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HER2 Expression in Salivary Gland Carcinomas: Dependence on Histological Subtype

  • Bonnie Glisson
  • , A. Dimitrios Colevas
  • , Robert Haddad
  • , Jeoffrey Krane
  • , Adel El-Naggar
  • , Merrill Kies
  • , Rosemary Costello
  • , Carmen Summey
  • , Matthew Arquette
  • , Corey Langer
  • , Philip C. Amrein
  • , Marshall Posner

Research output: Contribution to journalArticlepeer-review

201 Scopus citations

Abstract

Purpose: Previous evaluation of HER2 overexpression in salivary gland cancers indicated an incidence varying between 7 and 56%, with no clear difference among three histologically different subtypes. As part of a Phase II trial of trastuzumab for treatment of incurable salivary gland cancer, we screened 137 tumors for HER2 expression. Experimental Design: Unstained sections of paraffin-embedded tumor samples were stained with p185/HER2 receptor antibody. Tumors with moderate (2+) to strong (3+) complete membrane staining in at least 10% of the tumor cells were scored as positive for overexpression. Results: The overall frequency of overexpression for HER2 was 17% (23 of 137), whereas it was only 8% in the three most common histological subtypes screened. Overexpression was distinctly rare in the most common subtype screened, adenoid cystic carcinoma (4%, 3 of 70). Overexpression was very common in salivary duct cancers; 10 (83%) of 12 were positive for HER2. This observation is consistent with the typical high-grade histological features and aggressive behavior of this subtype as well as with its histogenetic similarity to breast cancer. Analysis based on histogenesis (intercalated duct versus excretory duct) indicated a higher frequency of overexpression in the latter (55%) than in the former (7%). Conclusions: Our overall results suggest that trastuzumab will not have a major role in treatment of salivary gland cancers of intercalated duct origin. Further systematic evaluation of trastuzumab in subtypes of excretory duct origin could be supported.

Original languageEnglish
Pages (from-to)944-946
Number of pages3
JournalClinical Cancer Research
Volume10
Issue number3
DOIs
StatePublished - 1 Feb 2004
Externally publishedYes

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