Lapatinib plus Capecitabine versus Trastuzumab plus Capecitabine in the Treatment of Human Epidermal Growth Factor Receptor 2-positive Metastatic Breast Cancer with Central Nervous System Metastases for Patients Currently or Previously Treated with Trastuzumab (LANTERN): a Phase II Randomised Trial.
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Breast Neoplasms
/ drug therapy
Capecitabine
/ administration & dosage
Central Nervous System Neoplasms
/ drug therapy
Female
Humans
Lapatinib
/ administration & dosage
Middle Aged
Prognosis
Receptor, ErbB-2
/ metabolism
Salvage Therapy
Survival Rate
Trastuzumab
/ administration & dosage
Brain metastases
HER2
breast cancer
lapatinib
radiotherapy
trastuzumab
Journal
Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902
Informations de publication
Date de publication:
10 2020
10 2020
Historique:
received:
02
01
2020
revised:
14
05
2020
accepted:
03
06
2020
pubmed:
1
7
2020
medline:
25
5
2021
entrez:
1
7
2020
Statut:
ppublish
Résumé
Brain (central nervous system; CNS) metastases occur in 30-50% of patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic breast cancer (MBC). A substantive evidence base for treatment is lacking, but activity with lapatinib plus capecitabine (lap-cap) has been reported. We compared lap-cap with trastuzumab plus capecitabine (tras-cap) in patients with HER2-positive MBC with CNS metastases previously treated with trastuzumab. This open-label randomised phase II screening trial aimed to randomise 130 participants over 2 years to receive lap-cap or tras-cap. Eligible patients had HER2-positive MBC with newly diagnosed or recently progressed CNS metastases; previous, or current, treatment included: trastuzumab, a taxane or anthracycline and recent completion of local cranial therapy. The primary end point was time to progression of CNS metastases within the 24-week trial period. Secondary objectives included CNS response rate, progression-free survival, steroid use for CNS symptoms and feasibility of recruitment to a large phase III trial. Between September 2011 and October 2013, 30 participants were randomised, 16 to lap-cap and 14 to tras-cap. Recruitment to a large phase III trial was determined not to be feasible. At 24 weeks, CNS disease progression was 41.8% (95% confidence interval 16.1-67.5%) in lap-cap and 41.2% (95% confidence interval 12.8-69.6%) in tras-cap arms; progression-free survival was 44.4% (95% confidence interval 18.1-70.8%) in lap-cap and 50.0% (95% confidence interval 20.9-79.1%) in tras-cap arms. Poor recruitment confirmed that a larger phase III trial would not be feasible and prohibited a preliminary evaluation of the superiority of lap-cap over tras-cap. Descriptive statistics are presented to inform the limited evidence base and future study design.
Identifiants
pubmed: 32600919
pii: S0936-6555(20)30237-5
doi: 10.1016/j.clon.2020.06.003
pii:
doi:
Substances chimiques
Lapatinib
0VUA21238F
Capecitabine
6804DJ8Z9U
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
Trastuzumab
P188ANX8CK
Types de publication
Clinical Trial, Phase II
Comparative Study
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
656-664Subventions
Organisme : Medical Research Council
ID : MC_U137686858
Pays : United Kingdom
Organisme : Cancer Research UK
ID : C8225/A21133
Pays : United Kingdom
Organisme : Cancer Research UK
ID : CRUKE/10/046
Pays : United Kingdom
Informations de copyright
Copyright © 2020 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.