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Navigating the clinical development landscape for oncolytic viruses and other cancer therapeutics: no shortcuts on the road to approval.

机译:浏览溶瘤病毒和其他癌症治疗剂的临床发展前景:获得批准的道路上没有捷径。

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Chemotherapy remains a common mode of anticancer treatment even though in most cancer indications the therapeutic approach is not effective and ultimately associated with the onset of chemoresistance. A better understanding of genetic differences in tumors ushered in the era of targeted therapy which has revolutionized the treatment of certain cancer types. However, generally targeted therapies are only cytostatic and a proportion of the patient population may be non-responsive to targeted therapy due to mutations of other genes in the same pathway (e.g. ras mutations in patients with colorectal cancer treated with EGFR targeted therapy). Therefore, there exists a need for a radically new approach to cancer therapy. Oncolytic viruses (OVs) possess many properties of an ideal cancer therapeutic. OVs are cytotoxic and target cancers via multiple mechanisms of action while at the same time exploiting validated genetic pathways known to be dysregulated in many cancers. Indeed, promising safety and efficacy data has emerged from Phase 1 and Phase 2 trials with diverse OVs (e.g. JX-594, a targeted oncolytic poxvirus). Though the field has lagged behind with pivotal, randomized Phase 3 trials, these are currently being initiated for a number of OVs. In addition, the field must ensure a continued clinical development of newly developed OVs; a strategy for the clinical development of novel cancer therapeutics is outlined.
机译:即使在大多数癌症适应症中,化学疗法仍然是抗癌治疗的一种常见方式,但该治疗方法并不有效,最终与化学抗药性的发作有关。对肿瘤遗传差异的更好理解迎来了靶向治疗时代,该时代彻底变革了某些癌症类型的治疗方法。然而,通常靶向疗法仅是细胞抑制疗法,并且由于同一途径中其他基因的突变(例如,EGFR靶向疗法治疗的结直肠癌患者中的ras突变),一部分患者群体可能对靶向疗法无反应。因此,需要一种全新的癌症治疗方法。溶瘤病毒(OVs)具有理想癌症治疗剂的许多特性。 OVs具有多种细胞毒性作用,并通过多种作用机制靶向癌症,同时利用已知在许多癌症中表达异常的已验证遗传途径。确实,具有多种OV的1期和2期试验(例如JX-594,一种靶向溶瘤性痘病毒)已经出现了有希望的安全性和有效性数据。尽管该领域在关键的,随机的3期临床试验方面落后于其他研究,但目前这些试验已在许多OVs中启动。此外,该领域必须确保新开发的OV的持续临床开发;概述了新型癌症治疗剂临床开发的策略。

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