Immunoprofiles and Oncologic Outcomes of 15 Patients with Androgen Receptor-Positive Salivary Duct Carcinoma

Author:

Gogineni Emile1ORCID,Sells Blake E.2ORCID,Dibs Khaled1,Jhawar Sachin R.1ORCID,Haring Catherine T.3,Limbach Abberly L.4,Konieczkowski David J.1,Ma Sung J.1ORCID,Zhu Simeng1,Baliga Sujith1,Mitchell Darrion L.1ORCID,Grecula John C.1,Bonomi Marcelo5ORCID,Bhateja Priyanka5ORCID,Old Matthew O.3,Seim Nolan B.3,Kang Stephen Y.3,Rocco James W.3,Chakravarti Arnab1,Blakaj Dukagjin M.1,Gamez Mauricio E.6

Affiliation:

1. Department of Radiation Oncology, The Ohio State University Wexner Medical Center, 460 W. 10th Ave, Columbus, OH 43210, USA

2. St. Louis School of Medicine, St. Louis, MO 63310, USA

3. Department of Otolaryngology, The Ohio State University Wexner Medical Center, 460 W. 10th Ave, Columbus, OH 43210, USA

4. Department of Pathology, The Ohio State University Wexner Medical Center, 460 W. 10th Ave, Columbus, OH 43210, USA

5. Department of Medical Oncology, The Ohio State University Wexner Medical Center, 460 W. 10th Ave, Columbus, OH 43210, USA

6. Department of Radiation Oncology, Mayo Clinic, 200 First St SW, Rochester, MN 55905, USA

Abstract

Background: Salivary duct carcinomas (SDC) are a rare and aggressive subtype of salivary gland neoplasm. They can present with distinct immunoprofiles, such as androgen receptor (AR) and HER-2/Neu-positivity. To date, no consensus exists on how to best manage this entity. Methods: All patients diagnosed with nonmetastatic AR+ SDC of the parotid from 2013 to 2019 treated with curative intent were included. Immunologic tumor profiling was conducted using 24 distinct markers. Kaplan–Meier analyses were used to estimate locoregional recurrence (LRR), distant control, and overall survival (OS). Results: Fifteen patients were included. Nine (60%) patients presented with T4 disease and eight (53%) had positive ipsilateral cervical lymphadenopathy. Ten (67%) patients underwent trimodality therapy, including surgery followed by adjuvant radiation and concurrent systemic therapy. The median follow-up was 5.5 years (interquartile range, 4.8–6.1). The estimated 5-year rates of LRR, distant progression, and OS were 6%, 13%, and 87%, respectively. Conclusion: Despite only including AR+ SDC of the parotid, immunoprofiles, such as expression of HER-2, were highly variable, highlighting the potential to tailor systemic regimens based on individual histologic profiles in the future. Studies with larger patient numbers using tumor-specific molecular profiling and tumor heterogeneity analyses are justified to better understand the biology of these tumors. Molecularly informed treatment approaches, including the potential use of AR- and HER-2/Neu-directed therapies upfront in the definitive setting, may hold future promise to further improve outcomes for these patients.

Publisher

MDPI AG

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