Evidence map›Paper›PMID 32720734›Full record

ArticleThe oncologist2020

Checkpoint Blockade Treatment May Sensitize Hodgkin Lymphoma to Subsequent Therapy.

Nicole A Carreau, Orrin Pail, Philippe Armand, Reid Merryman, Ranjana H Advani, Michael A Spinner, Alex Herrera, Robert Chen, Sarah Tomassetti, Radhakrishnan Ramchandren and 24 more

Abstract readMulticenter Study
In one paragraph

Article in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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  5. Pembrolizumab in Relapsed or Refractory Primary Mediastinal Large B-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2019
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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

34 authors.

Nicole A CarreauDivision of Hematology and Medical Oncology, Perlmutter Cancer Center at NYU Langone Health, New York, New York, USA.
Orrin PailDepartment of Medicine, New York University School of Medicine & Langone Medical Center, New York, New York, USA.
Philippe ArmandDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Reid MerrymanDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.
Ranjana H AdvaniDepartment of Medicine, Division of Oncology, Stanford University, Stanford, California, USA.
Michael A SpinnerDepartment of Medicine, Division of Oncology, Stanford University, Stanford, California, USA.
Alex HerreraDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.
Robert ChenDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.
Sarah TomassettiDepartment of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.
Radhakrishnan RamchandrenDivision of Hematology and Oncology, University of Tennessee Medical Center, Knoxville, Tennessee, USA.
Muhammad S HamidDepartment of Oncology, Karmanos Cancer Institute, Detroit, Michigan, USA.
Sarit AssoulineMcGill University, Montreal, Quebec, Canada.
Raoul SantiagoMcGill University, Montreal, Quebec, Canada.
Nina Wagner-JohnstonSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland, USA.
Suman PaulSidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland, USA.
Jakub SvobodaAbramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Steven BairAbramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Stefan BartaAbramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Yang LiuDepartment of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.
Sunita NathanRush University Medical Center, Chicago, Illinois, USA.
Reem KarmaliDivision of Hematology, Northwestern University, Chicago, Illinois, USA.
Madelyn BurkartDivision of Hematology, Northwestern University, Chicago, Illinois, USA.
Pallawi TorkaRoswell Park Comprehensive Cancer Center, Buffalo, New York, USA.
Kevin DavidRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
Catherine WeiRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.
Frederick LansiganDartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Lukas EmeryDartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.
Daniel PerskyDivision of Hematology/Oncology, University of Arizona Cancer Center, Tucson, Arizona, USA.
Sonali SmithUniversity of Chicago, Chicago, Illinois, USA.
James GodfreyUniversity of Chicago, Chicago, Illinois, USA.
Julio ChavezMoffitt Cancer Center, Tampa, Florida, USA.
Yuhe XiaNew York University School of Medicine, New York, New York, USA.
Andrea B TroxelNew York University School of Medicine, New York, New York, USA.
Catherine DiefenbachDivision of Hematology and Medical Oncology, Perlmutter Cancer Center at NYU Langone Health, New York, New York, USA.ORCID https://orcid.org/0000-0003-1116-3246

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTargeted therapies and checkpoint blockade therapy (CBT) have shown efficacy for patients with Hodgkin lymphoma (HL) in the relapsed and refractory (R/R) setting, but once discontinued owing to progression or side effects, it is unclear how successful further therapies will be. Moreover, there are no data on optimal sequencing of these treatments with standard therapies and other novel agents. In a multicenter, retrospective analysis, we investigated whether exposure to CBT could sensitize HL to subsequent therapy. MATERIALS AND

methodsSeventeen centers across the U.S. and Canada retrospectively queried medical records for eligible patients. The primary aim was to evaluate the overall response rate (ORR) to post-CBT treatment using the Lugano criteria. Secondary aims included progression-free survival (PFS), duration of response, and overall survival (OS).

resultsEighty-one patients were included. Seventy-two percent had stage III-IV disease, and the population was heavily pretreated with a median of four therapies before CBT. Most patients (65%) discontinued CBT owing to progression. The ORR to post-CBT therapy was 62%, with a median PFS of 6.3 months and median OS of 21 months. Post-CBT treatment regimens consisted of chemotherapy (44%), targeted agents (19%), immunotherapy (15%), transplant conditioning (14%), chemotherapy/targeted combination (7%), and clinical trials (1%). No significant difference in OS was found when stratified by post-CBT regimen.

conclusionIn a heavily pretreated R/R HL population, CBT may sensitize patients to subsequent treatment, even after progression on CBT. Post-CBT regimen category did not impact OS. This may be a novel treatment strategy, which warrants further investigation in prospective clinical trials. IMPLICATIONS FOR PRACTICE: Novel, life-prolonging treatment strategies in relapsed and refractory (R/R) Hodgkin lymphoma (HL) are greatly desired. The results of this multicenter analysis concur with a smaller, earlier report that checkpoint blockade therapy (CBT) use in R/R HL may sensitize patients to their subsequent treatment. This approach may potentially enhance therapeutic options or to bridge patients to transplant. Prospective data are warranted prior to practice implementation. As more work is done in this area, we may also be able to optimize sequencing of CBT and novel agents in the treatment paradigm to minimize treatment-related toxicity and thus improve patient quality of life.

Indexed as

Hodgkin DiseaseAntineoplastic Combined Chemotherapy ProtocolsCanadaHumansNeoplasm Recurrence, LocalProspective StudiesQuality of LifeRetrospective StudiesCheckpoint blockadeHodgkin lymphomaImmunotherapyRelapsedSensitization

Identifiers

PMID32720734
PMCPMC7543382

What OpenQuestion holds

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Registered trials

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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.