Evidence map›Paper›PMID 37130017›Full record

Trial reportBlood2023

Pembrolizumab in relapsed or refractory primary mediastinal large B-cell lymphoma: final analysis of KEYNOTE-170.

Pier Luigi Zinzani, Catherine Thieblemont, Vladimir Melnichenko, Krimo Bouabdallah, Jan Walewski, Alejandro Majlis, Laura Fogliatto, A Martin Garcia-Sancho, Beth Christian, Zafer Gulbas and 8 more

Erratum issued Registry-linked trialOpen access · hybridAbstract readClinical Trial
In one paragraph

Trial report in Blood, 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 NCT02576990 (A Phase II Study of Pembrolizumab), which is not on this map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
14.8field-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.

NCT02576990 phase2completednot on this map

A Phase II Study of Pembrolizumab (MK-3475) in Subjects With Relapsed or Refractory Primary Mediastinal Large B-cell Lymphoma (rrPMBCL) or Relapsed or Refractory Richter Syndrome (rrRS)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2015 to 2020Enrolled80ConditionsMediastinal Large B-cell Lymphoma, Richter SyndromeArmsPembrolizumab
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Incidence of B-cell Malignancies in Patients with Lung Cancer Receiving PD-1 Blockade Therapy.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
  6. Observational
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 15 institutions in 9 countries.

Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna Istituto di Ematologia "Seràgnoli," Bologna, Italy.ORCID 0000-0002-2112-2651
Catherine ThieblemontDepartment of Hemato-Oncology, Hôpital Saint-Louis APHP, Paris, France.
Vladimir MelnichenkoDepartment of Medical Oncology, Pirogov National Medical Surgical Center, Moscow, Russia.
Krimo BouabdallahDepartment of Hematology and Cellular Therapy, University Hospital, Bordeaux, France.
Jan WalewskiDepartment of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, European Reference Network, Warsaw, Poland.ORCID 0000-0003-4247-2674
Alejandro MajlisDepartment of Hemato-Oncology, Clinica Alemana de Santiago, Santiago, Chile.
Laura FogliattoDepartment of Clinical Hematology, Hospital de Clinicas de Porto Alegre, Porto Alegre, Brazil.
A Martin Garcia-SanchoDepartment of Hematology, Hospital Universitario de Salamanca, Institute of Biomedical Research of Salamanca, Centro de Investigación Biomédica en Red Cáncer, Salamanca, Spain.ORCID 0000-0001-6330-1028
Beth ChristianDivision of Hematology, The James Cancer Hospital and Solove Research Institute, The Ohio State University, Columbus, OH.
Zafer GulbasDepartment of Hematologic Oncology, Anadolu Medical Center, Gebze, Turkey.
Muhit ÖzcanDepartment of Hematology and Bone Marrow Transplantation Unit, Ankara University School of Medicine, Ankara, Turkey.ORCID 0000-0002-1326-1918
Guilherme Fleury PeriniDepartment of Hematology, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Herve GhesquieresDepartment of Clinical Hematology, Lyon-Sud Hospital Center, Lyon, France.
Margaret A ShippDepartment of Hematologic Oncology, Dana-Farber Cancer Institute, Boston, MA.ORCID 0000-0002-3949-6897
Seth ThompsonDepartment of Medical Oncology, Merck & Co, Inc, Rahway, NJ.
Samhita ChakrabortyDepartment of Medical Oncology, Merck & Co, Inc, Rahway, NJ.
Patricia MarinelloDepartment of Medical Oncology, Merck & Co, Inc, Rahway, NJ.
Philippe ArmandDepartment of Hematologic Oncology, Dana-Farber Cancer Institute, Boston, MA.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USDana-Farber Cancer Institute · USAnadolu University · TRAnkara University · TRAssistance Publique – Hôpitaux de Paris · FRClinica Santa Maria · CLComplejo Hospitalario de Salamanca · ESHôpital Lyon Sud · FRHospital de Clínicas de Porto Alegre · BRHospital Israelita Albert Einstein · BRIstituto di Ematologia di Bologna · ITLaboratoire de Génétique Cellulaire · FRNational Medical and Surgical Center named after N.I. Pirogov · RUThe Maria Sklodowska-Curie National Research Institute of Oncology · PLThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous analyses of the phase 2 KEYNOTE-170 (NCT02576990) study demonstrated effective antitumor activity and acceptable safety of pembrolizumab 200 mg given every 3 weeks for up to 35 cycles (∼2 years) in patients with relapsed/refractory (R/R) primary mediastinal B-cell lymphoma (PMBCL) whose disease progressed after or who were ineligible for autologous stem cell transplantation. The end points included objective response rate (ORR), progression-free survival (PFS), and duration of response (DOR) according to the investigator per 2007 Response Criteria; overall survival (OS); and safety. In this final analysis, median duration of follow-up was 48.7 months (range, 41.2-56.2). The ORR was 41.5% (complete response, 20.8%; partial response, 20.8%). The median DOR was not reached; no patients who achieved a complete response progressed at the data cutoff. The median PFS was 4.3 months; the 4-year PFS rate was 33.0%. The median OS was 22.3 months; the 4-year OS rate was 45.3%. At the data cutoff, 30 patients (56.6%) had any-grade treatment-related adverse events (AEs); the most common were neutropenia, asthenia, and hypothyroidism. Grade 3/4 treatment-related AEs occurred in 22.6% of the patients; no grade 5 AEs occurred. After 4 years of follow-up, pembrolizumab continued to provide durable responses, with promising trends for long-term survival and acceptable safety in R/R PMBCL.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Large B-Cell, DiffuseMediastinal NeoplasmsThymus NeoplasmsAdultAntibodies, Monoclonal, HumanizedHumansTransplantation, AutologousAntibodies, Monoclonal, Humanizedpembrolizumab

Identifiers

PMID37130017
PMCPMC10651864
OpenAlexW4367668321

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.