geir E Eide
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't     Date:  2011-05-12
Journal Detail:
Title:  International journal of colorectal disease     Volume:  26     ISSN:  1432-1262     ISO Abbreviation:  Int J Colorectal Dis     Publication Date:  2011 Oct 
Date Detail:
Created Date:  2011-09-20     Completed Date:  2012-01-11     Revised Date:  2013-06-30    
Medline Journal Info:
Nlm Unique ID:  8607899     Medline TA:  Int J Colorectal Dis     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  1299-307     Citation Subset:  IM    
Affiliation:
Department of Surgery, Haraldsplass Deaconal Hospital, University of Bergen, PO Box 6165, 5892, Bergen, Norway.
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Aged, 80 and over
Aging / pathology*
Cohort Studies
Colonic Neoplasms / mortality,  pathology*,  surgery*
Female
Hospitals, Teaching
Humans
Kaplan-Meier Estimate
Lymph Nodes / pathology*
Male
Middle Aged
Multivariate Analysis
Neoplasm Staging
Norway / epidemiology
Sex Characteristics*
Young Adult
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Full Text
Journal Information
Journal ID (nlm-ta): Int J Colorectal Dis
ISSN: 0179-1958
ISSN: 1432-1262
Publisher: Springer-Verlag, Berlin/Heidelberg
Article Information
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© The Author(s) 2011
Accepted Day: 3 Month: 5 Year: 2011
Electronic publication date: Day: 12 Month: 5 Year: 2011
pmc-release publication date: Day: 12 Month: 5 Year: 2011
Print publication date: Month: 10 Year: 2011
Volume: 26 Issue: 10
First Page: 1299 Last Page: 1307
ID: 3176397
PubMed Id: 21562744
Publisher Id: 1244
DOI: 10.1007/s00384-011-1244-2

Overall survival after resection for colon cancer in a national cohort study was adversely affected by TNM stage, lymph node ratio, gender, and old age
Kristian E. Storli1
Karl Søndenaa12 Address: +47-91-868877 +47-55-978555 kasoende@online.no
Ida R. K. Bukholm3
Idunn Nesvik4
Tore Bru4
Bjørg Furnes1
Bjarte Hjelmeland1
Knut B. Iversen1
Geir E. Eide56
1Department of Surgery, Haraldsplass Deaconal Hospital, University of Bergen, PO Box 6165, 5892 Bergen, Norway
2Department of Surgical Sciences, University of Bergen, Bergen, Norway
3Department of Surgery, Akershus University Hospital, Oslo, Norway
4Department of Surgery, Stavanger University Hospital, Stavanger, Norway
5Centre for Clinical Research, Haukeland University Hospital, Bergen, Norway
6Department of Public Health and Primary Care, University of Bergen, Bergen, Norway

Introduction

In recent years, the results after surgery for rectal cancer in Norway, with a 5-year overall survival (OS) rate of 60.1%, has surpassed that of colon cancer at 57.5% [1]. This has been achieved because the surgical technique has been standardized according to total mesorectal excision (TME) with subsequent dramatic reductions of local recurrences. Beginning in 2007, all colon cancers were to be reported separately to the Norwegian National Cancer Registry in an effort to systematically survey and hopefully improve results. Nevertheless, a national strategy to standardize surgical treatment along the lines of radical surgery has neither been implemented in detail nor been generally accepted [2, 3].

In this respect, the number of lymph nodes retrieved may act as a surrogate measure of radical surgery. The survival benefit of a large lymph node harvest has been shown in several reports [24]. It has been accepted nationally to offer patients with tumor–node–metastasis (TNM) stage III below a certain age, usually 75 years, adjuvant chemotherapy. This depends on adequate staging and lymph node sampling. It has been decided that a rather arbitrary level of 12 retrieved nodes is enough to obtain adequate surgery and staging. Pathologists may be a key factor for optimal lymph node harvest, and a conjoined effort between surgeon and pathologist would be ideal to improve results [26].

The aim of the study was to examine, after modest radical colon surgery removing mesocolic nodes and focus on lymph node yield, what would influence survival and where surgical improvement might be possible using data from a cohort of patients from three large Norwegian teaching hospitals.


Material and methods

Patients from a national cohort were operated in 2000, and follow-up was until December 2007, a mean of 7.5 years later. Three teaching community hospitals, Haraldsplass Deaconal Hospital, Stavanger University Hospital, and Akershus University Hospital contributed patients.

