Results of high-dose therapy for 1000 patients with multiple myeloma: durable complete remissions and superior survival in the absence of chromosome 13 abnormalities

Raman Desikan(Fred Hutch Cancer Center), Bart Barlogie(Fred Hutch Cancer Center), Jeffrey R. Sawyer(Fred Hutch Cancer Center), Dan Ayers(Fred Hutch Cancer Center), Guido Tricot(Fred Hutch Cancer Center), Ashraf Badros(Fred Hutch Cancer Center), Maurizio Zangari(Fred Hutch Cancer Center), Nikhil C. Munshi(Fred Hutch Cancer Center), Elias Anaissie(Fred Hutch Cancer Center), Dan Spoon(Fred Hutch Cancer Center), David S. Siegel(Fred Hutch Cancer Center), Sundar Jagannath(Fred Hutch Cancer Center), David H. Vesole(Fred Hutch Cancer Center), Joshua Epstein(Fred Hutch Cancer Center), John D. Shaughnessy(Fred Hutch Cancer Center), Athanasios Fassas(Fred Hutch Cancer Center), Seah H. Lim(Fred Hutch Cancer Center), Paula K. Roberson(Fred Hutch Cancer Center), John Crowley(Fred Hutch Cancer Center)
Blood
June 15, 2000
Cited by 319

Abstract

High-dose therapy (HDT) has increased complete remission (CR) rates and survival in multiple myeloma (MM). We now report on continuous CR (CCR) and associated prognostic factors in 1000 consecutive patients receiving melphalan-based tandem HDT. Five-year CCR was 52% among 112 CR patients without chromosome 13 (triangle up13) abnormalities and with beta-2-microglobulin </= 2.5 mg/L, C-reactive protein </= 4 mg/L, and pre-HDT standard chemotherapy </= 12 months. Of all 390 CR patients without triangle up13 abnormalities, 35% enjoyed 5-year CCR but none of 54 with triangle up13 abnormalities. triangle up13 abnormalities, present in overall 16%, reduced 5-year event-free survival from 20% to 0% and overall survival from 44% to 16% (both P <.0001). CR and a second HDT cycle applied within 6 months both extended event-free and overall survival significantly, justifying further pursuit of HDT, especially toward curing non-triangle up13 MM. (Blood. 2000;95:4008-4010)


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