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针对癌症干细胞(CSC)的抗体药物偶联物(ADC)——仍有乐观的空间吗?

Antibody-Drug Conjugates (ADC) Against Cancer Stem-Like Cells (CSC)-Is There Still Room for Optimism?

作者信息

Marcucci Fabrizio, Caserta Carmelo Antonio, Romeo Elisabetta, Rumio Cristiano

机构信息

Department of Pharmacological and Biomolecular Sciences, University of Milan, Milan, Italy.

Fondazione per la Medicina Solidale, Reggio Calabria, Italy.

出版信息

Front Oncol. 2019 Mar 29;9:167. doi: 10.3389/fonc.2019.00167. eCollection 2019.

Abstract

Cancer stem-like cells (CSC) represent a subpopulation of tumor cells with peculiar functionalities that distinguish them from the bulk of tumor cells, most notably their tumor-initiating potential and drug resistance. Given these properties, it appears logical that CSCs have become an important target for many pharma companies. Antibody-drug conjugates (ADC) have emerged over the last decade as one of the most promising new tools for the selective ablation of tumor cells. Three ADCs have already received regulatory approval and many others are in different phases of clinical development. Not surprisingly, also a considerable number of anti-CSC ADCs have been described in the literature and some of these have entered clinical development. Several of these ADCs, however, have yielded disappointing results in clinical studies. This is similar to the results obtained with other anti-CSC drug candidates, including native antibodies, that have been investigated in the clinic. In this article we review the anti-CSC ADCs that have been described in the literature and, in the following, we discuss reasons that may underlie the failures in clinical trials that have been observed. Possible reasons relate to the biology of CSCs themselves, including their heterogeneity, the lack of strictly CSC-specific markers, and the capacity to interconvert between CSCs and non-CSCs; second, inherent limitations of some classes of cytotoxins that have been used for the construction of ADCs; third, the inadequacy of animal models in predicting efficacy in humans. We conclude suggesting some possibilities to address these limitations.

摘要

癌症干细胞(CSC)是肿瘤细胞中的一个亚群,具有独特的功能,使其有别于大多数肿瘤细胞,最显著的是其肿瘤起始潜能和耐药性。鉴于这些特性,CSC成为许多制药公司的重要靶点似乎是合乎逻辑的。抗体药物偶联物(ADC)在过去十年中已成为选择性消除肿瘤细胞最有前景的新工具之一。已有三种ADC获得监管批准,许多其他产品正处于不同阶段的临床开发中。不出所料,文献中也描述了相当数量的抗CSC ADC,其中一些已进入临床开发阶段。然而,其中一些ADC在临床研究中产生了令人失望的结果。这与在临床上研究过的其他抗CSC候选药物(包括天然抗体)所获得的结果类似。在本文中,我们回顾了文献中描述的抗CSC ADC,接下来,我们将讨论可能导致已观察到的临床试验失败的原因。可能的原因与CSC本身的生物学特性有关,包括其异质性、缺乏严格的CSC特异性标志物以及CSC与非CSC之间相互转化的能力;其次,用于构建ADC的某些细胞毒素类别的固有局限性;第三,动物模型在预测人类疗效方面的不足。我们在结论中提出了一些解决这些局限性的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61f4/6449442/04b449dcd348/fonc-09-00167-g0001.jpg

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