Surgery

All three hospitals are teaching community hospitals, and the patients were operated with an open access by a large number of surgeons. At that time, extra radical surgery was unusual, and it is fair to assume that radical surgery usually constituted a moderate mesocolic resection. If metastases were diagnosed, patients and tumor conditions were assessed regarding feasibility for resection.

Follow-up

Patients usually went to the outpatient clinic every third month for the first 2 years and then every sixth month until 5 years had passed. Blood tests with carcino-embryonic antigen measurement and ultrasonography of the liver and chest X-ray were carried out. Elderly patients are stead-bound and even if a few of them were not followed up frequently, they could be tracked and life status ascertained through their identity number in the official National Population Registry. Death certificates for all deceased patients were available through Statistics, Norway.

Pathology

The specimen was examined and rinsed by the surgeons on the back table before being mounted on a board and placed in a box filled with enough formaldehyde for secure fixation. The specimen was examined by a junior pathologist; after 48–72 h, assisted by the consultant. Lymph nodes were harvested by sight and palpation. A minimum sampling of 12 lymph nodes was aimed for. Tissue was paraffin-embedded, and hematoxylin–eosin staining was used routinely before sections were examined microscopically. Metastatic deposits were defined as lymph nodes if these structures resembled nodes but without containing visible lymphatic tissue. The large intestine was defined as ending 16 cm from the anus. The TNM classification 5th edition was used for staging.

Oncology

Patients younger than 75 years of age that were classified as TNM stage III were offered 12 courses of adjuvant treatment with 5-fluorouracil plus calsiumfolinate (FLV).

Ethics

The Regional Committee for Medical and Health Research Ethics of Western Norway and the Data Inspectorate for National Registries approved the study. The study is part of a prospective project registered with clinicaltrials.gov (NCT00963352).

Statistical analysis

The chi-square test was used to compare groups with respect to categorical variables and analysis of variance for continuous variables. The following variables were analysed with respect to survival: hospital, age, gender, location, no of lymph nodes and lymph node ratio (LNR), T stage, and TNM stage. Survival curves were estimated by the Kaplan–Meier method [7] and compared using the log-rank test [8]. Multiple prognostic factors were analysed with the Cox proportional hazards model [9] using the SPSS 17 package.


Results

Two hundred sixty-nine patients, 152 (56.5%) women and 117 men, with a mean age of 71 years (range, 20–93 years) were studied. One of the hospitals operated male patients that were younger, with a mean of 67 years.

Surgery

The different tumor locations are shown in Table 1. Tumor locations were not different between the hospitals (p = 0.059). Right hemicolectomy and sigmoid resection were the most common procedures (78.4%). Locoregional R0 resections for a single tumor location were done in 264 patients, while double resections (n = 4) and a suspected locoregional R1 resection (n = 1) were done in five patients.

Pathology

There were no significant differences between hospitals relating to TNM stage distribution: 34 patients (12.6%) were stage I, 116 patients (43.1%) were stage II, 93 patients (34.6%) were stage III, and 26 patients (9.6%) were stage IV. The number of lymph nodes harvested for various stages were 8.7 (stage I), 10.3 (stage II), 10.9 (stage III), and 10.3 (stage IV). In 11 patients, the pathologist had classified the T category and TNM stage but omitted to specify the number of lymph nodes present. The mean number in 258 patients was 10.3 lymph nodes per specimen. Twelve or more lymph nodes were examined in 41.1% (106/258) of the resected specimens. Significantly fewer lymph nodes (p < 0.001) were harvested at one of the hospitals. Otherwise, the three patient populations had similar characteristics.

Survival analysis

Overall in-hospital mortality was 5.2% (14/269; range, 4.3–6.3%). Urgent surgery had a mortality of 12.5% (3/24), whereas the elective group had a mortality of 4.5% (11/245). The 5-year OS was 58.0% (Fig. 1) and did not differ between the hospitals (log-rank p = 0.372; Fig. 3).

