- Case report
- Open Access
Case report: anti-hormonal therapy in the treatment of ductal carcinoma of the parotid gland
BMC Cancer volume 14, Article number: 701 (2014)
Ductal carcinomas of the parotid gland are rare, highly aggressive, have a poor prognosis and are histologically similar to Ductal Breast Cancer. We report what we believe to be the first case in literature of metastatic salivary duct carcinoma (SDC) of the parotid gland with objective response to tamoxifen and aromatase inhibitors, achieving a long-term stability of disease with no associated toxicity.
A 70-year-old female was referred to our institution for treatment of a painless nodular lesion in the scalp, localized in the frontal region of the cranium. A biopsy was taken and tested positive for metastatic ductal carcinoma. On PET CT hypermetabolic nodules were localized in the left parotid gland (11 mm), right parotid gland (10 and 12 mm), submandibular node (11 mm) and left cervical node (10 mm). A salivary ductal carcinoma was considered to be the primary tumor. The patient was subsequently started on tamoxifen, with a complete response from the scalp nodule and left parotid nodule, while the right parotid nodule demonstrated a partial response that maintained stable for 2 years until progression. Anastrazol was chosen as the next line of treatment, achieving 6 more months of stable disease. As a pseudo-adjuvant treatment, surgical resection of the right parotid lesion was performed and helped achieve two years of disease stability.
Estrogen receptor antagonists such as tamoxifen or aromatase inhibitors may represent a target for the establishment of a safe alternative and novel therapy for SDC, however more accurate data obtained from larger studies are required.
Ductal carcinomas of the parotid gland are rare, highly aggressive, have a poor prognosis and are histologically similar to Ductal Breast Cancer. Salivary gland tumors metastasize most frequently to lymph nodes, lung, liver and bones. Distant metastases occur in 27%, independent of histology and 46% in adenoid cyst cell types and high-grade salivary ductal carcinoma . Surgical resection of solitary metastasis may be considered in select cases, but the goal of chemotherapy in metastatic or recurrent disease is palliative care, based on response rates that range from 10-30% and the lack of evidence benefiting survival .
Salivary ductal carcinomas are an uncommon and high-grade adenocarcinoma arising from the ductal epithelium, which Kleinsasser et al. reported in 1968 for the first time , and the World Health Organization classified as a distinct neoplasm in 1991 . Ductal carcinomas, typically present in the sixth or seventh decade of life and are more prevalent in males (3:1.8) [5, 6]. The parotid gland is involved in 80% of diagnosis, followed by the submandibular gland in 8% and the rest in the minor salivary glands [7, 8]. The aggressive behavior characterizing ductal carcinomas is associated with rapid progression, early lymph node metastasis, a high risk of local recurrence, distant metastasis and ultimately a low survival rate, 3 yrs. median [9, 10].
Due to SDC’s histological similarity to ductal carcinoma of the breast, hormonal receptor status and regulation has been a subject of interest. However, hormone receptor expression is virtually absent in most malignant salivary gland tumors, with the exception of the androgen receptor, which is present in approximately 92% of cases. Similar to invasive ductal carcinoma of the breast, overexpression and amplification of the HER-2 gene is present in SDC. Patients with SDC and HER-2 overexpression and amplification may be targeted with trastuzumab and obtain positive responses to therapy . SDC in comparison to ductal carcinoma of the breast expresses in a lower percentage estrogen (−8%) or progesterone receptors . Androgen receptor (AR) therapy however has emerged as a possible target, due to the fact that a majority of SDC lesions express AR and have demonstrated clinical benefit .
Cytotoxic chemotherapy has limited benefit in a subtype of SDC that is rare and aggressive, for which genotyping analysis has been pursued to help identify novel tumor-specific mutations that may help direct targeted therapies in these cases. There has been an interest in recently discovered PIK3CA, PTEN and BRAF V600E kinase mutations in subsets of HER2-negative SDC; due to these recent discoveries the aforementioned pathways have been suggested as therapeutic targets [11, 12].
The following case report is what we believe to be the first case in literature of metastatic salivary duct carcinoma of the parotid gland with objective response to tamoxifen and aromatase inhibitors, achieving a long-term stability of disease with no associated toxicity.
