Abstract
Purpose
Preclinical data indicate that the combination of docetaxel, cisplatin and trastuzumab (TCH) may have the potential for clinically significant activity against breast cancers that overexpress the her2/neu gene (HER2). An open-label phase II trial was designed to investigate the response rate and toxicity profile of TCH in breast cancer patients with a primary tumor 2–5 cm in diameter (T2) in its original size.
Methods
Thirty breast cancer patients with HER2-overexpressing tumors were enrolled. Patients received 6 cycles of docetaxel at 60 mg/m2 and cisplatin at 50 mg/m2 given on day 1 and then every 21 days. Trastuzumab was given on day 1, cycle 1 (4 mg/kg), and then continued weekly at 2 mg/kg for 1 year or until disease progression. Tumor measurements were obtained at baseline as well as after 3 and 6 cycles of chemotherapy.
Results
We identified 29 breast cancer patients in Taiwan, of whom 13 (44.8%) had pathological complete responses. No cardiac toxicity was observed. Hematologic grade 4 or 3 toxicities were observed in 1 of 28 patients. Non-hematologic grade 4 or 3 toxicities with a reverse pattern were observed in 6 of 29 patients.
Conclusions
The results of our study indicate that TCH neoadjuvant chemotherapy is feasible and active in T2 HER2-overexpressing breast cancer patients in terms of pathological complete response rate, complete response, partial response and manageable toxicities.
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Acknowledgments
This work was supported by grants from Sanofi-Aventis Taiwan Co. Ltd. and Roche Taiwan Co. Ltd. Editorial support was provided by Ms. Yu-Fen Wang for editing assistance.
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Lin, C., Chen, DR., Chang, KJ. et al. A phase II study of neoadjuvant chemotherapy with docetaxel, cisplatin and trastuzumab for T2 breast cancers. Cancer Chemother Pharmacol 69, 1363–1368 (2012). https://doi.org/10.1007/s00280-012-1841-y
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DOI: https://doi.org/10.1007/s00280-012-1841-y