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单药Val-boroPro(他拉泊司他)抑制转移性结直肠癌患者成纤维细胞活化蛋白的II期试验。

Phase II trial of single agent Val-boroPro (Talabostat) inhibiting Fibroblast Activation Protein in patients with metastatic colorectal cancer.

作者信息

Narra Kalyani, Mullins Stefanie R, Lee Hyung-Ok, Strzemkowski-Brun Brenda, Magalong Kimberly, Christiansen Victoria J, McKee Patrick A, Egleston Brian, Cohen Steven J, Weiner Louis M, Meropol Neal J, Cheng Jonathan D

机构信息

Department of Medical Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111, USA.

出版信息

Cancer Biol Ther. 2007 Nov;6(11):1691-9. doi: 10.4161/cbt.6.11.4874. Epub 2007 Aug 14.

Abstract

PURPOSE

Fibroblast Activation Protein (FAP) is a tumor fibroblast protease that has been shown to potentiate colorectal cancer growth. The clinical impact of FAP inhibition was tested using Val-boroPro (Talabostat), the first clinical inhibitor of FAP enzymatic activity, in a phase II study of patients with metastatic colorectal cancer.

METHODS

Patients with metastatic colorectal cancer who had previously received systemic chemotherapies were treated with single agent Val-boroPro 200 microg p.o. BID continuously. Eligibility included measurable disease, performance status of 0 to 2, and adequate organ function. Laboratory correlates evaluated the pharmacodynamic effects of Val-boroPro on FAP enzymatic function in the peripheral blood.

RESULTS

Twenty-eight patients (median age 62; 12 males, 16 females) were enrolled in this study. There were no objective responses. Six of 28 (21%) patients had stable disease for a median of 25 weeks (range 11-38 weeks). Laboratory analysis demonstrated significant, although incomplete inhibition of FAP enzymatic activity in the peripheral blood.

CONCLUSION

This phase II trial of Val-boroPro demonstrated minimal clinical activity in patients with previously treated metastatic colorectal cancer. However it provides the initial proof-of-concept that physiologic inhibition of FAP activity can be accomplished in patients with colorectal cancer, and lays the groundwork for future studies targeting the tumor stroma.

摘要

目的

成纤维细胞活化蛋白(FAP)是一种肿瘤成纤维细胞蛋白酶,已被证明可促进结直肠癌生长。在一项转移性结直肠癌患者的II期研究中,使用首个FAP酶活性临床抑制剂Val-boroPro(他拉泊司他)测试了FAP抑制的临床影响。

方法

先前接受过全身化疗的转移性结直肠癌患者接受单药Val-boroPro 200微克口服,每日两次,持续给药。入选标准包括可测量的疾病、0至2的体能状态以及足够的器官功能。实验室相关指标评估了Val-boroPro对外周血中FAP酶功能的药效学作用。

结果

28例患者(中位年龄62岁;男性12例,女性16例)入组本研究。无客观缓解。28例患者中有6例(21%)疾病稳定,中位持续时间为25周(范围11 - 38周)。实验室分析表明,外周血中FAP酶活性受到显著但不完全的抑制。

结论

Val-boroPro的这项II期试验在先前治疗过的转移性结直肠癌患者中显示出最小的临床活性。然而,它提供了初步的概念验证,即结直肠癌患者可以实现FAP活性的生理性抑制,并为未来针对肿瘤基质的研究奠定了基础。

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