Neratinib and Ado-Trastuzumab-Emtansine for Pre-treated and Untreated HER2-positive Breast Cancer Brain Metastases: Translational Breast Cancer Research Consortium Trial 022.

T-DM1 ado-trastuzumab-emtansine brain metastases breast cancer neratinib

Journal

Annals of oncology : official journal of the European Society for Medical Oncology
ISSN: 1569-8041
Titre abrégé: Ann Oncol
Pays: England
ID NLM: 9007735

Informations de publication

Date de publication:
06 Jul 2024
Historique:
received: 22 03 2024
revised: 27 06 2024
accepted: 02 07 2024
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 8 7 2024
Statut: aheadofprint

Résumé

Treatment options for HER2-positive breast cancer brain metastases (BCBM) remain limited. We previously reported central nervous system (CNS) activity for neratinib and neratinib-capecitabine. Preclinical data suggest that neratinib may overcome resistance to ado-trastuzumab-emtansine (T-DM1) when given in combination. In TBCRC 022's cohort 4, we examined the efficacy of neratinib plus T-DM1 in patients with HER2-positive BCBM. In this multicenter, phase II study, patients with measurable HER2-positive BCBM received neratinib 160 mg daily plus T-DM1 3.6 mg/kg intravenously every 21 days in three parallel-enrolling cohorts (cohort 4A-previously untreated BCBM, cohorts 4B and 4C- BCBM progressing after local CNS-directed therapy without [4B] and with [4C] prior exposure to T-DM1). Cycle 1 diarrheal prophylaxis was required. The primary endpoint was the Response Assessment in Neuro-Oncology-Brain Metastases (RANO-BM) by cohort. Overall survival (OS) and toxicity were also assessed. Between 2018-2021, 6, 17, and 21 patients enrolled to cohorts 4A, 4B, and 4C. Enrollment was stopped prematurely for slow accrual. The CNS objective response rate in cohorts 4A, 4B, and 4C was 33.3% (95% confidence interval [CI]: 4.3-77.7%), 35.3% (95% CI: 14.2-61.7%), and 28.6% (95% CI: 11.3-52.2%), respectively; 38.1-50% experienced stable disease for ≥6 months or response. Diarrhea was the most common grade 3 toxicity (22.7%). Median OS was 30.2 months (cohort 4A; 95% CI: 21.9, not reached [NR]), 23.3 months (cohort 4B; 95% CI: 17.6, NR), and 20.9 months (cohort 4C; 95% CI: 14.9, NR). We observed Intracranial activity for neratinib plus T-DM1, including those with prior T-DM1 exposure, suggesting synergistic effects with neratinib. Our data provide additional evidence for neratinib-based combinations in patients with HER2-positive BCBM, even those who are heavily pre-treated.

Identifiants

pubmed: 38977064
pii: S0923-7534(24)01015-9
doi: 10.1016/j.annonc.2024.07.245
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 European Society for Medical Oncology. Published by Elsevier Ltd. All rights reserved.

Auteurs

R A Freedman (RA)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA. Electronic address: Rachel_freedman@dfci.harvard.edu.

H M Heiling (HM)

Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.

T Li (T)

Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.

D Trapani (D)

Division of New Drug Development for innovative therapies, European Institute of Oncology IRCCS, Milan, Italy; University of Milan, department of oncology and hematology, Milan, Italy.

N Tayob (N)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.

K L Smith (KL)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

R Davis (R)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

A M Pereslete (AM)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

M K DeMeo (MK)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

C Cotter (C)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

W Y Chen (WY)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

H A Parsons (HA)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

C A Santa-Maria (CA)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

C Van Poznak (C)

University of Michigan, Ann Arbor, MI, USA.

B Moy (B)

Massachusetts General Hospital, Boston, MA, USA.

A M Brufsky (AM)

UPMC Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

M E Melisko (ME)

University of California at San Francisco, San Francisco, CA, USA.

C C O'Sullivan (CC)

Mayo Clinic, Rochester, MN, USA.

N Ashai (N)

MedStar/Georgetown University, Washington, DC, USA.

Y Rauf (Y)

University of North Carolina, Chapel Hill, NC, USA.

J R Nangia (JR)

Baylor College of Medicine, Houston, TX, USA.

R T Burns (RT)

The Emmes Corporation, Rockville, MD, USA.

J Savoie (J)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA; The Emmes Corporation, Rockville, MD, USA.

A C Wolff (AC)

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, MD, USA.

E P Winer (EP)

Yale Cancer Center, New Haven, CT, USA.

M F Rimawi (MF)

Baylor College of Medicine, Houston, TX, USA.

I E Krop (IE)

Yale Cancer Center, New Haven, CT, USA.

N U Lin (NU)

Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA; Breast Oncology Program, Dana-Farber Cancer Institute, Boston, MA, USA.

Classifications MeSH