Real-world ANASTASE study of atezolizumab+nab-paclitaxel as first-line treatment of PD-L1-positive metastatic triple-negative breast cancer.


Journal

NPJ breast cancer
ISSN: 2374-4677
Titre abrégé: NPJ Breast Cancer
Pays: United States
ID NLM: 101674891

Informations de publication

Date de publication:
08 Sep 2023
Historique:
received: 22 12 2022
accepted: 23 08 2023
medline: 9 9 2023
pubmed: 9 9 2023
entrez: 8 9 2023
Statut: epublish

Résumé

The combination of atezolizumab and nab-paclitaxel is recommended in the EU as first-line treatment for PD-L1-positive metastatic triple-negative breast cancer (mTNBC), based on the results of phase III IMpassion130 trial. However, 'real-world' data on this combination are limited. The ANASTASE study (NCT05609903) collected data on atezolizumab plus nab-paclitaxel in PD-L1-positive mTNBC patients enrolled in the Italian Compassionate Use Program. A retrospective analysis was conducted in 29 Italian oncology centers among patients who completed at least one cycle of treatment. Data from 52 patients were gathered. Among them, 21.1% presented de novo stage IV; 78.8% previously received (neo)adjuvant treatment; 55.8% patients had only one site of metastasis; median number of treatment cycles was five (IQR: 3-8); objective response rate was 42.3% (95% CI: 28.9-55.7%). The median time-to-treatment discontinuation was 5 months (95% CI: 2.8-7.1); clinical benefit at 12 months was 45.8%. The median duration of response was 12.7 months (95% CI: 4.1-21.4). At a median follow-up of 20 months, the median progression-free survival was 6.3 months (95% CI: 3.9-8.7) and the median time to next treatment or death was 8.1 months (95% CI: 5.5-10.7). At 12 months and 24 months, the overall survival rates were 66.3% and 49.1%, respectively. The most common immune-related adverse events included rash (23.1%), hepatitis (11.5%), thyroiditis (11.5%) and pneumonia (9.6%). Within the ANASTASE study, patients with PD-L1-positive mTNBC treated with first-line atezolizumab plus nab-paclitaxel achieved PFS and ORR similar to those reported in the IMpassion130 study, with no unexpected adverse events.

Identifiants

pubmed: 37684252
doi: 10.1038/s41523-023-00579-2
pii: 10.1038/s41523-023-00579-2
pmc: PMC10491680
doi:

Types de publication

Journal Article

Langues

eng

Pagination

73

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

Alessandra Fabi (A)

Precision Medicine Unit in Senology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy. alessandra.fabi@policlinicogemelli.it.

Luisa Carbognin (L)

Division of Gynecology Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Andrea Botticelli (A)

Medical Oncology Unit, La Sapienza, University of Rome, Policlinico Umberto I, Rome, Italy.

Ida Paris (I)

Division of Gynecology Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Paolo Fuso (P)

Division of Gynecology Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Maria Cristina Savastano (MC)

Medical Oncology Unit, A.O.U. San Giovanni di Dio e Ruggi D'Aragona, Salerno, Italy.

Nicla La Verde (N)

Medical Oncology Unit, ASST Fatebenefratelli Sacco PO Luigi Sacco - Polo Universitario, Milan, Italy.

Carla Strina (C)

Medical Oncology Unit Azienda Socio-Sanitaria Territoriale Cremona, Cremona, Italy.

Rebecca Pedersini (R)

Medical Oncology Unit ASST Spedali Civili, Brescia, Italy.

Stefania Guarino (S)

Medical Oncology Unit Santa Maria della Misericordia Hospital, Urbino, Italy.

Giuseppe Curigliano (G)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Division of Early Drug Development, European Institute of Oncology, IRCCS, Milan, Italy.

Carmen Criscitiello (C)

Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.
Division of Early Drug Development, European Institute of Oncology, IRCCS, Milan, Italy.

Mimma Raffaele (M)

Presidio Cassia Sant'andrea, Dipartimento Oncologico, Asl Roma1, Rome, Italy.

Alessandra Beano (A)

Department of Medical Oncology1, Città della Salute e della Scienza Hospital, Turin, Italy.

Antonio Franco (A)

Breast Unit, Department of Women, Children and Public Health Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Maria Rosaria Valerio (MR)

Medical Oncology, Policlinico Universitario P. Giaccone, Palermo, Italy.

Francesco Verderame (F)

Medical Oncology, AO Riuniti Villa Sofia, Cervello, Palermo, Italy.

Andrea Fontana (A)

Medical Oncology Unit 2, Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy.

Eva Regina Haspinger (ER)

Azienda Sanitaria dell'Alto Adige - Ospedale di Merano, Merano, Italy.

Alessia Caldara (A)

Santa Chiara Hospital, Trento, Italy.

Alba Di Leone (A)

Breast Unit, Department of Women, Children and Public Health Sciences, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.

Giampaolo Tortora (G)

Medical Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Medical Oncology, Department of Translational Medicine and Surgery, Università Cattolica del Sacro Cuore, Rome, Italy.

Diana Giannarelli (D)

Epidemiology and Biostatistics Facility, Fondazione Policlinico Universitario A. Gemelli IRCCS, Roma, Italy.

Giovanni Scambia (G)

Division of Gynecology Oncology, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.
Università Cattolica del Sacro Cuore, Rome, Italy.

Classifications MeSH