Checkpoint Blockade Treatment May Sensitize Hodgkin Lymphoma to Subsequent Therapy.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
10 2020
Historique:
received: 27 02 2020
accepted: 16 07 2020
pubmed: 29 7 2020
medline: 22 6 2021
entrez: 29 7 2020
Statut: ppublish

Résumé

Targeted 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. Seventeen 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). Eighty-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. In 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. 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.

Sections du résumé

BACKGROUND
Targeted 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 METHODS
Seventeen 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).
RESULTS
Eighty-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.
CONCLUSION
In 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.

Identifiants

pubmed: 32720734
doi: 10.1634/theoncologist.2020-0167
pmc: PMC7543382
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

878-885

Informations de copyright

© 2020 AlphaMed Press.

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Auteurs

Nicole A Carreau (NA)

Division of Hematology and Medical Oncology, Perlmutter Cancer Center at NYU Langone Health, New York, New York, USA.

Orrin Pail (O)

Department of Medicine, New York University School of Medicine & Langone Medical Center, New York, New York, USA.

Philippe Armand (P)

Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Reid Merryman (R)

Department of Medical Oncology, Dana Farber Cancer Institute, Boston, Massachusetts, USA.

Ranjana H Advani (RH)

Department of Medicine, Division of Oncology, Stanford University, Stanford, California, USA.

Michael A Spinner (MA)

Department of Medicine, Division of Oncology, Stanford University, Stanford, California, USA.

Alex Herrera (A)

Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.

Robert Chen (R)

Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.

Sarah Tomassetti (S)

Department of Hematology and Hematopoietic Cell Transplantation, City of Hope, Duarte, California, USA.

Radhakrishnan Ramchandren (R)

Division of Hematology and Oncology, University of Tennessee Medical Center, Knoxville, Tennessee, USA.

Muhammad S Hamid (MS)

Department of Oncology, Karmanos Cancer Institute, Detroit, Michigan, USA.

Sarit Assouline (S)

McGill University, Montreal, Quebec, Canada.

Raoul Santiago (R)

McGill University, Montreal, Quebec, Canada.

Nina Wagner-Johnston (N)

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland, USA.

Suman Paul (S)

Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins University, Baltimore, Maryland, USA.

Jakub Svoboda (J)

Abramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Steven Bair (S)

Abramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Stefan Barta (S)

Abramson Cancer Center, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Yang Liu (Y)

Department of Hematology/Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania, USA.

Sunita Nathan (S)

Rush University Medical Center, Chicago, Illinois, USA.

Reem Karmali (R)

Division of Hematology, Northwestern University, Chicago, Illinois, USA.

Madelyn Burkart (M)

Division of Hematology, Northwestern University, Chicago, Illinois, USA.

Pallawi Torka (P)

Roswell Park Comprehensive Cancer Center, Buffalo, New York, USA.

Kevin David (K)

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.

Catherine Wei (C)

Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA.

Frederick Lansigan (F)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.

Lukas Emery (L)

Dartmouth-Hitchcock Medical Center, Lebanon, New Hampshire, USA.

Daniel Persky (D)

Division of Hematology/Oncology, University of Arizona Cancer Center, Tucson, Arizona, USA.

Sonali Smith (S)

University of Chicago, Chicago, Illinois, USA.

James Godfrey (J)

University of Chicago, Chicago, Illinois, USA.

Julio Chavez (J)

Moffitt Cancer Center, Tampa, Florida, USA.

Yuhe Xia (Y)

New York University School of Medicine, New York, New York, USA.

Andrea B Troxel (AB)

New York University School of Medicine, New York, New York, USA.

Catherine Diefenbach (C)

Division of Hematology and Medical Oncology, Perlmutter Cancer Center at NYU Langone Health, New York, New York, USA.

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