Phase III, Randomized Study of Dual Human Epidermal Growth Factor Receptor 2 (HER2) Blockade With Lapatinib Plus Trastuzumab in Combination With an Aromatase Inhibitor in Postmenopausal Women With HER2-Positive, Hormone Receptor-Positive Metastatic Breast Cancer: Updated Results of ALTERNATIVE.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 01 2021
Historique:
pubmed: 22 8 2020
medline: 12 6 2021
entrez: 22 8 2020
Statut: ppublish

Résumé

Human epidermal growth factor receptor 2 (HER2) targeting plus endocrine therapy (ET) improved clinical benefit in HER2-positive, hormone receptor (HR)-positive metastatic breast cancer (MBC) versus ET alone. Dual HER2 blockade enhances clinical benefit versus single HER2 blockade. The ALTERNATIVE study evaluated the efficacy and safety of dual HER2 blockade plus aromatase inhibitor (AI) in postmenopausal women with HER2-positive/HR-positive MBC who received prior ET and prior neo(adjuvant)/first-line trastuzumab (TRAS) plus chemotherapy. This updated article reflects minor numerical corrections in some secondary efficacy analyses that resulted from programming errors and that do not change the major conclusions of the study. Patients were randomly assigned (1:1:1) to receive lapatinib (LAP) plus TRAS plus AI, TRAS plus AI, or LAP plus AI. Patients for whom chemotherapy was intended were excluded. The primary end point was progression-free survival (PFS; investigator assessed) with LAP plus TRAS plus AI versus TRAS plus AI. Secondary end points were PFS (comparison of other arms), overall survival (OS), overall response rate (ORR), clinical benefit rate (CBR), and safety. Three hundred fifty-five patients were included in this analysis: LAP plus TRAS plus AI (n = 120), TRAS plus AI (n = 117), and LAP plus AI (n = 118). Baseline characteristics were balanced. The study met its primary end point; superior PFS was observed with LAP plus TRAS plus AI versus TRAS plus AI (median PFS, 11 Dual HER2 blockade with LAP plus TRAS plus AI showed superior PFS benefit versus TRAS plus AI in patients with HER2-positive/HR-positive MBC. This combination offers an effective and safe chemotherapy-sparing alternative treatment regimen for this patient population.

Identifiants

pubmed: 32822287
doi: 10.1200/JCO.20.01894
doi:

Substances chimiques

Aromatase Inhibitors 0
Lapatinib 0VUA21238F
Fulvestrant 22X328QOC4
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Banques de données

ClinicalTrials.gov
['NCT01160211']
EudraCT
['2010-019577-16']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

79-89

Subventions

Organisme : Department of Health
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Stephen R D Johnston (SRD)

The Royal Marsden NHS Foundation Trust, London, United Kingdom.

Roberto Hegg (R)

Centro de Referência da Saúde da Mulher, São Paulo, Brazil.

Seock-Ah Im (SA)

Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.

In Hae Park (IH)

National Cancer Center, Gyeonggi-do, Korea.

Olga Burdaeva (O)

Regional Oncology Dispensary, Arkhangelsk, Russia.

Galina Kurteva (G)

University Cancer Center Hospital, Sofia, Bulgaria.

Michael F Press (MF)

University of Southern California, Los Angeles, Los Angeles, CA.

Sergei Tjulandin (S)

N.N. Blokhin Russian Cancer Research Center, Moscow, Russia.

Hiroji Iwata (H)

Aichi Cancer Center Hospital, Aichi, Japan.

Sergio D Simon (SD)

Hospital Israelita Albert Einstein, São Paulo, Brazil.

Sarah Kenny (S)

Novartis Pharma AG, Basel, Switzerland.

Severine Sarp (S)

Novartis Pharma AG, Basel, Switzerland.

Miguel A Izquierdo (MA)

Novartis Pharma AG, Basel, Switzerland.

Lisa S Williams (LS)

Novartis Pharmaceuticals UK Limited, Frimley, United Kingdom.

William J Gradishar (WJ)

Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL.

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Classifications MeSH