Trastuzumab for the Treatment of Salivary Duct Carcinoma

  • Limaye S
  • Posner M
  • Krane J
  • et al.
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Abstract

Objectives. Salivary duct carcinoma (SDC) is a rare and aggressive malignancy with high mortality and poor response to treatment. A significant fraction of SDCs are HER2 positive. This retrospective review examines HER2 testing in SDC and the outcome of trastuzumab-based therapy in adjuvant and palliative settings. Methods. A total of 13 patients with SDC and HER2/neu expression by immunohistochemistry of 1-3+ were treated with trastuzumab in adjuvant (n=8) or palliative (n=5) setting. Adjuvant therapy consisted of concurrent radiation and chemotherapy with weekly paclitaxel, carboplatin, and trastuzumab (TCH) for 6 weeks followed by TCH for 12 weeks and trastuzumab alone for 1 year. Palliative treatment for metastatic disease consisted of TCH every 3 weeks for 6 cycles followed by trastuzumab for variable time periods with or without second-line chemotherapy for progression. All patients had fluorescence in situ hybridization testing for HER2/ neu gene amplification. Results. The median duration of follow-up was 27 months (range: 8-48 months). In all, 62% of adjuvant patients (5/8) had no evidence of disease more than 2 years from completion of therapy. All patients with metastatic disease (5/5 patients) responded to treatment with TCH. One patient achieved a complete response and remains with no evidence of disease 52 months after initiation of TCH. The median duration of response was 18 months (range: 8-52 months). Conclusion. HER2/neu positivity and treatment with trastuzumab correlated well with long-term survivaland response in our patients. Based on this data, we propose that HER2/neu status be examined routinely in all patients with SDCs and the treatment be directed accordingly. © AlphaMed Press 2013.

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Limaye, S. A., Posner, M. R., Krane, J. F., Fonfria, M., Lorch, J. H., Dillon, D. A., … Haddad, R. I. (2013). Trastuzumab for the Treatment of Salivary Duct Carcinoma. The Oncologist, 18(3), 294–300. https://doi.org/10.1634/theoncologist.2012-0369

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