Evidence map›Paper›PMID 42351384›Full record

ArticleAmerican journal of hematology2026

Early Treatment Failure in Patients Receiving Ciltacabtagene-Autoleucel for Relapsed/Refractory Multiple Myeloma.

Kenneth J C Lim, Shaji Kumar, Ricardo Parrondo, Saurabh Chhabra, Melinda Tan, Katharine Dooley, Andre De Menezes Silva Corraes, Morie Gertz, Lisa Hwa, Haily Stephens and 15 more

Abstract readMulticenter Study
In one paragraph

Article in American journal of hematology, 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

25 authors.

Kenneth J C LimDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-2664-116X
Shaji KumarDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Ricardo ParrondoDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Jacksonville, Florida, USA.
Saurabh ChhabraDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona, USA.ORCID https://orcid.org/0000-0001-9117-8696
Melinda TanDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0003-1690-1447
Katharine DooleyDepartment of Research, Mayo Clinic, Rochester, Minnesota, USA.
Andre De Menezes Silva CorraesDepartment of Research, Mayo Clinic, Rochester, Minnesota, USA.
Morie GertzDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-3853-5196
Lisa HwaDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Haily StephensDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Prashant KapoorDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Taxiarchis KourelisDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Rahma WarsameDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Joselle CookDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0001-5335-9533
Moritz BinderDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0001-9014-9658
Nadine AbdallahDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0001-9195-1589
P Leif BergsagelDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona, USA.
Udit YadavDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona, USA.
J Erin Wiedmeier-NutorDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona, USA.ORCID https://orcid.org/0000-0001-9434-5269
Susan GeyerDepartment of Research, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0009-0002-5649-6909
S Vincent RajkumarDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0002-5862-1833
Sikander AilawadhiDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Jacksonville, Florida, USA.
Rafael FonsecaDivision of Hematology and Medical Oncology, Department of Medicine, Mayo Clinic, Phoenix, Arizona, USA.ORCID https://orcid.org/0000-0002-5938-3769
Yi LinDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Saurabh ZanwarDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.ORCID https://orcid.org/0000-0001-5074-8453

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ciltacabtagene autoleucel (cilta-cel) has demonstrated excellent efficacy and long-term disease control in patients with relapsed/refractory multiple myeloma (RRMM). However, a proportion of patients experience early treatment failures. We investigated clinical factors associated with early progression or death (within 12 months) in patients with RRMM receiving standard-of-care cilta-cel across the three Mayo clinic centers. Patients with a follow-up of at least 12 months or progression or death within 12 months from infusion were included. Of the patients with early treatment failure (n = 52), 69% had progressive disease and 31% had a non-relapse mortality (NRM) event. In patients without early treatment failure (n = 164), 13% of events were NRM. Among pretreatment factors, prior BCMA-directed therapy, presence of extramedullary disease and a CAR-HEMATOTOX score of ≥ 2 were independent predictors of early progression or death. The utilization of cilta-cel in earlier lines of treatment (1-3 vs. 4 or more) demonstrated comparable PFS (12-month PFS 73% vs. 77%, p = 0.94). Measurable residual disease positivity in the bone marrow at 3 months (11/197 patients) identified a small but high-risk group with an increased risk of early treatment failure (OR 5.68; p = 0.012). Patients with less than a complete response on a FDG PET/CT at 3 months also had an increased risk of early treatment failure (OR 11.8; p < 0.0001). Our findings may help identify patients at high-risk for early adverse outcomes despite receiving highly effective therapy, and support consideration of novel therapeutic strategies within a clinical trial setting.

Indexed as

Multiple MyelomaAdultAgedDisease ProgressionFemaleHumansMaleMiddle AgedRecurrenceTreatment Failure

Identifiers

PMID42351384
PMCPMC13428361

What OpenQuestion holds

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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.