<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16(6)</volume><submitter>Gogineni E</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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).&lt;h4>Results&lt;/h4>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.&lt;h4>Conclusion&lt;/h4>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.</pubmed_abstract><journal>Cancers</journal><pagination>1204</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10969601</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunoprofiles and Oncologic Outcomes of 15 Patients with Androgen Receptor-Positive Salivary Duct Carcinoma.</pubmed_title><pmcid>PMC10969601</pmcid><pubmed_authors>Jhawar SR</pubmed_authors><pubmed_authors>Kang SY</pubmed_authors><pubmed_authors>Chakravarti A</pubmed_authors><pubmed_authors>Baliga S</pubmed_authors><pubmed_authors>Mitchell DL</pubmed_authors><pubmed_authors>Grecula JC</pubmed_authors><pubmed_authors>Seim NB</pubmed_authors><pubmed_authors>Gamez ME</pubmed_authors><pubmed_authors>Gogineni E</pubmed_authors><pubmed_authors>Haring CT</pubmed_authors><pubmed_authors>Ma SJ</pubmed_authors><pubmed_authors>Sells BE</pubmed_authors><pubmed_authors>Konieczkowski DJ</pubmed_authors><pubmed_authors>Bonomi M</pubmed_authors><pubmed_authors>Rocco JW</pubmed_authors><pubmed_authors>Blakaj DM</pubmed_authors><pubmed_authors>Old MO</pubmed_authors><pubmed_authors>Limbach AL</pubmed_authors><pubmed_authors>Bhateja P</pubmed_authors><pubmed_authors>Dibs K</pubmed_authors><pubmed_authors>Zhu S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunoprofiles and Oncologic Outcomes of 15 Patients with Androgen Receptor-Positive Salivary Duct Carcinoma.</name><description>&lt;h4>Background&lt;/h4>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.&lt;h4>Methods&lt;/h4>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).&lt;h4>Results&lt;/h4>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.&lt;h4>Conclusion&lt;/h4>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.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2025-04-21T21:32:45.658Z</modification><creation>2025-04-05T18:23:01.287Z</creation></dates><accession>S-EPMC10969601</accession><cross_references><pubmed>38539538</pubmed><doi>10.3390/cancers16061204</doi></cross_references></HashMap>