Polatuzumab Vedotin in Relapsed or Refractory Diffuse Large B-Cell Lymphoma.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
10 01 2020
Historique:
pubmed: 7 11 2019
medline: 26 6 2020
entrez: 7 11 2019
Statut: ppublish

Résumé

Patients with transplantation-ineligible relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) fare poorly, with limited treatment options. The antibody-drug conjugate polatuzumab vedotin targets CD79b, a B-cell receptor component. Safety and efficacy of polatuzumab vedotin with bendamustine and obinutuzumab (pola-BG) was evaluated in a single-arm cohort. Polatuzumab vedotin combined with bendamustine and rituximab (pola-BR) was compared with bendamustine and rituximab (BR) in a randomly assigned cohort of patients with transplantation-ineligible R/R DLBCL (primary end point: independent review committee [IRC] assessed complete response [CR] rate at the end of treatment). Duration of response, progression-free survival (PFS), and overall survival (OS) were analyzed using Kaplan-Meier and Cox regression methods. Pola-BG and pola-BR had a tolerable safety profile. The phase Ib/II pola-BG cohort (n = 27) had a CR rate of 29.6% and a median OS of 10.8 months (median follow-up, 27.0 months). In the randomly assigned cohort (n = 80; 40 per arm), pola-BR patients had a significantly higher IRC-assessed CR rate (40.0% Polatuzumab vedotin combined with BR resulted in a significantly higher CR rate and reduced the risk of death by 58% compared with BR in patients with transplantation-ineligible R/R DLBCL.

Identifiants

pubmed: 31693429
doi: 10.1200/JCO.19.00172
pmc: PMC7032881
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antibodies, Monoclonal, Humanized 0
Biomarkers, Tumor 0
Immunoconjugates 0
Bendamustine Hydrochloride 981Y8SX18M
polatuzumab vedotin KG6VO684Z6
obinutuzumab O43472U9X8

Banques de données

ClinicalTrials.gov
['NCT02257567']

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

155-165

Subventions

Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

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Auteurs

Laurie H Sehn (LH)

BC Cancer Centre for Lymphoid Cancer and The University of British Columbia, Vancouver, British Columbia, Canada.

Alex F Herrera (AF)

City of Hope, Duarte, CA.

Christopher R Flowers (CR)

Winship Cancer Institute of Emory University, Atlanta, GA.

Manali K Kamdar (MK)

University of Colorado, Aurora, CO.

Andrew McMillan (A)

Nottingham University Hospitals, Nottingham, United Kingdom.

Mark Hertzberg (M)

Prince of Wales Hospital and University of NSW, Sydney, NSW, Australia.

Sarit Assouline (S)

Jewish General Hospital, Montreal, Quebec, Canada.

Tae Min Kim (TM)

Seoul National University Hospital, Seoul, South Korea.

Won Seog Kim (WS)

Samsung Medical Center, Seoul, South Korea.

Muhit Ozcan (M)

Ankara University, Ankara, Turkey.

Jamie Hirata (J)

Genentech, South San Francisco, CA.

Elicia Penuel (E)

Genentech, South San Francisco, CA.

Joseph N Paulson (JN)

Genentech, South San Francisco, CA.

Ji Cheng (J)

F. Hoffman-La Roche, Mississauga, Ontario, Canada.

Grace Ku (G)

Genentech, South San Francisco, CA.

Matthew J Matasar (MJ)

Memorial Sloan Kettering Cancer Center, New York, NY.

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Classifications MeSH