拓扑异构酶I抑制剂在治疗间充质恶性肿瘤中的作用及其作为肉瘤特异性抗体-药物偶联物有效载荷的潜在未来应用。

IF 2 4区 医学 Q3 ONCOLOGY
Oncology Research and Treatment Pub Date : 2024-01-01 Epub Date: 2023-11-28 DOI:10.1159/000535491
Patrick Schöffski, Chao-Chi Wang, Morris Patrick Schöffski, Agnieszka Wozniak
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引用次数: 0

摘要

背景:拓扑异构酶I是一种通过超螺旋双链DNA的松弛在DNA复制和转录中起关键作用的酶。拓扑异构酶I抑制剂与拓扑异构酶I切割复合物结合,从而稳定其结构,防止DNA链的断裂,从而导致DNA损伤、细胞周期阻滞和细胞凋亡。各种拓扑异构酶I抑制剂已经在实体肿瘤中进行了评估,伊立替康和拓扑替康已被批准用于治疗上皮恶性肿瘤。这些药物都没有被批准用于肉瘤,这是一种罕见的实体肿瘤,对有效治疗的需求尚未得到满足。摘要:拓扑异构酶I抑制剂已在临床前研究中作为实体肿瘤的单药或联合用药进行了评估,其中一些包括观察到活性的肉瘤。评估拓扑异构酶I抑制剂治疗肉瘤的临床试验显示,单一疗法的疗效有限。拓扑异构酶I抑制剂与其他细胞毒性药物联合使用,已成为部分肉瘤亚型临床常规治疗的一部分。伊立替康/长春新碱/替莫唑胺等方案用于复发性横纹肌肉瘤,伊立替康/替莫唑胺和长春新碱/拓扑替康/环磷酰胺常用于难治性尤文氏肉瘤,拓扑替康/卡铂在晚期软组织肉瘤中显示出一定的活性。本文综述了拓扑异构酶I抑制剂治疗肉瘤的关键研究。拓扑异构酶I抑制剂目前也被评估为抗体-药物偶联物(adc)的“有效载荷”,允许靶向表达特定抗原的肿瘤细胞,并将抑制剂直接递送到肿瘤细胞中,具有增强治疗效果的潜力,同时将全身毒性降到最低。在这里,我们也提供了拓扑异构酶i - adc的简要概述。关键信息:拓扑异构酶I抑制剂是某些肉瘤系统性治疗的重要组成部分,具有强大的细胞毒性和药理学特性,使其成为肉瘤特异性adc发展的相关候选有效载荷。adc是一种基于抗体的靶向药物,允许将给定的药物有效和特异性地递送到肿瘤细胞。拓扑异构酶I- adc是一种新的靶向递送方法,可能有潜力改善拓扑异构酶I抑制剂治疗肉瘤的治疗指数,值得在各种间质恶性肿瘤中进行研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current Role of Topoisomerase I Inhibitors for the Treatment of Mesenchymal Malignancies and Their Potential Future Use as Payload of Sarcoma-Specific Antibody-Drug Conjugates.

Background: Topoisomerase I is an enzyme that plays a crucial part in DNA replication and transcription by the relaxation of supercoiled double-stranded DNA. Topoisomerase I inhibitors bind to the topoisomerase I cleavage complex, thereby stabilizing it and preventing the religation of the DNA strands, leading to DNA damage, cell cycle arrest, and apoptosis. Various topoisomerase I inhibitors have been evaluated in solid tumors, and irinotecan and topotecan have been approved for the treatment of epithelial malignancies. None of them have been approved for sarcoma, a diverse group of rare solid tumors with an unmet need for effective treatments.

Summary: Topoisomerase I inhibitors have been evaluated in preclinical studies as single agents or in combination in solid tumors, some of which have included sarcomas where activity was observed. Clinical trials evaluating topoisomerase I inhibitors for the treatment of sarcoma have shown limited efficacy as monotherapy. In combination with other cytotoxic agents, topoisomerase I inhibitors have become part of clinical routine in selected sarcoma subtypes. Regimens such as irinotecan/vincristine/temozolomide are used in relapsed rhabdomyosarcoma, irinotecan/temozolomide and vincristine/topotecan/cyclophosphamide are commonly given in refractory Ewing sarcoma, and topotecan/carboplatin showed some activity in advanced soft tissue sarcoma. This review provides an overview of key studies with topoisomerase I inhibitors for the treatment of sarcoma. Topoisomerase I inhibitors are currently also being assessed as "payloads" for antibody-drug conjugates (ADCs), allowing for the targeting of specific antigen-expressing tumor cells and the delivery of the inhibitor directly to the tumor cells with the potential of enhancing therapeutic efficacy while minimizing systemic toxicity. Here, we also provide a brief overview on topoisomerase I-ADCs.

Key message: Topoisomerase I inhibitors are an important component of some systemic therapies for selected sarcomas and have potent cytotoxic properties and pharmacological characteristics that make them relevant candidates as payloads for the development of sarcoma-specific ADCs. ADCs are antibody-based targeted agents allowing for efficient and specific delivery of a given drug to the tumor cell. Topoisomerase I-ADCs are a novel targeted delivery approach which may have the potential to improve the therapeutic index of topoisomerase I inhibitors in the treatment of sarcoma and warrants investigation in a broad variety of mesenchymal malignancies.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
84
期刊介绍: With the first issue in 2014, the journal ''Onkologie'' has changed its title to ''Oncology Research and Treatment''. By this change, publisher and editor set the scene for the further development of this interdisciplinary journal. The English title makes it clear that the articles are published in English – a logical step for the journal, which is listed in all relevant international databases. For excellent manuscripts, a ''Fast Track'' was introduced: The review is carried out within 2 weeks; after acceptance the papers are published online within 14 days and immediately released as ''Editor’s Choice'' to provide the authors with maximum visibility of their results. Interesting case reports are published in the section ''Novel Insights from Clinical Practice'' which clearly highlights the scientific advances which the report presents.
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