P Nuciforo1, T Pascual2,3, J Cortés4,5, A Llombart-Cussac6, R Fasani1, L Paré3, M Oliveira5, P Galvan3, N Martínez4, B Bermejo7, M Vidal2, S Pernas8, R López9, M Muñoz2, I Garau10, L Manso11, J Alarcón12, E Martínez13, V Rodrik-Outmezguine14, J C Brase14, P Villagrasa15, A Prat2,3, E Holgado4,16,17. 1. Molecular Oncology Laboratory, Vall d'Hebron Institute of Oncology, Barcelona, Spain. 2. Department of Medical Oncology, Hospital Clínic de Barcelona, Barcelona, Spain. 3. Translational Genomics and Targeted Therapeutics in Solid Tumors, August Pi i Sunyer Biomedical Research Institute (IDIBAPS), Barcelona, Spain. 4. Department of Medical Oncology, Ramon y Cajal University Hospital, Madrid, Spain. 5. Department of Medical Oncology, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain. 6. Department of Medical Oncology, Arnau de Vilanova University Hospital, Valencia, Spain. 7. Department of Medical Oncology, Hospital Clínico de Valencia, Valencia, Spain. 8. Department of Medical Oncology, Instituto Catalán de Oncología, Hospitalet, Spain. 9. Department of Medical Oncology, Complejo Universitario de Santiago de Compostela, Santiago de Compostela, Spain. 10. Department of Medical Oncology, Hospital de Son Llàtzer, Palma de Mallorca, Spain. 11. Department of Medical Oncology, Hospital 12 de Octubre, Madrid, Spain. 12. Department of Medical Oncology, Hospital Universitario Son Espases, Palma de Mallorca, Spain. 13. Department of Medical Oncology, Hospital Provincial Centre de Castelló, Castelló de la Plana, Spain. 14. Novartis Oncology, Basel, Switzerland. 15. SOLTI Breast Cancer Research Group, Barcelona, Spain. 16. Department of Medical Oncology, Baselga Oncological Institute, Madrid, Spain. 17. Department of Medical Oncology, Baselga Oncological Institute, Barcelona, Spain.
Abstract
Background: The presence of stromal tumor-infiltrating lymphocytes (TILs) is associated with increased pathologic complete response (pCR) and improved outcomes in HER2-positive early-breast cancer (BC) treated with anti-HER2-based chemotherapy. In the absence of chemotherapy, the association of TILs with pCR following anti-HER2 therapy-only is largely unknown. Patients and methods: The PAMELA neoadjuvant trial treated 151 women with HER2-positive BC with lapatinib and trastuzumab [and hormonal therapy if hormone receptor (HR)-positive] for 18 weeks. Percentage of TILs and tumor cellularity were determined at baseline (N = 148) and at day 15 (D15) of treatment (N = 134). Associations of TILs and tumor cellularity with pCR in the breast were evaluated. A combined score based on tumor cellularity and TILs (CelTIL) measured at D15 was derived in PAMELA, and validated in D15 samples from 65 patients with HER2-positive disease recruited in the LPT109096 neoadjuvant trial, where anti-HER2 therapy-only was administer for 2 weeks, then standard chemotherapy was added for 24 weeks. Results: In PAMELA, baseline and D15 TILs were significantly associated with pCR in univariate analysis. In multivariable analysis, D15 TILs, but not baseline TILs, were significantly associated with pCR. At D15, TILs and tumor cellularity were found independently associated with pCR. A combined score (CelTIL) taking into account both variables was derived. CelTIL at D15 as a continuous variable was significantly associated with pCR, and patients with CelTIL-low and CelTIL-high scores had a pCR rate of 0% and 33%, respectively. In LPT109096, CelTIL at D15 was found associated with pCR both as a continuous variable and as group categories using a pre-defined cut-off (75.0% versus 33.3%). Conclusions: On-treatment TILs, but not baseline TILs, are independently associated with response following anti-HER2 therapy-only. A combined score of TILs and tumor cellularity measured at D15 provides independent predictive information upon completion of neoadjuvant anti-HER2-based therapy. Clinical trial number: NCT01973660.
Background: The presence of stromal tumor-infiltrating lymphocytes (TILs) is associated with increased pathologic complete response (pCR) and improved outcomes in HER2-positive early-breast cancer (BC) treated with anti-HER2-based chemotherapy. In the absence of chemotherapy, the association of TILs with pCR following anti-HER2 therapy-only is largely unknown. Patients and methods: The PAMELA neoadjuvant trial treated 151 women with HER2-positive BC with lapatinib and trastuzumab [and hormonal therapy if hormone receptor (HR)-positive] for 18 weeks. Percentage of TILs and tumor cellularity were determined at baseline (N = 148) and at day 15 (D15) of treatment (N = 134). Associations of TILs and tumor cellularity with pCR in the breast were evaluated. A combined score based on tumor cellularity and TILs (CelTIL) measured at D15 was derived in PAMELA, and validated in D15 samples from 65 patients with HER2-positive disease recruited in the LPT109096 neoadjuvant trial, where anti-HER2 therapy-only was administer for 2 weeks, then standard chemotherapy was added for 24 weeks. Results: In PAMELA, baseline and D15 TILs were significantly associated with pCR in univariate analysis. In multivariable analysis, D15 TILs, but not baseline TILs, were significantly associated with pCR. At D15, TILs and tumor cellularity were found independently associated with pCR. A combined score (CelTIL) taking into account both variables was derived. CelTIL at D15 as a continuous variable was significantly associated with pCR, and patients with CelTIL-low and CelTIL-high scores had a pCR rate of 0% and 33%, respectively. In LPT109096, CelTIL at D15 was found associated with pCR both as a continuous variable and as group categories using a pre-defined cut-off (75.0% versus 33.3%). Conclusions: On-treatment TILs, but not baseline TILs, are independently associated with response following anti-HER2 therapy-only. A combined score of TILs and tumor cellularity measured at D15 provides independent predictive information upon completion of neoadjuvant anti-HER2-based therapy. Clinical trial number: NCT01973660.
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