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E-Poster Display

221P - Long-term outcomes of patients with node-negative, ≤3cm, HER2+ breast cancer (BC) enrolled in ALTTO

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Breast Cancer

Presenters

Daniel Eiger

Citation

Annals of Oncology (2020) 31 (suppl_4): S303-S339. 10.1016/annonc/annonc267

Authors

D. Eiger1, Z. Tsourti2, R. Caparica3, M. Kassapian2, S. Napoleone1, S. Hultsch4, L. Korde5, Y. Wang6, S. Chumsri7, K. Pritchard8, M. Untch9, M. Bellet Ezquerra10, D.D. Rosa11, A. Moreno-Aspitia12, M. Piccart13, U. Dafni14, E. de Azambuja1

Author affiliations

  • 1 Clinical Trial Support Unit, Institute Jules Bordet, 1000 - Brussels/BE
  • 2 Statistical Analysis - Project Management, Frontier Science Foundation Hellas, 15773 - Athens/GR
  • 3 Clinical Trials Support Unit, Institute Jules Bordet, 1000 - Brussels/BE
  • 4 Na, Breast International Group (BIG), 1000 - Brussels/BE
  • 5 Head, Breast Cancer Therapeutics, CTEP, NCI, Seattle/US
  • 6 Oncology, Novartis Pharmaceuticals Corporation, East Hanover/US
  • 7 Na, Mayo Clinic, Jacksonville/US
  • 8 Medical Oncology/hematology, Sunnybrook Health Sciences Centre, Sunnybrook Research Institute, University of Toronto, Toronto/CA
  • 9 Clinic For Gynecology, Gynecologic Oncology And Obstetrics, Helios Klinikum Berlin Buch, 13125 - Berlin/DE
  • 10 Oncology Dept., Vall d'Hebron Institute of Oncology (VHIO)-Cellex Center, 8035 - Barcelona/ES
  • 11 Oncology Unit, Hospital Moinhos de Vento, 90560-030 - Porto Alegre/BR
  • 12 Division Of Hematology And Oncology, Mayo CLinic, Jacksonville/US
  • 13 Oncology, Institute Jules Bordet, 1000 - Brussels/BE
  • 14 Public Health Dept, University of Athens, 115 27 - Athens/GR

Resources

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Abstract 221P

Background

One year of trastuzumab (T) with 12 weeks of paclitaxel (APT) is recommended for patients (pts) with small, node-negative (N0) HER2+ BC, although the data supporting this indication comes from a single-arm phase II trial. ALTTO was a large phase III study evaluating the addition of lapatinib (L) to T for early-stage HER2+ BC pts, and its large dataset provides a unique opportunity to delineate the outcomes of pts with HER2+ BC with pathological tumour size (pT)≤3cm/N0.

Methods

Pts were randomized to receive L alone, T alone, T combined with L (T+L) or T followed by L (T→L). L arm was closed earlier due to futility and 54% of its pts went on to receive T. Our primary endpoint was disease-free survival (DFS), with overall survival (OS) as a key secondary one. A multivariable Cox model for DFS adjusted for all clinicopathological features was fitted and 2-sided p-value<0.05 set for significance.

Results

Among 8381 pts, 2821 were eligible: 707 in L, 725 in T, 702 in T+L and 687 in T→L arm. Baseline characteristics were balanced among treatment arms. Median age was 52 years (y), with most pts having pT≤2 cm (64%), histologic grade 3 (56%), hormone receptor positivity (61%), and received an anthracycline-based CT (93%). At a median follow-up of 7y (IQR: [6.1-7.2 y]), 291 DFS events were observed, with 7y DFS rate of 88% (95% CI [87-89]). Multivariate analysis showed Asian ethnicity, adjuvant radiotherapy and concomitant CT to yield a protective effect, while L alone to be detrimental (table). As such, for pts under concomitant CT (N=1235), 96 DFS events occurred for 7y DFS rates of 84% (95% CI [77-90]), 91% (86-94), 93% (89-96), and 89% (83-93) in L, T, T+L, and T⟶L, respectively (p=0.038). With 102 deaths, 7y OS rate was 96% (95% CI [95-97]). Table: 221P

Multivariable Cox model for DFS adjusted for all clinicopathological variables and stratification factors

n of pts=2820* n of DFS events=291 HR (95% CI) p-value
Anti-HER2 treatment arm
L vs. T 1.52 (1.11 - 2.09) 0.009
T + L vs. T 1.08 (0.77 - 1.52) 0.64
T ⟶ L vs. T 1.05 (0.74 - 1.47) 0.79
Ethnicity
Asian vs. White 0.66 (0.49 - 0.89) 0.007
Black/Other vs. White 0.65 (0.33 - 1.27) 0.2
Age
≥50 y vs. <50 y 0.80 (0.63 - 1.01) 0.058
Adjuvant radiotherapy
Yes vs. No 0.76 (0.60 - 0.97) 0.028
Timing of chemotherapy
Concomitant vs. Sequential 0.70 (0.55 - 0.90) 0.005

*One patient with missing menopausal status excluded Model selection based on backward method with p>10% Legends: CI= confidence interval; HR= hazard ratio

Conclusions

With most of its pts treated with anthracyclines, ALTTO shows that pts with pT≤3cm/N0 HER2+ BC treated with T and concomitant CT have long-term outcomes at best similar to that of those treated with APT, calling into question de-escalation of chemotherapy in this population.

Clinical trial identification

NCT00490139 (registration date: 22/06/2007); EudraCT Number: 2006–000562–36 (registration date: 04/05/2007); Sponsor Protocol Number: BIG2–06 /EGF106708/N063D.

