Evidence map›Paper›PMID 38583184›Full record

ArticleCancer discovery2024

CD70-Targeted Allogeneic CAR T-Cell Therapy for Advanced Clear Cell Renal Cell Carcinoma.

Sumanta K Pal, Ben Tran, John B A G Haanen, Michael E Hurwitz, Adrian Sacher, Nizar M Tannir, Lihua E Budde, Simon J Harrison, Sebastian Klobuch, Sagar S Patel and 15 more

Abstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing 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

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

  1. Pooled it
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  12. Adoptive cell therapy in lung cancer: progress, challenges, and prospects.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  13. Allogeneic CD70-Targeted Chimeric Antigen Receptor T-Cell Therapy for Advanced Renal Cell Carcinoma: Results From the Phase I TRAVERSE Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  14. [Chemical & biomedical imaging · 2026
    Article
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  19. Neurological complications of current and emerging CAR-T cell therapies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Review
  20. Review

51 more citing papers are in PubMed but not listed here.

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.

Sumanta K PalDepartment of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, California.ORCID 0000-0002-1712-0848
Ben TranDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.ORCID 0000-0001-9124-354X
John B A G HaanenNetherlands Cancer Institute, Amsterdam, the Netherlands.
Michael E HurwitzYale School of Medicine, New Haven, Connecticut.ORCID 0000-0002-1326-7308
Adrian SacherPrincess Margaret Cancer Centre, University Health Network, Toronto, Canada.ORCID 0000-0001-7865-2701
Nizar M TannirUniversity of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0001-5559-8060
Lihua E BuddeDepartment of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, California.ORCID 0000-0003-1464-5494
Simon J HarrisonDepartment of Medical Oncology, Peter MacCallum Cancer Centre, Melbourne, Australia.ORCID 0000-0003-4555-6582
Sebastian KlobuchNetherlands Cancer Institute, Amsterdam, the Netherlands.ORCID 0000-0003-1364-0763
Sagar S PatelDivision of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.ORCID 0000-0001-9949-3615
Luis MezaDepartment of Medical Oncology, City of Hope Comprehensive Cancer Center, Duarte, California.ORCID 0000-0002-0235-297X
Mary-Lee DequeantCRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0005-8385-3547
Anna MaCRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0005-4522-1768
Qiuling Ally HeCRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0002-7900-8736
Leah M WilliamsCRISPR Therapeutics, Boston, Massachusetts.ORCID 0000-0003-3121-1081
Alissa KeeganCRISPR Therapeutics, Boston, Massachusetts.ORCID 0000-0001-5560-9989
Ellen B GuraryFormerly employed by CRISPR Therapeutics, Boston, Massachusetts.ORCID 0000-0003-0217-260X
Henia DarCRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0006-8825-4081
Sushant KarnikCRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0001-8803-746X
Changan GuoFormerly employed by CRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0001-0611-3239
Heidi HeathCRISPR Therapeutics, Boston, Massachusetts.ORCID 0000-0002-9325-1268
Rachel R YuenCRISPR Therapeutics, Boston, Massachusetts.ORCID 0000-0001-8272-9185
Phuong K MorrowFormerly employed by CRISPR Therapeutics, Boston, Massachusetts.ORCID 0009-0007-5349-6344
Neeraj AgarwalDivision of Medical Oncology, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah.ORCID 0000-0003-1076-0428
Samer A SrourUniversity of Texas MD Anderson Cancer Center, Houston, Texas.ORCID 0000-0002-6693-2025

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
NCATS NIH HHS UL1 TR001863
6 · The paper itself

Abstract

Therapeutic approaches for clear cell renal cell carcinoma (ccRCC) remain limited; however, chimeric antigen receptor (CAR) T-cell therapies may offer novel treatment options. CTX130, an allogeneic CD70-targeting CAR T-cell product, was developed for the treatment of advanced or refractory ccRCC. We report that CTX130 showed favorable preclinical proliferation and cytotoxicity profiles and completely regressed RCC xenograft tumors. We also report results from 16 patients with relapsed/refractory ccRCC who received CTX130 in a phase I, multicenter, first-in-human clinical trial. No patients encountered dose-limiting toxicity, and disease control was achieved in 81.3% of patients. One patient remains in a durable complete response at 3 years. Finally, we report on a next-generation CAR T construct, CTX131, in which synergistic potency edits to CTX130 confer improved expansion and efficacy in preclinical studies. These data represent a proof of concept for the treatment of ccRCC and other CD70+ malignancies with CD70- targeted allogeneic CAR T cells. Significance: Although the role of CAR T cells is well established in hematologic malignancies, the clinical experience in solid tumors has been disappointing. This clinical trial demonstrates the first complete response in a patient with RCC, reinforcing the potential benefit of CAR T cells in the treatment of solid tumors.

Indexed as

Carcinoma, Renal CellCD27 LigandImmunotherapy, AdoptiveKidney NeoplasmsAdultAgedAnimalsCell Line, TumorFemaleHumansMaleMiceMiddle AgedReceptors, Chimeric AntigenXenograft Model Antitumor AssaysCD27 LigandCD70 protein, humanReceptors, Chimeric Antigen

Identifiers

PMID38583184
PMCPMC11215406

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.