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.


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
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

656-664

Subventions

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.

Auteurs

J F Seligmann (JF)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

A Wright-Hughes (A)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

A Pottinger (A)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

G Velikova (G)

St James's Institute of Oncology, St James University Hospital, Leeds, UK.

J B Oughton (JB)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

G Murden (G)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

M Rizwanullah (M)

Department of Clinical Oncology, The Beatson West of Scotland Cancer Centre, Glasgow, UK.

C Price (C)

Department of Medical Oncology, University Hospitals, Bristol, UK.

H Passant (H)

Department of Medical Oncology, Velindre Hospital, Cardiff, UK.

P Heudtlass (P)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

H Marshall (H)

Clinical Trials Research Unit, University of Leeds, Leeds, UK.

S Johnston (S)

Department of Medical Oncology, The Royal Marsden NHS Foundation Trust, London, UK.

D Dodwell (D)

St James's Institute of Oncology, St James University Hospital, Leeds, UK; Nuffield Department of Population Health, Oxford University, Oxford, UK. Electronic address: david.dodwell@nhs.net.

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Classifications MeSH