Mobilization in myeloma revisited: IMWG consensus perspectives on stem cell collection following initial therapy with thalidomide-, lenalidomide-, or bortezomib-containing regimens

Shaji Kumar(Mayo Clinic in Arizona), Sergio Giralt(The University of Texas MD Anderson Cancer Center), Edward A. Stadtmauer(University of Pennsylvania), Jean Luc Harousseau, Antonio Palumbo(Azienda Ospedaliero Universitaria San Giovanni Battista), William Bensinger(Fred Hutch Cancer Center), Raymond L. Comenzo(Memorial Sloan Kettering Cancer Center), Suzanne Lentzsch(UPMC Hillman Cancer Center), Nikhil C. Munshi(Dana-Farber Cancer Institute), Rubén Niesvizky(Cornell University), Jesús F. San Miguel(Centro de Investigación del Cáncer), Heinz Ludwig(Wilhelminen Hospital), Leif Bergsagel(Mayo Clinic in Arizona), Joan Bladé(Hospital Clínic de Barcelona), Sagar Lonial(Emory University), Kenneth C. Anderson(Dana-Farber Cancer Institute), Patrizia Tosi(University of Bologna), Pieter Sonneveld(Erasmus MC), Orhan Sezer(Berlin University of the Arts), David H. Vesole(Loyola University Chicago), Michèle Cavo(Istituto Oncologico Romagnolo), Hermann Einsele(University of Würzburg), Paul G. Richardson(Dana-Farber Cancer Institute), Brian G.M. Durie, S. Vincent Rajkumar(Mayo Clinic in Arizona)
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Abstract

The past decade has witnessed a paradigm shift in the initial treatment of multiple myeloma with the introduction of novel agents such as thalidomide, lenalidomide, and bortezomib, leading to improved outcomes. High-dose therapy and autologous stem cell transplantation remains an important therapeutic option for patients with multiple myeloma eligible for the procedure. Before the advent of the novel agents, patients underwent stem cell collection prior to significant alkylating agent exposure, given its potential deleterious effect on stem cell collection. With increasing use of the novel agents in the upfront setting, several reports have emerged raising concerns about their impact on the ability to collect stem cells. An expert panel of the International Myeloma Working Group (IMWG) was convened to examine the implications of these therapies on stem collection in patients with myeloma and to develop recommendations for addressing these issues. Here we summarize the currently available data and present our perspective on the problem and potential options to overcome this problem. Specifically, we recommend early mobilization of stem cells, preferably within the first 4 cycles of initial therapy, in patients treated with novel agents and encourage participation in clinical trials evaluating novel approaches to stem cell mobilization.


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