Surgery
Volume 147, Issue 3 , Pages 358-365, March 2010

Staging error does not explain the relationship between the number of lymph nodes in a colon cancer specimen and survival

  • Jesse Moore, MD

      Affiliations

    • Department of Surgery, University of Vermont College of Medicine, Burlington, VT
  • ,
  • Neil Hyman, MD

      Affiliations

    • Department of Surgery, University of Vermont College of Medicine, Burlington, VT
    • Corresponding Author InformationReprint requests: Neil Hyman, MD, Department of Surgery, Fletcher 464, University of Vermont College of Medicine, Burlington, VT 05401.
  • ,
  • Peter Callas, PhD

      Affiliations

    • Department of Biostatistics, University of Vermont College of Medicine, Burlington, VT
  • ,
  • Benjamin Littenberg, MD

      Affiliations

    • General Internal Medicine, University of Vermont College of Medicine, Burlington, VT

Accepted 2 October 2009. published online 04 December 2009.

Background

Survival in colon cancer is greater in those patients who have more lymph nodes identified at resection and may be due to stage migration, confounding by treatment, social, or clinical characteristics. Identifying factor(s) responsible for the effect may represent an opportunity to improve quality of care for patients with colon cancer by increasing node counts in specimens.

Methods

Cox proportional hazards models were created to analyze survival of 11,399 patients with stage I-III colon cancer from the Surveillance, Epidemiology and End Results (SEER)-Medicare database. The primary predictor variable was the number of lymph nodes identified. The models allowed adjustment for patient factors, use of chemotherapy, surgical specialty, and the average number of nodes identified by surgeon and hospital pathologist.

Results

The number of nodes identified was related to survival. Compared to those with less than 7 nodes, patients with 7 to 11 nodes had a 13% lesser risk of death (hazard ratio [HR], 0.87; 95% confidence interval [CI], 0.76–0.99; P = .037). Patients with more than 12 nodes had a 17% lesser risk (HR, 0.83; 95% CI, 0.73–0.95; P = .005). Adjusting for selected patient demographic characteristics, receipt of chemotherapy, surgical specialty, and the average number of nodes identified per specimen by the surgeon or hospital did not significantly alter the relationship between number of nodes and survival.

Conclusion

These findings argue against understaging or confounding as the explanation for the inferior survival observed in patients with fewer nodes identified. National initiatives to increase the number of nodes identified in colon cancer specimens may not improve substantially the cancer-specific outcomes.

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 Supported in part by research grants from the National Institutes of Health (K30 RR22260 and K24 DK68380).

PII: S0039-6060(09)00613-8

doi:10.1016/j.surg.2009.10.003

Surgery
Volume 147, Issue 3 , Pages 358-365, March 2010