Austin Health

Title
Safety and efficacy of atezolizumab with rituximab and CHOP in previously untreated diffuse large B-cell lymphoma.
Publication Date
2023-04-25
Author(s)
Younes, Anas
Burke, John M
Cheson, Bruce D
Diefenbach, Catherine
Ferrari, Silvia
Hahn, Uwe
Hawkes, Eliza A
Khan, Cyrus
Lossos, Izidore S
Musuraca, Gerardo
Tani, Monica
Vitolo, Umberto
Yuen, Sam L S
Raval, Aparna
Shivhare, Mahesh
Nielsen, Tina G
Sellam, Gila
Sharman, Jeff P
Subject
atezolizumab
rituximab
B-cell lymphoma
CHOP
Type of document
Journal Article
OrcId
#PLACEHOLDER_PARENT_METADATA_VALUE#
0000-0002-5144-6710
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
0000-0002-9917-2843
#PLACEHOLDER_PARENT_METADATA_VALUE#
0000-0002-0376-2559
#PLACEHOLDER_PARENT_METADATA_VALUE#
0000-0002-9346-9013
0000-0003-1947-1032
#PLACEHOLDER_PARENT_METADATA_VALUE#
0000-0001-7772-2747
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
#PLACEHOLDER_PARENT_METADATA_VALUE#
DOI
10.1182/bloodadvances.2022008344
Abstract
Rituximab plus cyclophosphamide, doxorubicin, vincristine and prednisone (R-CHOP) is the current standard therapy for patients with diffuse large B-cell lymphoma (DLBCL) and is curative in ∼60% of patients. Atezolizumab is a humanized immunoglobulin G1 monoclonal antibody that targets programmed death-ligand 1 and has previously shown anti-tumor activity in several tumor types. In a phase 1b/2 trial (NCT02596971) we evaluated the safety and efficacy of atezolizumab in combination with R-CHOP (atezo-R-CHOP; for 6 to 8 cycles) in patients with previously untreated DLBCL. Patients achieving a complete response at the end of induction received consolidation therapy with atezolizumab on Day 1 of each 21-day cycle for an additional 17 cycles. Overall, 42 patients with DLBCL were included in this analysis. The primary endpoint, complete response rate at end of induction, as assessed by an independent review committee (IRC; modified Lugano 2014) was 77.5% (95% confidence interval [CI], 64.0-87.7; n = 40). Investigator-assessed progression-free survival and overall survival at 3 years were 77.4% (95% CI, 59.7-88.0) and 87.2% (95% CI, 71.9-94.5), respectively. All treated patients experienced ≥1 adverse event (AE; 32 patients [76.2%] had a Grade 3-4 AE). One patient had a fatal AE (unconfirmed progressive multifocal leukoencephalopathy), that was considered related to atezolizumab and rituximab, and 17 (40.5%) patients experienced atezolizumab-related AEs of special interest. In previously untreated patients with DLBCL, atezo-R-CHOP demonstrated encouraging clinical efficacy and a safety profile consistent with the known toxicities of the individual drugs.
Link
Citation
Blood Advances 2023; 7(8)
Jornal Title
Blood Advances
ISSN
2473-9537

Files:

NameSizeformatDescriptionLink