Evidence map›Paper›PMID 40817326›Full record

ReviewBiomarker research2025

Targeting degradation of IKZF1 and IKZF3 through modulation of the E3 ligase substrates in the context of cellular therapies for multiple myeloma.

David Kegyes, Anamaria Bancos, Adrian Bogdan Tigu, Ioana Rus, Delia Dima, Diana Cenariu, Madalina Nistor, Raluca Munteanu, Diana Gulei, Alina Tanase and 9 more

Abstract readReview
In one paragraph

Review in Biomarker research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

19 authors.

David KegyesDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Anamaria BancosDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Adrian Bogdan TiguDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Ioana RusDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Delia DimaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Diana CenariuDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Madalina NistorDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Raluca MunteanuDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Diana GuleiDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Alina TanaseDepartment of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.
Anca ColitaDepartment of Stem Cell Transplantation, Fundeni Clinical Institute, Bucharest, Romania.
Anca BuzoianuDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Cristina IugaDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Mihnea ZdrengheaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania.
Evangelos TerposDepartment of Clinical Therapeutics, School of Medicine, National and Kapodistrian University of Athens, Alexandra General Hospital, Athens, Greece.
Stefan O CiureaHematopoietic Stem Cell Transplantation and Cellular Therapy Program, Division of Hematology/Oncology, Department of Medicine, University of California Irvine, Irvine, CA, USA.
Aaron CiechanoverDepartment of Cell Biology and Cancer Science, Rappaport Faculty of Medicine, Technion- Israel Institute of Technology, Haifa, Israel.
Hermann EinseleDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania.
Ciprian TomuleasaDepartment of Translational Medicine, Medfuture Institute of Medical Research and Life Sciences, Cluj-Napoca, Romania. ciprian.tomuleasa@umfcluj.ro.

Funding

European Hematology Association CAR NK cells for tumor associated macrophage immunomodulation-a new era of immunotherapyMinisterul Cercetării şi Inovării PNRR/2022/C9/MCID/18, Contract No. 760278/26.03.2024Professorship from the Israel Cancer Research Fund AC
6 · The paper itself

Abstract

Multiple myeloma (MM) is a blood cancer characterized by the clonal evolution of plasma cells. In 2022, there were an estimated 118 000 MM cases and 121 000 deaths worldwide. The treatment landscape of MM has undergone a dramatic transformation in recent decades, shifting from conventional chemotherapy to more targeted approaches. In order to overcome intrinsic and acquired resistance mechanisms that frequently restrict the efficacy of single-agent therapies, drug combination strategies have been developed to simultaneously target multiple pathogenetic pathways. Building on the success of immunomodulatory agents, CRBN E3 ligase modulators (CELMoDs), iberdomide (CC-220) and mezigdomide (CC-92480), have been designed as promising and more selective agents. CELMoDs demonstrate a 10-20 times higher binding capacity and they promote a more profound and rapid breakdown of Ikaros and Aiolos compared to traditional immunomodulatory agents. According to the National Cancer Institute Surveillance Program, the median survival for fit patients is greater than ten years, and the 5-year survival for the general MM patient population in the US approaches 60%. Despite these encouraging numbers, MM is still an incurable disease, and the majority of patients eventually relapse and require additional lines of therapy. Combining CELMoDs with cellular therapies significantly improves the response rate in MM patients. In this paper, based on the literature presented at the Annual Meeting of the American Society of Hematology (ASH), the American Society of Clinical Oncology (ASCO), the International Myeloma Society (IMS), and the European Hematology Association (EHA) in the 2020-2025 timeframe, we explore the rationale and emerging evidence of combining CELMoDs with immunotherapies, and their use as a bridge to transplant or as post-ASCT maintenance therapy in MM.

Indexed as

Autologous hematopoietic stem cell transplantationCAR t-cell therapyCC-220CC-92480CELMoDIberdomideImmunotherapiesMezigdomideMultiple myelomaT-cell engager

Identifiers

PMID40817326
PMCPMC12357425

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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.