Documenting the Natural History of Patients With Resected Stage II Adenocarcinoma of the Colon After Random Assignment to Adjuvant Treatment With Edrecolomab or Observation: Results From CALGB 9581

Author:

Niedzwiecki Donna1,Bertagnolli Monica M.1,Warren Robert S.1,Compton Carolyn C.1,Kemeny Nancy E.1,Benson Al Bowen1,Eckhardt S. Gail1,Alberts Steven1,Porjosh Gity N.1,Kerr David J.1,Fields Anthony1,Rougier Philippe1,Pipas J. Marc1,Schwartz Joel H.1,Atkins James1,O'Rourke Mark1,Perry Michael C.1,Goldberg Richard M.1,Mayer Robert J.1,Colacchio Thomas A.1

Affiliation:

1. Cancer and Leukemia Group B Statistical Center; Duke University Medical Center, Durham; Southeast Cancer Control Consortium, Goldsboro; University of North Carolina, Chapel Hill, NC; Brigham and Women's Hospital; Eastern Cooperative Oncology Group; Dana-Farber Cancer Institute, Boston; Massachusetts General, North Shore Cancer Center, Danvers, MA; University of California, San Francisco, San Francisco, CA; National Cancer Institute, Bethesda; National Cancer Institute Expanded Participation Project,...

Abstract

PurposeWe conducted a randomized trial comparing adjuvant treatment with edrecolomab versus observation in patients with resected, low-risk, stage II colon cancer. This study also prospectively studied patient- and tumor-specific markers of treatment outcome.Patients and MethodsAfter surgical resection, patients with stage II colon cancer were randomly assigned to either five infusions of edrecolomab at 28-day intervals or observation without adjuvant therapy.ResultsFinal accrual included 1,738 patients; 865 patients received edrecolomab, and 873 patients were observed without adjuvant treatment. Median follow-up time was 7.9 years. There were no significant outcome differences between study arms (overall survival [OS], P = .71; disease-free survival, P = .64). The combined 5-year all-cause OS was 0.86 (95% CI, 0.84 to 0.88), and the combined 5-year disease-specific OS was 0.93 (95% CI, 0.91 to 0.94). The relationships between demographic and histopathologic factors and survival differed for all-cause and disease-specific survival outcomes, but no combined prognostic factor model was found to adequately classify patients at higher risk of recurrence or death as a result of colon cancer.ConclusionEdrecolomab did not prolong survival. Consequently, this large study with a long duration of follow-up provided unique data concerning the natural history of resected stage II colon cancer. Prognostic factors identified in previous retrospective and pooled analyses were associated with survival outcomes in this stage II patient cohort. Results from ongoing molecular marker studies may enhance our ability to determine the risk profile of these patients.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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