Outcomes of patients with small and node-negative HER2-positive early breast cancer treated with adjuvant chemotherapy and anti-HER2 therapy-a sub-analysis of the ALTTO study.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
11 2022
Historique:
received: 07 04 2022
accepted: 17 08 2022
revised: 13 08 2022
pubmed: 2 9 2022
medline: 11 11 2022
entrez: 1 9 2022
Statut: ppublish

Résumé

Patients with small node-negative HER2-positive breast cancer are commonly treated with paclitaxel and 1 year of adjuvant trastuzumab. We performed a sub-analysis of the ALTTO trial to explore the long-term outcomes of patients with small node-negative tumours. The ALTTO trial randomised 8381 patients with early HER2-positive BC treated with adjuvant chemotherapy (anthracycline/taxane- or taxane/carboplatin-based), to trastuzumab (T), lapatinib (L), their sequence (T → L) or their combination (L + T). Patients with tumours ≤3 cm and node-negative were included in this sub-analysis. A total of 2821 patients were analysed (median follow-up of 7 years). The median age was 52 years, and most patients had tumours ≤2 cm (64.3%). The 7-year disease-free survival (DFS) was 88.1% (95% CI: 86.7-89.3%). DFS was similar for arms T, T + L and T⟶L and significantly lower for arm L (stratified log-rank P = 0.031). The 7-year overall survival rate was 95.9% (95% CI: [95.0-96.6%) and the 7-year time-to-distant recurrence was 93.4% (95% CI: 92.3-94.4%). With most patients treated with anthracycline-based regimens, ALTTO shows that patients with small tumours treated with trastuzumab and concomitant chemotherapy have excellent long-term outcomes, similar to those of the APT trial. Clinicaltrials.gov identifier NCT00490139.

Sections du résumé

BACKGROUND
Patients with small node-negative HER2-positive breast cancer are commonly treated with paclitaxel and 1 year of adjuvant trastuzumab. We performed a sub-analysis of the ALTTO trial to explore the long-term outcomes of patients with small node-negative tumours.
METHODS
The ALTTO trial randomised 8381 patients with early HER2-positive BC treated with adjuvant chemotherapy (anthracycline/taxane- or taxane/carboplatin-based), to trastuzumab (T), lapatinib (L), their sequence (T → L) or their combination (L + T). Patients with tumours ≤3 cm and node-negative were included in this sub-analysis.
RESULTS
A total of 2821 patients were analysed (median follow-up of 7 years). The median age was 52 years, and most patients had tumours ≤2 cm (64.3%). The 7-year disease-free survival (DFS) was 88.1% (95% CI: 86.7-89.3%). DFS was similar for arms T, T + L and T⟶L and significantly lower for arm L (stratified log-rank P = 0.031). The 7-year overall survival rate was 95.9% (95% CI: [95.0-96.6%) and the 7-year time-to-distant recurrence was 93.4% (95% CI: 92.3-94.4%).
CONCLUSION
With most patients treated with anthracycline-based regimens, ALTTO shows that patients with small tumours treated with trastuzumab and concomitant chemotherapy have excellent long-term outcomes, similar to those of the APT trial.
TRIAL REGISTRATION
Clinicaltrials.gov identifier NCT00490139.

Identifiants

pubmed: 36050448
doi: 10.1038/s41416-022-01963-8
pii: 10.1038/s41416-022-01963-8
pmc: PMC9643324
doi:

Substances chimiques

Anthracyclines 0
Receptor, ErbB-2 EC 2.7.10.1
Taxoids 0
Trastuzumab P188ANX8CK

Banques de données

ClinicalTrials.gov
['NCT00490139']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1799-1807

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180863
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA025224
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180821
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180882
Pays : United States

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

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Auteurs

Guilherme Nader-Marta (G)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium. guilherme.nadermarta@bordet.be.

Véronique Debien (V)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Daniel Eiger (D)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Zoi Tsourti (Z)

Frontier Science Foundation Hellas, Athens, Greece.

Rafael Caparica (R)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Marie Kassapian (M)

Frontier Science Foundation Hellas, Athens, Greece.

Sylvia Napoleone (S)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Susanne Hultsch (S)

Breast International Group (BIG), Brussels, Belgium.

Larissa Korde (L)

Breast Cancer Therapeutics, CTEP, NCI, Seattle, WA, USA.

Yingbo Wang (Y)

Oncology, Novartis Pharmaceuticals Corporation, Basel, Switzerland.

Saranya Chumsri (S)

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

Kathleen I Pritchard (KI)

Medical Oncology/Hematology, Sunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Toronto, ON, Canada.
Canadian Cancer Trials Group (CCTG), Kingston, ON, Canada.

Michael Untch (M)

Clinic for Gynecology, Gynecologic Oncology and Obstetrics, Helios Klinikum Berlin Buch, Berlin, Germany.

Meritxell Bellet-Ezquerra (M)

Oncology Department, Vall d'Hebron Institute of Oncology (VHIO) - Cellex Center, Barcelona, Spain.

Daniela Dornelles Rosa (D)

Oncology Unit, Hospital Moinhos de Vento, Porto Alegre, RS, Brazil.

Alvaro Moreno-Aspitia (A)

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

Martine Piccart (M)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

Urania Dafni (U)

Public Health Department, University of Athens, Athens, Greece.

Evandro de Azambuja (E)

Institut Jules Bordet, and l'Université Libre de Bruxelles (U.L.B.), Brussels, Belgium.

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Classifications MeSH