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Poster viewing and lunch

121TiP - LESS: Single-arm study to de-escalate adjuvant endocrine therapy duration in post-menopausal women with HR+ HER2- early breast cancer at very low risk of metastasis

Date

12 May 2023

Session

Poster viewing and lunch

Presenters

Magali Lacroix-Triki

Citation

Annals of Oncology (2023) 8 (1suppl_4): 101219-101219. 10.1016/esmoop/esmoop101219

Authors

E. Deluche1, S. Michiels2, D. Fric3, C. Perrin4, C. Bailleux5, T. Bachelot6, P. Ko Kivok Yun7, G. De Rauglaudre8, M.A. Mouret Reynier9, R. Le Scodan10, I.V. Vaz Luis11, M. Lacroix-Triki12, C. GUYONNEAU13, F. André14

Author affiliations

  • 1 CHU Limoges - Hopital Dupuytren, Limoges/FR
  • 2 Institut Gustave Roussy, Villejuif, Cedex/FR
  • 3 GHM - Groupe Hospitalier Mutualiste de Grenoble, Grenoble, cedex/FR
  • 4 Centre Eugene - Marquis, Rennes/FR
  • 5 Centre Anticancer Antoine Lacassagne, Nice/FR
  • 6 Centre Léon Bérard, Lyon/FR
  • 7 Centre Hospitalier International, Mont de Marsan/FR
  • 8 Institut Sainte-Catherine, Avignon, Cedex/FR
  • 9 Jean Perrin Center, 63011 - Clermont-Ferrand/FR
  • 10 Ctre De Radiotherapie St Vincent, St Gregoire/FR
  • 11 Institut Gustave Roussy, Villejuif/FR
  • 12 Institut Gustave Roussy, 94805 - Villejuif/FR
  • 13 R&D Unicancer, Paris, Cedex/FR
  • 14 Gustave Roussy - Cancer Campus, Villejuif/FR

Resources

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Abstract 121TiP

Background

Adjuvant Endocrine Therapy (AET) is the cornerstone treatment of localized hormone-receptor-positive (HR+) breast cancer, with demonstrated benefits on overall survival (30-40% relative decrease in mortality) but also on the risk of local and contralateral relapse (43-50% relative decrease). While the relative benefit of 5 years of ET is identical for small tumors as compared to larger ones, the absolute benefit is much lower, and the risk-benefit ratio becomes questionable given the frequent and impactful side effects of ET which are associated with non-adherence. If recent trials tested longer durations as compared to 5 years for high-risk cancers, older trials have tested shorter durations. Five years appeared at that time as the gold standard because of optimal benefit-risk ratios of tamoxifen among rather high-risk patients. However, shorter treatments of 2-3 years were already associated with substantial benefits. The purpose of this study is to demonstrate that AET limited to 2 years of aromatase inhibitor (AI) in postmenopausal women at very low risk of recurrence as determined with a MammaPrint/BluePrint Ultra Low Risk test result can ensure very high survival without metastatic relapse and allows a reduction of side effects and a better quality of life.

Trial design

LESS is a prospective, national, multicenter, single-arm, interventional, non-threshold crossing phase II study evaluating a therapeutic de-escalation that limits adjuvant ET to 2 years of AI. Approximately 696 post-menopausal patients with an invasive unilateral, HR+, HER2-negative, without indication of adjuvant chemotherapy and genomically-assessed MammaPrint/BluePrint Ultra Low risk luminal A breast cancer tumors, will be enrolled. LESS will include 2 sub cohorts: the majority of patients with Grade 2, pT1c-2, pN0/N1mic tumors, and up to 80 patients ≥65 years with Grade 1, pT1, pN0 and Ki67 ⩽ 10% tumors. The primary endpoint is distant metastasis free survival defined as the time from date of registration to date of 1st event of distant recurrence, death, or 2d primary non-breast invasive cancer. The 1st patient was included in Oct 2022, initiating the 2-year inclusion period.

Clinical trial identification

NCT05297617.

Legal entity responsible for the study

Unicancer.

Funding

Agendia.

Disclosure

E. Deluche: Financial Interests, Personal, Advisory Board: Novartis, Pfizer, FRESENIUS-KABI, Lilly; Financial Interests, Personal, Invited Speaker: MSD; Financial Interests, Personal, Other, scientific events: Lilly, GSK; Financial Interests, Personal, Other, funding for conference travel: AstraZeneca-Daiichi, Roche, AMGEN. S. Michiels: Financial Interests, Personal, Other, Statistical advice: Roche; Financial Interests, Personal, Other, DSMB member: Sensorion, Servier, Biophytis, Yuhan, IQVIA, Kedrion. C. Bailleux: Other, Travel, accommodations, expenses: AstraZeneca; Financial Interests, Advisory Role: Seagen, Novartis, AstraZeneca. T. Bachelot: Financial Interests, Personal, Advisory Board: Roche, Novartis, AstraZeneca, Pfizer, Seagen, Daiichi Sankyo; Financial Interests, Institutional, Research Grant: Novartis, Roche, AstraZeneca, Seagen, Pfizer; Financial Interests, Personal, Invited Speaker: Roche; Financial Interests, Institutional, Invited Speaker: AstraZeneca. I.V. Vaz Luis: Financial Interests, Institutional, Invited Speaker: Amgen, Pfizer/Edimark, Pfizer/Edimark, AstraZeneca; Financial Interests, Institutional, Advisory Board, Consulting/ AB: Novartis; Financial Interests, Institutional, Expert Testimony: Sandoz; Financial Interests, Institutional, Funding: Resilience; Non-Financial Interests, Member, Member of WG: ASCO. F. André: Financial Interests, Institutional, Research Grant: AstraZeneca, Lilly, Novartis, Pfizer, Roche, Daiichi; Financial Interests, Institutional, Other, advisory board: Guardant Health; Financial Interests, Institutional, Other, Advisory board: MEDIMMUNE, Gilead, Relay therapeutics; Other, Founder: Pegacsy. All other authors have declared no conflicts of interest.

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