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首页> 外文期刊>Breast cancer research and treatment. >A systematic review on topoisomerase 1 inhibition in the treatment of metastatic breast cancer.
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A systematic review on topoisomerase 1 inhibition in the treatment of metastatic breast cancer.

机译:拓扑异构酶1抑制治疗转移性乳腺癌的系统评价。

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Following treatment with anthracyclines and taxanes, few established options exist for the treatment of metastatic breast cancer (MBC). Although the topoisomerase 1 inhibitors irinotecan, etirinotecan, and topotecan have been used in clinical trials on MBC, the drugs have never been introduced as standard treatment for the disease. We performed a systematic review on topoisomerase 1 inhibitors in MBC and found 22 prospective trials and three retrospective ones. No phase III trials were identified. Only one study was randomized, and generally studies were small. Response rates (RR) for irinotecan monotherapy varied from 5 to 23?%, whereas RRs for etirinotecan were 26-32?%. Only four trials on topotecan monotherapy were reported with RRs of 6-31?%. Combination therapy with irinotecan and various chemotherapeutics resulted in RRs ranging from 14 to 64?%, whereas irinotecan combined with biologic agents showed very limited effect. Topotecan was studied in combination with either another chemotherapeutic or a biologic agent in two trials, both studies failing to show any effect of topotecan. The most common grade 3 and 4 adverse events (AE) for irinotecan were neutropenia, diarrhea, and nausea/vomiting. The dosing schedule appears to affect the toxicity profile of the drug. Hematologic AEs are most frequently reported for topotecan. Conclusively, topotecan does not seem to be efficient in the treatment of MBC. Irinotecan seem to be effective in some patients previously treated with anthracyclines and taxanes. RRs of 23?% for irinotecan and 32?% for etirinotecan are comparable to some of the more commonly used treatments for MBC. However, a large proportion of patients do not respond, thus emphasizing the need for a biomarker predictive of response to irinotecan in order to introduce this drug as the standard treatment for MBC.
机译:用蒽环类药物和紫杉烷类药物治疗后,很少有确定的治疗转移性乳腺癌(MBC)的选择。尽管拓扑异构酶1抑制剂伊立替康,依立替康和托泊替康已用于MBC的临床试验,但从未引入该药物作为该疾病的标准治疗方法。我们对MBC中的拓扑异构酶1抑制剂进行了系统评价,发现22项前瞻性试验和3项回顾性试验。没有发现III期试验。只有一项研究是随机的,一般来说研究很小。伊立替康单药治疗的缓解率(RR)为5%至23 %%,而依立替康的缓解率为26-32%。仅报道了四项有关拓扑替康单药治疗的试验,其RRs为6-31%。伊立替康与各种化学疗法的联合治疗导致RRs范围为14%至64%,而伊立替康与生物制剂的结合则显示出非常有限的效果。在两项试验中对托泊替康与另一种化学治疗剂或生物制剂的组合进行了研究,但两项研究均未显示托泊替康具有任何作用。伊立替康最常见的3级和4级不良事件(AE)是中性粒细胞减少,腹泻和恶心/呕吐。给药时间表似乎会影响药物的毒性。血液学不良事件最常报道为拓扑替康。最后,托泊替康似乎在MBC的治疗中似乎无效。伊立替康似乎对以前用蒽环类药物和紫杉烷类药物治疗过的患者有效。伊立替康和依立替康的RRs为23%,与MBC的一些较常用治疗相当。但是,很大一部分患者没有反应,因此强调需要一种生物标志物来预测对伊立替康的反应,以便将该药物作为MBC的标准治疗方法。

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