IMMUNOHISTOCHEMICAL DETECTION OF E-CADHERIN IN DIFFERENTIATED THYROIDCARCINOMAS CORRELATES WITH CLINICAL OUTCOME

Citation
R. Vonwasielewski et al., IMMUNOHISTOCHEMICAL DETECTION OF E-CADHERIN IN DIFFERENTIATED THYROIDCARCINOMAS CORRELATES WITH CLINICAL OUTCOME, Cancer research, 57(12), 1997, pp. 2501-2507
Citations number
46
Categorie Soggetti
Oncology
Journal title
ISSN journal
00085472
Volume
57
Issue
12
Year of publication
1997
Pages
2501 - 2507
Database
ISI
SICI code
0008-5472(1997)57:12<2501:IDOEID>2.0.ZU;2-E
Abstract
A retrospective immunohistochemical analysis of the adhesion molecule E-cadherin (E-CD) was performed in 112 differentiated thyroid carcinom as and 38 synchronous and 20 relapse metastases primarily from operati ons performed at the Medical School Hanover between 1982 and 1992. E-C D-specific antibody 5H9 was applied to paraffin-embedded tissues. All patients were clinically followed for a maximal period of 12 years. La ck of E-CD expression (i.e., <5% of tumor cells positive) occurred in 18 of 112 (16.1%) cases, whereas the majority showed either low (24.1% ), medium (35.7%), or high (24.1%) positivity. No difference was found between papillary (n = 88) and follicular (n = 24) carcinomas. Univar iate statistical analysis for survival (Kaplan-Meier) showed that lack of E-CD expression (P < 0.024) is an adverse prognostic factor for di fferentiated thyroid carcinomas. The highest significance was seen amo ng patients without lymph node involvment at first presentation (pN(0) ; P = 0.0068) and among females (P = 0.0033). Multivariate analysis (C ox model) indicated that E-CD staining is an independent prognostic fa ctor (corrected risk factor, 3.7; P < 0.03) in addition to distant met astasis (pM1) and tumor size. A comparison of E-CD stainings between p rimary tumors and their metastatic lesions showed similar results in b oth synchronous and relapse metastases after therapy. In conclusion, E -CD immunostaining is an independent prognostic indicator for differen tiated thyroid carcinomas. It may help to uncover the small group of p atients with differentiated thyroid carcinomas carrying a high risk of suffering an unfavorable clinical outcome.