Final analysis of the ALTTO trial: adjuvant trastuzumab in sequence or in combination with lapatinib in patients with HER2-positive early breast cancer [BIG 2-06/NCCTG N063D (Alliance)].

HER2-positive adjuvant chemotherapy early breast cancer lapatinib trastuzumab

Journal

ESMO open
ISSN: 2059-7029
Titre abrégé: ESMO Open
Pays: England
ID NLM: 101690685

Informations de publication

Date de publication:
16 Oct 2024
Historique:
received: 15 07 2024
revised: 11 09 2024
accepted: 12 09 2024
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 17 10 2024
Statut: aheadofprint

Résumé

Dual anti-human epidermal growth factor receptor 2 (HER2) blockade has improved the outcomes of patients with early and metastatic HER2-positive breast cancer. Here we present the final 10-year analysis of the ALTTO trial. The ALTTO trial (NCT00490139) is a prospective randomized, phase III, open-label, multicenter study that investigated the role of adjuvant chemotherapy and trastuzumab alone, in combination or sequentially with lapatinib. The primary endpoint was disease-free survival (DFS) and secondary endpoints included overall survival (OS), time to distant recurrence and safety. Overall, 6281 patients with HER2-positive early breast cancer were included in the final efficacy analysis in three treatment groups: trastuzumab (T), lapatinib + trastuzumab (L + T) and trastuzumab followed by lapatinib (T→L). Baseline characteristics were well balanced between groups. At a median follow-up of 9.8 years, the addition of lapatinib to trastuzumab and chemotherapy did not significantly improve DFS nor OS. The 10-year DFS was 77% in T, 79% in L + T and 79% in T→L, and the 10-year OS was 87%, 89% and 89%, respectively. The incidence of any cardiac event was low and similar in the three treatment groups. With a longer follow-up, no significant improvement was observed in DFS in patients treated with dual anti-HER2 blockade with lapatinib + trastuzumab compared to trastuzumab alone. The 10-year survival rates for the combination group are consistent with other studies that have explored dual anti-HER2 therapy.

Sections du résumé

BACKGROUND BACKGROUND
Dual anti-human epidermal growth factor receptor 2 (HER2) blockade has improved the outcomes of patients with early and metastatic HER2-positive breast cancer. Here we present the final 10-year analysis of the ALTTO trial.
PATIENTS AND METHODS METHODS
The ALTTO trial (NCT00490139) is a prospective randomized, phase III, open-label, multicenter study that investigated the role of adjuvant chemotherapy and trastuzumab alone, in combination or sequentially with lapatinib. The primary endpoint was disease-free survival (DFS) and secondary endpoints included overall survival (OS), time to distant recurrence and safety.
RESULTS RESULTS
Overall, 6281 patients with HER2-positive early breast cancer were included in the final efficacy analysis in three treatment groups: trastuzumab (T), lapatinib + trastuzumab (L + T) and trastuzumab followed by lapatinib (T→L). Baseline characteristics were well balanced between groups. At a median follow-up of 9.8 years, the addition of lapatinib to trastuzumab and chemotherapy did not significantly improve DFS nor OS. The 10-year DFS was 77% in T, 79% in L + T and 79% in T→L, and the 10-year OS was 87%, 89% and 89%, respectively. The incidence of any cardiac event was low and similar in the three treatment groups.
CONCLUSIONS CONCLUSIONS
With a longer follow-up, no significant improvement was observed in DFS in patients treated with dual anti-HER2 blockade with lapatinib + trastuzumab compared to trastuzumab alone. The 10-year survival rates for the combination group are consistent with other studies that have explored dual anti-HER2 therapy.

Identifiants

pubmed: 39418883
pii: S2059-7029(24)01708-3
doi: 10.1016/j.esmoop.2024.103938
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103938

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.

Auteurs

E de Azambuja (E)

Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (H.U.B), Institut Jules Bordet, Service d'oncologie médicale, Brussels. Electronic address: evandro.deazambuja@hubruxelles.be.

