Developments in continuous therapy and maintenance treatment approaches for patients with newly diagnosed multiple myeloma.


Journal

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

Informations de publication

Date de publication:
13 02 2020
Historique:
received: 13 05 2019
accepted: 18 09 2019
revised: 13 09 2019
entrez: 15 2 2020
pubmed: 15 2 2020
medline: 31 10 2020
Statut: epublish

Résumé

The evolving paradigm of continuous therapy and maintenance treatment approaches in multiple myeloma (MM) offers prolonged disease control and improved outcomes compared to traditional fixed-duration approaches. Potential benefits of long-term strategies include sustained control of disease symptoms, as well as continued cytoreduction and clonal control, leading to unmeasurable residual disease and the possibility of transforming MM into a chronic or functionally curable condition. "Continuous therapy" commonly refers to administering a doublet or triplet regimen until disease progression, whereas maintenance approaches typically involve single-agent or doublet treatment following more intensive prior therapy with autologous stem cell transplant (ASCT) or doublet, triplet, or even quadruplet induction therapy. However, the requirements for agents and regimens within these contexts are similar: treatments must be tolerable for a prolonged period of time, should not be associated with cumulative or chronic toxicity, should not adversely affect patients' quality of life, should ideally be convenient with a minimal treatment burden for patients, and should not impact the feasibility or efficacy of subsequent treatment at relapse. Multiple agents have been and are being investigated as long-term options in the treatment of newly diagnosed MM (NDMM), including the immunomodulatory drugs lenalidomide and thalidomide, the proteasome inhibitors bortezomib, carfilzomib, and ixazomib, and the monoclonal antibodies daratumumab, elotuzumab, and isatuximab. Here we review the latest results with long-term therapy approaches in three different settings in NDMM: (1) maintenance treatment post ASCT; (2) continuous frontline therapy in nontransplant patients; (3) maintenance treatment post-frontline therapy in the nontransplant setting. We also discuss evidence from key phase 3 trials. Our review demonstrates how the paradigm of long-term treatment is increasingly well-established across NDMM treatment settings, potentially resulting in further improvements in patient outcomes, and highlights key clinical issues that will need to be addressed in order to provide optimal benefit.

Identifiants

pubmed: 32054831
doi: 10.1038/s41408-020-0273-x
pii: 10.1038/s41408-020-0273-x
pmc: PMC7018731
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

17

Subventions

Organisme : NCI NIH HHS
ID : P01 CA155258
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180888
Pays : United States

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Auteurs

Meletios A Dimopoulos (MA)

Hematology & Medical Oncology, Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. mdimop@med.uoa.gr.

Andrzej J Jakubowiak (AJ)

University of Chicago Medical Center, Chicago, IL, USA.

Philip L McCarthy (PL)

Roswell Park Comprehensive Cancer Center, Buffalo, NY, USA.

Robert Z Orlowski (RZ)

Department of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Michel Attal (M)

Hematology Department, University Hospital Purpan, Toulouse, France.

Joan Bladé (J)

Hematology Department, Hospital Clinic, Institut de Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.

Hartmut Goldschmidt (H)

Department of Internal Medicine V, University Medical Hospital and National Center of Tumor Diseases, University of Heidelberg, Heidelberg, Germany.

Katja C Weisel (KC)

Department of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Karthik Ramasamy (K)

Oxford University Hospitals, NHS Foundation Trust, Oxford, UK.

Sonja Zweegman (S)

Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Center, VU University Amsterdam, Amsterdam, The Netherlands.

Andrew Spencer (A)

Malignant Haematology and Stem Cell Transplantation Service, Alfred Health-Monash University, Melbourne, Australia.

Jeffrey S Y Huang (JSY)

National Taiwan University, Taipei, Taiwan.

Jin Lu (J)

Department of Hematology, Peking University People's Hospital and Peking University Institute of Hematology, Beijing, China.

Kazutaka Sunami (K)

Department of Hematology, National Hospital Organization Okayama Medical Center, Okayama, Japan.

Shinsuke Iida (S)

Department of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Wee-Joo Chng (WJ)

Department of Haematology-Oncology, National University Cancer Institute, National University Health System, and Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.

Sarah A Holstein (SA)

Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.

Alberto Rocci (A)

Department of Haematology, Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
Faculty of Biology, Medicine and Health, School of Medical Science, Division of Cancer Science, University of Manchester, Manchester, UK.

Tomas Skacel (T)

Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.

Richard Labotka (R)

Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.

Antonio Palumbo (A)

Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.

Kenneth C Anderson (KC)

Dana-Farber Cancer Institute, Boston, MA, USA.

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