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OPTIM 试验:一项 III 期临床试验,评估一种携带 GM-CSF 的溶瘤单纯疱疹病毒治疗不可切除的 III 期或 IV 期黑色素瘤。

OPTIM trial: a Phase III trial of an oncolytic herpes virus encoding GM-CSF for unresectable stage III or IV melanoma.

机构信息

The Tumor Immunology Laboratory & Department of General Surgery, Rush University Medical Center, Chicago, IL 60612, USA.

出版信息

Future Oncol. 2010 Jun;6(6):941-9. doi: 10.2217/fon.10.66.

Abstract

There are few effective treatment options available for patients with advanced melanoma. An oncolytic herpes simplex virus type 1 encoding granulocyte macrophage colony-stimulating factor (GM-CSF; Oncovex(GM-CSF)) for direct injection into accessible melanoma lesions resulted in a 28% objective response rate in a Phase II clinical trial. Responding patients demonstrated regression of both injected and noninjected lesions highlighting the dual mechanism of action of Oncovex(GM-CSF) that includes both a direct oncolytic effect in injected tumors and a secondary immune-mediated anti-tumor effect on noninjected tumors. Based on these preliminary results a prospective, randomized Phase III clinical trial in patients with unresectable Stage IIIb or c and Stage IV melanoma has been initiated. The rationale, study design, end points and future development of the Oncovex(GM-CSF) Pivotal Trial in Melanoma (OPTIM) trial are discussed in this article.

摘要

对于晚期黑色素瘤患者,有效的治疗选择有限。一种复制型单纯疱疹病毒 1 编码粒细胞巨噬细胞集落刺激因子(GM-CSF;Oncovex[GM-CSF]),可直接注射到可触及的黑色素瘤病变部位,在 II 期临床试验中,客观缓解率为 28%。有反应的患者表现为注射和未注射病变的消退,突出了 Oncovex[GM-CSF]的双重作用机制,包括对注射肿瘤的直接溶瘤作用和对未注射肿瘤的继发免疫介导的抗肿瘤作用。基于这些初步结果,一项针对不可切除的 IIIb 或 c 期和 IV 期黑色素瘤患者的前瞻性、随机 III 期临床试验已经启动。本文讨论了 Oncovex[GM-CSF]在黑色素瘤中的关键性试验(OPTIM)的基本原理、研究设计、终点和未来发展。

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