Gaps and opportunities in the treatment of relapsed-refractory multiple myeloma: Consensus recommendations of the NCI Multiple Myeloma Steering Committee.


Journal

Blood cancer journal
ISSN: 2044-5385
Titre abrégé: Blood Cancer J
Pays: United States
ID NLM: 101568469

Informations de publication

Date de publication:
29 06 2022
Historique:
received: 13 02 2022
accepted: 08 06 2022
revised: 29 05 2022
entrez: 29 6 2022
pubmed: 30 6 2022
medline: 2 7 2022
Statut: epublish

Résumé

A wide variety of new therapeutic options for Multiple Myeloma (MM) have recently become available, extending progression-free and overall survival for patients in meaningful ways. However, these treatments are not curative, and patients eventually relapse, necessitating decisions on the appropriate choice of treatment(s) for the next phase of the disease. Additionally, an important subset of MM patients will prove to be refractory to the majority of the available treatments, requiring selection of effective therapies from the remaining options. Immunomodulatory agents (IMiDs), proteasome inhibitors, monoclonal antibodies, and alkylating agents are the major classes of MM therapies, with several options in each class. Patients who are refractory to one agent in a class may be responsive to a related compound or to a drug from a different class. However, rules for selection of alternative treatments in these situations are somewhat empirical and later phase clinical trials to inform those choices are ongoing. To address these issues the NCI Multiple Myeloma Steering Committee formed a relapsed/refractory working group to review optimal treatment choices, timing, and sequencing and provide recommendations. Additional issues considered include the role of salvage autologous stem cell transplantation, risk stratification, targeted approaches for genetic subsets of MM, appropriate clinical trial endpoints, and promising investigational agents. This report summarizes the deliberations of the working group and suggests potential avenues of research to improve the precision, timing, and durability of treatments for Myeloma.

Identifiants

pubmed: 35768410
doi: 10.1038/s41408-022-00695-5
pii: 10.1038/s41408-022-00695-5
pmc: PMC9243011
doi:

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

98

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© 2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.

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Auteurs

Shaji Kumar (S)

Hematologic Malignancies, Mayo Clinic College of Medicine and Science, Rochester, USA.

Lawrence Baizer (L)

Division of Lung Diseases, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, MD, USA. baizerl@mail.nih.gov.

Natalie S Callander (NS)

Myeloma Clinical Program, University of Wisconsin Carbone Cancer Center, Madison, USA.

Sergio A Giralt (SA)

Division of Hematologic Malignancies, Memorial Sloan Kettering Cancer Center, Madison, USA.

Jens Hillengass (J)

Oncology and Internal Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, USA.

Boris Freidlin (B)

Biometric Research Program, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Antje Hoering (A)

Cancer Research and Biostatistics and University of Washington School of Public Health, Seattle, USA.

Paul G Richardson (PG)

Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Boston, USA.

Elena I Schwartz (EI)

Coordinating Center for Clinical Trials, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Anthony Reiman (A)

University of New Brunswick, Department of Medicine, Dalhousie University Department of Oncology, Saint John Regional Hospital, Fredericton, Canada.

Suzanne Lentzsch (S)

Multiple Myeloma and Amyloidosis Service, Department of Medicine, Columbia University Medical Center, New York, USA.

Philip L McCarthy (PL)

Department of Medicine, Oncology and Internal Medicine, Transplant & Cellular Therapy Center, Roswell Park Comprehensive Cancer Center, Buffalo, USA.

Sundar Jagannath (S)

Division of Hematology and Medical Oncology, Mount Sinai School of Medicine, Center of Excellence for Multiple Myeloma, New York, USA.

Andrew J Yee (AJ)

Department of Medicine, Harvard Medical School, Multiple Myeloma Program, Medical Oncology, Massachusetts General Hospital, Boston, USA.

Richard F Little (RF)

Clinical Investigations Branch, Cancer Therapy Evaluation Program, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Noopur S Raje (NS)

Department of Medicine, Harvard Medical School, Multiple Myeloma Program, Medical Oncology, Massachusetts General Hospital, Boston, USA.

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