Evidence map›Paper›PMID 38985302›Full record

ArticleBlood advances2024

CD19-directed CART therapy for T-cell/histiocyte-rich large B-cell lymphoma.

Priyanka A Pophali, Joshua A Fein, Kwang W Ahn, Molly Allbee-Johnson, Nausheen Ahmed, Farrukh T Awan, Shatha Farhan, Natalie S Grover, Talal Hilal, Madiha Iqbal and 9 more

Abstract read
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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Priyanka A PophaliDivision of Hematology, Medical Oncology and Palliative Care, University of Wisconsin, Carbone Cancer Center, Madison, WI.ORCID 0000-0002-2410-9540
Joshua A FeinDivision of Hematology and Oncology, Weill Cornell Medicine, New York, NY.
Kwang W AhnDivision of Biostatistics, Institute for Health and Equity, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0003-4567-8037
Molly Allbee-JohnsonCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.
Nausheen AhmedDivision of Hematologic Malignancies and Cellular Therapeutics, The University of Kansas Cancer Center, Kansas City, KS.ORCID 0000-0003-4336-4982
Farrukh T AwanHarold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0003-1813-9812
Shatha FarhanHenry Ford Health System Stem Cell Transplant & Cellular Therapy Program, Detroit, MI.ORCID 0000-0002-5723-7442
Natalie S GroverDivision of Hematology, University of North Carolina, Chapel Hill, NC.ORCID 0000-0002-1346-3157
Talal HilalDivision of Hematology and Oncology, Mayo Clinic, Phoenix, AZ.ORCID 0000-0001-8249-4128
Madiha IqbalDivision of Hematology/Oncology, Mayo Clinic, Jacksonville, FL.
Joseph MaakaronDivision of Hematology, Oncology and Transplantation, University of Minnesota, Minneapolis, MN.
Dipenkumar ModiKarmanos Cancer Institute, Wayne State University, Detroit, MI.ORCID 0000-0001-6525-8844
Elham NasrollahiDepartment of Internal Medicine, University of Pittsburgh Medical Center in Central Pa., Harrisburg, PA.
Levanto G SchachterUniversity of California Los Angeles, Los Angeles, CA.
Craig SauterDepartment of Hematology and Medical Oncology, Blood and Marrow Transplant Program, Taussig Cancer Center, Cleveland Clinic, Cleveland, OH.
Mehdi HamadaniCenter for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, WI.ORCID 0000-0001-5372-510X
Alex HerreraDivision of Lymphoma, Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, CA.ORCID 0000-0002-9665-7415
Roni ShouvalDepartment of Medicine, Adult Bone Marrow Transplantation Service, Memorial Sloan Kettering Cancer Center, New York, NY.
Mazyar ShadmanFred Hutchinson Cancer Center and University of Washington, Seattle, WA.ORCID 0000-0002-3365-6562

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Data Resource for Analyzing Blood &Marrow TransplantsU24CA076518 · NCI · MEDICAL COLLEGE OF WISCONSIN · PI Amy M Moskop, Bronwen Shaw · 1998 to 2026
$105.2M
A multimodal approach for precision immuno-oncology in lymphoma treated with CAR-T cellsK08CA282987 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI Roni Shouval · 2023 to 2026
$1.1M
NCI NIH HHS K08 CA282987NCI NIH HHS P30 CA008748NCI NIH HHS U24 CA076518
6 · The paper itself

Abstract

abstractT-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) is a rare histologic variant of LBCL. Limited data regarding CD19-directed chimeric antigen receptor T-cell (CART) therapy in relapsed/refractory (R/R) THRLBCL suggest poor efficacy. We investigated CART outcomes for R/R THRLBCL through the Center for International Blood and Marrow Transplant Research registry. A total of 58 adult patients with R/R THRLBCL who received commercial CD19-CART therapy between 2018 and 2022 were identified. Most patients (67%) had early relapse of disease (45% primary refractory) with a median of 3 (range, 1-7) prior therapies and were treated with axicabtagene ciloleucel (69%). At median follow-up of 23 months after CART therapy, 2-year overall and progression-free survival were 42% (95% confidence interval [CI], 27-57) and 29% (95% CI, 17-43), respectively. In univariable analysis, poor performance status before CART therapy was associated with higher mortality (hazard ratio, 2.35; 95%CI, 1.02-5.5). The 2-year cumulative incidences of relapse/progression and nonrelapse mortality were 69% and 2%, respectively. Grade ≥3 cytokine release syndrome and immune effector cell-associated neurologic syndrome occurred in 7% and 15% of patients, respectively. In this largest analysis of CD19-CART therapy for R/R THRLBCL, ∼30% of patients were alive and progression free 2 years after CART therapy. Despite a high incidence of progression (69% at 2 years), these results suggest a subset of patients with R/R THRLBCL may have durable responses with CARTs.

Indexed as

Antigens, CD19Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseAdultAgedFemaleHistiocytesHumansMaleMiddle AgedReceptors, Chimeric AntigenT-LymphocytesTreatment OutcomeYoung AdultAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID38985302
PMCPMC11497379

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.