Journal article
IGF-1R expression is associated with HPV-negative status and adverse survival in head and neck squamous cell cancer
- Abstract:
- Head and neck squamous cell carcinomas (HNSCC) are treated with surgery, radiotherapy and cisplatin-based chemotherapy, but survival from locally-advanced disease remains poor, particularly in patients whose tumors are negative for Human papillomavirus (HPV). Type 1 IGF receptor (IGF-1R) is known to promote tumorigenesis and resistance to cancer therapeutics. Here, we assessed IGF-1R immunohistochemistry on tissue microarrays containing 852 cores from 346 HNSCC patients with primary tumors in the oropharynx (n = 231), larynx (85), hypopharynx (28), oral cavity (2). Of these, 236 (68%) were HPV-negative, 110 (32%) positive. IGF-1R was detected in the cell membrane of 36% and cytoplasm of 92% of HNSCCs; in 64 cases with matched normal tonsillar epithelium, IGF-1R was overexpressed in the HNSCCs (P < 0.001). Overall survival (OS) and disease-specific survival (DSS) were reduced in patients whose tumors contained high membrane IGF-1R [OS: hazard ratio (HR) = 1.63, P = 0.006; DSS: HR = 1.63, P = 0.016], cytoplasmic IGF-1R (OS: HR = 1.58, P = 0.009; DSS: HR = 1.58, P = 0.024) and total IGF-1R (OS: HR = 2.02, P < 0.001; DSS: HR = 2.2, P < 0.001). High tumor IGF-1R showed significant association with high-tumor T-stage (P < 0.001) and HPV-negativity (P < 0.001), and was associated with shorter OS when considering patients with HPV-positive (P = 0.01) and negative (P = 0.006) tumors separately. IGF-1R was independently associated with survival in multivariate analysis including HPV, but not when lymphovascular invasion, perineural spread and T-stage were included. Of these factors, only IGF-1R can be manipulated; the association of IGF-1R with aggressive disease supports experimental incorporation of anti-IGF-1R agents into multimodality treatment programs for HPV-negative and high IGF-1R HPV-positive HNSCC.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
Actions
Authors
- Publisher:
- Oxford University Press
- Journal:
- Carcinogenesis More from this journal
- Volume:
- 36
- Issue:
- 6
- Pages:
- 648-655
- Publication date:
- 2015-04-20
- Acceptance date:
- 2015-03-21
- DOI:
- EISSN:
-
1460-2180
- ISSN:
-
0143-3334
- Pmid:
-
25896444
- Language:
-
English
- Keywords:
- Pubs id:
-
pubs:521614
- UUID:
-
uuid:6eb0a5cf-78db-46ca-af8d-f309924de3d4
- Local pid:
-
pubs:521614
- Source identifiers:
-
521614
- Deposit date:
-
2017-12-18
Terms of use
- Copyright holder:
- Dale et al
- Copyright date:
- 2015
- Rights statement:
- © The Author 2015
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