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Amrubicin for relapsed small-cell lung cancer: a systematic review and meta-analysis of 803 patients

机译:阿姆比星治疗复发性小细胞肺癌:803例患者的系统评价和荟萃分析

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Currently, amrubicin is permitted for relapsed small-cell lung carcinoma (SCLC) only in Japan. The efficacy and adverse effects of amrubicin as reported by previous studies varied greatly. The inclusion criterion was a prospective study that was able to provide data for efficacy and safety by the AMR single agent regimen as second-line chemotherapy for a patient with SCLC. Binary data were meta-analyzed with the random-model generic inverse variance method. We included nine articles consisted of 803 patients. The pooled three-, six-, and nine-month progression-free survival were 63% (95% CI 57–69%, I2?=?53%), 28% (95% CI 21–35%, I2?=?71%), and 10% (95% CI 6–14%, I2?=?41%), respectively. The pooled six-, 12-, and 18-month overall survival were 69% (95% CI 61–78%, I2?=?83%), 36% (95% CI 28–44%, I2?=?80%), and 15% (95% CI 8–21%, I2?=?81%), respectively. Amrubicin seemed much more beneficial for Japanese patients. However, compared to the efficacy of topotecan presented in a previous meta-analysis, amrubicin may be a better treatment option than topotecan for both Japanese and Euro-American. Adverse effects by amrubicin were almost exclusively observed to be hematological. Notably, grade III/IV neutropenia incidence was 70% and febrile neutropenia incidence was 12%.
机译:目前,仅在日本允许氨柔比星用于复发性小细胞肺癌(SCLC)。如先前研究报道的氨柔比星的疗效和不良反应差异很大。纳入标准是一项前瞻性研究,能够通过AMR单药方案作为SCLC患者的二线化疗提供疗效和安全性数据。使用随机模型通用逆方差方法对二进制数据进行荟萃分析。我们纳入了包括803名患者的9篇文章。合并的三个月,六个月和九个月的无进展生存期分别为63%(95%CI 57–69%,I 2 ?=?53%),28%(95%CI 21–35%,I 2 ?=?71%)和10%(95%CI 6–14%,I 2 ?=?41%) 。汇总的六个月,十二个月和十八个月的总生存期分别为69%(95%CI 61–78%,I 2 ?=?83%),36%(95%CI 28-分别为44%,I 2 ?=?80%)和15%(95%CI 8–21%,I 2 ?=?81%)。对于日本患者而言,氨柔比星似乎更为有益。但是,与先前的荟萃分析中显示的拓扑替康的疗效相比,对于日本人和欧美人而言,氨柔比星可能比拓扑替康更好的治疗选择。几乎完全观察到氨柔比星的不良反应是血液学的。值得注意的是,III / IV级中性粒细胞减少症的发生率为70%,高热性中性粒细胞减少症的发生率为12%。

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