Evidence map›Paper›PMID 24311149›Full record

ReviewInternational journal of hematology2014

Chimeric antigen receptors for the adoptive T cell therapy of hematologic malignancies.

Marco L Davila, Diana C G Bouhassira, Jae H Park, Kevin J Curran, Eric L Smith, Hollie J Pegram, Renier Brentjens

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in International journal of hematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02782351 (Humanized CAR-T Therapy for Treatment of Recurrent or Refractory B Cell Malignancy by Targeting CD19), which is not on this map. Cited by 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
6.3field-weighted citation impact, top 3% of its field
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.

NCT02782351 phase1 / phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

Humanized CAR-T Therapy for Treatment of Recurrent or Refractory B Cell Malignancy by Targeting CD19

TypeinterventionalSponsorKai Lin Xu; Jun Nian ZhengRan2016 to 2018Enrolled50ConditionsLeukemia, Lymphocytic, Chronic, B-CellArmsCAR-T
3 · Its place in the literature

Who cites it

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 108 citations in OpenAlex.

  1. The growing world of CAR T cell trials: a systematic review.Cancer immunology, immunotherapy : CII · 2016
    Pooled it
  2. Bioactivity and Safety of IL13Rα2-Redirected Chimeric Antigen Receptor CD8+ T Cells in Patients with Recurrent Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2015
    Trial
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  10. The research status and prospects of MUC1 in immunology.Human vaccines & immunotherapeutics · 2023
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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Marco L DavilaLeukemia Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, New York, NY, 10065, USA, davilam@mskcc.org.
Diana C G Bouhassira
Jae H Park
Kevin J Curran
Eric L Smith
Hollie J Pegram
Renier Brentjens
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI KENNETH Lynn WRIGHT · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

The genetic modification of autologous T cells with chimeric antigen receptors (CARs) represents a breakthrough for gene engineering as a cancer therapy for hematologic malignancies. By targeting the CD19 antigen, we have demonstrated robust and rapid anti-leukemia activity in patients with heavily pre-treated and chemotherapy-refractory B cell acute lymphoblastic leukemia (B-ALL). We demonstrated rapid induction of deep molecular remissions in adults, which has been recently confirmed in a case report involving a child with B-ALL. In contrast to the results when treating B-ALL, outcomes have been more modest in patients with chronic lymphocytic leukemia (CLL) or other non-hodgkin's lymphoma (NHL). We review the clinical trial experience targeting B-ALL and CLL and speculate on the possible reasons for the different outcomes and propose potential optimization to CAR T cell therapy when targeting CLL or other indolent NHL. Lastly, we discuss the pre-clinical development and potential for clinical translation for using CAR T cells against multiple myeloma and acute myeloid leukemia. We highlight the potential risks and benefits by targeting these poor outcome hematologic malignancies.

Indexed as

Immunotherapy, AdoptiveAnimalsAntigens, CD19Genetic TherapyHematologic NeoplasmsHumansLeukemia, Myeloid, AcuteMultiple MyelomaPrecursor B-Cell Lymphoblastic Leukemia-LymphomaReceptors, AntigenRecombinant Fusion ProteinsT-LymphocytesAntigens, CD19Receptors, AntigenRecombinant Fusion Proteins

Identifiers

PMID24311149
PMCPMC4684946
OpenAlexW2030311815

What OpenQuestion holds

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Registered trials

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.