Evidence map›Paper›PMID 34644372›Full record

ArticleBlood advances2022

Quality-of-life analysis of pembrolizumab vs brentuximab vedotin for relapsed/refractory classical Hodgkin lymphoma.

Pier Luigi Zinzani, Radhakrishnan Ramchandren, Armando Santoro, Ewa Paszkiewicz-Kozik, Robin Gasiorowski, Nathalie A Johnson, Jose S R de Oliveira, Valeria Buccheri, Guilherme Fleury Perini, Michael Dickinson and 8 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article 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 NCT02684292 (A Phase III, Randomized, Open-label, Clinical Trial to Compare Pembrolizumab With Brentuximab Vedotin in Subjects With Relapsed or Refractory Classical Hodgkin Lymphoma), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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.

NCT02684292 phase3completednot on this map

A Phase III, Randomized, Open-label, Clinical Trial to Compare Pembrolizumab With Brentuximab Vedotin in Subjects With Relapsed or Refractory Classical Hodgkin Lymphoma

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2016 to 2026Enrolled304ConditionsHodgkin LymphomaArmspembrolizumab, brentuximab vedotin
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Quality of Life and Survivorship in Lymphoma.Current oncology reports · 2022
    Review
  8. Review
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

18 authors at 14 institutions in 8 countries.

Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna Istituto di Ematologia "Seràgnoli", Bologna, Italy.ORCID 0000-0002-2112-2651
Radhakrishnan RamchandrenDepartment of Medicine, University of Tennessee, Knoxville, TN.
Armando SantoroDepartment of Biomedical Sciences, Humanitas University and IRCCS Humanitas Research Hospital, Humanitas Cancer Center, Milan, Italy.ORCID 0000-0003-1709-9492
Ewa Paszkiewicz-KozikDepartment of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.ORCID 0000-0003-2629-3932
Robin GasiorowskiDepartment of Hematology, Concord Hospital, University of Sydney, Sydney, NSW, Australia.ORCID 0000-0003-1225-8757
Nathalie A JohnsonDepartment of Medicine, Jewish General Hospital Montreal, Montreal, QC, Canada.
Jose S R de OliveiraCasa de Saúde Santa Marcelina, São Paulo, Brazil.
Valeria BuccheriDepartment of Medicine, Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil.ORCID 0000-0002-6999-4109
Guilherme Fleury PeriniDepartment of Medical Oncology, Hospital Israelita Albert Einstein, São Paulo, Brazil.
Michael DickinsonClinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, and The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia.ORCID 0000-0002-1492-5966
Andrew McDonaldDepartment of Medical Oncology, Pretoria East Hospital, Pretoria, South Africa.
Muhit ÖzcanDepartment of Medical Oncology, Ankara University School of Medicine, Ankara, Turkey.ORCID 0000-0002-1326-1918
Naohiro SekiguchiDepartment of Hematology, National Hospital Organization Disaster Medical Center, Tokyo, Japan.
Ying ZhuMerck & Co., Inc., Kenilworth, NJ; and.
Monika RautMerck & Co., Inc., Kenilworth, NJ; and.
Todd L SaretskyMerck & Co., Inc., Kenilworth, NJ; and.
Akash NaharMerck & Co., Inc., Kenilworth, NJ; and.
John KuruvillaPrincess Margaret Cancer Centre, Toronto, ON, Canada.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USAnkara University · TRHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRHospital Israelita Albert Einstein · BRHospital Santa Marcelina · BRHumanitas University · ITIstituto di Ematologia di Bologna · ITJewish General Hospital · CANational Hospital Organization · JPPrincess Margaret Cancer Centre · CAThe Maria Sklodowska-Curie National Research Institute of Oncology · PLThe Royal Melbourne Hospital · AUThe University of Sydney · AUUniversity of Tennessee at Knoxville · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

KEYNOTE-204 (NCT02684292) demonstrated a progression-free survival advantage for pembrolizumab over brentuximab vedotin (BV) in patients who had relapsed or refractory classical Hodgkin lymphoma (R/R cHL) following, or who were ineligible for, autologous stem cell transplantation (ASCT). Health-related quality of life (HRQoL), measured by patient-reported outcomes (PROs) from KEYNOTE-204, are reported from patients who received ≥1 dose of study treatment and completed ≥1 PRO assessment. The EORTC QoL Questionnaire Core 30 (QLQ-C30) and EuroQoL EQ-5D were administered at baseline, every 6 weeks until week 24, and every 12 weeks thereafter. Prespecified end points included least squares mean (LSM) changes from baseline to week 24 and time to true deterioration (TTD; ≥10-point decline from baseline). Comparisons were evaluated using 2-sided P values uncontrolled for multiplicity. High compliance at baseline (>90%) and through week 24 (>80%) was demonstrated across treatment groups (PRO analysis set: pembrolizumab, n = 146; BV, n = 150). The EORTC QLQ-C30 global health status (GHS)/quality of life (QoL) score improved from baseline to week 24 on pembrolizumab and worsened on BV and demonstrated significant LSM differences at 24 weeks (GHS/QoL: 8.60 [95% confidence interval, 3.89-13.31]; P = .0004). Significant improvements were observed in each QLQ-C30 domain except emotional and cognitive functioning. Compared with BV, pembrolizumab prolonged TTD for GHS/QoL (hazard ratio, 0.40 [95% CI, 0.22-0.74]; P = .003) and each QLQ-C30 domain except cognitive functioning. In conclusion, pembrolizumab demonstrated overall improvements in PROs of HRQoL measures over BV in the KEYNOTE-204 study. These data and previously reported efficacy results support pembrolizumab as the preferred treatment option for patients with R/R cHL who are ineligible for or experience relapse after ASCT.

Indexed as

Hematopoietic Stem Cell TransplantationHodgkin DiseaseAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsBrentuximab VedotinChronic DiseaseHumansNeoplasm Recurrence, LocalQuality of LifeTransplantation, AutologousAntibodies, Monoclonal, HumanizedBrentuximab Vedotinpembrolizumab

Identifiers

PMID34644372
PMCPMC8791579
OpenAlexW3205072810

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.