Atezolizumab, obinutuzumab and venetoclax for the treatment of patients with relapsed/refractory B non‐Hodgkin lymphoma: Final analysis of a phase II trial from the <scp>LYSA</scp> group

Developing new therapeutic regimens for relapsed/refractory (R/R) B non-Hodgkin lymphoma (NHL) patients remains a significant unmet clinical need. Our objective was to evaluate atezolizumab (ATE), obinutuzumab (OBI) and venetoclax (VEN) combination in patients with R/R NHL who had received at least one prior anti-CD20-containing immunochemotherapy regimen. We report here the final analysis of the phase II LYSA-promoted multicentre trial (NCT03276468) of this combination in follicular lymphoma (FL, n = 58), diffuse large B-cell lymphoma (DLBCL, n = 58) and marginal zone lymphoma (MZL, n = 20). The primary end-point for FL and DLBCL was not met: ATE, OBI, and VEN resulted in an overall response rate (ORR) at the end of induction (EOI) of 53.6% for FL (cohort 1) and 23.6% for DLBCL (cohort 2) when a minimum of 70% and 48% was expected respectively. The median progression-free survival was 11.0 and 2.7 months in cohorts 1 and 2 respectively. In cohort 3 (MZL), the ORR at the EOI was evaluated at 66.7%. The most frequent adverse events (AEs) were cytopenias. We also observed 7.4% of autoimmune AE imputable to the combination. In this phase II study, ATE, OBI and VEN demonstrated moderate efficacy and a manageable toxicity profile when used as induction and maintenance therapy.

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Journal
British Journal of Haematology
Published
2025-04-26
DOI
https://doi.org/10.1111/bjh.20109
Citations
1
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
1.47

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article

Atezolizumab, obinutuzumab and venetoclax for the treatment of patients with relapsed/refractory B non‐Hodgkin lymphoma: Final analysis of a phase II trial from the LYSA group

Hervé Tilly, Emmanuelle Nicolas‐Virelizier, Loïc Ysebaert, Steven Le Gouill et al.
1 citations
British Journal of Haematology
Lymphoma Diagnosis and Treatment
1.47
article

Atezolizumab, obinutuzumab and venetoclax for the treatment of patients with relapsed/refractory B non‐Hodgkin lymphoma: Final analysis of a phase II trial from the LYSA group

Hervé Tilly, Emmanuelle Nicolas‐Virelizier, Loïc Ysebaert, Steven Le Gouill, Morgane Cheminant, Luc‐Matthieu Fornecker, Corinne Haïoun, Guillaume Cartron, Charles Herbaux, Franck Morschhauser, Emmanuel Bachy, Olivier Casasnovas, Gandhi Laurent Damaj, Catherine Thieblemont, Rémy Gressin, Emmanuel Gyan, Nadine Morineau, Stéphanie Guidez, Nicolas Daguindau, Roch Houot, Pierre Feugier, Réda Bouabdallah
article en
1 citations

Abstract

Developing new therapeutic regimens for relapsed/refractory (R/R) B non-Hodgkin lymphoma (NHL) patients remains a significant unmet clinical need. Our objective was to evaluate atezolizumab (ATE), obinutuzumab (OBI) and venetoclax (VEN) combination in patients with R/R NHL who had received at least one prior anti-CD20-containing immunochemotherapy regimen. We report here the final analysis of the phase II LYSA-promoted multicentre trial (NCT03276468) of this combination in follicular lymphoma (FL, n = 58), diffuse large B-cell lymphoma (DLBCL, n = 58) and marginal zone lymphoma (MZL, n = 20). The primary end-point for FL and DLBCL was not met: ATE, OBI, and VEN resulted in an overall response rate (ORR) at the end of induction (EOI) of 53.6% for FL (cohort 1) and 23.6% for DLBCL (cohort 2) when a minimum of 70% and 48% was expected respectively. The median progression-free survival was 11.0 and 2.7 months in cohorts 1 and 2 respectively. In cohort 3 (MZL), the ORR at the EOI was evaluated at 66.7%. The most frequent adverse events (AEs) were cytopenias. We also observed 7.4% of autoimmune AE imputable to the combination. In this phase II study, ATE, OBI and VEN demonstrated moderate efficacy and a manageable toxicity profile when used as induction and maintenance therapy.

British Journal of HaematologyVol. 207(1)
Université de Tours (FR), Hôpital Necker-Enfants Malades (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Université de Versailles Saint-Quentin-en-Yvelines (FR), Université de Montpellier (FR), Centre Hospitalier Universitaire de Lille (FR), Institut de Cancérologie Strasbourg (FR), Centre Hospitalier Universitaire de Tours (FR), Assistance Publique – Hôpitaux de Paris (FR), Institut universitaire du cancer de Toulouse Oncopole (FR), Centre Hospitalier Régional et Universitaire de Nancy (FR), Centre Léon Bérard (FR), Roche (France) (FR), Centre Hospitalier Universitaire de Poitiers (FR), Hôpital Lyon Sud (FR), Centre Hospitalier Universitaire de Caen Normandie (FR), CHU Dijon Bourgogne (FR), Centre Hospitalier Annecy Genevois (FR), Hôpital Saint-Louis (FR), Centre Hospitalier Départemental Vendée (FR), Institut Paoli-Calmettes (FR), Hôpital Claude Huriez (FR), Centre Hospitalier Universitaire de Rennes (FR), Institut de Génétique Humaine (FR), Université de Rennes (FR), Institut Curie (FR), Université Grenoble Alpes (FR), Université de Caen Normandie (FR)
Roche
Good health and well-being
Openalex Percentile: Top 20%
Lymphoma Diagnosis and Treatment
1.47
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