Evidence map›Paper›PMID 40144211›Full record

SynthesisFrontiers in oncology2025

Clinical outcomes associated with anti-CD38-based retreatment in relapsed/refractory multiple myeloma: a systematic literature review.

Francesca Gay, Elena Zamagni, Craig Emmitt Cole, Christof Scheid, Malin Hultcrantz, Justyna Chorazy, Ike Iheanacho, Anuja Pandey, Jacopo Bitetti, Natalie Boytsov and 3 more

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

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

13 authors.

Francesca GayUniversity Division of Hematology, Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino, Torino, Italy.
Elena ZamagniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Istituto di Ematologia "Seràgnoli", Bologna, Italy.
Craig Emmitt ColeDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI, United States.
Christof ScheidDepartment I of Medicine, University Hospital Cologne, Cologne, Germany.
Malin HultcrantzMyeloma Service, Memorial Sloan Kettering Cancer Center, New York, NY, United States.
Justyna ChorazyEvidera, London, United Kingdom.
Ike IheanachoEvidera, London, United Kingdom.
Anuja PandeyEvidera, London, United Kingdom.
Jacopo BitettiGlobal Medical Affairs, GSK, Zug, Switzerland.
Natalie BoytsovValue Evidence and Outcomes, GSK, Upper Providence, PA, United States.
Molly PurserValue Evidence and Outcomes, GSK, Upper Providence, PA, United States.
Simon McNamaraGlobal Real World Evidence and Health Outcomes Research, GSK, Stevenage, United Kingdom.
Shinsuke IidaDepartment of Hematology and Oncology, Nagoya City University Institute of Medical and Pharmaceutical Sciences, Nagoya, Japan.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Introduction: Anti-CD38-based therapy has become a backbone regimen for the treatment of multiple myeloma (MM), approved in first-, second-, and third-line settings. The effectiveness of anti-CD38-based retreatment after an initial relapse on previous anti-CD38-based therapy is unclear. Here we present the results of a systematic literature review investigating the clinical outcomes of anti-CD38-based retreatment in patients with relapsed/refractory MM. Methods: Medline/Embase, congress publications, and other sources were searched (to December 8, 2023) for relevant articles in English and screened for eligibility criteria using the Population, Intervention, Comparator, Outcomes, Study Design (PICOS) framework, and data were then extracted for outcomes including progression-free survival (PFS), overall survival (OS), and overall response rate (ORR). Results: In total, 2938 records were identified from the initial Medline/Embase search and 11 were identified from other sources; 34 were eligible for inclusion, representing 24 studies (6 clinical [n=18-307] and 18 real-world evidence [RWE; n=19-583]). Where reported, median follow-up ranged from 1.9-43.0 months across 6 clinical and 8.7-53.0 months across 10 RWE studies. For clinical trials, anti-CD38-based retreatment resulted in a median PFS of 1.0-2.8 months in all but one trial (19.4 months), a median OS of 10.7-19.1 months (not reached in one trial), and ORRs of 0-75%. RWE studies reported a median PFS of 1.5-8.4 months, a median OS of 8.4-19.0 months (not reached in one study), and ORRs of 24.6-90.0%. Discussion: Findings from this systematic literature review indicate that clinical outcomes with anti-CD38-based retreatment are variable and offer limited clinical benefit in patients with relapsed/refractory MM, including in those refractory to anti-CD38-based treatment.

Indexed as

anti-CD38multiple myelomarelapsed/refractoryretreatmentsystematic literature review

Identifiers

PMID40144211
PMCPMC11938063

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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.