Haematologica
(Sep 2015)
Four genes predict high risk of progression from smoldering to symptomatic multiple myeloma (SWOG S0120)
Rashid Khan,
Madhav Dhodapkar,
Adam Rosenthal,
Christoph Heuck,
Xenofon Papanikolaou,
Pingping Qu,
Frits van Rhee,
Maurizio Zangari,
Yogesh Jethava,
Joshua Epstein,
Shmuel Yaccoby,
Antje Hoering,
John Crowley,
Nathan Petty,
Clyde Bailey,
Gareth Morgan,
Bart Barlogie
Affiliations
Rashid Khan
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Madhav Dhodapkar
Yale School of Medicine, New Haven, CT, USA
Adam Rosenthal
Cancer Research And Biostatistics, Seattle, WA, USA
Christoph Heuck
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Xenofon Papanikolaou
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Pingping Qu
Cancer Research And Biostatistics, Seattle, WA, USA
Frits van Rhee
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Maurizio Zangari
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Yogesh Jethava
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Joshua Epstein
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Shmuel Yaccoby
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Antje Hoering
Cancer Research And Biostatistics, Seattle, WA, USA
John Crowley
Cancer Research And Biostatistics, Seattle, WA, USA
Nathan Petty
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Clyde Bailey
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Gareth Morgan
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
Bart Barlogie
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR, USA
DOI
https://doi.org/10.3324/haematol.2015.124651
Journal volume & issue
Vol. 100,
no. 9
Abstract
Read online
Multiple myeloma is preceded by an asymptomatic phase, comprising monoclonal gammopathy of uncertain significance and smoldering myeloma. Compared to the former, smoldering myeloma has a higher and non-uniform rate of progression to clinical myeloma, reflecting a subset of patients with higher risk. We evaluated the gene expression profile of smoldering myeloma plasma cells among 105 patients enrolled in a prospective observational trial at our institution, with a view to identifying a high-risk signature. Baseline clinical, bone marrow, cytogenetic and radiologic data were evaluated for their potential to predict time to therapy for symptomatic myeloma. A gene signature derived from four genes, at an optimal binary cut-point of 9.28, identified 14 patients (13%) with a 2-year therapy risk of 85.7%. Conversely, a low four-gene score (
Published in Haematologica
ISSN
0390-6078 (Print)
1592-8721 (Online)
Publisher
Ferrata Storti Foundation
Country of publisher
Italy
LCC subjects
Medicine: Internal medicine: Specialties of internal medicine: Diseases of the blood and blood-forming organs
Website
http://www.haematologica.org
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