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Impact, mechanisms, and novel chemotherapy strategies for overcoming resistance to anthracyclines and taxanes in metastatic breast cancer.

机译:在转移性乳腺癌中克服对蒽环类和紫杉烷类药物的耐药性的影响,机制和新颖的化学疗法策略。

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摘要

Despite advances in treatment of patients with metastatic breast cancer (MBC), prognosis remains poor and median survival is 2-3 years. Resistance to antineoplastics mediated by many factors, potentially including overexpression of drug efflux proteins or altered beta-tubulin isotype expression limits the effectiveness of MBC chemotherapy. Capecitabine, approved for anthracycline- and taxane-resistant MBC, has produced modest responses, highlighting the need for more effective treatments for MBC resistant to multiple chemotherapeutic agents. Agents with potential to reverse drug resistance have not proven effective. Albumin-bound paclitaxel is a formulation that may enhance delivery to tumor tissues. Conversely, ixabepilone, an epothilone analog, has been reported to have lower susceptibility to at least some mechanisms of tumor resistance and clinical activity in resistant/refractory MBC. The topoisomerase-I inhibitor irinotecan also has low cross-resistance with other antineoplastics, and has shown some activity against refractory MBC. Development of new agents and identification of genetic biomarkers in translational studies promise to improve management of patients with resistant/refractory breast cancer.
机译:尽管转移性乳腺癌(MBC)患者的治疗取得了进步,但预后仍然很差,中位生存期为2-3年。由许多因素介导的对抗肿瘤药的耐药性,可能包括药物外排蛋白的过表达或β-微管蛋白同种型表达的改变,限制了MBC化疗的有效性。卡培他滨已被批准用于耐蒽环类和紫杉烷类的MBC,但其反应却不明显,这表明需要针对多种化学治疗剂的MBC更有效的治疗方法。具有逆转耐药性潜力的药物尚未证明有效。结合白蛋白的紫杉醇是可以增强向肿瘤组织的递送的制剂。相反,据报道,埃博霉素的类似物ixabepilone对耐药/难治性MBC的至少一些肿瘤耐药性和临床活性机制的敏感性较低。拓扑异构酶-I抑制剂伊立替康与其他抗肿瘤药的交叉耐药性也较低,并且对难治性MBC表现出一定的活性。在转化研究中新药的开发和遗传生物标记的鉴定有望改善对耐药/难治性乳腺癌患者的管理。

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