Polatuzumab Vedotin in Relapsed or Refractory Diffuse Large B-Cell Lymphoma.
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal
/ administration & dosage
Antibodies, Monoclonal, Humanized
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Bendamustine Hydrochloride
/ administration & dosage
Biomarkers, Tumor
/ metabolism
Female
Humans
Immunoconjugates
/ administration & dosage
Immunohistochemistry
Lymphoma, Large B-Cell, Diffuse
/ drug therapy
Male
Middle Aged
Progression-Free Survival
Survival Rate
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
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
155-165Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Commentaires et corrections
Type : CommentIn
Type : CommentIn
Références
Blood. 2017 Oct 19;130(16):1800-1808
pubmed: 28774879
N Engl J Med. 2002 Jan 24;346(4):235-42
pubmed: 11807147
J Clin Oncol. 2015 Sep 10;33(26):2848-56
pubmed: 26240231
J Clin Oncol. 2010 Sep 20;28(27):4184-90
pubmed: 20660832
Leukemia. 2015 Jul;29(7):1578-86
pubmed: 25708834
J Clin Oncol. 2013 Jun 10;31(17):2103-9
pubmed: 23650408
Ann Hematol. 2014 Mar;93(3):403-9
pubmed: 23955074
J Clin Oncol. 2012 Oct 1;30(28):3452-9
pubmed: 22851565
Lancet Haematol. 2019 May;6(5):e254-e265
pubmed: 30935953
N Engl J Med. 2017 Dec 28;377(26):2531-2544
pubmed: 29226797
J Clin Oncol. 2017 Nov 1;35(31):3529-3537
pubmed: 28796588
Blood. 2009 Sep 24;114(13):2721-9
pubmed: 19633198
Mol Cancer Ther. 2013 Oct;12(10):2031-42
pubmed: 23873847
Blood. 2010 Jun 3;115(22):4393-402
pubmed: 20194898
J Clin Oncol. 2014 Sep 20;32(27):3059-68
pubmed: 25113753
Lancet Oncol. 2015 Jun;16(6):704-15
pubmed: 25925619
Blood. 1993 Jan 1;81(1):84-94
pubmed: 8417805
J Clin Oncol. 1998 Aug;16(8):2780-95
pubmed: 9704731
J Biol Chem. 1990 Oct 5;265(28):17141-9
pubmed: 2211617