Whether categorizing number of lymph nodes harvested in three groups (<10, 10–19, 20 or more) or in two (<12, 12 or more), no differences was found in OS (log-rank p = 0.423 and 0.270, respectively). This was still the case after adjusting for hospital or TNM stage (log-rank p = 0.449). The uncategorized number of lymph nodes was not significant in a simple Cox regression (likelihood ratio p = 0.129). However, in one hospital, better survival was found when the lymph node harvest was ≥12 compared to <12 (log-rank p = 0.037) as shown in Fig. 2. Stage II patients had OS of 72.7% with ≥12 nodes harvested and 58.3% with <12 nodes (p = 0.124), and stage III patients had a 5-year OS of 61.5% and 55.6%, respectively (p = 0.508).

In stage III patients, the lymph node ratio (LNR) was highly significant for patient survival, and OS for LNR 1 (<0.25) was 83.3.5%, LNR 2 (0.25–0.50) 63.3%, LNR 3 (0.51–0.75) 18.8%, and LNR 4 (0.76–1) 18.2% (log-rank test p < 0.001). The total number of lymph nodes was not significant for stage III patients.

Two of the hospitals did more resections of T4 tumors (chi-square test p = 0.021). Adjusted for hospital, T4 tumors compared to T1–T3, was a significant adverse factor for survival in the log-rank test (p = 0.049).

Survival according to the different TNM stages is shown in Table 2. The 5-year OS was 58.1% for stage III and 63.8% for stage II without differences between the hospitals in uni- and multivariate analyses. OS for stage IV was significantly worse (p < 0.001).

The results of univariate and multivariate Cox-regression analyses are shown in Table 3. In the univariate Cox regression old age, T category, high LNR, and TNM stage were adverse factors for survival. Age as a variable was highly significant both as a continuous variable and with a cutoff value of 69 years. Locations of the tumors with regard to the various resected segments were not significant (Table 3).

In the multivariate model age, male gender, high LNR, and TNM stage were adverse factors (Figs. 4, 5, and 6). In the fully adjusted multivariate analysis, T category was not significant, but when removing TNM stage from the multivariate model, the T category again became significant (p = 0.047). These variables were not significant: hospital, tumor location, or number of harvested lymph nodes in these categories (<10, 10–19, ≥20). LNR was also highly significant for stage III patients (n = 93) when adjusted for all the variables in Table 3 in a multivariate Cox regression with HRs (95% CIs) of 1.72 (0.80, 3.67), 5.16 (2.48, 10.74), and 4.80 (1.92, 11.99) for LNR 2–4 vs. LNR 1, respectively (p < 0.001).

Statistical analysis

The study may have been underpowered for detection of an assumed difference between patients with a lymph node harvest of <12 lymph nodes and those with >12. With the number of patients included in our study, a power of at least 0.84 would be necessary to detect a difference in 5-year survival of 50% vs. 68%. An increase in sample size to detect a difference of 50% vs. 60% with a power of 0.80 in a one-tailed chi-square test would require 305 patients in each group.


Discussion

Even though several groups have pioneered radical surgery for colon cancer (complete mesocolic excision and a central tie) with its potential benefits similar to (TME) of rectal cancer surgery, such an approach has not been widely adopted in our country. Therefore, we wanted to examine our background results based on a less standardized approach and potential areas for improvement before embarking on more radical procedures as championed by others [2].

The 5-year overall survival (OS) for all three hospitals was 58.0%. Advanced TNM stage had an adverse influence on outcome, as the results for stage IV versus I–III and stage III versus I–II were significant in the multivariate analysis. For stage III patients, the 5-year OS was 58.1%. In one hospital, the 5-year OS for stage III was worse with 47.8%. In the multivariate analysis, however, when adjusted for hospital, there was no significant survival difference. A recently published international multicenter study of a colorectal population [10] reported an identical OS of 58.8% for patients treated in 2000–2002. Others have found a 5-year OS of 90.7–96.3% for stage II and 64.6–71.7% for stage III using radical surgical procedures [2]. Thus, we consider our figures to show room for improvement, although where improvement may be best realised is debatable.

