# Complete Response in Salivary Duct Carcinoma Ex Pleomorphic Adenoma With Upfront Combination of Trastuzumab and Chemo-Hormonal Therapy

**Authors:** Ajay Gupta, Aadithya Lakshmi Narayanan, Vikas Kashyap, Surabhi Gupta

PMC · DOI: 10.7759/cureus.82742 · Cureus · 2025-04-21

## TL;DR

A rare aggressive cancer showed a complete response to a combination of trastuzumab, hormone therapy, and chemotherapy.

## Contribution

A novel treatment combination achieved a durable complete response in a rare and aggressive salivary duct carcinoma.

## Key findings

- A 48-year-old male with advanced SDC ex pleomorphic adenoma achieved complete response after treatment.
- Combination therapy included trastuzumab, CAB, and docetaxel, showing durable results over 17 months.
- The case highlights a potential treatment strategy for rare cancers where large studies are impractical.

## Abstract

Salivary duct carcinoma (SDC) is one of the rarest malignancies. It can arise de novo or from pre-existing pleomorphic adenoma (carcinoma ex pleomorphic adenoma - CXPA) and can be very aggressive.

Here, we present one such case of a 48-year-old male with relapsed, widely invasive SDC ex pleomorphic adenoma of the parotid that was locally advanced with intracranial extension that was refractory to chemo-radiation. Immunohistochemistry confirmed positivity for human epidermal growth factor receptor-2 (HER2) and androgen receptor (AR). He was started on a combination of trastuzumab, Combined Androgen Blockade (CAB) with leuprolide and bicalutamide, and docetaxel. Follow-up imaging at three months and nine months from treatment initiation demonstrated a complete response, ongoing at 17 months at follow-up. The upfront combination of anti-HER2 therapy, CAB, and chemotherapy resulted in a durable complete response in an aggressive disease.

The result obtained from our experience provides valuable insight into the management of a rare and treatment-resistant entity, where large prospective studies without heterogeneity are not possible.

## Linked entities

- **Proteins:** ERBB2 (erb-b2 receptor tyrosine kinase 2)
- **Chemicals:** leuprolide (PubChem CID 657181), bicalutamide (PubChem CID 2375), docetaxel (PubChem CID 148124)
- **Diseases:** salivary duct carcinoma (MONDO:0044915), pleomorphic adenoma (MONDO:0008401), carcinoma ex pleomorphic adenoma (MONDO:0002472)

## Full-text entities

- **Genes:** AR (androgen receptor) [NCBI Gene 367] {aka AIS, AR8, DHTR, HPCX3, HUMARA, HYSP1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** Carcinoma Ex Pleomorphic Adenoma (MESH:D008949), malignancies (MESH:D009369), SDC (MESH:D012465)
- **Chemicals:** docetaxel (MESH:D000077143), Chemo (-), Trastuzumab (MESH:D000068878), bicalutamide (MESH:C053541)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12094920/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12094920/full.md

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Source: https://tomesphere.com/paper/PMC12094920