Ten-year survival of neoadjuvant dual HER2 blockade in patients with HER2-positive breast cancer.


Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
03 2023
Historique:
received: 07 11 2022
revised: 20 12 2022
accepted: 20 12 2022
pubmed: 16 1 2023
medline: 15 2 2023
entrez: 15 1 2023
Statut: ppublish

Résumé

Dual anti-HER2-targeted therapy in breast cancer (BC) significantly increased the rate of pathological complete response (pCR) compared to single blockade when added to chemotherapy. However, limited data exist on the long-term impact on survival of the additional increase in pCR. Neoadjuvant lapatinib and/or trastuzumab treatment optimisation (NCT00553358) is an international, randomised, open-label, phase III study investigating the addition of lapatinib to chemotherapy plus trastuzumab in HER2-positive early BC. Ten-year event-free survival (EFS), overall survival (OS) and safety were assessed on intention-to-treat population. The association between pCR and EFS or OS was investigated in landmark population. A total of 455 patients were randomised to receive lapatinib (154), trastuzumab (149) or the combination (152). Ten-year EFS estimates were 63% (95% confidence interval [CI], 54%-71%) in the lapatinib group, 64% (95% CI, 55%-72%) in the trastuzumab group and 67% (95% CI, 58%-74%) in the combination group. Ten-year OS rates were 76% (95% CI, 67%-83%), 75% (95% CI, 66%-82%) and 80% (95% CI, 73%-86%) in the lapatinib, trastuzumab and combination groups, respectively. Women who achieved a pCR had improved EFS (hazard ratio 0.48, 95% CI, 0.31-0.73) and OS (hazard ratio 0.37, 95% CI, 0.20-0.63) compared with those who did not. The numerical difference in survival according to pCR status was greater in women treated with the combination and those with hormone-receptor-negative tumours. There were no new or long-term safety concerns. Patients with HER2-positive BC showed a durable survival benefit of neoadjuvant anti-HER2, irrespective of treatment arm. Patients who achieve pCR have significantly better outcomes than patients without pCR.

Sections du résumé

BACKGROUND
Dual anti-HER2-targeted therapy in breast cancer (BC) significantly increased the rate of pathological complete response (pCR) compared to single blockade when added to chemotherapy. However, limited data exist on the long-term impact on survival of the additional increase in pCR.
METHODS
Neoadjuvant lapatinib and/or trastuzumab treatment optimisation (NCT00553358) is an international, randomised, open-label, phase III study investigating the addition of lapatinib to chemotherapy plus trastuzumab in HER2-positive early BC. Ten-year event-free survival (EFS), overall survival (OS) and safety were assessed on intention-to-treat population. The association between pCR and EFS or OS was investigated in landmark population.
RESULTS
A total of 455 patients were randomised to receive lapatinib (154), trastuzumab (149) or the combination (152). Ten-year EFS estimates were 63% (95% confidence interval [CI], 54%-71%) in the lapatinib group, 64% (95% CI, 55%-72%) in the trastuzumab group and 67% (95% CI, 58%-74%) in the combination group. Ten-year OS rates were 76% (95% CI, 67%-83%), 75% (95% CI, 66%-82%) and 80% (95% CI, 73%-86%) in the lapatinib, trastuzumab and combination groups, respectively. Women who achieved a pCR had improved EFS (hazard ratio 0.48, 95% CI, 0.31-0.73) and OS (hazard ratio 0.37, 95% CI, 0.20-0.63) compared with those who did not. The numerical difference in survival according to pCR status was greater in women treated with the combination and those with hormone-receptor-negative tumours. There were no new or long-term safety concerns.
CONCLUSIONS
Patients with HER2-positive BC showed a durable survival benefit of neoadjuvant anti-HER2, irrespective of treatment arm. Patients who achieve pCR have significantly better outcomes than patients without pCR.

Identifiants

pubmed: 36641898
pii: S0959-8049(22)01831-7
doi: 10.1016/j.ejca.2022.12.020
pii:
doi:

Substances chimiques

Lapatinib 0VUA21238F
Receptor, ErbB-2 EC 2.7.10.1
Trastuzumab P188ANX8CK

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

92-101

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Paolo Nuciforo (P)

Vall d'Hebron Institute of Oncology, Barcelona Spain. SOLTI, Barcelona, Spain. Electronic address: pnuciforo@vhio.net.

John Townend (J)

Frontier Science (Scotland) Ltd, Kincraig, Kingussie, UK.

Martine J Piccart (MJ)

Institut Jules Bordet, Université Libre de Bruxelles (ULB) Brussels, Belgium.

Shona Fielding (S)

Frontier Science (Scotland) Ltd, Kincraig, Kingussie, UK.

Panagiota Gkolfi (P)

Global Drug Development, Novartis, Basel, Switzerland.

Sarra El-Abed (S)

Breast International Group, Brussels, Belgium.

Evandro de Azambuja (E)

Institut Jules Bordet, Université Libre de Bruxelles (ULB) Brussels, Belgium.

Gustavo Werutsky (G)

Latin American Cooperative Oncology Group (LACOG), Porto Alegre, Brazil.

Judith Bliss (J)

The Institute of Cancer Research ICR-CTSU, London, UK.

Volker Moebus (V)

Dept. of Medicine II, Hematology & Oncology University of Frankfurt, Frankfurt, Germany.

Marco Colleoni (M)

Division of Medical Senology, IEO, European Institute of Oncology, IRCCS, Milan, Italy.

Alvaro Moreno Aspitia (AM)

Jacoby Center for Breast Health, Mayo Clinic, Jacksonville, FL, USA.

Henry Gomez (H)

National Institute of Neoplastic Diseases Ricardo Palma University Lima, Peru.

Andrea Gombos (A)

Institut Jules Bordet, Université Libre de Bruxelles (ULB) Brussels, Belgium.

Maria A Coccia-Portugal (MA)

Coccia-Portugal M, Eastleigh Breast Care Centre, Pretoria, South Africa.

Ling-Ming Tseng (LM)

Taipei-Veterans General Hospital, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Georg Kunz (G)

Dept. Obstet./Gyn., St.-Johannes-Hospital, Dortmund, Germany.

Guillermo Lerzo (G)

Fundación CENIT Para La Investigación Ciudad Autónoma de Buenos Aires, Argentina.

Joohyuk Sohn (J)

Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, South Korea.

Vladimir Semiglazov (V)

Breast Cancer Department, N.N. Petrov National Medical Research Center of Oncology, St. Petersburg, Russian Federation.

Cristina Saura (C)

Vall d'Hebron Institute of Oncology, Barcelona Spain. SOLTI, Barcelona, Spain.

Judith Kroep (J)

Department Medical Oncology, Leiden University Medical Center, Leiden, The Netherlands. Dutch Breast Cancer Oncology Group (BOOG), the Netherlands.

Antonella Ferro (A)

Department of Medical Oncology, Rete Clinica Senologica- Santa Chiara Hospital, Trento, Italy.

David Cameron (D)

Edinburgh Cancer Research, The University of Edinburgh, Institute of Genetics and Cancer, Crewe Road South, Edinburgh, UK.

Richard Gelber (R)

Department of Data Science, Dana-Farber Cancer Institute, Harvard Medical School, Harvard TH Chan School of Public Health, Frontier Science Foundation, Boston, MA, USA.

Jens Huober (J)

Cantonal Hospital St.Gallen | Breast Center | St.Gallen, Switzerland. University of Ulm, Breast Center, Ulm, Germany.

Serena Di Cosimo (S)

Integrated Biology Platform, Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH