Skip to main navigation Skip to search Skip to main content

Conversion surgery following trastuzumab and docetaxel combination therapy for unresectable HER2-positive parotid gland cancer

  • Satoshi Kano
  • , Jun Taguchi
  • , Taku Maeda
  • , Takayoshi Suzuki
  • , Seijiro Hamada
  • , Shun Kato
  • , Atsuhiko Saito
  • , Yasushi Shimizu
  • , Akihiro Homma

Research output: Contribution to journal › Article › peer-review

Abstract

Salivary gland cancers (SGCs) are rare and histologically diverse tumors. Among them, salivary duct carcinoma and carcinoma ex pleomorphic adenoma frequently exhibit HER2 overexpression, for which trastuzumab (Tmab) combined with docetaxel (DTX) has shown clinical efficacy. We report two cases of initially unresectable, HER2-positive parotid gland carcinoma successfully treated with Tmab and DTX, enabling curative surgery. In Case 1, a 68-year-old woman with T4bN2bM0 parotid carcinoma experienced marked tumor shrinkage, allowing surgical resection while preserving the skin and facial nerve. In Case 2, a 46-year-old woman with T4bN2cM0 disease discontinued systemic therapy after four cycles due to toxicity but subsequently underwent successful resection with skin reconstruction. These cases suggest that systemic HER2-targeted therapy can serve as an effective neoadjuvant approach for locally advanced HER2-positive SGCs. Conversion surgery following Tmab and DTX treatment may offer a curative option in selected patients initially deemed inoperable.

Original languageEnglish
Pages (from-to)328-331
Number of pages4
JournalAuris Nasus Larynx
Volume53
Issue number3
DOIs
Publication statusPublished - 06-2026
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

All Science Journal Classification (ASJC) codes

  • Surgery
  • Otorhinolaryngology

Fingerprint

Dive into the research topics of 'Conversion surgery following trastuzumab and docetaxel combination therapy for unresectable HER2-positive parotid gland cancer'. Together they form a unique fingerprint.

Cite this