SIGNIFICANCE OF BETA-HCG IN THE SERUM AS A TUMOR-MARKER FOR GASTRIC-CANCER

Citation
B. Rau et al., SIGNIFICANCE OF BETA-HCG IN THE SERUM AS A TUMOR-MARKER FOR GASTRIC-CANCER, Langenbecks Archiv fur Chirurgie, 380(6), 1995, pp. 359-364
Citations number
NO
Categorie Soggetti
Surgery
ISSN journal
00238236
Volume
380
Issue
6
Year of publication
1995
Pages
359 - 364
Database
ISI
SICI code
0023-8236(1995)380:6<359:SOBITS>2.0.ZU;2-B
Abstract
Introduction: Recent investigations indicate that in 50% of patients w ith gastric cancer, beta-hCG-positive cells can be found in the tumour by immunohistochemical investigations. The objective of this study wa s to investigate how often beta-hCG-immunoreactive gastric carcinomas were accompanied by an elevation in serum beta-hCG, that could have be en used as a course control variable. Methods: In 54 patients with gas tric carcinoma a monoclonal antibody directed against beta-hCG was use d for immunohistochemical marking in the APAAP system. The evaluation was graded positive or negative. In parallel, serum beta-hCG was deter mined preoperatively using an enzyme immunoassay (MEIA). Tumour stage, grading and tumour localization were determinants in the evaluation. Results: We found that 41% (22 of 54) of the carcinomas induced a posi tive immunohistochemical response to beta-hCG, regardless of their loc ation in the stomach. In relation to tumour stage, a positive beta-hCG immunoreactivity was apparent in 27% (6/22) of tumours without lymph node or distant metastases (T1 - 4N0M0), in 54% (7/13) of tumours with lymph node and without distant metastases (T1 - 4N greater than or eq ual to 1M0) and in 47% (9/35) of tumours with distant metastases. Poor ly differentiated tumours (G3-4) were positive in 42% (15/36) and well -differentiated tumors (G1-2) in 39% (7/18) of cases. In only 1 patien t was the beta-hCG level in serum elevated, however. Conclusions. beta -hCG-Positive gastric carcinomas are found more frequently in advanced tumour stages and poorly differentiated carcinomas. These carcinomas, however, seem not to excrete beta-hCG in sufficient amounts to produc e measurable serum values. Therefore, beta-hCG cannot be used a progno stic factor or for course control. The relevance of beta-hCG expressio n of tumour cells to the patients' prognosis remains obscure.