Evidence map›Paper›PMID 38776397›Full record

ArticleBlood advances2024

Absolute lymphocyte count after BCMA CAR-T therapy is a predictor of response and outcomes in relapsed multiple myeloma.

Mateo Mejia Saldarriaga, Darren Pan, Caitlin Unkenholz, Tarek H Mouhieddine, Juan Esteban Velez-Hernandez, Katherine Engles, Joshua A Fein, Jorge Monge, Cara Rosenbaum, Roger Pearse and 15 more

Abstract readMulticenter Study
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
–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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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.

Mateo Mejia SaldarriagaDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-3504-5597
Darren PanDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Caitlin UnkenholzDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0009-0005-8972-7883
Tarek H MouhieddineDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0002-1190-5978
Juan Esteban Velez-HernandezDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-0800-5709
Katherine EnglesDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Joshua A FeinDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0001-5441-1516
Jorge MongeDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0003-0854-0768
Cara RosenbaumDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.
Roger PearseDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.
David JayabalanDepartment of Internal Medicine, Universidad de Antioquia, Medellin, Colombia.
Christian GordilloDivision of Hematology & Oncology, Columbia University Irving Cancer Center, New York, NY.
Hei Ton ChanDivision of Hematology & Oncology, Columbia University Irving Cancer Center, New York, NY.
Samuel YamshonDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.
Santiago ThibaudDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0001-8454-5136
Markus MaparaDivision of Hematology & Oncology, Columbia University Irving Cancer Center, New York, NY.
Giorgio InghiramiDepartment of Pathology, Weill Cornell Medicine, New York, NY.ORCID 0000-0001-5566-0864
Suzanne LentzschDivision of Hematology & Oncology, Columbia University Irving Cancer Center, New York, NY.
Ran ReshefDivision of Hematology & Oncology, Columbia University Irving Cancer Center, New York, NY.
Adriana RossiDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Samir ParekhDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Sundar JagannathDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0003-2934-6518
Shambavi RichardDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
Ruben NiesvizkyDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.
Mark BustorosDivision of Hematology & Medical Oncology, Meyer Cancer Center, Weill Cornell Medicine, New York, NY.ORCID 0000-0002-4652-5449

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
Multidisciplinary Training in Gastrointestinal CancersT32CA285274 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Julian Abrams, Anil K Rustgi · 2024 to 2026
$897k
NCI NIH HHS P30 CA013696NCI NIH HHS T32 CA285274
6 · The paper itself

Abstract

abstractB-cell maturation antigen (BCMA)-targeting chimeric antigen receptor T cells (CAR-Ts) used in multiple myeloma (MM) are rapidly becoming a mainstay in the treatment of relapsed/refractory (R/R) disease, and CAR-T expansion after infusion has been shown to inform depth and duration of response (DoR), but measuring this process remains investigational. This multicenter study describes the kinetics and prognostic impact of absolute lymphocyte count (ALC) in the first 15 days after CAR-T infusion in 156 patients with relapsed MM treated with the BCMA-targeting agents ciltacabtagene autoleucel and idecabtagene vicleucel. Patients with higher maximum ALC (ALCmax) had better depth of response, progression-free survival (PFS), and DoR. Patients with ALCmax >1.0 × 103/μL had a superior PFS (30.5 months vs 6 months; P < .001) compared with those with ≤1.0 × 103/μL, whereas patients with ALCmax ≤0.5 × 103/μL represent a high-risk group with early disease progression and short PFS (hazard ratio, 3.4; 95% confidence interval, 2-5.8; P < .001). In multivariate analysis, ALCmax >1.0 × 103/μL and nonparaskeletal extramedullary disease were the only independent predictors of PFS and DoR after accounting for international staging systemic staging, age, CAR-T product, high-risk cytogenetics, and the number of previous lines. Moreover, our flow cytometry data suggest that ALC is a surrogate for BCMA CAR-T expansion and can be used as an accessible prognostic marker. We report, to our knowledge, for the first time the association of ALC after BCMA CAR-T infusion with clinical outcomes and its utility in predicting response in patients with R/R MM.

Indexed as

B-Cell Maturation AntigenImmunotherapy, AdoptiveMultiple MyelomaAdultAgedFemaleHumansLymphocyte CountMaleMiddle AgedPrognosisReceptors, Chimeric AntigenTreatment OutcomeB-Cell Maturation AntigenReceptors, Chimeric AntigenTNFRSF17 protein, human

Identifiers

PMID38776397
PMCPMC11321283

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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.