Efficacy of Neratinib Plus Capecitabine in the Subgroup of Patients with Central Nervous System Involvement from the NALA Trial.


Journal

The oncologist
ISSN: 1549-490X
Titre abrégé: Oncologist
Pays: England
ID NLM: 9607837

Informations de publication

Date de publication:
08 2021
Historique:
received: 01 12 2020
accepted: 03 05 2021
pubmed: 25 5 2021
medline: 29 9 2021
entrez: 24 5 2021
Statut: ppublish

Résumé

Neratinib has efficacy in central nervous system (CNS) metastases from HER2-positive metastatic breast cancer (MBC). We report outcomes among patients with CNS metastases at baseline from the phase III NALA trial of neratinib plus capecitabine (N + C) versus lapatinib plus capecitabine (L + C). NALA was a randomized, active-controlled trial in patients who received two or more previous HER2-directed regimens for HER2-positive MBC. Patients with asymptomatic/stable brain metastases (treated or untreated) were eligible. Patients were assigned to N + C (neratinib 240 mg per day, capecitabine 750 mg/m Of 621 patients enrolled, 101 (16.3%) had known CNS metastases at baseline (N + C, n = 51; L + C, n = 50); 81 had received prior CNS-directed radiotherapy and/or surgery. In the CNS subgroup, mean PFS through 24 months was 7.8 months with N + C versus 5.5 months with L + C (hazard ratio [HR], 0.66; 95% confidence interval [CI], 0.41-1.05), and mean OS through 48 months was 16.4 versus 15.4 months (HR, 0.90; 95% CI, 0.59-1.38). At 12 months, cumulative incidence of interventions for CNS disease was 25.5% for N + C versus 36.0% for L + C, and cumulative incidence of progressive CNS disease was 26.2% versus 41.6%, respectively. In patients with target CNS lesions at baseline (n = 32), confirmed intracranial objective response rates were 26.3% and 15.4%, respectively. No new safety signals were observed. These analyses suggest improved PFS and CNS outcomes with N + C versus L + C in patients with CNS metastases from HER2-positive MBC. In a subgroup of patients with central nervous system (CNS) metastases from HER2-positive breast cancer after two or more previous HER2-directed regimens, the combination of neratinib plus capecitabine was associated with improved progression-free survival and CNS outcomes compared with lapatinib plus capecitabine. These findings build on previous phase II and III studies describing efficacy of neratinib in the prevention and treatment of CNS metastases, and support a role for neratinib as a systemic treatment option in the management of patients with HER2-positive brain metastases following antibody-based HER2-directed therapies.

Sections du résumé

BACKGROUND
Neratinib has efficacy in central nervous system (CNS) metastases from HER2-positive metastatic breast cancer (MBC). We report outcomes among patients with CNS metastases at baseline from the phase III NALA trial of neratinib plus capecitabine (N + C) versus lapatinib plus capecitabine (L + C).
MATERIALS AND METHODS
NALA was a randomized, active-controlled trial in patients who received two or more previous HER2-directed regimens for HER2-positive MBC. Patients with asymptomatic/stable brain metastases (treated or untreated) were eligible. Patients were assigned to N + C (neratinib 240 mg per day, capecitabine 750 mg/m
RESULTS
Of 621 patients enrolled, 101 (16.3%) had known CNS metastases at baseline (N + C, n = 51; L + C, n = 50); 81 had received prior CNS-directed radiotherapy and/or surgery. In the CNS subgroup, mean PFS through 24 months was 7.8 months with N + C versus 5.5 months with L + C (hazard ratio [HR], 0.66; 95% confidence interval [CI], 0.41-1.05), and mean OS through 48 months was 16.4 versus 15.4 months (HR, 0.90; 95% CI, 0.59-1.38). At 12 months, cumulative incidence of interventions for CNS disease was 25.5% for N + C versus 36.0% for L + C, and cumulative incidence of progressive CNS disease was 26.2% versus 41.6%, respectively. In patients with target CNS lesions at baseline (n = 32), confirmed intracranial objective response rates were 26.3% and 15.4%, respectively. No new safety signals were observed.
CONCLUSION
These analyses suggest improved PFS and CNS outcomes with N + C versus L + C in patients with CNS metastases from HER2-positive MBC.
IMPLICATIONS FOR PRACTICE
In a subgroup of patients with central nervous system (CNS) metastases from HER2-positive breast cancer after two or more previous HER2-directed regimens, the combination of neratinib plus capecitabine was associated with improved progression-free survival and CNS outcomes compared with lapatinib plus capecitabine. These findings build on previous phase II and III studies describing efficacy of neratinib in the prevention and treatment of CNS metastases, and support a role for neratinib as a systemic treatment option in the management of patients with HER2-positive brain metastases following antibody-based HER2-directed therapies.

Identifiants

pubmed: 34028126
doi: 10.1002/onco.13830
pmc: PMC8342591
doi:

Substances chimiques

Quinolines 0
Capecitabine 6804DJ8Z9U
Receptor, ErbB-2 EC 2.7.10.1
neratinib JJH94R3PWB

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1327-e1338

Informations de copyright

© 2021 The Authors. The Oncologist published by Wiley Periodicals LLC on behalf of AlphaMed Press.

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Auteurs

Sara A Hurvitz (SA)

University of California Los Angeles/Jonsson Comprehensive Cancer Center, Los Angeles, California, USA.

Cristina Saura (C)

Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, SOLTI Breast Cancer Cooperative Group, Barcelona, Spain.

Mafalda Oliveira (M)

Vall d'Hebron University Hospital, Vall d'Hebron Institute of Oncology, SOLTI Breast Cancer Cooperative Group, Barcelona, Spain.

Maureen E Trudeau (ME)

Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.

Beverly Moy (B)

Massachusetts General Hospital Cancer Center, Boston, Massachusetts, USA.

Suzette Delaloge (S)

Gustave Roussy, Villejuif, France.

William Gradishar (W)

Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Chicago, Illinois, USA.

Sung-Bae Kim (SB)

Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.

Barbara Haley (B)

University of Texas Southwestern, Dallas, Texas, USA.

Larisa Ryvo (L)

Sourasky Medical Center (Ichilov), Tel Aviv, Israel.

Ming-Shen Dai (MS)

Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.

Vladimir Milovanov (V)

Tambov Regional Oncology Center, Tambov, Russia.

Jesús Alarcón (J)

Hospital Universitario Son Espases, Palma de Mallorca, Balearic Islands, Spain.

Sujith Kalmadi (S)

Ironwood Cancer and Research Centers, Chandler, Arizona, USA.

Eduardo Cronemberger (E)

Centro Regional Integrado de Oncologia, Fortaleza, Ceará, Brazil.

Cristiano Souza (C)

Hospital de Câncer de Barretos, Barretos, São Paulo, Brazil.

Luciana Landeiro (L)

Nucleo de Oncologia Da Bahia, Ondina, Bahia, Brazil.

Ron Bose (R)

Washington University School of Medicine, St Louis, Missouri, USA.

Judith Bebchuk (J)

Puma Biotechnology, Inc., Los Angeles, California, USA.

Fairooz Kabbinavar (F)

Puma Biotechnology, Inc., Los Angeles, California, USA.

Richard Bryce (R)

Puma Biotechnology, Inc., Los Angeles, California, USA.

Kiana Keyvanjah (K)

Puma Biotechnology, Inc., Los Angeles, California, USA.

Adam M Brufsky (AM)

Magee-Womens Hospital of UPMC, Pittsburgh, Pennsylvania, USA.

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Classifications MeSH