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Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma
Obinutuzumab (G) chemoimmunotherapy demonstrated improved progression-free survival (PFS) vs rituximab-based chemoimmunotherapy in patients with previously untreated follicular lymphoma (FL) in the GALLIUM trial. Atezolizumab (atezo) is a programmed death-ligand 1 inhibitor with a complementary mech...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society of Hematology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582582/ https://www.ncbi.nlm.nih.gov/pubmed/35359000 http://dx.doi.org/10.1182/bloodadvances.2021006131 |
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author | Younes, Anas Burke, John M. Diefenbach, Catherine Ferrari, Silvia Khan, Cyrus Sharman, Jeff P. Tani, Monica Ujjani, Chaitra Vitolo, Umberto Yuen, Sam Raval, Aparna Shivhare, Mahesh Nielsen, Tina G. Sellam, Gila Gilbertson, Michael |
author_facet | Younes, Anas Burke, John M. Diefenbach, Catherine Ferrari, Silvia Khan, Cyrus Sharman, Jeff P. Tani, Monica Ujjani, Chaitra Vitolo, Umberto Yuen, Sam Raval, Aparna Shivhare, Mahesh Nielsen, Tina G. Sellam, Gila Gilbertson, Michael |
author_sort | Younes, Anas |
collection | PubMed |
description | Obinutuzumab (G) chemoimmunotherapy demonstrated improved progression-free survival (PFS) vs rituximab-based chemoimmunotherapy in patients with previously untreated follicular lymphoma (FL) in the GALLIUM trial. Atezolizumab (atezo) is a programmed death-ligand 1 inhibitor with a complementary mechanism of action to G by restoring cytotoxic T-cell function. We evaluated the safety and efficacy of atezo-G-bendamustine in patients with previously untreated FL in a phase Ib/II trial (#NCT02596971). A safety run-in phase was followed by an expansion phase with atezo-G-bendamustine induction and atezo-G maintenance for ≤24 months. Forty patients with previously untreated FL were enrolled and treated with atezo-G-bendamustine. The primary endpoint, complete response (CR) rate, assessed by an independent review committee (IRC; modified Lugano 2014 criteria) was 75.0% (95% confidence interval [CI], 61.3% to 85.8%). Three-year investigator-assessed PFS and overall survival rates were 80.9% (95% CI, 63.9% to 90.5%) and 89.3% (95% CI, 73.9% to 95.9%), respectively. At baseline, 21/40 patients had circulating lymphoma-specific clonotypes and underwent repeat testing at end of induction; all were minimal residual disease negative (10(−5) sensitivity), with 16 (76.2%) CRs, 3 (14.3%) partial responses, and 2 (9.5%) with stable disease (IRC assessed). Grade 5 (fatal) adverse events (AEs) were reported in 5 patients. The efficacy of atezo-G-bendamustine in previously untreated FL did not appear superior to G-bendamustine efficacy as seen in the GALLIUM trial, and the addition of atezo to G-bendamustine was associated with an increased risk of AEs. Particularly due to the unfavorable safety profile, this regimen cannot be recommended in patients with previously untreated FL. This trial was registered at www.clinicaltrials.gov as #NCT02596971. |
format | Online Article Text |
id | pubmed-9582582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-95825822022-10-28 Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma Younes, Anas Burke, John M. Diefenbach, Catherine Ferrari, Silvia Khan, Cyrus Sharman, Jeff P. Tani, Monica Ujjani, Chaitra Vitolo, Umberto Yuen, Sam Raval, Aparna Shivhare, Mahesh Nielsen, Tina G. Sellam, Gila Gilbertson, Michael Blood Adv Regular Article Obinutuzumab (G) chemoimmunotherapy demonstrated improved progression-free survival (PFS) vs rituximab-based chemoimmunotherapy in patients with previously untreated follicular lymphoma (FL) in the GALLIUM trial. Atezolizumab (atezo) is a programmed death-ligand 1 inhibitor with a complementary mechanism of action to G by restoring cytotoxic T-cell function. We evaluated the safety and efficacy of atezo-G-bendamustine in patients with previously untreated FL in a phase Ib/II trial (#NCT02596971). A safety run-in phase was followed by an expansion phase with atezo-G-bendamustine induction and atezo-G maintenance for ≤24 months. Forty patients with previously untreated FL were enrolled and treated with atezo-G-bendamustine. The primary endpoint, complete response (CR) rate, assessed by an independent review committee (IRC; modified Lugano 2014 criteria) was 75.0% (95% confidence interval [CI], 61.3% to 85.8%). Three-year investigator-assessed PFS and overall survival rates were 80.9% (95% CI, 63.9% to 90.5%) and 89.3% (95% CI, 73.9% to 95.9%), respectively. At baseline, 21/40 patients had circulating lymphoma-specific clonotypes and underwent repeat testing at end of induction; all were minimal residual disease negative (10(−5) sensitivity), with 16 (76.2%) CRs, 3 (14.3%) partial responses, and 2 (9.5%) with stable disease (IRC assessed). Grade 5 (fatal) adverse events (AEs) were reported in 5 patients. The efficacy of atezo-G-bendamustine in previously untreated FL did not appear superior to G-bendamustine efficacy as seen in the GALLIUM trial, and the addition of atezo to G-bendamustine was associated with an increased risk of AEs. Particularly due to the unfavorable safety profile, this regimen cannot be recommended in patients with previously untreated FL. This trial was registered at www.clinicaltrials.gov as #NCT02596971. The American Society of Hematology 2022-03-29 /pmc/articles/PMC9582582/ /pubmed/35359000 http://dx.doi.org/10.1182/bloodadvances.2021006131 Text en © 2022 by The American Society of Hematology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Regular Article Younes, Anas Burke, John M. Diefenbach, Catherine Ferrari, Silvia Khan, Cyrus Sharman, Jeff P. Tani, Monica Ujjani, Chaitra Vitolo, Umberto Yuen, Sam Raval, Aparna Shivhare, Mahesh Nielsen, Tina G. Sellam, Gila Gilbertson, Michael Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title | Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title_full | Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title_fullStr | Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title_full_unstemmed | Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title_short | Safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
title_sort | safety and efficacy of atezolizumab with obinutuzumab and bendamustine in previously untreated follicular lymphoma |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582582/ https://www.ncbi.nlm.nih.gov/pubmed/35359000 http://dx.doi.org/10.1182/bloodadvances.2021006131 |
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