Evidence map›Paper›PMID 38750138›Full record

ArticleLeukemia2024

Chimeric antigen receptor T-cell infusion for large B-cell lymphoma in complete remission: a center for international blood and marrow transplant research analysis.

Trent P Wang, Kwang W Ahn, Mazyar Shadman, Manmeet Kaur, Nausheen Ahmed, Ulrike Bacher, Jan Cerny, Andy Chen, Narendranath Epperla, Matthew Frigault and 19 more

Abstract read
In one paragraph

Article in Leukemia, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
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  5. Article
  6. 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

29 authors.

Trent P WangDivision of Transplantation and Cellular Therapy, Department of Medicine, University of Miami Miller School of Medicine, Miami, USA.ORCID 0000-0001-5685-7204
Kwang W AhnBMT & Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA.
Mazyar ShadmanClinical Research Division, Fred Hutchinson Cancer Center, University of Washington, Seattle, WA, USA.
Manmeet KaurDivision of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI, USA.
Nausheen AhmedUniversity of Kansas Cancer Center, Division of Hematologic Malignancies and Cellular Therapeutics, Kansas City, KS, USA.ORCID 0000-0003-4336-4982
Ulrike BacherDepartment of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
Jan CernyDivision of Hematology/Oncology, Department of Medicine, University of Massachusetts Medical Center, Worcester, MA, USA.
Andy ChenDivision of Hematology and Medical Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR, USA.ORCID 0000-0001-5204-9445
Narendranath EpperlaDivision of Hematology, Department of Medicine, Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.ORCID 0000-0002-8216-3457
Matthew FrigaultMassachusetts General Hospital Cancer Center, Harvard Medical School, Division of Hematology & Oncology, Boston, MA, USA.
Natalie GroverLineberger Comprehensive Cancer Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Bradley HaverkosUniversity of Colorado Cancer Center, Aurora, CO, USA.ORCID 0000-0003-0056-6023
Brian HillDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
Nasheed HossainCell Therapy and Transplant Program, Division of Hematology/Oncology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-3278-655X
Madiha IqbalDivision of Hematology and Oncology, Mayo Clinic, Jacksonville, FL, USA.
Tania JainDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0000-0001-6854-773X
Maxwell M KremKansas City VA Medical Center, Kansas City, MO, USA.
Joseph MaakaronDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN, USA.ORCID 0000-0002-1732-6694
Dipenkumar ModiDivision of Hematology/Oncology, Karmanos Cancer Institute, Detroit, MI, USA.ORCID 0000-0001-6525-8844
Muhamad Alhaj MoustafaDivision of Hematology and Oncology, Mayo Clinic, Jacksonville, FL, USA.ORCID 0000-0001-8582-1219
Peter RiedellThe David and Etta Jonas Center for Cellular Therapy, University of Chicago, Chicago, IL, USA.
Bipin SavaniDivision of Hematology/Oncology, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-3304-9965
R Alejandro SicaDepartment of Oncology, Montefiore Medical Center, Albert Einstein Cancer Center, Bronx, NY, USA.
Anna SuredaInstitut Català d'Oncologia, Hospital Duran i Reynals, Barcelona, Spain.ORCID 0000-0002-1238-6970
Kitsada WudhikarnDivision of Hematology and Center of Excellence in Translational Hematology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID 0000-0001-9528-8681
Alex F HerreraDepartment of Hematology and Hematopoietic Stem Cell Transplantation, City of Hope National Medical Center, Duarte, CA, USA.ORCID 0000-0002-9665-7415
Craig SauterDepartment of Hematology and Medical Oncology, Cleveland Clinic, Cleveland, OH, USA.
Mehdi HamadaniBMT & Cellular Therapy Program, Department of Medicine, Medical College of Wisconsin, Milwaukee, WI, USA. mhamadani@mcw.edu.ORCID 0000-0001-5372-510X
Antonio Jimenez JimenezDivision of Transplantation and Cellular Therapy, Department of Medicine, University of Miami Miller School of Medicine, Miami, USA.ORCID 0000-0003-2817-6836

Funding

Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
UM Calabresi Clinical Oncology Research Career Development AwardK12CA226330 · NCI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Alan Pollack · 2018 to 2026
$5.1M
NCI NIH HHS K12 CA226330NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

CD19 CAR T-cell (CAR-T) therapy is commonly administered to patients with relapsed or refractory large B-cell lymphomas (LBCL), but salvage or bridging therapy can sometimes lead to a complete response (CR) prior to infusion. Limited studies have assessed the outcomes of patients infused in CR. A total of 134 patients with LBCL in CR prior to CAR-T infusion were identified from the CIBMTR registry, with median prior lines of therapy of 3 (range 2-9). At two years post-infusion, the probability of progression-free survival was 43.5% (95% CI 34.4-52.8) and the probability of overall survival was 63.8% (95% CI 54.4-72.6). The cumulative incidence rates of non-relapse mortality and relapse/progression at two years were 9.2% (95% CI 4.5-15.4) and 47.3% (95% CI 38.2-56.6), respectively. The rate of grade 3 or higher cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were 2.2% and 8.2%, respectively. In summary, CAR-T in heavily pretreated patients with LBCL who are in CR following two or more lines of prior therapy demonstrate that a subset of patients may remain free of progression at two years. Additionally, the toxicity profile was impressive with very low rates of grade 3 CRS and ICANS.

Indexed as

Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseRemission InductionAdultAgedAntigens, CD19FemaleFollow-Up StudiesHumansMaleMiddle AgedPathologic Complete ResponseReceptors, Chimeric AntigenSurvival RateYoung AdultAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID38750138
PMCPMC11271761

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.