Belli Valentina, Sforza Vincenzo, Cardone Claudia, Martinelli Erika, Barra Giusi, Matrone Nunzia, Napolitano Stefania, Morgillo Floriana, Tuccillo Concetta, Federico Alessandro, Dallio Marcello, Loguercio Carmelina, Gravina Antonietta Gerarda, De Palma Raffaele, Ciardiello Fortunato, Troiani Teresa
Oncologia Medica, Dipartimento di Internistica Clinica e Sperimentale "F. Magrassi", Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
Medicina Interna, Dipartimento di Internistica Clinica e Sperimentale "F. Magrassi", Università degli Studi della Campania "Luigi Vanvitelli", Napoli, Italy.
Oncotarget. 2017 Aug 7;8(40):68305-68316. doi: 10.18632/oncotarget.20054. eCollection 2017 Sep 15.
Regorafenib, an oral multikinase inhibitor, has demonstrated survival benefit in metastatic colorectal cancer (mCRC) patients that have progressed after all standard therapies. However, novel strategies to improve tolerability and enhance anti-cancer efficacy are needed.
We have evaluated the effects of regorafenib in combination with silybin, a biologically active component extracted from the seeds of Silybum marianum, in a panel of human colon cancer cells. Furthermore, we have prospectively treated a cohort of 22 refractory mCRC patients with regorafenib plus silybin.
Treatment with regorafenib determined a dose-dependent growth inhibition whereas treatment with silybin had no anti-proliferative effects among all cancer cells tested. The combined treatment with regorafenib and silybin induced synergistic anti-proliferative and apoptotic effects by blocking PI3K/AKT/mTOR intracellular pathway. Moreover, combined treatment with regorafenib and silybin increased the production of reactive oxygen species levels within cells. In an exploratory proof of concept clinical study in a cohort of 22 mCRC patients after failure of all standard therapies, the clinical activity of regorafenib in combination with silybin was assessed. A median progression-free survival of 10.0 months and a median overall survival of 17.6 months were observed in these patients. These results suggest that the combined treatment potentially increases the clinical efficacy of regorafenib. Moreover, due to its anti-oxidative properties, silybin could protect patients from drug-induced liver damages, allowing to continue an effective anti-cancer therapy.
The present study suggests that silybin in combination with regorafenib is a promising strategy for treatment of metastatic colorectal patients.
瑞戈非尼是一种口服多激酶抑制剂,已在所有标准治疗后病情进展的转移性结直肠癌(mCRC)患者中显示出生存获益。然而,需要新的策略来提高耐受性并增强抗癌疗效。
我们评估了瑞戈非尼与水飞蓟宾(从水飞蓟种子中提取的一种生物活性成分)联合使用对一组人结肠癌细胞的影响。此外,我们前瞻性地对22例难治性mCRC患者采用瑞戈非尼加 水飞蓟宾进行治疗。
瑞戈非尼治疗可导致剂量依赖性生长抑制,而水飞蓟宾治疗在所有测试癌细胞中均无抗增殖作用。瑞戈非尼与水飞蓟宾联合治疗通过阻断PI3K/AKT/mTOR细胞内途径诱导协同抗增殖和凋亡作用。此外,瑞戈非尼与水飞蓟宾联合治疗增加了细胞内活性氧水平的产生。在一项针对22例所有标准治疗均失败的mCRC患者的探索性概念验证临床研究中,评估了瑞戈非尼与水飞蓟宾联合使用的临床活性。这些患者的中位无进展生存期为10.0个月,中位总生存期为17.6个月。这些结果表明联合治疗可能会提高瑞戈非尼的临床疗效。此外,由于其抗氧化特性,水飞蓟宾可以保护患者免受药物性肝损伤,从而能够继续进行有效的抗癌治疗。
本研究表明,水飞蓟宾与瑞戈非尼联合使用是治疗转移性结直肠癌患者的一种有前景的策略。