Cancers (Mar 2022)

Negative Relationship between Post-Treatment Stromal Tumor-Infiltrating Lymphocyte (TIL) and Survival in Triple-Negative Breast Cancer Patients Treated with Dose-Dense Dose-Intense NeoAdjuvant Chemotherapy

  • Sylvie Giacchetti,
  • Lilith Faucheux,
  • Charlotte Gardair,
  • Caroline Cuvier,
  • Anne de Roquancourt,
  • Luca Campedel,
  • David Groheux,
  • Cedric de Bazelaire,
  • Jacqueline Lehmann-Che,
  • Catherine Miquel,
  • Laurence Cahen Doidy,
  • Malika Amellou,
  • Isabelle Madelaine,
  • Fabien Reyal,
  • Laetitia Someil,
  • Hamid Hocini,
  • Christophe Hennequin,
  • Luis Teixeira,
  • Marc Espié,
  • Sylvie Chevret,
  • Vassili Soumelis,
  • Anne-Sophie Hamy

DOI
https://doi.org/10.3390/cancers14051331
Journal volume & issue
Vol. 14, no. 5
p. 1331

Abstract

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Background: Patients with triple-negative breast cancers (TNBC) have a poor prognosis unless a pathological complete response (pCR) is achieved after neoadjuvant chemotherapy (NAC). Few studies have analyzed changes in TIL levels following dose-dense dose-intense (dd-di) NAC. Patients and methods: From 2009 to 2018, 117 patients with TNBC received dd-di NAC at our institution. We aimed to identify factors associated with pre- and post-NAC TIL levels, and oncological outcomes relapse-free survival (RFS), and overall survival (OS). Results: Median pre-NAC and post-NAC TIL levels were 15% and 3%, respectively. Change in TIL levels with treatment was significantly correlated with metabolic response (SUV) and pCR. High post-NAC TIL levels were associated with a weak metabolic response after two cycles of NAC, with the presence of residual disease and nodal involvement at NAC completion. In multivariate analyses, high post-NAC TIL levels independently predicted poor RFS and poor OS (HR = 1.4 per 10% increment, 95%CI (1.1; 1.9) p = 0.014 and HR = 1.8 per 10% increment 95%CI (1.3–2.3), p Conclusion: Our results suggest that TNBC patients with TIL enrichment after NAC are at higher risk of relapse. These patients are potential candidates for adjuvant treatment, such as immunotherapy, in clinical trials.

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