An advanced stage may theoretically be better treated with more radical surgery even though the presence of skip lesions in rare instances may hardly explain this [11]. Radical or complete mesocolic excision has been shown to increase both the absolute lymph node harvest and prognosis for the patients [2, 3]. However, it has been contested that patients will benefit from more radical surgery in advanced cases [12]. In a Swedish population-based retrospective study [13], a median number of six lymph nodes were detected in the specimens from 1,856 patients operated between 1996 and 2000. The patients in that study had a high local recurrence rate of 11.5%. Locations in the right flexure or left colon were independent risk factors for outcome. There were a very low number of nodes in the specimens from the left colon, whereas in the right flexure tumors, the lymph node count was not inferior. In both instances, the feeding vessel areas were not divided completely, i.e., the inferior mesenteric artery proximally and the root of the medial colic artery. In a population-based study from The Netherlands by Kelder and co-workers, the median lymph node harvest was six and in only 21% of the specimens were 12 or more nodes examined [14]. Thus, we consider that the principle of radical colon surgery may have been violated in these studies when tumors were in those locations. More radical surgery for colon cancer has been recommended in reports from the USA, Europe, and Japan [2, 15, 16]. A retrospective national report based on a small number with supposedly radical colon surgery found that this approach significantly increased survival compared with a much larger and older group subject to a “standard” procedure [17].

The number of lymph nodes may be seen only as a surrogate marker for the extent of surgery without a proper oncologic explanation for the importance of a large harvest [2, 3]. The node count has been correlated to survival both for stage II and III disease [2, 18]. The oncologic explanation is particularly lacking for stage II tumors [12]. The Ontario Cancer Registry study [19] showed better survival with a lymph node harvest of more than ten lymph nodes. Increasing the number even more did not improve survival. In contrast, there is good evidence reported by others that increasing the total number of lymph nodes increases survival significantly [2, 4]. In one study, a mean harvest of more than 28 lymph nodes was reported [2]. Data from the SEER database demonstrated that a cutoff value of 15 was useful, and perhaps, there is an inherent limit to the number of nodes necessary to achieve this effect on survival [20]. Nevertheless, the hypothesis that a larger (negative) lymph node yield is beneficial is contradicted even from highly rated institutions [21]. Only 41% of our patients had more than 12 nodes detected in the specimen. In the univariate analysis, one of the hospitals achieved a significantly better survival with a harvest of more than 12 lymph nodes. However, no significant survival benefit was found with harvest of more than 12 lymph nodes in the multivariate analysis. Several confounding factors may have been present [21, 22]. Many pathologists were involved in this trial even though the specimen handling was supposed to be equal. In a recent study, the pathologist was found to be the dependent factor in lymph node harvest in multivariate analysis, not the operating surgeon [6]. The overall poor lymph node harvest may also indicate that more extensive surgery is one way to improve outcome as found in one of the hospitals. It may be speculated that the poorer outcome in the other two hospitals may have levelled out any benefit by an improved lymph node harvest, i.e., more radical surgery. The power of the study may have concealed such a result [21].

Patients below 75 years were given FLV chemotherapy, and staging was considered important for that reason. For proper staging of colon cancer, the minimum number of lymph nodes needed has been somewhat arbitrarily suggested as 12 by a National Cancer Institute expert panel [15]. Although some authors [14, 18] have concluded with stage migration as an explanation for an increased survival benefit, other studies have shown that detection of positive nodes beyond six or seven lymph nodes examined had no effect on staging [19, 23]. Thus, stage migration is debatable and should not be taken for granted [24]. Patient and tumor factors may also contribute to a variable lymph node presence [18]. Doubtless, a standardized surgical approach in cooperation with a dedicated pathology service is necessary if a minimum number of nodes shall be found and consequently help in outcome assessment. The mean number of lymph nodes in our series was 10.3. Therefore, under-staging was not considered important in our study [24]. The share of stage III tumors equalled that reported by others from large cohorts [12].

Studies have shown that the LNR is an independent and better marker than pN+ for survival [25]. In our study, LNR was highly significant for OS when adjusted for hospitals in the multivariate analysis. Five-year OS varied from 83.5% in LNR group 1, 63.3% in LNR 2, to 18.8% in LNR group 3. According to Wang et al. [26, 27], the prognostic effect of LNR did not depend on the total number of lymph nodes nor on the number of positive nodes. In contrast, Berger et al. [25] found that LNR was not a significant prognostic indicator with less than ten examined nodes but became highly significant for OS and disease-free survival with more than ten lymph nodes harvested. A Mayo Clinic study [21] found a positive correlation between the number of positive lymph nodes and survival but did not analyze the effect of LNR. Fifty-eight percent of our stage III patients had less than 12 lymph nodes examined. Still, we found a significant survival difference of 44.5% between LNR group 2 and 3 and 65.3% between group 1 and 4. A study from New Zealand [22] found that both the absolute number of lymph nodes retrieved up to 16, as well as the LNR, were important for prognosis. The share of stage III compared to stage II cancers in their patients amounted to 54.9%, higher than in most other reports. It seems obvious that a large negative lymph node yield will down-regulate LNR, but the importance of this with regard to outcome may need to be examined in more detail.

