Alberto Ocana1,2,3, Marta Gil-Martin4,5, Silvia Antolín4,6, María Atienza7, Álvaro Montaño4,7, Nuria Ribelles4,8, Ander Urruticoechea4,9, Alejandro Falcón7, Sonia Pernas4,5, Javier Orlando6, Juan Carlos Montero10,11, Maria José Escudero4, Sara Benito4, Rosalía Caballero4, Eva Carrasco4, Federico Rojo4,10,12, Atanasio Pandiella4,10,11, Manuel Ruiz-Borrego4,7. 1. Department of Medical Oncology, Hospital Clínico San Carlos, Madrid and Centro Regional de Investigaciones Biomédicas, Universidad de Castilla La Mancha, 02006, Albacete, Spain. albertoo@sescam.jccm.es. 2. GEICAM, Spanish Breast Cancer Group, Madrid, Spain. albertoo@sescam.jccm.es. 3. Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Madrid, Spain. albertoo@sescam.jccm.es. 4. GEICAM, Spanish Breast Cancer Group, Madrid, Spain. 5. Department of Medical Oncology, Institut Català d'Oncologia (ICO)-IDIBELL, L'Hospitalet, Barcelona, Spain. 6. Department of Medical Oncology, Complejo Hospitalario Universitario A Coruña, A Coruña, Spain. 7. Department of Medical Oncology, Hospital Universitario Virgen del Rocío, Sevilla, Spain. 8. Department of Medical Oncology, Hospital Universitario Virgen de la Victoria, Institute of Biomedical Reasearch in Malaga, Malaga, Spain. 9. Department of Medical Oncology, Fundación Onkologikoa, Donostia, Spain. 10. Centro de Investigación Biomédica en Red de Oncología, CIBERONC-ISCIII, Madrid, Spain. 11. Instituto de Biología Molecular y Celular del Cáncer, IBSAL, CSIC-Universidad de Salamanca, Salamanca, Spain. 12. Fundación Jiménez Díaz, Madrid, Spain.
Abstract
BACKGROUND: An important proportion of HER2-positive metastatic breast cancer patients do not respond to trastuzumab. The combination of dasatinib and trastuzumab has shown to be synergistic in preclinical models. METHODS: We conducted a phase II trial combining dasatinib 100 mg once daily with trastuzumab 2 mg/kg and paclitaxel 80 mg/m2 weekly. Primary objective was objective response rate (ORR) and secondary included safety, other efficacy parameters and pharmacodynamics in tumour tissue, blood samples and skin biopsies. RESULTS: From June 2013 to December 2015, 29 patients were included. Median number of cycles was 12 (1-49). Only 6 patients discontinued due to adverse events. ORR was 79.3% (95% CI 60.3-92), clinical benefit rate 82.8% (95% CI 64.2-94.2). Median time to progression 23.9 months (95% CI 14.9-not reached [NR]), median progression-free survival 23.9 months (95% CI 10.3-NR). No grade 4 toxicity was seen. Grade 3 toxicities included: ejection fraction decrease, neutropenia, hyponatremia, fatigue and sensory neuropathy and one left ventricular systolic dysfunction. Phosphorylated (p)-SRC was reduced in peripheral blood mononuclear cells. Phosphorylated SRC, ERK and AKT were also reduced in epidermal keratinocytes. CONCLUSIONS: Dasatinib can be safely combined with trastuzumab and paclitaxel. The combination is active with an ORR of almost 80%. TRIAL REGISTRATION: NCT01306942, EudraCT 2010-023304-27.
BACKGROUND: An important proportion of HER2-positive metastatic breast cancerpatients do not respond to trastuzumab. The combination of dasatinib and trastuzumab has shown to be synergistic in preclinical models. METHODS: We conducted a phase II trial combining dasatinib 100 mg once daily with trastuzumab 2 mg/kg and paclitaxel 80 mg/m2 weekly. Primary objective was objective response rate (ORR) and secondary included safety, other efficacy parameters and pharmacodynamics in tumour tissue, blood samples and skin biopsies. RESULTS: From June 2013 to December 2015, 29 patients were included. Median number of cycles was 12 (1-49). Only 6 patients discontinued due to adverse events. ORR was 79.3% (95% CI 60.3-92), clinical benefit rate 82.8% (95% CI 64.2-94.2). Median time to progression 23.9 months (95% CI 14.9-not reached [NR]), median progression-free survival 23.9 months (95% CI 10.3-NR). No grade 4 toxicity was seen. Grade 3 toxicities included: ejection fraction decrease, neutropenia, hyponatremia, fatigue and sensory neuropathy and one left ventricular systolic dysfunction. Phosphorylated (p)-SRC was reduced in peripheral blood mononuclear cells. Phosphorylated SRC, ERK and AKT were also reduced in epidermal keratinocytes. CONCLUSIONS:Dasatinib can be safely combined with trastuzumab and paclitaxel. The combination is active with an ORR of almost 80%. TRIAL REGISTRATION: NCT01306942, EudraCT 2010-023304-27.
Entities:
Keywords:
Dasatinib; HER2-positive breast cancer; Metastatic breast cancer; Phase II; SRC kinase inhibitor; Trastuzumab resistance
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