M Piccart-Gebhart (M)

Université libre de Bruxelles (ULB), Hôpital Universitaire de Bruxelles (H.U.B), Institut Jules Bordet, Brussels, Belgium.

S Fielding (S)

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

J Townend (J)

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

D W Hillman (DW)

Department of Quantitative Health Sciences, Mayo Clinic, Rochester, USA.

M Colleoni (M)

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

R Roylance (R)

Department of Oncology, UCLH Foundation Trust, London, UK.

C M Kelly (CM)

Cancer Trials Ireland, Dublin, Ireland; Mater Private Hospital, Dublin, Ireland.

J Lombard (J)

Breast Cancer Trials (Australia New Zealand), Newcastle, Australia.

S El-Abed (S)

Breast International Group (BIG), Brussels, Belgium.

A Choudhury (A)

Novartis Healthcare Pvt Ltd, Hyderabad, India.

L Korde (L)

Cancer Therapy Evaluation Program, Division of Cancer Treatment and Diagnosis, National Cancer Institute, Bethesda, USA.

M Vicente (M)

Institut Jules Bordet, Brussels, Belgium.

S Chumsri (S)

Mayo Clinic, Jacksonville, USA.

R Rodeheffer (R)

Mayo Clinic College of Medicine and Science, Rochester, USA.

S L Ellard (SL)

BC Cancer Kelowna, Kelowna, Canada.

A C Wolff (AC)

The Johns Hopkins Kimmel Cancer Center, Baltimore, USA.

J Holtschmidt (J)

German Breast Group (GBG) Forschungs GmbH, Neu-Isenburg, Germany.

I Lang (I)

Clinexpert Research, Gyongyos, Hungary.

M Untch (M)

Helios Klinikum Berlin-Buch, Head of Clinic for Gynecology, Gynecologic Oncology and Obstetrics, Breast Cancer Center, Berlin, Germany; AGO B Study Group, Study Center of the Women's Clinic, Erlangen University Hospital, Erlangen, Germany.

F Boyle (F)

Patricia Ritchie Centre for Cancer Care and Research, Mater Hospital, North Sydney, Australia; University of Sydney, Sydney, Australia.

B Xu (B)

National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

G Werutsky (G)

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

J Tujakowski (J)

Chemotherapy, Centre of Oncology, Bydgoszcz, Poland.

C-S Huang (CS)

National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.

N B Baruch (NB)

Holy Family Hospital, Nazareth, Israel.

J Bliss (J)

The Institute of Cancer Research, London, UK.

A Ferro (A)

Breast Unit, Department of Medical Oncology, APSS, Trento, Italy.

J Gralow (J)

American Society of Clinical Oncology, Alexandria, USA.

S-B Kim (SB)

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

J R Kroep (JR)

Leiden University Medical Center, Leiden, The Netherlands.

I Krop (I)

Yale Cancer Center, New Haven, Connecticut, USA.

S Kuemmel (S)

Breast Unit, Kliniken Essen-Mitte, Essen; Clinic for Gynecology with Breast Center, Charité-Universitätsmedizin, Berlin, Germany.

R McConnell (R)

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

L Moscetti (L)

Department of Oncology-Hematology, University Hospital of Modena, Modena; GOIRC (Gruppo Oncologico Italiano di Ricerca Clinica), Parma, Italy.

A S Knop (AS)

Department of Oncology, Copenhagen University Hospital, Copenhagen, Denmark.

F van Duijnhoven (F)

Netherlands Cancer Institute/Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands.

H Gomez (H)

Instituto Nacional de Enfermedades Neoplasicas, Lima, Peru.

D Cameron (D)

Edinburgh University Cancer Centre, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

S Di Cosimo (S)

Department of Advanced Diagnostics, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milano, Italy.

R D Gelber (RD)

Department of Data Science, Division of Biostatistics, Dana-Farber Cancer Institute, Harvard Medical School, Harvard T.H. Chan School of Public Health, Boston; Frontier Science Foundation, Boston, USA.

A Moreno-Aspitia (A)

Mayo Clinic, Jacksonville, USA.

Classifications MeSH