Obinutuzumab plus CHOP is effective and has a tolerable safety profile in previously untreated, advanced diffuse large B-cell lymphoma: the phase II GATHER study.


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
04 2019
Historique:
pubmed: 3 10 2018
medline: 23 6 2020
entrez: 3 10 2018
Statut: ppublish

Résumé

This study investigated the safety and efficacy of obinutuzumab plus cyclophosphamide, doxorubicin, vincristine, and prednisone (G-CHOP) in patients with advanced diffuse large B-cell lymphoma (DLBCL) and explored the impact of cell-of-origin (COO) on patient outcomes. Patients (N = 100) received obinutuzumab (1000 mg on the days 1, 8, and 15 of cycle 1, and day 1 of cycles 2-8) plus CHOP (cycles 1-6). For patients without grade ≥3 infusion-related reactions (IRRs) to standard-rate obinutuzumab infusion, a shorter duration of infusion (SDI) was evaluated. Overall and complete response rates, as determined according to the Cheson et al. criteria by investigators/independent radiological facility, were 82.0/75.0% and 55.0/58.0%, respectively. SDI of 120 minutes and 90 minutes were well tolerated with no grade ≥3 IRRs. Among all patients, IRRs typically occurred during cycle 1, day 1. G-CHOP is active and has an acceptable safety profile in the first-line treatment of patients with advanced DLBCL. Clinical Trials: NCT01414855DLBCL.

Identifiants

pubmed: 30277102
doi: 10.1080/10428194.2018.1515940
pmc: PMC6445782
mid: NIHMS1514696
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
obinutuzumab O43472U9X8
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT01414855']

Types de publication

Clinical Trial, Phase II 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

894-903

Subventions

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

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Auteurs

Jeff P Sharman (JP)

a Willamette Valley Cancer Institute and Research Center , US Oncology Research , Eugene , OR , USA.

Andres Forero-Torres (A)

b University of Alabama School of Medicine , Birmingham , AL , USA.

Luciano J Costa (LJ)

c Division of Hematology/Oncology , Medical University of South Carolina , Charleston , SC , USA.

Ian W Flinn (IW)

d Sarah Cannon Research Institute , Nashville , TN , USA.

Lowell Inhorn (L)

e Blue Ridge Cancer Care , Roanoke , VA , USA.

Kevin Kelly (K)

f USC Norris Comprehensive Cancer Center , Los Angeles , CA , USA.

Alberto Bessudo (A)

g California Cancer Associates for Research and Excellence , San Diego , CA , USA.

Luis E Fayad (LE)

h Department of Lymphoma and Myeloma , M.D. Anderson Cancer Center, University of Texas , Houston , TX , USA.

Mark S Kaminski (MS)

i Division of Hematology/Oncology , University of Michigan Comprehensive Cancer Center, Ann Arbor , MI , USA.

Andrew M Evens (AM)

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

Christopher R Flowers (CR)

k Winship Cancer Institute , Atlanta , GA , USA.

Deniz Sahin (D)

l F. Hoffmann-La Roche Ltd , Basel , Switzerland.

Kirsten E Mundt (KE)

l F. Hoffmann-La Roche Ltd , Basel , Switzerland.

Thomas Sandmann (T)

m Genentech Inc. , South San Francisco , CA , USA.

Günter Fingerle-Rowson (G)

l F. Hoffmann-La Roche Ltd , Basel , Switzerland.

Charlotte Vignal (C)

l F. Hoffmann-La Roche Ltd , Basel , Switzerland.

Mehrdad Mobasher (M)

m Genentech Inc. , South San Francisco , CA , USA.

Andrew D Zelenetz (AD)

n Memorial Sloan Kettering Cancer Center and Weill Cornell Medical Center , New York , NY , USA.

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Classifications MeSH