Evidence map›Paper›PMID 36779512›Full record

ArticleFuture oncology (London, England)2023

A phase II multi-arm study of magrolimab combinations in patients with relapsed/refractory multiple myeloma.

Barry Paul, Michaela Liedtke, Jack Khouri, Robert Rifkin, Mitul D Gandhi, Andrew Kin, Moshe Y Levy, Rebecca Silbermann, Francesca Cottini, Douglas W Sborov and 7 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial Protocol
In one paragraph

Article in Future oncology (London, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04892446 (A Phase 2 Multi-Arm Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma), which is not on this map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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.

NCT04892446 phase2terminatednot on this map

A Phase 2 Multi-Arm Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma

TypeinterventionalSponsorGilead SciencesRan2021 to 2024Enrolled36ConditionsMultiple MyelomaArmsMagrolimab, Daratumumab, Pomalidomide, Dexamethasone, Bortezomib
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Immunotherapy of Multiple Myeloma: Current Status as Prologue to the Future.International journal of molecular sciences · 2023
    Review
  10. Review
  11. 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

17 authors at 13 institutions in 2 countries.

Barry PaulLevine Cancer Institute, Department of Hematologic Oncology and Blood Disorders, Charlotte, NC 28204, USA.ORCID 0000-0003-2702-8225
Michaela LiedtkeStanford Cancer Institute, Stanford Comprehensive Cancer Center, Stanford, CA 94305, USA.ORCID 0000-0001-8945-5850
Jack KhouriTaussig Cancer Institute, Cleveland Clinic, Department of Hematology and Medical Oncology, Cleveland, OH 44195, USA.ORCID 0000-0002-2473-6528
Robert RifkinRocky Mountain Cancer Centers, US Oncology Research, Denver, CO 80218, USA.ORCID 0000-0003-3141-1518
Mitul D GandhiVirginia Cancer Specialists, Gainesville, VA 20155, USA.ORCID 0000-0002-3263-2374
Andrew KinBarbara Ann Karmanos Cancer Institute, Wayne State University, Department of Oncology, Detroit, MI 48201, USA.
Moshe Y LevyBaylor University Medical Center, Department of Hematology and Medical Oncology, Dallas, TX 75246, USA.
Rebecca SilbermannOregon Health & Science University, Division of Hematology/Medical Oncology, Portland, OR 97239, USA.ORCID 0000-0002-7571-1523
Francesca CottiniThe Ohio State University Comprehensive Cancer Center, Department of Internal Medicine, Columbus, OH 43210, USA.ORCID 0000-0001-8676-7840
Douglas W SborovHuntsman Cancer Institute, University of Utah, Department of Internal Medicine, Salt Lake City, UT 84112, USA.ORCID 0000-0003-4268-2698
Irwindeep SandhuCross Cancer Institute, University of Alberta, Department of Oncology, Edmonton, Alberta, T6G 1Z2, Canada.ORCID 0000-0001-9407-6265
Lyssa VillarrealGilead Sciences, Inc, Foster City, CA 94404, USA.
Michael MurphyGilead Sciences, Inc, Foster City, CA 94404, USA.ORCID 0000-0001-6529-6824
Lin GuGilead Sciences, Inc, Foster City, CA 94404, USA.ORCID 0000-0003-4593-8572
Ann ChenGilead Sciences, Inc, Foster City, CA 94404, USA.
Nishanthan RajakumaraswamyGilead Sciences, Inc, Foster City, CA 94404, USA.ORCID 0000-0002-0226-0637
Saad Z UsmaniMemorial Sloan Kettering Cancer Center, New York City, NY 10065, USA.ORCID 0000-0002-5484-8731
Gilead Sciences (United States) · USBaylor University Medical Center · USCleveland Clinic · USLevine Cancer Institute · USMemorial Sloan Kettering Cancer Center · USOregon Health & Science University · USRocky Mountain Cancer Centers · USStanford Cancer InstituteThe Ohio State University · USUniversity of Alberta · CAUniversity of Utah · USVirginia Cancer Specialists · USWayne State University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Network Lead Academic Participating Site: Memorial Sloan Kettering Cancer CenterUG1CA233290 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CAROL AGHAJANIAN, Darren Feldman · 2019 to 2026
$10.2M
NCI NIH HHS P30 CA008748NCI NIH HHS UG1 CA233290
6 · The paper itself

Abstract

Magrolimab is a monoclonal antibody that blocks CD47, a 'do not eat me' signal overexpressed on tumor cells. CD47 is overexpressed in multiple myeloma (MM), which contributes to its pathogenesis. Preclinical studies have shown that CD47 blockade induces macrophage activation, resulting in elimination of myeloma cells, and that there is synergy between magrolimab and certain anticancer therapies. These findings suggest that magrolimab-based combinations may have a therapeutic benefit in MM. This phase II study investigates magrolimab in combination with commonly used myeloma therapies in patients with relapsed/refractory MM and includes a safety run-in phase followed by a dose-expansion phase. Primary end points include the incidence of dose-limiting toxicities and adverse events (safety run-in) and the objective response rate (dose expansion).

Indexed as

Multiple MyelomaAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCD47 AntigenClinical Trials, Phase I as TopicClinical Trials, Phase II as TopicDexamethasoneHumansNeoplasm Recurrence, LocalAntibodies, Monoclonal, HumanizedCD47 AntigenDexamethasonemagrolimabbortezomibcarfilzomibCD47daratumumabdexamethasoneimmunotherapymagrolimabmultiple myelomapomalidomide

Identifiers

PMID36779512
PMCPMC10463212
OpenAlexW4320491137

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.