Safety and Efficacy of Ribociclib in Combination with Letrozole in Patients with HR+, HER2- Advanced Breast Cancer: Results from the Italian Subpopulation of Phase 3b CompLEEment-1 Study.


Journal

Targeted oncology
ISSN: 1776-260X
Titre abrégé: Target Oncol
Pays: France
ID NLM: 101270595

Informations de publication

Date de publication:
11 2022
Historique:
accepted: 10 08 2022
pubmed: 25 9 2022
medline: 26 11 2022
entrez: 24 9 2022
Statut: ppublish

Résumé

Ribociclib plus letrozole demonstrated manageable safety and efficacy profiles in hormone receptor-positive (HR+), human epidermal growth factor receptor-2-negative (HER2-) advanced breast cancer (ABC) in the Phase 3b CompLEEment-1 trial. To evaluate the safety and efficacy of ribociclib plus letrozole in the Italian subpopulation with HR+, HER2- ABC from the CompLEEment-1 trial. Patients with HR+, HER2- ABC received ribociclib (600 mg/day, 3 weeks on/1 week off) plus letrozole (2.5 mg/day) while men and premenopausal women additionally received goserelin. Patients were allowed with ≤ 1 line of prior chemotherapy and an Eastern Cooperative Oncology Group performance status of ≤ 2. The primary outcome included safety and tolerability. Of the 554 Italian patients, 246 (44.4 %) patients completed treatment. The reasons for treatment discontinuation included progressive disease (PD; 36.6 %), adverse events (AEs; 11.9 %), and death (1.6 %). All-grade AEs and grade ≥ 3 AEs occurred in 98.9 % and 77.8 % patients, respectively. The most common treatment-related AEs were neutropenia (73.6 %), followed by leukopenia (32.1 %), and nausea (25.3 %). The overall response rate was 28.2 % (95 % confidence interval [CI], 24.4-32.1); clinical benefit rate was 71.7 % (95 % CI, 67.7-75.4); and median time to progression was 26.7 months (95 % CI, 24.8-non-estimable). Health-related quality of life scores were maintained during treatment. The safety and efficacy profiles of ribociclib plus letrozole in the Italian subpopulation was found to be consistent with the CompLEEment-1 global population result, MONALEESA-2, and MONALEESA-7 outcomes, which reaffirm ribociclib plus letrozole as the frontline treatment option in patients with HR+, HER2- ABC. NCT02941926 (30 November 2016).

Sections du résumé

BACKGROUND
Ribociclib plus letrozole demonstrated manageable safety and efficacy profiles in hormone receptor-positive (HR+), human epidermal growth factor receptor-2-negative (HER2-) advanced breast cancer (ABC) in the Phase 3b CompLEEment-1 trial.
OBJECTIVE
To evaluate the safety and efficacy of ribociclib plus letrozole in the Italian subpopulation with HR+, HER2- ABC from the CompLEEment-1 trial.
PATIENTS AND METHODS
Patients with HR+, HER2- ABC received ribociclib (600 mg/day, 3 weeks on/1 week off) plus letrozole (2.5 mg/day) while men and premenopausal women additionally received goserelin. Patients were allowed with ≤ 1 line of prior chemotherapy and an Eastern Cooperative Oncology Group performance status of ≤ 2. The primary outcome included safety and tolerability.
RESULTS
Of the 554 Italian patients, 246 (44.4 %) patients completed treatment. The reasons for treatment discontinuation included progressive disease (PD; 36.6 %), adverse events (AEs; 11.9 %), and death (1.6 %). All-grade AEs and grade ≥ 3 AEs occurred in 98.9 % and 77.8 % patients, respectively. The most common treatment-related AEs were neutropenia (73.6 %), followed by leukopenia (32.1 %), and nausea (25.3 %). The overall response rate was 28.2 % (95 % confidence interval [CI], 24.4-32.1); clinical benefit rate was 71.7 % (95 % CI, 67.7-75.4); and median time to progression was 26.7 months (95 % CI, 24.8-non-estimable). Health-related quality of life scores were maintained during treatment.
CONCLUSION
The safety and efficacy profiles of ribociclib plus letrozole in the Italian subpopulation was found to be consistent with the CompLEEment-1 global population result, MONALEESA-2, and MONALEESA-7 outcomes, which reaffirm ribociclib plus letrozole as the frontline treatment option in patients with HR+, HER2- ABC.
TRIAL REGISTRATION NUMBER AND DATE OF REGISTRATION
NCT02941926 (30 November 2016).

