Evidence map›Paper›PMID 34666347›Full record

Trial reportBlood advances2022

Pretherapy metabolic tumor volume is associated with response to CD30 CAR T cells in Hodgkin lymphoma.

Timothy J Voorhees, Beibo Zhao, Jorge Oldan, George Hucks, Amir Khandani, Christopher Dittus, Jennifer Smith, J Kaitlin Morrison, Catherine J Cheng, Anastasia Ivanova and 7 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02690545 (Phase Ib/II Study of the Administration of T Lymphocytes Expressing the CD30 Chimeric Antigen Receptor), which is not on this map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
2.9field-weighted citation impact, top 7% 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.

NCT02690545 phase1 / phase2active not recruitingnot on this map

Phase Ib/II Study of the Administration of T Lymphocytes Expressing the CD30 Chimeric Antigen Receptor (CAR) for Relapsed/Refractory CD30+ Hodgkin's Lymphoma and CD30+ Non-Hodgkin's Lymphoma

TypeinterventionalSponsorUNC Lineberger Comprehensive Cancer CenterRan2016 to 2039Enrolled38ConditionsLymphoma, Lymphoma, Non-Hodgkin, Immune System Diseases, Immunoproliferative DisordersArmsATLCAR.CD30 cells
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Baseline and interimCancer imaging : the official publication of the International Cancer Imaging Society · 2026
    Article
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  7. Review
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  9. Observational
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  15. Prognostic value of baseline and interim [European journal of nuclear medicine and molecular imaging · 2024
    Article
  16. Review
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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

17 authors at 3 institutions in 2 countries.

Timothy J VoorheesLineberger Comprehensive Cancer Center.ORCID 0000-0001-7603-6454
Beibo ZhaoGillings School of Public Health.
Jorge OldanDepartment of Radiology, and.
George HucksLineberger Comprehensive Cancer Center.
Amir KhandaniDepartment of Radiology, and.ORCID 0000-0003-3629-5472
Christopher DittusLineberger Comprehensive Cancer Center.
Jennifer SmithGillings School of Public Health.
J Kaitlin MorrisonLineberger Comprehensive Cancer Center.
Catherine J ChengLineberger Comprehensive Cancer Center.
Anastasia IvanovaLineberger Comprehensive Cancer Center.
Steven ParkDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Charlotte, NC.ORCID 0000-0001-5674-6408
Thomas C SheaLineberger Comprehensive Cancer Center.
Anne W BeavenLineberger Comprehensive Cancer Center.
Gianpietro DottiLineberger Comprehensive Cancer Center.
Jonathan SerodyLineberger Comprehensive Cancer Center.ORCID 0000-0003-4568-1092
Barbara SavoldoLineberger Comprehensive Cancer Center.
Natalie GroverLineberger Comprehensive Cancer Center.ORCID 0000-0002-1346-3157
Segeberger Kliniken · DEUniversity of North Carolina at Chapel Hill · USLevine Cancer Institute · US

Funding

Tissue Procurement & PathologyP50CA058223 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHARLES M PEROU · 1992 to 2026
$59.3M
Tailoring CAR T cell therapy for Hodgkin LymphomaR01CA247497 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SAVOLDO, BARBARA · 2020 to 2024
$3.1M
Enhancement of stem cell transplants using CAR.CD30-redirected T lymphocytesR01HL114564 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SAVOLDO, BARBARA · 2013 to 2017
$2.2M
Duke-UNC Chapel Hill Immunotherapy Training GrantT32CA211056 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CHAO, NELSON J., SERODY, JONATHAN S. · 2017 to 2021
$2.2M
Cellular Immunotherapy of Ovarian CancerR01CA243543 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DOTTI, GIANPIETRO · 2019 to 2023
$2.0M
NCI NIH HHS P50 CA058223NCI NIH HHS R01 CA243543NCI NIH HHS R01 CA247497NCI NIH HHS T32 CA211056NHLBI NIH HHS R01 HL114564
6 · The paper itself

Abstract

Our group has recently demonstrated that chimeric antigen receptor T-cell therapy targeting the CD30 antigen (CD30.CAR-T) is highly effective in patients with relapsed and refractory (r/r) classical Hodgkin lymphoma (cHL). Despite high rates of clinical response, relapses and progression were observed in a subset of patients. The objective of this study was to characterize clinical and correlative factors associated with progression-free survival (PFS) after CD30.CAR-T cell therapy. We evaluated correlatives in 27 patients with r/r cHL treated with lymphodepletion and CD30.CAR-T cells. With a median follow-up of 9.5 months, 17 patients (63%) progressed, with a median PFS of 352 days (95% confidence interval: 116-not reached), and 2 patients died (7%) with a median overall survival of not reached. High metabolic tumor volume (MTV, >60 mL) immediately before lymphodepletion and CD30.CAR-T cell infusion was associated with inferior PFS (log rank, P = .02), which persisted after adjusting for lymphodepletion and CAR-T dose (log rank, P = .01 and P = .006, respectively). In contrast, receiving bridging therapy, response to bridging therapy, CD30.CAR-T expansion/persistence, and percentage of CD3+PD-1+ lymphocytes over the first 6 weeks of therapy were not associated with differences in PFS. In summary, this study reports an association between high baseline MTV immediately before lymphodepletion and CD30.CAR-T cell infusion and worse PFS in patients with r/r cHL. This trial was registered at www.clinicaltrials.gov as #NCT02690545.

Indexed as

Hodgkin DiseaseReceptors, Chimeric AntigenHumansKi-1 AntigenNeoplasm Recurrence, LocalT-LymphocytesTumor BurdenKi-1 AntigenReceptors, Chimeric Antigen

Identifiers

PMID34666347
PMCPMC8864661
OpenAlexW3205154971

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.