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可溶性 FAS 在预测晚期结直肠癌患者接受西妥昔单抗和伊立替康治疗获益中的作用。

Soluble FAS in the prediction of benefit from cetuximab and irinotecan for patients with advanced colorectal cancer.

机构信息

Medical Oncology Department, Hospital Clínic Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Catalonia, Spain.

出版信息

Med Oncol. 2013 Mar;30(1):428. doi: 10.1007/s12032-012-0428-0. Epub 2013 Jan 22.

Abstract

The FAS/FASL system, comprising membrane-bound (mFAS and mFASL) and soluble forms (sFAS and sFASL), has been related to apoptosis driven by chemotherapy administration. In vitro experiments show chemotherapy upregulating membrane-bound forms, leading to an increase of receptor availability (at 24-72 h) and favoring apoptosis. The regulatory effect of chemotherapy on sFAS in patients has never been explored prospectively in advanced colorectal cancer (ACRC). We performed a pharmacodynamic study to address sFAS/sFASL variation. A prospective phase II translational multicenter study was designed to evaluate progression-free rate (PFR) in patients with ACRC treated with irinotecan and cetuximab in third-line therapy. The effect of sFAS was studied in vitro in colorectal cancer cell lines. Our results showed that statistically significant changes were observed in sFAS at 24-72 h compared to baseline levels in the pharmacodynamic study. Of the 93 patients enrolled in the prospective study in third-line therapy with cetuximab-irinotecan, 85 were evaluated for sFAS/sFASL changes at 48 h. There was no difference in PFR at 4 months between patients with sFAS and sFASL changes. In vitro analysis showed that although LoVo cell lines were sensitive to oxaliplatin and fluorouracil due to modulation of sFAS and FAS, HT29 lines were not. In summary, chemotherapy regulates FAS soluble fractions in vitro and in vivo, but does not predict PFR in ACRC patients undergoing third-line therapy with the combination of cetuximab and irinotecan.

摘要

FAS/FASL 系统由膜结合形式(mFAS 和 mFASL)和可溶性形式(sFAS 和 sFASL)组成,与化疗药物诱导的细胞凋亡有关。体外实验表明,化疗药物上调膜结合形式,导致受体可用性增加(24-72 小时),并促进细胞凋亡。在晚期结直肠癌(ACRC)患者中,化疗药物对 sFAS 的调节作用从未在前瞻性研究中探讨过。我们进行了一项药效学研究来探讨 sFAS/sFASL 的变化。设计了一项前瞻性 II 期转化多中心研究,以评估在三线治疗中接受伊立替康和西妥昔单抗治疗的 ACRC 患者的无进展率(PFR)。我们在结直肠癌细胞系中进行了 sFAS 的体外研究。我们的结果表明,在药效学研究中,与基线水平相比,sFAS 在 24-72 小时观察到统计学上的显著变化。在三线治疗中接受西妥昔单抗-伊立替康的 93 例前瞻性研究患者中,85 例患者在 48 小时时评估了 sFAS/sFASL 的变化。在 4 个月时,sFAS 和 sFASL 变化患者的 PFR 无差异。体外分析表明,尽管 LoVo 细胞系由于 sFAS 和 FAS 的调节而对奥沙利铂和氟尿嘧啶敏感,但 HT29 系却不是。总之,化疗在体外和体内调节 FAS 可溶性部分,但不能预测接受西妥昔单抗和伊立替康联合治疗的三线治疗 ACRC 患者的 PFR。

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