Trastuzumab for the Treatment of Salivary Duct Carcinoma

Author:

Limaye Sewanti A.1,Posner Marshall R.2,Krane Jeffrey F.3,Fonfria Maria1,Lorch Jochen H.1,Dillon Deborah A.3,Shreenivas Aditya V.1,Tishler Roy B.4,Haddad Robert I.1

Affiliation:

1. a Department of Medical Oncology, Dana-Farber Cancer Institute/Harvard Medical School, Boston, Massachusetts, USA;

2. c Department of Medical Oncology, Mount Sinai School of Medicine, New York, New York, USA;

3. d Department of Pathology, Brigham and Women's Hospital/Harvard Medical School, Boston, Massachusetts, USA

4. b Department of Radiation Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, Massachusetts, USA;

Abstract

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 survival and 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.

Funder

Head and Neck Cancer Research Fund at the Dana-Farber Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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