Another national report of colon cancer from a single institution found that an emergency operation, some colon locations, blood transfusion of more than two units, old age, and TNM stage were negative predictive factors [28]. No information about lymph node harvest was given. We did not study the effect of blood transfusion, and emergency operations were not separated from the rest partly because they were few, i.e., 15% reported by Sjo et al. [28], and the definition may be debatable. Information about tumor obstruction or perforation would be more appropriate in our opinion. The different colon locations found to be statistically significant (transverse, left flexure, and descending colon) were not so in our multivariate analysis. We suspect that this is partly because they were too few, 20%, to make an impact [28].

Old age was another adverse factor in our study. The overall in-hospital mortality in our series was 5%. Even though the number of urgently operated patients was small in this series, as expected, this small group had a higher mortality of 12.5% compared to 4.5% in the elective patients. Severe co-morbidities in old age may have contributed to these figures as has been reported by others [29]. However, it should be possible to set an optimal target of <3% in elective cases [2]. The average age of our study population was 71 years and that may be older than in series of selected patients. The average age of men and women in our country for those that have reached the age of 62 (earliest OAP retirement age) is 81 and 85 years. To circumvent the analytic problem of age, Sjo et al. [28] used relative survival. Thus, their survival figures improved from 62% actuarial survival to 74% for women and 79% for men. The method is cumbersome, as it necessitates life tables to calculate this for every patient year. Three-year disease-free survival has been shown to parallel overall 5-year survival [30]. However, it requires close follow-up with CT instead of the conventional ultrasonography and chest X-ray examinations. Close follow-up may even result in better treatment of metastases according to Japanese results [31].


Conclusion

Only 41% had a lymph node harvest of 12 or more lymph nodes, and although this influenced OS in one hospital, it did not overall. The lymph node ratio was significant for stage III patients. More radical surgery may increase the lymph node yield, but if this has the potential to increase overall survival in our patients remains to be seen in the prospective registry. Mortality should be kept low with adequate assessment and treatment of co-morbidities as well as meticulous surgery to avoid complications.


Acknowledgment

The study was supported by a grant from the Western Norway Health Authority, the University of Bergen and Haraldsplass Deaconal Hospital. Cand. med. Malte Schmidt helped organise data.

Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.


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30.. Sargent DJ,Wieand HS,Haller DG,Gray R,Benedetti JK,Buyse M,Labianca R,Seitz JF,O'Callaghan CJ,Francini G,Grothey A,O'Connell M,Catalano PJ,Blanke CD,Kerr D,Green E,Wolmark N,Andre T,Goldberg RM,Gramont A. Disease-free survival versus overall survival as a primary end point for adjuvant colon cancer studies: individual patient data from 20,898 patients on 18 randomized trialsJ Clin OncolYear: 200523348664867010.1200/JCO.2005.01.607116260700
31.. Kobayashi H,Mochizuki H,Sugihara K,Morita T,Kotake K,Teramoto T,Kameoka S,Saito Y,Takahashi K,Hase K,Oya M,Maeda K,Hirai T,Kameyama M,Shirouzu K,Muto T. Characteristics of recurrence and surveillance tools after curative resection for colorectal cancer: a multicenter studySurgeryYear: 20071411677510.1016/j.surg.2006.07.02017188169

Figures

[Figure ID: Fig1]
Fig. 1 

Kaplan–Meier survival curve for 269 patients resected for colon cancer in three Norwegian hospitals in 2000



[Figure ID: Fig2]
Fig. 2 

Kaplan–Meier survival curve for 103 patients resected for colon cancer in one of three Norwegian hospitals in 2000. Patients with a lymph node harvest of 12 or more showed significantly better overall survival (log-rank test p = 0.037)



[Figure ID: Fig3]
Fig. 3 

Kaplan–Meier survival curves for 269 patients resected for colon cancer in three Norwegian hospitals in 2000 according to hospital (log-rank test p = 0.372)



[Figure ID: Fig4]
Fig. 4 

Kaplan–Meier survival curves for 269 patients resected for colon cancer in three Norwegian hospitals in 2000 according to age (log-rank test p < 0.001)



