Combined Nivolumab and Ipilimumab in ...
Document type :
Article dans une revue scientifique: Article original
DOI :
PMID :
Title :
Combined Nivolumab and Ipilimumab in Octogenarian and Nonagenarian Melanoma Patients
Author(s) :
Reichert, Constance [Auteur]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
Baldini, Capucine [Auteur]
Analyse moléculaire, modélisation et imagerie de la maladie cancéreuse [AMMICa]
Institut Gustave Roussy [IGR]
Mezghani, Sarah [Auteur]
Institut Curie [Paris]
Maubec, Eve [Auteur]
Université Sorbonne Paris Nord
Hôpital Avicenne [AP-HP]
Longvert, Christine [Auteur]
Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie [BECCOH]
Université Paris-Saclay
Hôpital Ambroise Paré [AP-HP]
Mortier, Laurent [Auteur]
Thérapies Assistées par Lasers et Immunothérapies pour l'Oncologie - U 1189 [OncoThAI]
Service des Maladies de l'Appareil Digestif et de la Nutrition [CHRU Lille]
Quereux, Gaëlle [Auteur]
Centre d’Investigation Clinique de Nantes [CIC Nantes]
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital [CHU Nantes]
Immunology and New Concepts in ImmunoTherapy [INCIT]
Jannic, Arnaud [Auteur]
Service d'immunologie clinique et maladies infectieuses [Hôpitaux universitaires CHU Henri Mondor]
Machet, Laurent [Auteur]
Centre Hospitalier Régional Universitaire de Tours [CHRU Tours]
de Quatrebarbes, Julie [Auteur]
Centre Hospitalier Annecy-Genevois [Saint-Julien-en-Genevois]
Nardin, Charlée [Auteur]
Etablissement français du sang [Bourgogne-Franche-Comté] [EFS BFC]
Centre Hospitalier Régional Universitaire de Besançon [CHRU Besançon]
Interactions hôte-greffon-tumeur, ingénierie cellulaire et génique - UFC (UMR INSERM 1098) [RIGHT]
Beneton, Nathalie [Auteur]
Centre Hospitalier Le Mans (CH Le Mans)
Amini Adle, Mona [Auteur]
Centre Léon Bérard [Lyon]
Funck-Brentano, Elisa [Auteur]
Université Paris-Saclay
Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie [BECCOH]
Hôpital Ambroise Paré [AP-HP]
Descamps, Vincent [Auteur]
Université Paris Cité [UPCité]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
Hachon, Lorry [Auteur]
CIC Hôpital Bichat
Malissen, Nausicaa [Auteur]
Hôpital de la Timone [CHU - APHM] [TIMONE]
Centre de Recherche en Cancérologie de Marseille [CRCM]
Baroudjian, Barouyr [Auteur]
Immunologie humaine, physiopathologie & immunothérapie [HIPI (UMR_S_976 / U976)]
Hopital Saint-Louis [AP-HP] [AP-HP]
Brunet-Possenti, Florence [Auteur]
Université Paris Cité [UPCité]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
Baldini, Capucine [Auteur]
Analyse moléculaire, modélisation et imagerie de la maladie cancéreuse [AMMICa]
Institut Gustave Roussy [IGR]
Mezghani, Sarah [Auteur]
Institut Curie [Paris]
Maubec, Eve [Auteur]
Université Sorbonne Paris Nord
Hôpital Avicenne [AP-HP]
Longvert, Christine [Auteur]
Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie [BECCOH]
Université Paris-Saclay
Hôpital Ambroise Paré [AP-HP]
Mortier, Laurent [Auteur]

Thérapies Assistées par Lasers et Immunothérapies pour l'Oncologie - U 1189 [OncoThAI]
Service des Maladies de l'Appareil Digestif et de la Nutrition [CHRU Lille]
Quereux, Gaëlle [Auteur]
Centre d’Investigation Clinique de Nantes [CIC Nantes]
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital [CHU Nantes]
Immunology and New Concepts in ImmunoTherapy [INCIT]
Jannic, Arnaud [Auteur]
Service d'immunologie clinique et maladies infectieuses [Hôpitaux universitaires CHU Henri Mondor]
Machet, Laurent [Auteur]
Centre Hospitalier Régional Universitaire de Tours [CHRU Tours]
de Quatrebarbes, Julie [Auteur]
Centre Hospitalier Annecy-Genevois [Saint-Julien-en-Genevois]
Nardin, Charlée [Auteur]
Etablissement français du sang [Bourgogne-Franche-Comté] [EFS BFC]
Centre Hospitalier Régional Universitaire de Besançon [CHRU Besançon]
Interactions hôte-greffon-tumeur, ingénierie cellulaire et génique - UFC (UMR INSERM 1098) [RIGHT]
Beneton, Nathalie [Auteur]
Centre Hospitalier Le Mans (CH Le Mans)
Amini Adle, Mona [Auteur]
Centre Léon Bérard [Lyon]
Funck-Brentano, Elisa [Auteur]
Université Paris-Saclay
Biomarqueurs et essais cliniques en Cancérologie et Onco-Hématologie [BECCOH]
Hôpital Ambroise Paré [AP-HP]
Descamps, Vincent [Auteur]
Université Paris Cité [UPCité]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
Hachon, Lorry [Auteur]
CIC Hôpital Bichat
