Evidence map›Paper›PMID 42846987›Full record

ArticleHemaSphere2026

Dual targeting of BCMA and GPRC5D with the trispecific antibody ramantamig addresses antigenic heterogeneity in myeloma.

Chloe O'Neill, Marloes E C Broekmans, Charlotte L B M Korst, Maria Krevvata, Giada Dal Collo, Richard W Groen, Bing Li, Serena R Baglio, Ulrike Philippar, Kodandaram Pillarisetti and 4 more

Abstract read
In one paragraph

Article in HemaSphere, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Chloe O'NeillDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.ORCID https://orcid.org/0000-0003-3301-2932
Marloes E C BroekmansDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
Charlotte L B M KorstDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.ORCID https://orcid.org/0009-0005-0191-4343
Maria KrevvataJohnson&Johnson Spring House Pennsylvania United States.
Giada Dal ColloDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
Richard W GroenDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
Bing LiDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
Serena R BaglioDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC Vrije Universiteit Amsterdam Amsterdam The Netherlands.ORCID https://orcid.org/0000-0003-0503-8908
Ulrike PhilipparJohnson&Johnson Beerse Belgium.
Kodandaram PillarisettiJohnson&Johnson Spring House Pennsylvania United States.
Sonja ZweegmanDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.
Deeksha VishwamitraJohnson&Johnson Spring House Pennsylvania United States.
Tuna MutisDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.ORCID https://orcid.org/0000-0002-5557-7187
Niels W C J van de DonkDepartment of Hematology, Cancer Center Amsterdam Amsterdam UMC, Vrije Universiteit Amsterdam Amsterdam The Netherlands.ORCID https://orcid.org/0000-0002-7445-2603

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite advances in terms of bispecific antibodies (BsAbs) targeting single tumor-associated antigens in multiple myeloma (MM), not all patients respond, and most eventually relapse. Using flow cytometry, we found that BCMA and GPRC5D expression is highly heterogeneous within and between patients. Dual targeting with ramantamig (JNJ-79635322), a trispecific antibody targeting both BCMA and GPRC5D on the tumor cell surface, has been hypothesized to improve efficacy by overcoming heterogeneous target expression and preventing resistance due to antigen escape. Using T-cells from healthy donors, ramantamig was significantly more effective than mono-targeting antibodies against BCMA

Identifiers

PMID42846987
PMCPMC13644706

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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.