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Anticancer Res ; 26(3B): 2281-7, 2006.
Artículo en Inglés | MEDLINE | ID: mdl-16821603

RESUMEN

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.


Asunto(s)
Antígenos de Neoplasias/biosíntesis , Neoplasias Esofágicas/inmunología , Neoplasias de Células Escamosas/inmunología , Adulto , Anciano , Neoplasias Esofágicas/patología , Femenino , Humanos , Masculino , Antígenos Específicos del Melanoma , Proteínas de la Membrana/biosíntesis , Persona de Mediana Edad , Proteínas de Neoplasias/biosíntesis , Estadificación de Neoplasias , Neoplasias de Células Escamosas/patología , Modelos de Riesgos Proporcionales
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