Alpelisib for PIK3CA-mutated advanced gynecological cancers: First clues of clinical activity.

Alpelisib Endometrial cancer Gynecological cancers Ovarian cancer PIK3CA mutation

Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
21 Mar 2024
Historique:
received: 15 12 2023
revised: 20 02 2024
accepted: 28 02 2024
medline: 23 3 2024
pubmed: 23 3 2024
entrez: 22 3 2024
Statut: aheadofprint

Résumé

Recurrent gynecological tumors (e.g., endometrial, and ovarian cancers) are incurable diseases; therefore, new treatment options are urgently needed. The PTEN-AKT-PI3K pathway is frequently altered in these tumors, representing a potential treatment target. Alpelisib is an α-specific PI3K inhibitor approved in PIK3CA-mutated advanced breast cancer. We report outcomes from a large series of patients with PIK3CA-mutated gynecological cancers prospectively treated with alpelisib within a controlled program. From April 2021 to December 2022, 36 patients with PIK3CA-mutated advanced gynecological cancers received alpelisib 300 mg orally once daily. Objective response (ORR) and disease control (DCR) rates provided measure of the antitumor activity of alpelisib, the primary objective of the study. Included patients had endometrial (17/36 [47%]), ovarian (10/36 [28%]), or other gynecological cancers (9/36 [25%]). Most patients had received 2-3 prior systemic treatments (endometrial, 47·2%; ovarian, 60%; other, 56%), and presented with visceral metastases at baseline (82%, 70%, and 56%, respectively). Overall, 17 different PIK3CA mutations were found, including 53% in the kinase domain (most commonly H1047R) and 36% in the helical domain (most commonly E545K). Overall, the ORR was 28% and DCR was 61%, with the greatest benefit observed in patients with endometrial cancer (35% and 71%, respectively). Alpelisib represents an active treatment option in patients with recurrent gynecological cancers harboring a PIK3CA mutation. These findings support the need of biomarker-driven randomized trials of PI3K inhibitors in gynecological cancers.

Identifiants

pubmed: 38518529
pii: S0090-8258(24)00139-2
doi: 10.1016/j.ygyno.2024.02.029
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

61-67

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Anna Passarelli (A)

Department of Urology and Gynecology, Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Naples, Italy.

Vittoria Carbone (V)

Department of Women and Child Health, Division of Gynecologic Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Sandro Pignata (S)

Department of Urology and Gynecology, Istituto Nazionale Tumori Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Fondazione G. Pascale, Naples, Italy. Electronic address: s.pignata@istitutotumori.na.it.

Roberta Mazzeo (R)

Unit of Medical Oncology and Cancer Prevention, Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), Aviano, Italy.

Domenica Lorusso (D)

Department of Women and Child Health, Division of Gynecologic Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy; Department of Life Science and Public Health, Catholic University of Sacred Heart Largo Agostino Gemelli, Rome, Italy.

Giovanni Scambia (G)

Department of Women and Child Health, Division of Gynecologic Oncology, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy; Department of Life Science and Public Health, Catholic University of Sacred Heart Largo Agostino Gemelli, Rome, Italy.

Stefania Canova (S)

Medical Oncology Unit, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Teresa Di Palma (T)

Medical Oncology Unit, Ospedale S Maria Goretti, Latina, Italy.

Giulia Tasca (G)

Division of Oncology 2, Veneto Institute of Oncology IOV - IRCCS, Padua, Italy.

Mara Mantiero (M)

Department of Gynecologic Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Emanuele Naglieri (E)

Department of Oncology, Istituto Oncologico Giovanni Paolo II, Bari, Italy.

Claudia Andreetta (C)

Department of Oncology, ASU FC S. Maria della Misericordia, Udine, Italy.

Martina Rauso (M)

Oncological Medical and Specialists Department, Oncology Unit, University Hospital of Ferrara, Ferrara, Italy.

Anna Elisabetta Brunetti (AE)

ASL Taranto, PO San Pio, Castellaneta, Taranto, Italy.

Letizia Laera (L)

Department of Medical Oncology, Miulli General Regional Hospital, Acquaviva delle Fonti, Italy.

Chiara Abeni (C)

Department of Clinical Oncology, Fondazione Poliambulanza, Brescia, Italy.

Giuseppa Scandurra (G)

Medical Oncology Unit, Cannizzaro Hospital, Catania, Italy.

Anna Rita Gambaro (AR)

Medical Oncology Unit, ASST Fatebenefratelli Sacco, Ospedale Sacco Polo Universitario, Milano, Italy.

Alessia Pastore (A)

Medical Oncology Unit, Azienda Ospedaliera S. Anna, Como, Italy.

Carmelo Bengala (C)

Medical Oncology Unit, Misericordia Hospital, Grosseto, Italy.

Marco Gunnellini (M)

Medical Oncology Unit, Presidio Ospedaliero Alto Chiascio, Gubbio, Italy.

Alberto Farolfi (A)

Department of Medical Oncology, IRCCS- Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Emilia-Romagna, Italy.

Maurizio Spinello (M)

Novartis Farma S.p.A., Milan, Italy.

Michele Bartoletti (M)

Unit of Medical Oncology and Cancer Prevention, Department of Medical Oncology, Centro di Riferimento Oncologico di Aviano (CRO), Aviano, Italy.

Classifications MeSH