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膀胱移行细胞癌患者的辅助性贝司他汀免疫疗法。一项随机试验的临床结果。

Adjuvant Bestatin immunotherapy in patients with transitional cell carcinoma of the bladder. Clinical results of a randomized trial.

作者信息

Blomgren H, Näslund I, Esposti P L, Johansen L, Aaskoven O

出版信息

Cancer Immunol Immunother. 1987;25(1):41-6. doi: 10.1007/BF00199299.

Abstract

The first clinical results of an ongoing, prospective trial to determine the value of adjuvant Bestatin immunotherapy in the management of bladder cancer are presented. Patients with nonmetastatic transitional cell carcinoma of the bladder, scheduled for full dose local radiation therapy (64 Gy), were randomly allocated to adjuvant oral Bestatin treatment (30 mg daily for at least 1 year), starting at completion of irradiation, or no Bestatin. The longest follow-up period of the 151 evaluable patients is 6 years. The results have shown that the disease-free survival of the patients taking Bestatin is significantly improved compared to the controls (p = 0.04). However, the overall survival of the patients was not affected by the Bestatin treatment. The beneficial effect of Bestatin seemed to be more marked among men than women. Furthermore, statistical analyses of the patient material according to T tumor categories suggested that compared to the controls, patients with less advanced disease (T1 and T2) benefitted more from Bestatin treatment than those with more advanced tumors (T3 and T4). The results of this ongoing trial thus show that patients with bladder cancer benefit from adjuvant Bestatin treatment in terms of disease-free survival.

摘要

本文展示了一项正在进行的前瞻性试验的首批临床结果,该试验旨在确定辅助性贝司他汀免疫疗法在膀胱癌治疗中的价值。计划接受全剂量局部放射治疗(64 Gy)的非转移性膀胱移行细胞癌患者,在放疗结束后随机分配接受辅助性口服贝司他汀治疗(每日30 mg,至少持续1年)或不接受贝司他汀治疗。151例可评估患者的最长随访期为6年。结果显示,服用贝司他汀的患者无病生存期与对照组相比有显著改善(p = 0.04)。然而,患者的总生存期不受贝司他汀治疗的影响。贝司他汀的有益效果在男性中似乎比女性更明显。此外,根据T肿瘤类别对患者资料进行的统计分析表明,与对照组相比,病情较轻(T1和T2)的患者比病情较重(T3和T4)的患者从贝司他汀治疗中获益更多。因此,这项正在进行的试验结果表明,膀胱癌患者在无病生存期方面可从辅助性贝司他汀治疗中获益。

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