Evidence map›Paper›PMID 37530622›Full record

Trial reportBlood advances2023

Nivolumab for relapsed/refractory classical Hodgkin lymphoma: 5-year survival from the pivotal phase 2 CheckMate 205 study.

Stephen M Ansell, Paul J Bröckelmann, Gottfried von Keudell, Hun Ju Lee, Armando Santoro, Pier Luigi Zinzani, Graham P Collins, Jonathon B Cohen, Jan Paul de Boer, John Kuruvilla and 11 more

Erratum issued Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Blood advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02181713, which is not on this map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
19.6field-weighted citation impact, top 1% 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.

NCT02181713 no registry record found
3 · Its place in the literature

Who cites it

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 77 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Outcomes of Brentuximab Vedotin Monotherapy in Refractory/Relapsed Classical Hodgkin's Lymphoma: A Multi-Center Retrospective Study on Survival and Safety.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2026
    Article
  14. Article
  15. Review
  16. Review
  17. Classical Hodgkin Lymphoma Today.Mediterranean journal of hematology and infectious diseases · 2026
    Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 18 institutions in 10 countries.

Stephen M AnsellMayo Clinic, Rochester, MN.
Paul J BröckelmannUniversity of Cologne, Cologne, Germany and Center for Integrated Oncology Aachen Bonn Duesseldorf, Bonn, Germany.
Gottfried von KeudellMemorial Sloan Kettering Cancer Center, New York, NY.
Hun Ju LeeUniversity of Texas MD Anderson Cancer Center, Houston, TX.ORCID 0000-0001-7219-5562
Armando SantoroHumanitas University, Pieve Emanuele, Milan, Italy and IRCCS Humanitas Research Hospital, Humanitas Cancer Center, Rozzano, Milan, Italy.ORCID 0000-0003-1709-9492
Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna, Instituto di Ematologia "Seràgnoli" and Università di Bologna, Bologna, Italy.ORCID 0000-0002-2112-2651
Graham P CollinsChurchill Hospital, Oxford, United Kingdom.
Jonathon B CohenWinship Cancer Institute, Atlanta, GA.ORCID 0000-0002-2723-6481
Jan Paul de BoerNetherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.
John KuruvillaPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Kerry J SavageBC Cancer, Vancouver, BC, Canada.ORCID 0000-0002-5835-9863
Marek TrněnýCharles University in Prague, Prague, Czech Republic.
Mariano ProvencioUniversity Hospital Puerta de Hierro, Majadahonda, Spain.
Ulrich JägerMedical University of Vienna, Vienna, Austria.ORCID 0000-0001-9826-1062
Wolfgang WillenbacherInnsbruck Medical University and Sydena GmbH, Connect to Cure, Innsbruck, Austria.ORCID 0000-0001-7702-1721
Rachael WenBristol Myers Squibb, Princeton, NJ.
Alev AkyolBristol Myers Squibb, Princeton, NJ.
Joanna Mikita-GeoffroyBristol Myers Squibb, Boudry, Switzerland.
Margaret A ShippDana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-3949-6897
Andreas EngertUniversity of Cologne, Cologne, Germany and Center for Integrated Oncology Aachen Bonn Duesseldorf, Bonn, Germany.
Philippe ArmandDana-Farber Cancer Institute, Boston, MA.
Bristol-Myers Squibb (United States) · USDana-Farber Cancer Institute · USUniversity of Cologne · DEBeth Israel Deaconess Medical Center · USBristol-Myers Squibb (Switzerland) · CHCharles University · CZEmory University · USHospital Universitario Puerta de Hierro Majadahonda · ESHumanitas University · ITInnsbruck Medical University · ATIstituto di Ematologia di Bologna · ITMayo Clinic · USMedical University of Vienna · ATPrincess Margaret Cancer Centre · CASpinal Cord Injury BC · CAThe Netherlands Cancer Institute · NLThe University of Texas MD Anderson Cancer Center · USWhitchurch Hospital · GB

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Patients with relapsed/refractory (R/R) classical Hodgkin lymphoma (cHL) for whom autologous hematopoietic cell transplantation (auto-HCT) had failed experienced frequent and durable responses to nivolumab in the phase 2 CheckMate 205 trial. We present updated results (median follow-up, ∼5 years). Patients with R/R cHL who were brentuximab vedotin (BV)-naive (cohort A), received BV after auto-HCT (cohort B), or received BV before and/or after auto-HCT (cohort C) were administered with nivolumab 3 mg/kg IV every 2 weeks until progression or unacceptable toxicity. Patients in cohort C with complete remission (CR) for 1 year could discontinue nivolumab and resume upon relapse. Among 243 patients (cohort A, n = 63; B, n = 80; and C, n = 100), the objective response rate (ORR) was 71.2% (95% confidence interval [CI], 65.1-76.8); the CR rate was 21.4% (95% CI, 16.4-27.1). Median duration of response, CR, and partial remission were 18.2 (95% CI, 14.7-26.1), 30.3, and 13.5 months, respectively. Median progression-free survival was 15.1 months (95% CI, 11.3-18.5). Median overall survival (OS) was not reached; OS at 5 years was 71.4% (95% CI, 64.8-77.1). In cohort C, all 3 patients who discontinued in CR and were subsequently re-treated achieved objective response. No new or unexpected safety signals were identified. This 5-year follow-up of CheckMate 205 demonstrated favorable OS and confirmed efficacy and safety of nivolumab in R/R cHL after auto-HCT failure. Results suggest patients may discontinue treatment after persistent CR and reinitiate upon progression. This trial was registered at www.clinicaltrials.gov as #NCT02181713.

Indexed as

Hodgkin DiseaseImmunoconjugatesBrentuximab VedotinChronic DiseaseHumansNeoplasm Recurrence, LocalNivolumabBrentuximab VedotinImmunoconjugatesNivolumab

Identifiers

PMID37530622
PMCPMC10589773
OpenAlexW4385476260

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.