Evidence map›Paper›PMID 42237881›Full record

Observational studyBritish journal of haematology2026

Cesni-cel (ARI0002h) in ultra-high-risk multiple myeloma with plasma cell leukaemia or central nervous system involvement.

Carlos Jimenez-Mira, Natalia Tovar, Núria Martínez-Cibrián, Verónica González-Calle, Nil Albiol, Nieves López-Muñoz, Aina Oliver-Caldés, Azucena González, José Miguel Mateos, Marta Español-Rego and 16 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in British journal of haematology, 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
–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

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

26 authors.

Carlos Jimenez-MiraHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0009-0004-6293-2716
Natalia TovarHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Núria Martínez-CibriánHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Verónica González-CalleComplejo Asistencial Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca, Salamanca, Spain.
Nil AlbiolHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0003-2942-1362
Nieves López-MuñozHospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Universidad Complutense de Madrid, Madrid, Spain.
Aina Oliver-CaldésHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0002-7921-5420
Azucena GonzálezHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
José Miguel MateosHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Marta Español-RegoHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Laura RosiñolHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Manel JuanHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Paola CharryHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
José María Sanchez-PinaHospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Universidad Complutense de Madrid, Madrid, Spain.
Sergio NavarroHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Daniel MunárrizHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Lucía López-CorralComplejo Asistencial Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca, Salamanca, Spain.
Valentín Ortiz-MaldonadoHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Sara VareaHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Eulalia OlestiHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Julio DelgadoHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Álvaro Urbano-IspizuaHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Joaquín Martínez-LópezHospital Universitario 12 de Octubre, Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Universidad Complutense de Madrid, Madrid, Spain.
María Victoria MateosComplejo Asistencial Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca (IBSAL), Universidad de Salamanca, Salamanca, Spain.ORCID https://orcid.org/0000-0003-2390-1218
Luis Gerardo Rodríguez-LobatoHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Carlos Fernández de LarreaHospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.ORCID https://orcid.org/0000-0003-4930-9255

Funding

CRIS Cancer Foundation TRANSPHYSTALENT_23_6Instituto de Salud Carlos III ICI19/00025Instituto de Salud Carlos III PI22/00647Instituto de Salud Carlos III PI25/00571
6 · The paper itself

Abstract

Ultra-high-risk multiple myeloma (uHRMM), defined by extra-medullary disease (EMD, including central nervous system [CNS] or plasma cell leukaemia [PCL]), remains as a predictor of early relapse after chimeric antigen receptor T cell (CAR-T) therapy. We analysed the characteristics, toxicities, response and survival of patients with PCL/CNS-multiple myeloma (MM) treated with cesnicabtagene autoleucel (ARI0002h) at three Spanish centres (2020-2025). PCL was defined as per International Myeloma Working Group (IMWG) 2021 criteria; CNS-MM by leptomeningeal and/or intraparenchymal involvement. Nineteen patients (68% female; median age 61) were included: 12 patients had PCL, 5 had CNS-MM, and 2 had dual involvement. Fifty per cent had primary PCL. In CNS-MM, all had leptomeningeal disease and one had also intraparenchymal lesions. Fifty-seven per cent received CNS-directed therapy. Seventy four per cent harboured high-risk cytogenetics. Median prior lines: 3; 74% had haematopoietic stem cell transplantation (HSCT); two had prior B-cell maturation antigen (BCMA) exposure. One patient died pre-apheresis and one during manufacturing; 17 (89%) received ARI0002h. Cytokine release syndrome (CRS) occurred in 76% (none ≥G3), G3 immune effector cell (IEC)-associated neurotoxicity syndrome (ICANS) occurred in one case (not CNS-MM) and IEC-associated haemophagocytic lymphohistiocytosis-like syndrome (IEC-HS) occurred in 18% (one fatal). Overall response rate (ORR) was 88% at day +100, of which 87% achieved ≥ very good partial response (VGPR) and 80% complete CNS response. Median progression-free survival (PFS) and overall survival (OS) were 10.5 and 15.9 months respectively. ARI0002h induces deep responses in relapsed uHRMM, supporting inclusion of PCL and CNS-MM in clinical trials.

Indexed as

Central Nervous System NeoplasmsImmunotherapy, AdoptiveLeukemia, Plasma CellMultiple MyelomaAdultAgedFemaleHumansMaleMiddle AgedBCMACAR‐Tcentral nervous systemmyelomaplasma cell leukaemia

Identifiers

PMID42237881
PMCPMC13462260

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