Malissen, Nausicaa [Auteur]
Hôpital de la Timone [CHU - APHM] [TIMONE]
Centre de Recherche en Cancérologie de Marseille [CRCM]
Baroudjian, Barouyr [Auteur]
Immunologie humaine, physiopathologie & immunothérapie [HIPI (UMR_S_976 / U976)]
Hopital Saint-Louis [AP-HP] [AP-HP]
Brunet-Possenti, Florence [Auteur]
Université Paris Cité [UPCité]
AP-HP - Hôpital Bichat - Claude Bernard [Paris]
Journal title :
Cancers
Pages :
4330
Publisher :
MDPI
Publication date :
2023-09
ISSN :
2072-6694
English keyword(s) :
anti-CTLA-4
anti-PD-1
elderly
immune checkpoint inhibitors
melanoma
nonagenarian
octogenarian
anti-PD-1
elderly
immune checkpoint inhibitors
melanoma
nonagenarian
octogenarian
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
Data regarding elderly melanoma patients treated with anti-PD-1 or anti-CTLA-4 antibodies are in favor of tolerability outcomes that are similar to those of younger counterparts. However, there are very few studies focusing ...
Show more >Data regarding elderly melanoma patients treated with anti-PD-1 or anti-CTLA-4 antibodies are in favor of tolerability outcomes that are similar to those of younger counterparts. However, there are very few studies focusing on elderly patients receiving nivolumab combined with ipilimumab (NIVO + IPI). Here, we ask what are the current prescribing patterns of NIVO + IPI in the very elderly population and analyze the tolerance profile. This French multicenter retrospective study was conducted on 60 melanoma patients aged 80 years and older treated with NIVO + IPI between January 2011 and June 2022. The mean age at first NIVO + IPI administration was 83.7 years (range: 79.3–93.3 years). Fifty-five patients (92%) were in good general condition and lived at home. Two dosing regimens were used: NIVO 1 mg/kg + IPI 3 mg/kg Q3W (NIVO1 + IPI3) in 27 patients (45%) and NIVO 3 mg/kg + IPI 1 mg/kg Q3W (NIVO3 + IPI1) in 33 patients (55%). NIVO + IPI was a first-line treatment in 39 patients (65%). The global prevalence of immune-related adverse events was 63% (38/60), with 27% (16/60) being of grade 3 or higher. Grade ≥ 3 adverse events were less frequent in patients treated with NIVO3 + IPI1 compared with those treated with NIVO1 + IPI3 (12% versus 44%, p = 0.04). In conclusion, the prescribing patterns of NIVO + IPI in very elderly patients are heterogeneous in terms of the dosing regimen and line of treatment. The safety profile of NIVO + IPI is reassuring; whether or not the low-dose regimen NIVO3 + IPI1 should be preferred over NIVO1 + IPI3 in patients aged 80 years or older remains an open question.Show less >
Show more >Data regarding elderly melanoma patients treated with anti-PD-1 or anti-CTLA-4 antibodies are in favor of tolerability outcomes that are similar to those of younger counterparts. However, there are very few studies focusing on elderly patients receiving nivolumab combined with ipilimumab (NIVO + IPI). Here, we ask what are the current prescribing patterns of NIVO + IPI in the very elderly population and analyze the tolerance profile. This French multicenter retrospective study was conducted on 60 melanoma patients aged 80 years and older treated with NIVO + IPI between January 2011 and June 2022. The mean age at first NIVO + IPI administration was 83.7 years (range: 79.3–93.3 years). Fifty-five patients (92%) were in good general condition and lived at home. Two dosing regimens were used: NIVO 1 mg/kg + IPI 3 mg/kg Q3W (NIVO1 + IPI3) in 27 patients (45%) and NIVO 3 mg/kg + IPI 1 mg/kg Q3W (NIVO3 + IPI1) in 33 patients (55%). NIVO + IPI was a first-line treatment in 39 patients (65%). The global prevalence of immune-related adverse events was 63% (38/60), with 27% (16/60) being of grade 3 or higher. Grade ≥ 3 adverse events were less frequent in patients treated with NIVO3 + IPI1 compared with those treated with NIVO1 + IPI3 (12% versus 44%, p = 0.04). In conclusion, the prescribing patterns of NIVO + IPI in very elderly patients are heterogeneous in terms of the dosing regimen and line of treatment. The safety profile of NIVO + IPI is reassuring; whether or not the low-dose regimen NIVO3 + IPI1 should be preferred over NIVO1 + IPI3 in patients aged 80 years or older remains an open question.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Source :