An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy.

An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy.
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DOI:
10.3390/molecules26195847
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发表时间:
2021-09-27
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
通讯作者:
Kavianinia I
Kavianinia I
中科院分区:
其他
文献类型:
--
作者:
Tong JTW;Harris PWR;Brimble MA;Kavianinia I

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用于癌症治疗的大量新兴抗体药物偶联物(ADC)带来了显着的市场“繁荣”,引起了全世界的关注。尽管 ADC 给研究人员带来了巨大挑战,特别是在确定抗体、接头和有效负载的合适组合方面,但截至 2021 年 9 月,已有 11 种 ADC 获得 FDA 批准,其中 8 种自 2017 年以来就获得批准。尽管出现了 COVID-19 大流行,但对这种治疗方法的乐观情绪是显而易见的,2020 年对于 ADC 领域的交易和合作伙伴关系来说是具有里程碑意义的一年,这表明大型制药公司仍然表现出浓厚的兴趣。在此,我们通过重点关注 FDA 批准的 ADC 的功能来回顾人们对 ADC 的热情,并就该领域的发展方向提出一些想法。
The large number of emerging antibody-drug conjugates (ADCs) for cancer therapy has resulted in a significant market ‘boom’, garnering worldwide attention. Despite ADCs presenting huge challenges to researchers, particularly regarding the identification of a suitable combination of antibody, linker, and payload, as of September 2021, 11 ADCs have been granted FDA approval, with eight of these approved since 2017 alone. Optimism for this therapeutic approach is clear, despite the COVID-19 pandemic, 2020 was a landmark year for deals and partnerships in the ADC arena, suggesting that there remains significant interest from Big Pharma. Herein we review the enthusiasm for ADCs by focusing on the features of those approved by the FDA, and offer some thoughts as to where the field is headed.
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