Background: HER family receptors play a key role in tumor progression in several malignancies, such as colorectal, lung or breast cancer. The aims of this study were to investigate expression of HER-1, HER-2 and HER-3 in pancreatic cancer (PC) samples and evaluate the association between HER-family receptor expression and patients’ clinical outcomes. Methods: Tissue samples from 91 PC patients were subjected to immunohistochemical staining to assess the expression of HER-1, HER-2 and HER-3. Semiquantitative scores of zero (no staining or staining in less than 10% of cancer cells), 1+, 2+ or 3+ were assigned to each sample based on the intensity of staining for HER receptors. Scores of 2+ or 3+ were defined as positive staining. Results: HER-1 overexpression was observed in 41 out of 91 samples (45.1%), while HER-2 was not overexpressed in any of the analyzed samples. HER-3 was overexpressed in 37 samples (40.7%) and was found to be associated with advanced TNM stage. In particular, HER-3 was overexpressed in 12 out of 16 stage IV patients (75%) compared with only 33.3% of stage I-III patients (p = 0.02). Among 79 patients with available survival data, the 6 patients with strong HER-3 expression (score 3+) had a shorter survival compared with remaining patients (median overall survival 6.9 months vs. 12.3 months, respectively). Conclusions: HER-1 and HER-3 were found to be expressed in a significant proportion of PC patients. Strong HER- 3 expression represents an indicator of poor prognosis in PC patients, being associated with advanced stage and shorter survival.

HER family receptor expression and prognosis in pancreatic cancer / Bittoni, A.; Mandolesi, A.; Andrikou, K.; Santoni, M.; Alfonsi, S.; Lanese, A.; Loretelli, C.; Pellei, C.; Piva, F.; Scarpelli, M.; Cascinu, S.. - In: THE INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS. - ISSN 0393-6155. - 30:3(2015), pp. e327-e332. [10.5301/jbm.5000157]

HER family receptor expression and prognosis in pancreatic cancer

Cascinu S.
2015-01-01

Abstract

Background: HER family receptors play a key role in tumor progression in several malignancies, such as colorectal, lung or breast cancer. The aims of this study were to investigate expression of HER-1, HER-2 and HER-3 in pancreatic cancer (PC) samples and evaluate the association between HER-family receptor expression and patients’ clinical outcomes. Methods: Tissue samples from 91 PC patients were subjected to immunohistochemical staining to assess the expression of HER-1, HER-2 and HER-3. Semiquantitative scores of zero (no staining or staining in less than 10% of cancer cells), 1+, 2+ or 3+ were assigned to each sample based on the intensity of staining for HER receptors. Scores of 2+ or 3+ were defined as positive staining. Results: HER-1 overexpression was observed in 41 out of 91 samples (45.1%), while HER-2 was not overexpressed in any of the analyzed samples. HER-3 was overexpressed in 37 samples (40.7%) and was found to be associated with advanced TNM stage. In particular, HER-3 was overexpressed in 12 out of 16 stage IV patients (75%) compared with only 33.3% of stage I-III patients (p = 0.02). Among 79 patients with available survival data, the 6 patients with strong HER-3 expression (score 3+) had a shorter survival compared with remaining patients (median overall survival 6.9 months vs. 12.3 months, respectively). Conclusions: HER-1 and HER-3 were found to be expressed in a significant proportion of PC patients. Strong HER- 3 expression represents an indicator of poor prognosis in PC patients, being associated with advanced stage and shorter survival.
2015
EGFR
HER-2
HER-3
Pancreatic adenocarcinoma
Prognosis
Adenocarcinoma
Aged
Aged, 80 and over
Dimerization
ErbB Receptors
Female
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Molecular Targeted Therapy
Neoplasm Proteins
Neoplasm Staging
Pancreatectomy
Pancreatic Neoplasms
Prognosis
Proportional Hazards Models
Single-Blind Method
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/108772
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 9
  • ???jsp.display-item.citation.isi??? 10
social impact