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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.
  • Younes A; Memorial Sloan-Kettering Cancer Center, New York, NY.
  • Burke JM; US Oncology Research, The Woodlands, TX.
  • Diefenbach C; Rocky Mountain Cancer Center, Aurora, CO.
  • Ferrari S; Perlmutter Cancer Center of NYU Langone Health, New York, NY.
  • Khan C; Azienda Ospedaliera Papa Giovanni XXIII, Bergamo, Italy.
  • Sharman JP; Allegheny Health Network Cancer Institute, Pittsburgh, PA.
  • Tani M; US Oncology Research, The Woodlands, TX.
  • Ujjani C; Willamette Valley Cancer Institute, Eugene, OR.
  • Vitolo U; Ospedale Santa Maria delle Croci, Ravenna, Italy.
  • Yuen S; Seattle Cancer Care Alliance/Fred Hutchinson Cancer Research Center, Seattle, WA.
  • Raval A; Multidisciplinary Oncology Outpatient Clinic, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
  • Shivhare M; Calvary Mater Newcastle Hospital, Newcastle, NSW, Australia.
  • Nielsen TG; Genentech, Inc., South San Francisco, CA.
  • Sellam G; Roche Products, Welwyn Garden City, United Kingdom.
  • Gilbertson M; F. Hoffmann-La Roche Ltd., Basel, Switzerland.
Blood Adv ; 6(20): 5659-5667, 2022 10 25.
Article en En | MEDLINE | ID: mdl-35359000
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Folicular Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Linfoma Folicular Límite: Humans Idioma: En Año: 2022 Tipo del documento: Article