Atezolizumab and paclitaxel as first line ...
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Atezolizumab and paclitaxel as first line therapy in advanced triple-negative breast cancer patients included in the French early access program.
Auteur(s) :
de Moura, Alexandre [Auteur]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Vuagnat, P. [Auteur]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Renouf, B. [Auteur]
Pierga, J. Y. [Auteur]
Loirat, D. [Auteur]
Institut Curie [Paris]
Vaflard, Pauline [Auteur]
Institut Curie [Paris]
Lafayolle De La Bruyère, C. [Auteur]
Chaumard-Billotey, N. [Auteur]
Hajjaji, Nawale [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Ladoire, Sylvain [Auteur]
Département d'oncologie médicale [Centre Georges-François Leclerc]
Dabakuyo-Yonli, Tienhan Sandrine [Auteur]
Département d'oncologie médicale [Centre Georges-François Leclerc]
Patsouris, A. [Auteur]
Institut de Cancérologie de l'Ouest [Angers/Nantes] [UNICANCER/ICO]
Frenel, J. S. [Auteur]
Nicolai, V. [Auteur]
Institut Claudius Regaud [ICR]
Alexandre, M. [Auteur]
Institut régional de Cancérologie de Montpellier [ICM]
Dohollou, N. [Auteur]
Polyclinique Bordeaux Nord Aquitaine [PBNA]
Grenier, J. [Auteur]
Institut Sainte Catherine [Avignon]
Bourien, H. [Auteur]
Département d'oncologie médicale [Rennes]
Bidard, F. C. [Auteur]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Vuagnat, P. [Auteur]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Renouf, B. [Auteur]
Pierga, J. Y. [Auteur]
Loirat, D. [Auteur]
Institut Curie [Paris]
Vaflard, Pauline [Auteur]
Institut Curie [Paris]
Lafayolle De La Bruyère, C. [Auteur]
Chaumard-Billotey, N. [Auteur]
Hajjaji, Nawale [Auteur]
Protéomique, Réponse Inflammatoire, Spectrométrie de Masse (PRISM) - U1192
Ladoire, Sylvain [Auteur]
Département d'oncologie médicale [Centre Georges-François Leclerc]
Dabakuyo-Yonli, Tienhan Sandrine [Auteur]
Département d'oncologie médicale [Centre Georges-François Leclerc]
Patsouris, A. [Auteur]
Institut de Cancérologie de l'Ouest [Angers/Nantes] [UNICANCER/ICO]
Frenel, J. S. [Auteur]
Nicolai, V. [Auteur]
Institut Claudius Regaud [ICR]
Alexandre, M. [Auteur]
Institut régional de Cancérologie de Montpellier [ICM]
Dohollou, N. [Auteur]
Polyclinique Bordeaux Nord Aquitaine [PBNA]
Grenier, J. [Auteur]
Institut Sainte Catherine [Avignon]
Bourien, H. [Auteur]
Département d'oncologie médicale [Rennes]
Bidard, F. C. [Auteur]
Institut Curie [Paris]
Université de Versailles Saint-Quentin-en-Yvelines [UVSQ]
Titre de la revue :
Scientific Reports
Nom court de la revue :
Sci Rep
Numéro :
13
Pagination :
13427
Date de publication :
2023-08-28
ISSN :
2045-2322
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Following the results of the IMpassion130 trial, an early access program (EAP) was opened in France, allowing patients with PD-L1-positive advanced triple negative breast cancer (aTNBC) to receive a combination of paclitaxel ...
Lire la suite >Following the results of the IMpassion130 trial, an early access program (EAP) was opened in France, allowing patients with PD-L1-positive advanced triple negative breast cancer (aTNBC) to receive a combination of paclitaxel and atezolizumab as first line therapy. This EAP was later discontinued when the IMpassion131 trial read out with negative results. We performed a retrospective multicentric analysis in patients who were prospectively enrolled in the French EAP. Efficacy and toxicity data were obtained on 64 patients treated from August 2019 to August 2020 in 10 French cancer centers. Median progression-free survival (PFS) and overall survival (OS) were 4.1 months (95% CI [3.0–5.8]) and 17.9 months (95% CI [12.4–NR]), respectively. The 6-months PFS rate was 28% (95% CI [16–40%]) (N = 18/64), while N = 33/64 patients (52%, 95% CI [38–63%]) experienced a tumor response. Exploratory subgroup analyses retrieved that corticosteroid use at inclusion in the EAP, before treatment initiation, was the only independent unfavorable prognostic factor for PFS (HR 2.7, 95% CI [1.3–5.6]). No new safety signal was observed. This real-life study, unique by its setting (EAP granted by anticipation and later withdrawn), suggests atezolizumab and paclitaxel has a limited efficacy in PD-L1-positive aTNBC, especially in patients receiving corticosteroids as comedication before treatment start.Lire moins >
Lire la suite >Following the results of the IMpassion130 trial, an early access program (EAP) was opened in France, allowing patients with PD-L1-positive advanced triple negative breast cancer (aTNBC) to receive a combination of paclitaxel and atezolizumab as first line therapy. This EAP was later discontinued when the IMpassion131 trial read out with negative results. We performed a retrospective multicentric analysis in patients who were prospectively enrolled in the French EAP. Efficacy and toxicity data were obtained on 64 patients treated from August 2019 to August 2020 in 10 French cancer centers. Median progression-free survival (PFS) and overall survival (OS) were 4.1 months (95% CI [3.0–5.8]) and 17.9 months (95% CI [12.4–NR]), respectively. The 6-months PFS rate was 28% (95% CI [16–40%]) (N = 18/64), while N = 33/64 patients (52%, 95% CI [38–63%]) experienced a tumor response. Exploratory subgroup analyses retrieved that corticosteroid use at inclusion in the EAP, before treatment initiation, was the only independent unfavorable prognostic factor for PFS (HR 2.7, 95% CI [1.3–5.6]). No new safety signal was observed. This real-life study, unique by its setting (EAP granted by anticipation and later withdrawn), suggests atezolizumab and paclitaxel has a limited efficacy in PD-L1-positive aTNBC, especially in patients receiving corticosteroids as comedication before treatment start.Lire moins >
Comité de lecture :
Oui
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
Université de Lille
Inserm
CHU Lille
Inserm
CHU Lille
Date de dépôt :
2023-12-13T03:39:14Z
2024-01-23T15:10:41Z
2024-01-23T15:10:41Z
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- s41598-023-40569-9.pdf
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