Evidence map›Paper›PMID 38065967›Full record

ArticleBlood cancer journal2023

Real world data on outcomes of anti-CD38 antibody treated, including triple class refractory, patients with multiple myeloma: a multi-institutional report from the Canadian Myeloma Research Group (CMRG) Database.

A Visram, A De La Torre, D White, J Su, E Masih-Khan, M Chu, V Jimenez-Zepeda, A McCurdy, R LeBlanc, K Song and 12 more

Abstract readMulticenter Study
In one paragraph

Article in Blood cancer journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Trial
  2. Article
  3. Observational
  4. Article
  5. Review
  6. Review
  7. Review
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.

A VisramDepartment of Medicine, The Ottawa Hospital, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID http://orcid.org/0000-0002-7201-4642
A De La TorreDivision of Hematology, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada.
D WhiteDivision of Hematology, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, NS, Canada.
J SuCanadian Myeloma Research Group, Toronto, ON, Canada.
E Masih-KhanCanadian Myeloma Research Group, Toronto, ON, Canada.
M ChuDepartment of Oncology, Cross Cancer Institute, Edmonton, Alberta, Edmonton, AB, Canada.
V Jimenez-ZepedaTom Baker Cancer Center, Department of Hematology, University of Calgary, Calgary, AB, Canada.
A McCurdyDepartment of Medicine, The Ottawa Hospital, The Ottawa Hospital Research Institute, Ottawa, ON, Canada.ORCID http://orcid.org/0000-0002-8809-4368
R LeBlancHôpital Maisonneuve-Rosemont, Université de Montréal, Montreal, QC, Canada.
K SongThe Leukemia/Bone Marrow Transplant Program of BC, British Columbia Cancer Agency, Vancouver, Canada.
H MianJuravinski Cancer Centre (Hamilton-CCO), Hamilton, ON, Canada.ORCID http://orcid.org/0000-0003-1584-1067
M LouzadaUniversity of Western Ontario, London Health Sciences Centre, London, ON, Canada.
M SebagDivision of Hematology, McGill University Health Centre, Montreal, QC, Canada.
D BergstromDivision of Hematology, Memorial University of Newfoundland, St John's, Newfoundland and Labrador, Canada.
J StakiwSaskatoon Cancer Centre, Saskatoon, SK, Canada.
A ReimanOncology, Saint John Regional Hospital, Saint John, NB, Canada.
R KotbMedical Oncology and Hematology, Cancer Care Manitoba, Winnipeg, MB, Canada.
M AslamAllan Blair Cancer Center, Regina, SK, Canada.
C VennerBC Cancer - Vancouver Centre, Lymphoma and Myeloma Program, University of British Columbia, Vancouver, BC, Canada.
R KaedbeySegal Cancer Centre, Jewish General Hospital, McGill University, Montreal, Montreal, QC, Canada.
E GulCanadian Myeloma Research Group, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-3922-3215
D ReeceCanadian Myeloma Research Group, Toronto, ON, Canada. donna.reece@uhn.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) remains incurable despite the availability of novel agents. This multi-center retrospective cohort study used the Canadian Myeloma Research Group Database to describe real-world outcomes of patients withanti-CD38 monoclonal antibody (mAb) refractory MM subsequently treated with standard of care (SoC) regimens. Patients with triple class refractory (TCR) disease (refractory to a proteasome inhibitor, immunomodulatory drug, and anti-CD38 mAb) were examined as a distinct cohort. Overall, 663 patients had disease progression on anti-CD38 mAb therapy, 466 received further treatment (346 with SoC regimens were included, 120 with investigational agents on clinical trial and were excluded). The median age at initiation of subsequent SoC therapy of 67.9 (range 39.6-89.6) years with a median of 3 prior lines (range 1-9). The median PFS and OS from the start of subsequent therapy was 4.6 (95% CI 4.1-5.6) months and 13.3 (95% CI 10.6-16.6) months, respectively. The median PFS and OS of patients with TCR disease (n = 199) was 4.4 (95% CI 3.6-5.3) months and 10.5 (95% CI 8.5-13.8) months. Our results reinforce that real-world patients with relapsed MM, particularly those with TCR disease, have dismal outcomes. There remains an urgent unmet need for the development of and access to effective therapeutics for these patients.

Indexed as

Antineoplastic AgentsMultiple MyelomaAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsCanadaHumansMiddle AgedReceptors, Antigen, T-CellRetrospective StudiesAntineoplastic AgentsReceptors, Antigen, T-Cell

Identifiers

PMID38065967
PMCPMC10709576

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Registered trials

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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.