Expression of MAGE-A Cancer/Testis Antigens in Esophageal Squamous Cell Carcinomas
Background: Although the diagnosis and therapy of esophageal cancer have improved over the past decade, the prognosis remains dismal. Since MAGE-A cancer/testis antigens (CTA) are potential targets for immunotherapy, this study was aimed at evaluating their expression in these patients and its progn...
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Veröffentlicht in: | Anticancer research 2006-05, Vol.26 (3B), p.2281-2287 |
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Zusammenfassung: | Background: Although the diagnosis and therapy of esophageal cancer have improved over the past decade, the prognosis remains
dismal. Since MAGE-A cancer/testis antigens (CTA) are potential targets for immunotherapy, this study was aimed at evaluating
their expression in these patients and its prognostic value. Materials and Methods: Using 57B monoclonal antibody, MAGE-A
CTA expression was analyzed in paraffin-embedded tumor specimens of 98 patients with esophageal squamous cell carcinoma or
adenocarcinomas who had undergone surgical resection. For all patients, a postoperative follow-up of at least 4 years was
available. The expression was quantified using a scoring system considering intensity and homogeneity of the immunostaining.
The prognostic relevance of MAGE-A expression was analyzed in univariate analyses as well as Cox proportional hazard regression
analysis. Results: 57B positivity could be detected in 38 tumors (38.8%). Positive staining was observed in five out of 32
adenocarcinomas (15.2%) and in 33 out of 66 (50%) squamous cell carcinomas. MAGE-A expression did not correlate with the TNM
classification, grading or age of the patients. Both univariate (p=0.88) and multivariate analyses (p=0.82) revealed that
MAGE-A expression lacked prognostic significance in esophageal carcinomas. Conclusion: MAGE-A was expressed in half of the
squamous cell carcinomas of the esophagus, but rarely in adenocarcinomas. Although its immunodetection was insufficient for
prognostic evaluation, the high expression rate suggests MAGE-A as a potential target for immunotherapy in the first group
with the ability for pretherapeutic testing. |
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ISSN: | 0250-7005 1791-7530 |