Identifiants

pubmed: 36152144
doi: 10.1007/s11523-022-00913-x
pii: 10.1007/s11523-022-00913-x
pmc: PMC9684264
doi:

Substances chimiques

Letrozole 7LKK855W8I
ribociclib TK8ERE8P56
Receptors, Progesterone 0
Receptor, ErbB-2 EC 2.7.10.1
Receptors, Estrogen 0

Banques de données

ClinicalTrials.gov
['NCT02941926']

Types de publication

Clinical Trial, Phase III Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

615-625

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Michelino De Laurentiis (M)

Breast Oncology, Istituto Nazionale Tumori, IRCCS, Fondazione Pascale, Napoli, Italy. m.delaurentiis@breastunit.org.

Roberta Caputo (R)

Istituto Nazionale Tumori "Fondazione Pascale", Napoli, Italy.

Manuelita Mazza (M)

Senologia Medica, Istituto Europeo di Oncologia, Milano, Italy.

Mauro Mansutti (M)

Department of Oncology, Santa Maria della Misericordia hospital, Udine, Italy.

Riccardo Masetti (R)

Dipartimento di Scienze della Salute della Donna e del Bambino e di Sanità Pubblica, Fondazione Policlinico Gemelli IRCSS, Roma, Italy.

Zelmira Ballatore (Z)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, AOU Ospedali Riuniti Ancona Università Politecnica delle Marche, Ancona, Italy.

Rosalba Torrisi (R)

Department of Medical Oncology, IRCCS-Humanitas Clinical and Research Hospital, Rozzano, Italy.

Andrea Michelotti (A)

U.O. Oncologia Medica I, Azienda Ospedaliera Universitaria Pisana, Ospedale S. Chiara, Pisa, Italy.

Alberto Zambelli (A)

Humanitas University, IRCCS Research Hospital, Rozzano, Italy.

Antonella Ferro (A)

Medical Oncology, Ospedale Santa Chiara, Trento, Italy.

Daniele Generali (D)

U.O.C. Multidisciplinare di Patologia Mammaria, Istituti Ospitalieri di Cremona, ASST di Cremona, Cremona, Italy.

Patrizia Vici (P)

UOSD Sperimentazioni di fase IV, IRCCS Regina Elena National Cancer Institute, Roma, Italy.

Luigi Coltelli (L)

U.O.C. di Oncologia Medica, Presidio Ospedaliero Livorno, Livorno, Italy.

Alessandra Fabi (A)

Division of Medical Oncology 1, IRCCS Regina Elena National Cancer Institute, Roma, Italy.

Paolo Marchetti (P)

UOC Oncologia Medica, Azienda Ospedaliera St. Andrea, Rome, Italy.

Alberto Ballestrero (A)

Dipartimento di Medicina Interna DIMI, Ospedale Policlinico San Martino IRCCS, Genova, Italy.

Simon Spazzapan (S)

S.O.C. Oncologia Medica e Prevenzione Oncologica, Centro di Riferimento Oncologico IRCCS, Aviano, Italy.

Antonio Frassoldati (A)

U.O.C. Oncologia Clinica, Azienda Ospedaliero, Universitaria di Ferrara - Arcispedale Sant'Anna, Ferrara, Italy.

Maria Giuseppina Sarobba (MG)

UOC Oncologia, Presidio Ospedaliero S. Francesco, ASL Nuoro, Nuoro, Italy.

Donatella Grasso (D)

Oncology, Novartis Farma SpA, Origgio, Italy.

Claudio Zamagni (C)

Addarii Medical Oncology Unit IRCCS Azienda Ospedaliero-universitaria di Bologna, Bologna, Italy.

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