|
|||||
|
|
||||||
Journal of Clinical Oncology, Vol 22, No 13 (July 1), 2004: pp. 2567-2575 © 2004 American Society of Clinical Oncology. DOI: 10.1200/JCO.2004.11.141 Tree-Based Model for Breast Cancer PrognosticationFrom the Department of Biostatistics, University of Michigan, Ann Arbor; Barbara Ann Karmanos Cancer Institute and the Center for Healthcare Effectiveness Research, Wayne State University, Detroit, MI; and the Department of Management Science and Statistics, The University of Texas at San Antonio, San Antonio, TX Address reprint requests to Mousumi Banerjee, PhD, Department of Biostatistics, University of Michigan, 1420 Washington Heights, Ann Arbor, MI 48109-2029; e-mail: mousumib{at}umich.edu PURPOSE: To define prognostic groups for recurrence-free survival in breast cancer, assess relative effects of prognostic factors, and examine the influence of treatment variations on recurrence-free survival in patients with similar prognostic-factor profiles. PATIENTS AND METHODS: We analyzed 1,055 patients diagnosed with stage I-III breast cancer between 1990 and 1996. Variables studied included socioeconomic factors, tumor characteristics, concurrent medical conditions, and treatment. The primary end point was recurrence-free survival (RFS). Multivariable analyses were performed using recursive partitioning and Cox proportional hazards regression.
RESULTS: The most significant difference in prognosis was between patients with fewer than four and those with at least four positive nodes (P < .0001). Four distinct prognostic groups (5-year RFS, 97%, 78%, 58%, and 27%) were developed, defined by the number of positive nodes, tumor size, progesterone receptor (PR) status, differentiation, race, and marital status. Patients with fewer than four positive nodes and tumor CONCLUSION: Lymph node status, PR status, tumor size, differentiation, race, and marital status are valuable for prognostication in breast cancer. The prognostic groups derived can provide guidance for clinical trial design, patient management, and future treatment policy. Supported by grants from the National Science Foundation (DMS 9973410; M.B.) and the Ford Motor Company Foundation (W.H. and E.Y.S.). Authors' disclosures of potential conflicts of interest are found at the end of this article. This article has been cited by other articles:
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||
|
Copyright © 2004 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
|