Evidence map›Paper›PMID 31409671›Full record

Trial reportBlood2019

Pembrolizumab in relapsed or refractory Hodgkin lymphoma: 2-year follow-up of KEYNOTE-087.

Robert Chen, Pier Luigi Zinzani, Hun Ju Lee, Philippe Armand, Nathalie A Johnson, Pauline Brice, John Radford, Vincent Ribrag, Daniel Molin, Theodoros P Vassilakopoulos and 8 more

2 registry-linked trialsAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Blood, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 189 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
189citing papers in PubMed, 3 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.

NCT02453594 phase2completednot on this map

A Phase II Clinical Trial of MK-3475 (Pembrolizumab) in Subjects With Relapsed or Refractory (R/R) Classical Hodgkin Lymphoma (cHL)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2015 to 2023Enrolled211ConditionsHodgkin LymphomaArmspembrolizumab
NCT04419441 unknown statusnot on this mapstarted 2020, after this paper: background citation

Retrospective, Multicentric, Observational Study to Evaluate the Efficacy and Safety of the Combination of an Immune Checkpoint Inhibitor (ICI) and Radiotherapy (RT) in Patients With Relapsed/Refractory (R/R) Classical Hodgkin Lymphoma (cHL)

TypeobservationalSponsorOspedale Maggiore Di TriesteRan2020 to 2020Enrolled12ConditionsHodgkin Lymphoma, Immune Checkpoint Inhibitor, RadiotherapyArmsImmune checkpoint inhibitor
3 · Its place in the literature

Who cites it

189 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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  10. Tislelizumab for Relapsed/Refractory Classical Hodgkin Lymphoma: 3-Year Follow-up and Correlative Biomarker Analysis.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
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  15. Anti-CD30 CAR-T Cell Therapy in Relapsed and Refractory Hodgkin Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
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  18. Pembrolizumab in relapsed or refractory Richter syndrome.British journal of haematology · 2020
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129 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Robert ChenDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
Pier Luigi ZinzaniDepartment of Experimental, Diagnostic and Specialty Medicine, Institute of Hematology "Seràgnoli" University of Bologna, Bologna, Italy.
Hun Ju LeeDepartment of Lymphoma and Myeloma, The University of Texas, MD Anderson Cancer Center, Houston, TX.
Philippe ArmandDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, MA.
Nathalie A JohnsonDepartment of Hematology, Jewish General Hospital, Montreal, QC, Canada.
Pauline BriceDepartment of Hematology-Oncology, Hopital Saint Louis, Paris, France.
John RadfordDivision of Cancer Sciences, The University of Manchester and The Christie NHS Foundation Trust, Manchester, United Kingdom.
Vincent RibragDepartment of Drug Development and Hematology, Institut Gustave Roussy, Villejuif, France.
Daniel MolinSection of Experimental and Clinical Oncology, Department of Immunology, Genetics, and Pathology, Uppsala University, Uppsala, Sweden.
Theodoros P VassilakopoulosDepartment of Hematology and Bone Marrow Transplantation, General Hospital of Athens, Athens, Greece.
Akihiro TomitaDepartment of Hematology, Fujita Health University School of Medicine, Toyoake, Japan.
Bastian von TresckowDepartment of Internal Medicine, University of Cologne and University Hospital of Cologne, Cologne, Germany.
Margaret A ShippDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, MA.
Jianxin LinMedical Oncology, Merck & Co, Inc, Kenilworth, NJ; and.
Eunhee KimMedical Oncology, Merck & Co, Inc, Kenilworth, NJ; and.
Akash NaharMedical Oncology, Merck & Co, Inc, Kenilworth, NJ; and.
Arun BalakumaranMedical Oncology, Merck & Co, Inc, Kenilworth, NJ; and.
Craig H MoskowitzDepartment of Medicine, University of Miami Sylvester Comprehensive Cancer Center, Miami, FL.

Funding

Targetable Immune Evasion Pathways in Hodgkin LymphomaR01CA161026 · NCI · DANA-FARBER CANCER INST · PI SHIPP, MARGARET A · 2011 to 2020
$4.0M
NCI NIH HHS R01 CA161026
6 · The paper itself

Abstract

Programmed death-1 inhibitors are approved for patients with relapsed or refractory classic Hodgkin lymphoma (RRcHL). We present the 2-year follow-up of the phase 2 KEYNOTE-087 study of pembrolizumab in 210 patients, based on HL progression after autologous stem cell transplantation (ASCT) and subsequent brentuximab vedotin (BV; cohort 1); salvage chemotherapy and BV, with ineligibility for SCT owing to chemorefractory disease (cohort 2); and progression after SCT without BV (cohort 3). With a median follow-up of 27.6 months, the objective response rate (ORR) by blinded independent central review was 71.9% (95% CI, 65.3-77.9), the complete response rate (CRR) was 27.6%, and the partial response (PR) rate was 44.3%. Median duration of response was 16.5 months (range, 0.0+ to 27.0+ [+, no progressive disease at last assessment]) in all patients, 22.1 months in cohort 1, 11.1 months in cohort 2, and 24.4 months in cohort 3. Median progression-free survival was not reached in all patients with CR: 13.8 months (95% CI, 12.0-22.1) for patients with PR and 10.9 months (95% CI, 5.6-11.1) for patients with stable disease. Median overall survival was not reached in all patients or in any cohort. Treatment-related adverse events (TRAEs) of any grade occurred in 153 (72.9%) patients; grades 3 and 4 occurred in 25 (12.0%) patients; none resulted in death. Results confirmed effective antitumor activity, durability of response, and manageable safety of pembrolizumab monotherapy in RRcHL, regardless of prior treatment and including chemoresistant cHL. This trial was registered at www.clinicaltrials.gov as #NCT02453594.

Indexed as

AdolescentAdultAgedAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDisease-Free SurvivalFemaleFollow-Up StudiesHodgkin DiseaseHumansMaleMiddle AgedNeoplasm Recurrence, LocalTreatment OutcomeYoung AdultAntibodies, Monoclonal, HumanizedAntineoplastic Agents, Immunologicalpembrolizumab

Identifiers

PMID31409671
PMCPMC6776792

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.