化学病毒治疗:将化学治疗与溶瘤病毒治疗相结合。

IF 6.7
Oncolytic Virotherapy Pub Date : 2015-02-23 eCollection Date: 2015-01-01 DOI:10.2147/OV.S54780
Eike Binz, Ulrich M Lauer
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引用次数: 21

摘要

溶瘤病毒治疗近年来取得了重大进展,然而,广泛批准的病毒治疗仍然有限。这主要是由于目前可用的病毒疗法大多只在单一治疗的临床试验中进行测试(即,不与其他疗法联合),到目前为止只取得了很小的、通常临床上不显著的反应。鉴于病毒治疗的主要免疫治疗机制在一定程度上是时间依赖性的,并且快速生长的肿瘤因此只有很小的机会被及时捕获,因此假设联合伙伴的方案更有效。组合设置将有助于实现快速稳定甚至减少肿瘤肿块,同时为实现免疫(病毒)治疗成功提供足够的时间(数个月)。由于这个原因,病毒治疗与高遗传毒性方案(如化疗)的联合策略是主要的兴趣。许多临床试验将化疗和病毒治疗的概念结合在一起,但化疗和病毒治疗的最佳调度(最大限度地提高抗肿瘤效果,同时最大限度地降低重叠毒性的风险)仍然是一个主要挑战。因此,对已发表的和正在进行的I-III期试验的概述应该能提高我们对该领域当前挑战和未来发展的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chemovirotherapy: combining chemotherapeutic treatment with oncolytic virotherapy.

Chemovirotherapy: combining chemotherapeutic treatment with oncolytic virotherapy.

Oncolytic virotherapy has made significant progress in recent years, however, widespread approval of virotherapeutics is still limited. Primarily, this is due to the fact that currently available virotherapeutics are mostly tested in monotherapeutic clinical trials exclusively (ie, not in combination with other therapies) and so far have achieved only small and often clinically insignificant responses. Given that the predominantly immunotherapeutic mechanism of virotherapeutics is somewhat time-dependent and rapidly growing tumors therefore exhibit only minor chances of being captured in time, scenarios with combination partners are postulated to be more effective. Combinatory settings would help to achieve a rapid stabilization or even reduction of onset tumor masses while providing enough time (numerous months) for achieving immuno(viro)therapeutic success. For this reason, combination strategies of virotherapy with highly genotoxic regimens, such as chemotherapy, are of major interest. A number of clinical trials bringing the concepts of chemotherapy and virotherapy together have previously been undertaken, but optimal scheduling of chemovirotherapy (maximizing the anti-tumor effect while minimizing the risk of overlapping toxicity) still constitutes a major challenge. Therefore, an overview of published as well as ongoing Phase I-III trials should improve our understanding of current challenges and future developments in this field.

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