A Phase I Study of the Combination of Rituximab and Ipilimumab in Patients with Relapsed/Refractory B-Cell Lymphoma.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
01 12 2019
Historique:
received: 04 02 2019
revised: 03 06 2019
accepted: 28 08 2019
pubmed: 5 9 2019
medline: 22 9 2020
entrez: 5 9 2019
Statut: ppublish

Résumé

Based on the potential for ipilimumab (I) to augment T-cell activation, we hypothesize that ipilimumab would augment the efficacy of rituximab (R) in patients with relapsed/refractory (R/R) CD20 Thirty-three patients with R/R CD20 Toxicity was manageable; no dose-limiting toxicity was observed at the doses studied. When considering the entire cohort, efficacy was modest, with an objective response rate (ORR) of 24% and median progression-free survival (PFS) of 2.6 months. However, in follicular lymphoma patients, the ORR was 58% with a median PFS of 5.6 months. The randomized comparison of R with R+I demonstrated that R+I resulted in more effective B-cell depletion (BCD). Both B-cell depletion and the ratio of CD45RA The combination of R+I has manageable toxicity and encouraging efficacy in R/R follicular lymphoma. The ratio of CD45RA

Identifiants

pubmed: 31481504
pii: 1078-0432.CCR-19-0438
doi: 10.1158/1078-0432.CCR-19-0438
pmc: PMC7354236
mid: NIHMS1539041
doi:

Substances chimiques

Ipilimumab 0
Rituximab 4F4X42SYQ6

Types de publication

Clinical Trial, Phase I Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7004-7013

Subventions

Organisme : NCI NIH HHS
ID : P30 CA093373
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014089
Pays : United States
Organisme : NIH HHS
ID : DP2 OD008752
Pays : United States
Organisme : NCI NIH HHS
ID : U01 CA062505
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA033572
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA186717
Pays : United States

Informations de copyright

©2019 American Association for Cancer Research.

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Auteurs

Joseph M Tuscano (JM)

UC Davis Comprehensive Cancer Center, Sacramento, California. jtuscano@ucdavis.edu.
Veterans Administration Northern California Healthcare System, Sacramento, California.

Emanual Maverakis (E)

Department of Dermatology, UC Davis, Sacramento, California.

Susan Groshen (S)

Biostatistics Core, University of Southern California/Norris Cancer Center, Los Angeles, California.

Denice Tsao-Wei (D)

Biostatistics Core, University of Southern California/Norris Cancer Center, Los Angeles, California.

Guillaume Luxardi (G)

Department of Dermatology, UC Davis, Sacramento, California.

Alexander A Merleev (AA)

Department of Dermatology, UC Davis, Sacramento, California.

Anne Beaven (A)

University of North Carolina Comprehensive Cancer Center, Chapel Hill, North Carolina.

John F DiPersio (JF)

Washington University School of Medicine, St. Louis, Missouri.

Leslie Popplewell (L)

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.

Mark Kirschbaum (M)

Taiho Oncology, Princeton, New Jersey.

Mark A Schroeder (MA)

Washington University School of Medicine, St. Louis, Missouri.

Edward M Newman (EM)

Division of Molecular Pharmacology, Department of Medical Oncology, City of Hope, Duarte, California, USA.

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Classifications MeSH