Window of opportunity trials with immune checkpoint inhibitors in triple-negative breast cancer

Other authors

Institut Català de la Salut

[Quintana A] Breast Cancer Unit, Vall d’Hebron Institute of Oncology (VHIO), Barcelona, Spain. [Saini KS] Fortrea, Inc., Durham, USA. Addenbrooke’s Hospital, Cambridge University Hospitals National Health Service (NHS) Foundation Trust, Cambridge, UK. [Vidal L] Fortrea, Inc., Durham, USA. [Peg V] Biomedical Research Network Centre in Oncology (CIBERONC), Madrid, Spain. Servei d’Anatomia Patològica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Departament of Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain. [Slebe S] Medica Scientia Innovation Research (MedSIR), Barcelona, Spain. Oncoclínicas & Co, Jersey City, New Jersey and Sao Paulo, Brazil. [Loibl S] German Breast Group, GBG Forschungs GmbH, Neu-Isenburg, Germany

Vall d'Hebron Barcelona Hospital Campus

Publication date

2024-11-06T11:31:50Z

2024-11-06T11:31:50Z

2024-10



Abstract

Immune checkpoint inhibitors; Triple-negative breast cancer; Tumor-infiltrating lymphocytes


Inhibidors del punt de control immunitari; Càncer de mama triple negatiu; Limfòcits infiltrants de tumors


Inhibidores del punto de control inmunitario; Cáncer de mama triple negativo; Linfocitos infiltrantes de tumores


Patients with triple-negative breast cancer (TNBC) have a relatively poor clinical outcome. The immune checkpoint inhibitor (ICI) pembrolizumab combined with chemotherapy is the current standard of care in TNBC patients with stage II and III. Monotherapy with ICIs has not been comprehensively assessed in the neoadjuvant setting in TNBC patients, given unfavorable results in metastatic trials. ICIs, however, have been tested in the window of opportunity (WOO) before surgery or standard chemotherapy-based neoadjuvant treatment. The WOO design is well suited to assess an ICI alone or in combination with other ICIs, targeted therapy, radiotherapy or cryotherapy, and measure their pharmacodynamic and clinical effect in this treatment-naive population. Some patients show a good response to ICIs in WOO studies. Biomarkers like tumor-infiltrating lymphocytes, programmed death ligand-1, and interferon-γ signature may predict activity and may identify patients likely to benefit from ICIs. Moreover, an increase in tumor-infiltrating lymphocytes, programmed death ligand-1 expression or T cell receptor expansion following administration of ICIs in the WOO setting could potentially inform of immunotherapy benefit, which would allow tailoring further treatment. This article reviews WOO trials that assessed immunotherapy in the early-stage TNBC population, and how these results could be translated to test de-escalation strategies of neoadjuvant chemotherapy and immunotherapy without compromising a patient's prognosis.

Document Type

Article


Published version

Language

English

Publisher

Elsevier

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ESMO Open;9(10)

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Attribution-NonCommercial-NoDerivatives 4.0 International

http://creativecommons.org/licenses/by-nc-nd/4.0/

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