Editorial acknowledgement

Legal entity responsible for the study

Breast International Group (BIG).

Funding

GSK/Novartis.

Disclosure

D. Eiger: Research grant/Funding (self), Research grant/Funding (institution), Funding for my ESMO Fellowship (2018-2019): Novartis; Research grant/Funding (institution): Roche/GNE; Research grant/Funding (institution): AstraZeneca; Research grant/Funding (institution): Radius; Research grant/Funding (institution): Lilly; Research grant/Funding (institution): MSD; Research grant/Funding (institution): Synthon; Research grant/Funding (institution): Servier; Research grant/Funding (institution): Pfizer. R. Caparica: Research grant/Funding (institution): Roche/GNE; Research grant/Funding (institution): Radius; Speaker Bureau/Expert testimony, Research grant/Funding (institution), Travel/Accommodation/Expenses: AstraZeneca; Research grant/Funding (institution): Lilly; Research grant/Funding (institution): MSD; Research grant/Funding (institution): Novartis; Research grant/Funding (institution): Synthon; Research grant/Funding (institution): Servier; Research grant/Funding (institution), Travel/Accommodation/Expenses: Pfizer; Speaker Bureau/Expert testimony: Boehringer-Ingelheim; Speaker Bureau/Expert testimony: Janssen-Cilag. S. Hultsch: Research grant/Funding (institution): GSK/Novartis. Y. Wang: Shareholder/Stockholder/Stock options, Full/Part-time employment: Novartis. S. Chumsri: Research grant/Funding (self): Merck and Co.; Research grant/Funding (self): Array BioPharma; Advisory/Consultancy: Novartis; Advisory/Consultancy: Syndax Pharmaceuticals Inc.; Advisory/Consultancy: Puma Biotechnology; Advisory/Consultancy: Immunomedics. K. Pritchard: Advisory/Consultancy: Pfizer; Advisory/Consultancy: Roche; Advisory/Consultancy: Novartis; Advisory/Consultancy: Eisai; Advisory/Consultancy: Amgen; Advisory/Consultancy: Genomic Health Inc.; Advisory/Consultancy: Myriad Genetic Laboratories. M. Untch: Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: AbbVie; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Amgen; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: AstraZeneca; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Celgene; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Daichi Sankyo; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Eisai; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Lilly Germany; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Lilly International; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Merck; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: MSD Mundipharma; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Myriad Genetics; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Odonate; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Pierre Fabre; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Pfizer; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: PUMA Biotechnology; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: F. Hoffmann-La Roche; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: Sanofi Aventis; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses, Paid directly to my Institution: TEVA Pharmaceuticals. M. Bellet Ezquerra: Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Pfizer; Advisory/Consultancy, Speaker Bureau/Expert testimony: Lilly; Advisory/Consultancy, Speaker Bureau/Expert testimony: Novartis; Travel/Accommodation/Expenses: Roche. D.D. Rosa: Advisory/Consultancy, Speaker Bureau/Expert testimony, Research grant/Funding (self), Travel/Accommodation/Expenses: Roche; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Novartis; Advisory/Consultancy, Speaker Bureau/Expert testimony: AstraZeneca; Advisory/Consultancy, Speaker Bureau/Expert testimony, Travel/Accommodation/Expenses: Lilly; Advisory/Consultancy, Research grant/Funding (self): GSK; Advisory/Consultancy: Sanofi; Advisory/Consultancy: Libbs; Advisory/Consultancy: Eisai; Advisory/Consultancy, Speaker Bureau/Expert testimony: Pfizer; Advisory/Consultancy: Dr Reddy`s; Research grant/Funding (self), Travel/Accommodation/Expenses: Amgen. A. Moreno-Aspitia: Research grant/Funding (institution): Genentech; Research grant/Funding (institution): GSK; Research grant/Funding (institution): Sermonix; Research grant/Funding (institution): Daiichi. M. Piccart: Honoraria (self), Scientific Board: Oncolytics; Honoraria (self), Research grant/Funding (institution), Scientific Board: Radius; Honoraria (self), Research grant/Funding (institution): AstraZeneca; Honoraria (self): Camel-IDS; Honoraria (self): Crescendo Biologics; Honoraria (self): Debiopharm; Honoraria (self): G1 Therapeutics; Honoraria (self), Research grant/Funding (institution): Genentech; Honoraria (self): Huya; Honoraria (self): Immunomedics; Honoraria (self), Research grant/Funding (institution): Lilly; Honoraria (self): Menarini; Honoraria (self), Research grant/Funding (institution): MSD; Honoraria (self), Research grant/Funding (institution): Novartis; Honoraria (self): Odonate; Honoraria (self): Oncolytics; Honoraria (self), Research grant/Funding (institution): Pfizer; Honoraria (self), Research grant/Funding (institution): Roche; Honoraria (self): Seattle Genetics; Research grant/Funding (institution): Servier; Research grant/Funding (institution): Synthon. U. Dafni: Advisory/Consultancy, Tumor Agnostic Evidence Working Group 2020: Roche. E. de Azambuja: Honoraria (self), Advisory/Consultancy, Research grant/Funding (institution), Travel/Accommodation/Expenses: Roche/GNE; Travel/Accommodation/Expenses: GSK/Novartis; Research grant/Funding (institution): Radius; Research grant/Funding (institution): AstraZeneca; Research grant/Funding (institution): Lilly; Research grant/Funding (institution): MSD; Research grant/Funding (institution): Novartis; Research grant/Funding (institution): Synthon; Research grant/Funding (institution): Servier; Research grant/Funding (institution): Pfizer. All other authors have declared no conflicts of interest.

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