A 70-year-old female was referred for treatment of a painless nodular lesion with a diameter of 2 cm in the scalp, localized in the frontal region of the cranium. Her past medical history was unremarkable. A biopsy was taken and tested positive for metastatic ductal carcinoma. Further analysis revealed Estrogen Receptor positivity. Mastrography and CT did not demonstrate any evidence of a primary tumor, while PET CT showed hypermetabolic nodules localized as follows: 11 mm in the left parotid gland, 10 and 12 mm in the right parotid gland, 11 mm submandibular node and 10 mm left cervical node. At this point, there was clinical suspicion of a primary salivary ductal carcinoma. The patient was started on tamoxifen, 20 mg daily, with a complete response in the scalp nodule and left parotid nodule, although a partial response was observed on the right parotid lesions (Figure 1B). The patient continued stable for two years, after which progression of the right parotid nodule was observed through clinical palpation and through CT as a lesion 2 cms in diameter located in the right periaricular area (Figure 1C), without cranial nerve involvement or palpable cervical lymphadenopathy. There was no evidence of any metastatic lesions. Anastrozole 1 mg/day was started, achieving stable disease within 8 months of treatment (Figure 1D). Local control of the parotid lesion was obtained via surgical resection (Figure 1E), tissue was sent to pathology, where a Hematoxylin and Eosin (H & E) stained section showed ductal structures (Figure 2A). Immunohistochemistry was performed using standard procedures with monoclonal antibodies: 6 F11 (Novacastra Laboratories Ltd., Burlingame, CA) for ER and 1A6 (Novacastra Laboratories Ltd., Burlingame) for PR and AB-8 monoclonal antibody (NeoMarker Lab Vision Co., Fremont, CA) for Her2, which proved negative for Her2neu and positive for Estrogen and Progesterone Receptors (Figure 2B, C, D). The tumor was classified as a salivary duct carcinoma of the parotid gland. At this time, the patient had been receiving anastrozole as pseudo adjuvancy for two years without further evidence of disease (Figure 1F).
The histologic similarities between salivary duct carcinoma and ductal carcinoma of the breast in addition to the low response rates to chemotherapy have led to antihormonal therapies being considered for treatment. Salivary duct carcinomas responding to antiandrogen therapies and advanced adenoid cystic salivary tumors to Tamoxifen have been reported in the literature [13, 14]. However, Tamoxifen and Aromatase inhibitors (estrogen signaling inhibitor agents) have not been reported in the literature, due to the low expression of ER in Ductal Carcinoma of the Salivary Gland.
Tamoxifen and anastrazole have proven to be effective in Ductal Carcinoma of the Breast and were considered a potential novel therapy in this case, stopping the progression of salivary gland carcinoma (SGC) and achieving long-term stability of ductal parotid carcinoma. Tamoxifen prevents the activation of estrogen responsive genes by inhibiting both translocation and nuclear binding of the receptor itself. Aromatase inhibitors like Anastrozole on the other hand prevent ER activation by inhibiting the conversion of androgens to estrogens by binding to the aromatase enzyme.
Due to limited management options in salivary gland carcinoma and low rates of response to chemotherapy the goal of treatment for metastatic salivary gland carcinoma is palliation, since there is not strong evidence that survival is prolonged with systemic treatment. Targeted cancer therapies represent a promising strategy to treat these rare aggressive malignancies. Albeit, the expression of sex steroid hormone receptors in salivary gland carcinoma and the evidence of linking hormone receptors and growth factor receptors to the disease may lead to the use of hormone therapy in these specific cases. Estrogen receptor antagonists such as tamoxifen or aromatase inhibitors may represent a target for the establishment of a safe alternative therapy for SDC but more accurate data obtained from larger studies are required.
Genetic profiling is a valuable approach to identify actionable mutations (BRAF or PIK3CA mutations) which could have a significant impact in this rare in highly aggressive malignancy.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
Salivary Ductal Carcinoma
Epidermal growth factor receptor
- H & E:
Hematoxylin and Eosin
Salivary gland carcinoma.
Sung M-W, Kim KH, Kim J-W, Min Y-G, Seong W-J, Roh J-L, Lee SJ, Kwon TK, Park SW: Clinicopathologic predictors and impact of distant metastasis from adenoid cystic carcinoma of the head and neck. Arch Otolaryngol Head Neck Surg. 2003, 129 (11): 1193-1197. 10.1001/archotol.129.11.1193.
Belsky JL, Tachikawa K, Cihak RW, Yamamoto T: Salivary gland tumors in atomic bomb survivors, Hiroshima-Nagasaki, 1957 to 1970. JAMA. 1972, 219 (7): 864-868. 10.1001/jama.1972.03190330034007.
