Evidence map›Paper›PMID 32054831›Full record

ReviewBlood cancer journal2020

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

Meletios A Dimopoulos, Andrzej J Jakubowiak, Philip L McCarthy, Robert Z Orlowski, Michel Attal, Joan Bladé, Hartmut Goldschmidt, Katja C Weisel, Karthik Ramasamy, Sonja Zweegman and 12 more

Open access · goldAbstract readReview
In one paragraph

Review in Blood cancer journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
10.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 117 citations in OpenAlex.

  1. Pooled it
  2. A Novel Digital Educational Strategy Improves Treatment Adherence and Quality of Life in Patients with Multiple Myeloma.Journal of cancer education : the official journal of the American Association for Cancer Education · 2024
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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 19 institutions in 11 countries.

Meletios A DimopoulosHematology & Medical Oncology, Department of Clinical Therapeutics, National and Kapodistrian University of Athens, School of Medicine, Athens, Greece. mdimop@med.uoa.gr.
Andrzej J JakubowiakUniversity of Chicago Medical Center, Chicago, IL, USA.
Philip L McCarthyRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Robert Z OrlowskiDepartment of Lymphoma/Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michel AttalHematology Department, University Hospital Purpan, Toulouse, France.
Joan BladéHematology Department, Hospital Clinic, Institut de Investigacions Biomediques August Pi I Sunyer (IDIBAPS), Barcelona, Spain.
Hartmut GoldschmidtDepartment of Internal Medicine V, University Medical Hospital and National Center of Tumor Diseases, University of Heidelberg, Heidelberg, Germany.
Katja C WeiselDepartment of Oncology, Hematology and Bone Marrow Transplantation with Section of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Karthik RamasamyOxford University Hospitals, NHS Foundation Trust, Oxford, UK.
Sonja ZweegmanDepartment of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Center, VU University Amsterdam, Amsterdam, The Netherlands.
Andrew SpencerMalignant Haematology and Stem Cell Transplantation Service, Alfred Health-Monash University, Melbourne, Australia.
Jeffrey S Y HuangNational Taiwan University, Taipei, Taiwan.
Jin LuDepartment of Hematology, Peking University People's Hospital and Peking University Institute of Hematology, Beijing, China.
Kazutaka SunamiDepartment of Hematology, National Hospital Organization Okayama Medical Center, Okayama, Japan.ORCID http://orcid.org/0000-0002-8229-7439
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Wee-Joo ChngDepartment 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 HolsteinDepartment of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, USA.
Alberto RocciDepartment of Haematology, Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
Tomas SkacelMillennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.
Richard LabotkaMillennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.
Antonio PalumboMillennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA.
Kenneth C AndersonDana-Farber Cancer Institute, Boston, MA, USA.
Takeda (United States) · USAlfred Health · AUConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESDana-Farber Cancer Institute · USHeidelberg University · DEHôpital Purpan · FRManchester Academic Health Science Centre · GBNagoya City University · JPNational and Kapodistrian University of Athens · GRNational Hospital Organization · JPNational Taiwan University · TWNational University of Singapore · SGOxford University Hospitals NHS Trust · GBPeking University · CNRoswell Park Comprehensive Cancer Center · USThe University of Texas MD Anderson Cancer Center · USUniversität Hamburg · DEUniversity of Chicago Medical Center · USUniversity of Nebraska Medical Center · US

Funding

SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
NCI NIH HHS P01 CA155258NCI NIH HHS U10 CA180888
6 · The paper itself

Abstract

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.

Indexed as

Quality of LifeHematopoietic Stem Cell TransplantationHumansMaintenance ChemotherapyMultiple MyelomaPrognosis

Identifiers

PMID32054831
PMCPMC7018731
OpenAlexW3006419152

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.