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Efficacy and toxicities of gemcitabine and cisplatin combined with endostar in advanced thymoma and thymic carcinoma

机译:吉西他滨联合顺铂联合恩度星治疗晚期胸腺瘤和胸腺癌的疗效和毒性

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Background Thymoma and thymic carcinoma are rare thymic epithelial tumors. We investigated the efficacy of first‐line gemcitabine and cisplatin (GP) chemotherapy versus gemcitabine and cisplatin chemotherapy combined with the anti‐angiogenic drug endostar (GP + E) in advanced thymoma and thymic carcinoma. Methods The records of 45 patients with invasive metastatic thymomas or thymic carcinomas treated with GP as first‐line therapy between August 2008 and July 2017 at the Department of Respiratory Medicine, Peking University Cancer Hospital and Institute were retrospectively reviewed. Results Eighteen patients (75%) in the GP + E group achieved a partial response and six (25%) had stable disease. In GP only group, nine (42.8%) patients achieved a partial response, 11 (52.4%) had stable disease, and one (4.8%) had progressive disease. The GP + E group had a significantly higher overall response rate (75% vs. 42.9%; P = 0.028), and median progression‐free survival (PFS) and overall survival (OS) of 19 and 76 months, respectively. In the GP only group, median PFS and OS were 16 and 29 months, respectively. PFS and OS were not significantly different between the groups. Conclusions GP has moderate efficacy and could represent a suitable first‐line therapy for thymic carcinoma and thymoma. Chemotherapy combined with endostar could improve the overall response rate, but did not prolong PFS or OS.
机译:背景胸腺瘤和胸腺癌是罕见的胸腺上皮肿瘤。我们研究了吉西他滨和顺铂(GP)一线化疗与吉西他滨和顺铂化疗联合抗血管生成药物endostar(GP + E)在晚期胸腺瘤和胸腺癌中的疗效。方法回顾性分析2008年8月至2017年7月在北京大学肿瘤医院和研究所呼吸内科行一线治疗的45例浸润性转移性胸腺瘤或胸腺癌患者的病历。结果GP + E组18例(75%)获得部分缓解,6例(25%)病情稳定。在仅GP组中,有9名(42.8%)患者获得了部分缓解,11名(52.4%)患者病情稳定,1名(4.8%)患者病情进展。 GP + E组的总缓解率显着更高(75%比42.9%; P = 0.028),中位无进展生存期(PFS)和总体生存期(OS)分别为19个月和76个月。在仅GP组,中位PFS和OS分别为16个月和29个月。两组之间的PFS和OS没有显着差异。结论GP具有中等的疗效,可以作为胸腺癌和胸腺瘤的一线治疗药物。化学疗法联合endostar可以提高总体缓解率,但不能延长PFS或OS。

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