Distribution of PD-L1, TROP2 and HER2- “lowness” in early triple-negative breast cancer: an opportunity for treatment de-escalation
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Maria Jose Bueno [3] ; Silvana Mouron [3] ; Eduardo Caleiras [4] ; Mario Martínez [1] ; Luis Manso [1] ; Ramón Colomer [2] ; Miguel Quintela-Fandino [3]
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[1] Hospital Universitario 12 de Octubre
Hospital Universitario 12 de Octubre
Madrid, España
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[2] Hospital Universitario de la Princesa
Hospital Universitario de la Princesa
Madrid, España
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[3] Breast Cancer Clinical Research Unit, CNIO Spanish National Cancer Research Center, Madrid, Spain
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[4] Histopathology Unit, CNIO Spanish National Cancer Research Center, Madrid, Spain
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- Localización: Clinical & translational oncology, ISSN 1699-048X, Vol. 26, Nº. 5, 2024, págs. 1273-1279
- Idioma: inglés
- Texto completo no disponible (Saber más ...)
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Resumen
Background HER2, TROP2 and PD-L1 are novel targets in triple-negative breast cancer (TNBC). The combined expression status of these targets, and whether they can define prognostic subgroups, is currently undefined.
Methods Immunohistochemistry was used to determine HER2, TROP2 and PD-L1 levels in 459 TNBC cases, that received in the adjuvant/neoadjuvant setting active surveillance, CMF, anthracycline-, anthracycline plus taxane-, or carboplatin-containing regimes.
Results HER2-low patients with PD-L1 > 1 CPS (double-positive, herein “DP”) had a mean PFS of 4768 days (95% CI: 4267–5268) versus 3522 days (95% CI: 3184–3861) for non-DP patients (P = 0.002). Regarding the received adjuvant treatment, DP patients (versus non-DP) receiving anthracyclines plus taxanes exhibited a mean PFS time of 4726 (95% CI: 4022–5430) versus 3302 (95% CI: 2818–3785) days (P = 0.039). Finally, 100% of DP patients that received a carboplatin-based regimen were long-term disease-free.
Conclusions Early HER2-low, PD-L1-positive TNBC patients have a very good prognosis, particularly if treated with anthracycline/taxane- or carboplatin-containing regimes.
