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= .007), with median PFS of 20.6 vs 15.6 months. This PFS benefit was consistent across subgroups with individual high-risk cytogenetic abnormalities, including patients with del(17p) (HR, 0.596; 95% CI, 0.286-1.243). PFS was also longer with IRd vs placebo-Rd in patients with 1q21 amplification (HR, 0.781; 95% CI, 0.492-1.240), and in the "expanded high-risk" group, defined as those with high-risk cytogenetic abnormalities and/or 1q21 amplification (HR, 0.664; 95% CI, 0.474-0.928). IRd demonstrated substantial benefit compared with placebo-Rd in relapsed and/or refractory MM (RRMM) patients with high-risk and standard-risk cytogenetics, and improves the poor PFS associated with high-risk cytogenetic abnormalities. This trial was registered at www.clinicaltrials.gov as #NCT01564537.
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Hervé Avet‐Loiseau
Boston University
Nizar J. Bahlis
University of Calgary
Wee Joo Chng
National University of Singapore
Blood
Dana-Farber Cancer Institute
University of Calgary
Mayo Clinic in Arizona
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Avet‐Loiseau et al. (Fri,) studied this question.
synapsesocial.com/papers/6a0e9ac6686442d1c4c8621a — DOI: https://doi.org/10.1182/blood-2017-06-791228