Author:
Jethava Y,Mitchell A,Zangari M,Waheed S,Schinke C,Thanendrarajan S,Sawyer J,Alapat D,Tian E,Stein C,Khan R,Heuck C J,Petty N,Avery D,Steward D,Smith R,Bailey C,Epstein J,Yaccoby S,Hoering A,Crowley J,Morgan G,Barlogie B,van Rhee F
Abstract
Abstract
Multiple myeloma (MM) is a heterogeneous disease with high-risk patients progressing rapidly despite treatment. Various definitions of high-risk MM are used and we reported that gene expression profile (GEP)-defined high risk was a major predictor of relapse. In spite of our best efforts, the majority of GEP70 high-risk patients relapse and we have noted higher relapse rates during drug-free intervals. This prompted us to explore the concept of less intense drug dosing with shorter intervals between courses with the aim of preventing inter-course relapse. Here we report the outcome of the Total Therapy 5 trial, where this concept was tested. This regimen effectively reduced early mortality and relapse but failed to improve progression-free survival and overall survival due to relapse early during maintenance.
Publisher
Springer Science and Business Media LLC
Cited by
27 articles.
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