Abstract
Purpose: In multiple myeloma, many prognostic parameters have been proposed. However, all of these predict shorter survival. To identify patients with a longer life expectancy, we updated the data of patients treated in the IFM (Intergroupe Francophone du Myelome) 99-02 and 99-04 trials. Patients and Methods: A series of 520 patients was analyzed. Median follow-up was 90.5 months. To perform a comprehensive analysis of the major prognostic factors, we reanalyzed all patients for 1q gains [in addition to updating del(13), t(4;14), and del(17p) analyses]. Results: It was possible to identify a subgroup of patients (representing 20% of total patients) with an 8-year survival of 75%. These patients were defined by the absence of t(4;14), del(17p), and 1q gain and β 2-microglobulin less than 5.5 mg/L. Conclusion: We propose that all patients with newly diagnosed multiple myeloma be evaluated for these three chromosomal changes, not only to define high-risk patients but also to identify those with a longer life expectancy. © 2012 by American Society of Clinical Oncology.
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CITATION STYLE
Avet-Loiseau, H., Attal, M., Campion, L., Caillot, D., Hulin, C., Marit, G., … Moreau, P. (2012). Long-term analysis of the ifm 99 trials for myeloma: Cytogenetic abnormalities [t(4;14), del(17p), 1q gains] play a major role in defining long-term survival. Journal of Clinical Oncology, 30(16), 1949–1952. https://doi.org/10.1200/JCO.2011.36.5726
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