Kleinsasser O, Klein HJ, Hübner G: Salivary duct carcinoma. A group of salivary gland tumors analogous to mammary duct carcinoma. Arch Klin Exp Ohren Nasen Kehlkopfheilkd. 1968, 192 (1): 100-105. 10.1007/BF00301495.
Seifert G, Brocheriou C, Cardesa A, Eveson JW: WHO International Histological Classification of Tumours. Tentative Histological Classification of Salivary Gland Tumours. Pathol Res Pract. 1990, 186 (5): 555-581. 10.1016/S0344-0338(11)80220-7.
Murrah VA, Batsakis JG: Salivary duct carcinoma. Ann Otol Rhinol Laryngol. 1994, 103 (3): 244-247.
Madrigal B, García J, De Vicente JC: Salivary duct carcinoma: an unusual case of long-term evolution. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1999, 88 (5): 597-602. 10.1016/S1079-2104(99)70092-2.
Guzzo M, Di Palma S, Grandi C, Molinari R: Salivary duct carcinoma: clinical characteristics and treatment strategies. Head Neck. 1997, 19 (2): 126-133. 10.1002/(SICI)1097-0347(199703)19:2<126::AID-HED7>3.0.CO;2-6.
Nardi V, Sadow PM, Juric D, Zhao D, Cosper AK, Bergethon K, Scialabba VL, Batten JM, Borger DR, Iafrate AJ, Heist RS, Lawrence DP, Flaherty KT, Bendell JC, Deschler D, Li Y, Wirth LJ, Dias-Santagata D: Detection of novel actionable genetic changes in salivary duct carcinoma helps direct patient treatment. Clin Cancer Res. 2013, 19 (2): 480-490. 10.1158/1078-0432.CCR-12-1842.
Barnes L, Rao U, Krause J, Contis L, Schwartz A, Scalamogna P: Salivary duct carcinoma. Part I. A clinicopathologic evaluation and DNA image analysis of 13 cases with review of the literature. Oral Surg Oral Med Oral Pathol. 1994, 78 (1): 64-73. 10.1016/0030-4220(94)90119-8.
Jaspers HCJ, Verbist BM, Schoffelen R, Mattijssen V, Slootweg PJ, van der Graaf WTA, van Herpen CML: Androgen receptor-positive salivary duct carcinoma: a disease entity with promising new treatment options. J Clin Oncol. 2011, 29 (16): e473-e476. 10.1200/JCO.2010.32.8351.
Griffith CC, Seethala RR, Luvison A, Miller M, Chiosea SI: PIK3CA mutations and PTEN loss in salivary duct carcinomas. Am J Surg Pathol. 2013, 37 (8): 1201-1207. 10.1097/PAS.0b013e3182880d5a.
Cros J, Sbidian E, Hans S, Roussel H, Scotte F, Tartour E, Brasnu D, Laurent-Puig P, Bruneval P, Blons H, Badoual C: Expression and mutational status of treatment-relevant targets and key oncogenes in 123 malignant salivary gland tumours. Ann Oncol. 2013, 24 (10): 2624-2629. 10.1093/annonc/mdt338.
Shadaba A, Gaze MN, Grant HR: The response of adenoid cystic carcinoma to tamoxifen. J Laryngol Otol. 1997, 111 (12): 1186-1189.
van der Hulst RW, van Krieken JH, van der Kwast TH, Gerritsen JJ, de Jong RJ B, Nijeholt AA L à, Meinders AE: Partial remission of parotid gland carcinoma after goserelin. Lancet. 1994, 344 (8925): 817-
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/701/prepub
The authors wish to acknowledge the valuable contributions of Mrs. Elizabeth Guadarrama-Beltrán through her kindness and social work provided to this and many other patients at our institution. JH Flores-Arredondo, MD is currently supported by a National Institutes of Health (NIH) National Heart Lung and Blood Institute (NHLBI) T32 HL007812 training grant.
The authors declare that they have no competing interests.
CS treated the patient, participated in conception, acquisition of data and drafting the article. FJ participated in drafting and revision. DR participated in histological examination of sample. CM participated in radiological examination of images. DP participated in critical review and supervision. All the authors read and approved the final paper.
About this article
Cite this article
Campos-Gómez, S., Flores-Arredondo, J.H., Dorantes-Heredia, R. et al. Case report: anti-hormonal therapy in the treatment of ductal carcinoma of the parotid gland. BMC Cancer 14, 701 (2014). https://doi.org/10.1186/1471-2407-14-701
- Salivary gland
- Ductal carcinoma
- Estrogen receptor antagonist