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A pilot study of pembrolizumab in smoldering myeloma: report of the clinical, immune, and genomic analysis.

Authors :
Manasanch EE
Han G
Mathur R
Qing Y
Zhang Z
Lee H
Weber DM
Amini B
Berkova Z
Eterovic K
Zhang S
Zhang J
Song X
Mao X
Morgan M
Feng L
Baladandayuthapani V
Futreal A
Wang L
Neelapu SS
Orlowski RZ
Source :
Blood advances [Blood Adv] 2019 Aug 13; Vol. 3 (15), pp. 2400-2408.
Publication Year :
2019

Abstract

Multiple myeloma is, in most patients, an incurable cancer. Its precursors can be identified with routine tests setting the stage for early intervention to prevent active myeloma. We investigated the efficacy and safety of pembrolizumab, an antiprogrammed cell death 1 antibody, in smoldering myeloma patients with intermediate/high risk of progression to symptomatic myeloma. Thirteen patients were treated with a median number of 8 cycles. One patient achieved a stringent complete response with bone marrow next-generation sequencing negativity at 10 <superscript>-4</superscript> that is ongoing at 27 months (8%); 11 had stable disease (85%), and 1 progressed (8%). Three patients discontinued therapy due to immune-related adverse events: 2 with transaminitis and 1 due to tubulointerstitial nephritis. Immune profiling of bone marrow samples at baseline showed markers associated with a preexisting immune response in the responder compared with nonresponders and features of increased T-cell exhaustion in nonresponders. Consistent with this, transcriptome sequencing of bone marrow samples at baseline revealed an increased interferon-γ signature in the responder compared with the nonresponders. In summary, our results suggest that smoldering myeloma may be immunogenic in a subset of patients, and therapies that enhance antitumor T-cell responses may be effective in preventing its progression. This trial was registered at www.clinicaltrials.gov as #NCT02603887.<br /> (© 2019 by The American Society of Hematology.)

Details

Language :
English
ISSN :
2473-9537
Volume :
3
Issue :
15
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
31405950
Full Text :
https://doi.org/10.1182/bloodadvances.2019000300