[Figure ID: Fig5]
Fig. 5 

Kaplan–Meier survival curves for 93 patients resected for colon cancer in three Norwegian hospitals in 2000 according to lymph node ratio groups: <0.25 (group 1), 0.25–0.5 (group 2), 0.51–0.75 (group 3), and >0.75 (group 4) (log-rank test p < 0.001)



[Figure ID: Fig6]
Fig. 6 

Kaplan–Meier survival curves for 269 patients resected for colon cancer in three Norwegian hospitals in 2000 according to TNM stage (log-rank test p < 0.001)



Tables
[TableWrap ID: Tab1] Table 1 

Tumor locations and pathology variables of patients resected for colon cancer at three teaching community hospitals in 2000


Variables All patients Chi-square test
n = 269 p value
Location 0.059
 Right hemicolon 115 (42.8)
 Transverse colon including flexures 44 (16.4)
 Descending colon 9 (3.3)
 Sigmoid colon and rectosigmoid 96 (35.7)
 Multiplea or R1–2b 5 (1.9)
T category 0.021
 T1 11 (4.1)
 T2 30 (11.2)
 T3 180 (66.9)
 T4 48 (17.8)
TNM stage 0.098
 I 34 (12.6)
 II 116 (43.1)
 III 93 (34.6)
 IV 26 (9.7)

aResection of two tumors in separate locations

bNo radical loco-regional tumor resection


[TableWrap ID: Tab2] Table 2 

Five-year overall survival (OS) according to the different TNM stages for 269 patients treated with resection for colon cancer in three Norwegian teaching community hospitals in 2000


TNM stage n (%) % OS
I 34 (12.6) 76.5
II 116 (43.1) 63.8
III 93 (34.6) 58.1
IV 26 (9.7) 7.7
All stages 269 (100) 58.0

[TableWrap ID: Tab3] Table 3 

Univariate (n = 269 patients) and multivariate (n = 258) Cox regression models for analysis of overall survival for patients resected for colon cancer in three Norwegian teaching community hospitals in 2000


  Univariate Multivariatea LR test
HR 95% CI p value HR 95% CI p value
No. of sampled lymph nodes per increments of 10a 0.79 (0.58, 1.08) 0.129 0.82 (0.57, 1.17) 0.266
T category <0.001 0.129
 T1–T2 1 (reference) 1 (reference)
 T3 1.69 (0.94, 3.03) 1.84 (0.55, 6.15)
 T4 3.38 (1.79, 6.40) 2.64 (0.78, 8.99)
Tumor location 0.568 0.716
 Right colon 1 (reference) 1 (reference)
 Transverse colon 0.89 (0.55, 1.46) 0.79 (0.47, 1.32)
 Descending colon 0.97 (0.39, 2.42) 1.44 (0.57, 3.66)
 Sigmoid colon 0.70 (0.45, 1.10) 0.81 (0.50, 1.31)
 Rectosigmoid 0.82 (0.44, 1.53) 0.62 (0.31, 1.26)
 Other/double 0.96 (0.23, 3.93) 0.67 (0.15, 2.91)
 R2 5.83 (0.79, 42.81) 0.61 (0.08, 4.94)
Age per 10 years 1.46 (1.23, 1.74) 0.001 1.68 (1.38, 2.03) <0.001
Gender 0.192 0.031
 Females 1 (reference) 1 (reference)
 Males 1.26 (0.89, 1.77) 1.52 (1.04, 2.23)
TNM stage <0.001 <0.001
 I 1 (reference) 1 (reference)
 II 1.61 (0.82, 3.18) 0.91 (0.23, 3.69)
 III 2.07 (1.05, 4.12) 1.49 (0.39, 5.66)
 IV 10.50 (4.94, 22.32) 9.26 (2.15, 39.85)
Hospital 0.390 0.169
 AHUS 1 (reference) 1 (reference)
 SUS 1.06 (0.71, 1.60) 0.72 (0.46, 1.14)
 HDS 1.34 (0.87, 2.07) 0.62 (0.37, 1.03)

HR hazard ratio; CI confidence interval; LR likelihood ratio; SUS Stavanger University Hospital; HDS Haraldsplass Deaconal Hospital; AHUS Akershus University Hospital

aAnalyses based on 258 patients because of lack of specified number of lymph nodes



Article Categories:
  • Original Article

Keywords: Keywords Colon cancer, Lymph nodes, TNM stage, Surgery, Survival.

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