International Staging System for Multiple Myeloma

Philip R. Greipp(Spanish Head & Neck Cancer Cooperative Group), Jesús F. San Miguel(Spanish Head & Neck Cancer Cooperative Group), Brian G.M. Durie(Spanish Head & Neck Cancer Cooperative Group), John J. Crowley(Spanish Head & Neck Cancer Cooperative Group), Bart Barlogie(Spanish Head & Neck Cancer Cooperative Group), Joan Bladé(Spanish Head & Neck Cancer Cooperative Group), Mario Boccadoro(Spanish Head & Neck Cancer Cooperative Group), J. A. Child(Spanish Head & Neck Cancer Cooperative Group), Hervé Avet‐Loiseau(Spanish Head & Neck Cancer Cooperative Group), Robert A. Kyle(Spanish Head & Neck Cancer Cooperative Group), Juan José Lahuerta(Spanish Head & Neck Cancer Cooperative Group), Heinz Ludwig(Spanish Head & Neck Cancer Cooperative Group), Gareth J. Morgan(Spanish Head & Neck Cancer Cooperative Group), Raymond Powles(Spanish Head & Neck Cancer Cooperative Group), Kazuyuki Shimizu(Spanish Head & Neck Cancer Cooperative Group), Chaim Shustik(Spanish Head & Neck Cancer Cooperative Group), Pieter Sonneveld(Spanish Head & Neck Cancer Cooperative Group), Patrizia Tosi(Spanish Head & Neck Cancer Cooperative Group), Ingemar Turesson(Spanish Head & Neck Cancer Cooperative Group), Jan Westin(Spanish Head & Neck Cancer Cooperative Group)
Journal of Clinical Oncology
April 5, 2005
Cited by 2,913

Abstract

PURPOSE: There is a need for a simple, reliable staging system for multiple myeloma that can be applied internationally for patient classification and stratification. PATIENTS AND METHODS: Clinical and laboratory data were gathered on 10,750 previously untreated symptomatic myeloma patients from 17 institutions, including sites in North America, Europe, and Asia. Potential prognostic factors were evaluated by univariate and multivariate techniques. Three modeling approaches were then explored to develop a staging system including two nontree and one tree survival assessment methodologies. RESULTS: Serum beta2-microglobulin (Sbeta2M), serum albumin, platelet count, serum creatinine, and age emerged as powerful predictors of survival and were then used in the tree analysis approach. A combination of Sbeta2M and serum albumin provided the simplest, most powerful and reproducible three-stage classification. This new International Staging System (ISS) was validated in the remaining patients and consists of the following stages: stage I, Sbeta2M less than 3.5 mg/L plus serum albumin > or = 3.5 g/dL (median survival, 62 months); stage II, neither stage I nor III (median survival, 44 months); and stage III, Sbeta2M > or = 5.5 mg/L (median survival, 29 months). The ISS system was further validated by demonstrating effectiveness in patients in North America, Europe, and Asia; in patients less than and > or = 65 years of age; in patients with standard therapy or autotransplantation; and in comparison with the Durie/Salmon staging system. CONCLUSION) The new ISS is simple, based on easy to use variables (Sbeta2M and serum albumin), and recommended for early adoption and widespread use.


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