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抗体药物偶联物作为靶向治疗药物:我们已经做到了吗?对当前临床现状的批判性评价。

Antibody-drug conjugates as targeted therapies: Are we there yet? A critical review of the current clinical landscape.

机构信息

AbbVie Bioresearch Center, 100 Research Dr., Worcester, MA, 01605, USA.

AbbVie Inc., 1 North Waukegan Rd, North Chicago, IL, 60064, USA.

出版信息

Drug Discov Today Technol. 2020 Dec;37:13-22. doi: 10.1016/j.ddtec.2020.07.002. Epub 2020 Sep 29.

Abstract

Antibody-drug conjugates (ADCs) are targeted therapies with the expectation of broadened therapeutic window due to tumor-specific drug delivery. Recent approvals, including ADCs with a novel payload class, topoisomerase-1 inhibitors, generated renewed excitement in the field. We provide a critical review of approved and late-stage molecules, discuss strategies in solid tumors and ADCs outside oncology. Our pharmacokinetics-based assessment of targeting suggests that ADCs, especially in solid tumors, rely on additional mechanisms for efficacy including slow-release of the payload to the circulation at potentially efficacious levels. Further adjustments in the technology are needed to fulfill the promise of true targeted drug delivery.

摘要

抗体药物偶联物 (ADC) 是一种靶向治疗药物,由于其具有肿瘤特异性的药物递送作用,有望扩大治疗窗口。最近的批准,包括具有新型有效载荷类别的 ADC 和拓扑异构酶 1 抑制剂,为该领域带来了新的兴奋点。我们对已批准和晚期的分子进行了批判性的评估,讨论了在肿瘤学以外的实体瘤和 ADC 中的策略。我们基于药代动力学的靶向评估表明,ADC 尤其是在实体瘤中,需要额外的疗效机制,包括有效载荷在循环中以潜在有效的水平缓慢释放。需要进一步调整技术,以实现真正的靶向药物递送的承诺。

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