Kast Richard E, Ramiro Susana, Lladó Sandra, Toro Salvador, Coveñas Rafael, Muñoz Miguel
IIAIGC Headquarters, Dean of Studies, 22 Church St, Burlington, VT, 05401, USA.
Research Laboratory on Neuropeptides (IBIS), Virgen del Rocío University Hospital, Avda. Manuel Siurot s/n, 41013, Seville, Spain.
J Neurooncol. 2016 Feb;126(3):425-31. doi: 10.1007/s11060-015-1996-6. Epub 2015 Nov 24.
In the effort to find better treatments for glioblastoma we tested several currently marketed non-chemotherapy drugs for their ability to enhance the standard cytotoxic drug currently used to treat glioblastoma- temozolomide. We tested four antiviral drugs- acyclovir, cidofovir, maraviroc, ritonavir, and an anti-emetic, aprepitant. We found no cytotoxicity of cidofovir and discussed possible reasons for discrepancy from previous findings of others. We also found no cytotoxicity from acyclovir or maraviroc also in contradistinction to predictions. Cytotoxicity to glioma cell line GAMG for temozolomide alone was 14%, aprepitant alone 7%, ritonavir alone 14%, while temozolomide + aprepitant was 19%, temozolomide + ritonavir 34%, ritonavir + aprepitant 64 %, and all three, temozolomide + ritonavir + aprepitant 78%. We conclude that a remarkable synergy exists between aprepitant and ritonavir. Given the long clinical experience with these two well-tolerated drugs in treating non-cancer conditions, and the current median survival of glioblastoma of 2 years, a trial is warranted of adding these two simple drugs to current standard treatment with temozolomide.
为了找到治疗胶质母细胞瘤的更好方法,我们测试了几种目前市场上销售的非化疗药物,看它们是否有能力增强目前用于治疗胶质母细胞瘤的标准细胞毒性药物——替莫唑胺的疗效。我们测试了四种抗病毒药物——阿昔洛韦、西多福韦、马拉维若、利托那韦,以及一种止吐药阿瑞匹坦。我们发现西多福韦没有细胞毒性,并讨论了与其他人先前研究结果存在差异的可能原因。我们还发现阿昔洛韦或马拉维若也没有细胞毒性,这也与预测结果相反。单独使用替莫唑胺对胶质瘤细胞系GAMG的细胞毒性为14%,单独使用阿瑞匹坦为7%,单独使用利托那韦为14%,而替莫唑胺+阿瑞匹坦为19%,替莫唑胺+利托那韦为34%,利托那韦+阿瑞匹坦为64%,三种药物联合使用,即替莫唑胺+利托那韦+阿瑞匹坦为78%。我们得出结论,阿瑞匹坦和利托那韦之间存在显著的协同作用。鉴于这两种耐受性良好的药物在治疗非癌症疾病方面有着长期的临床经验,且目前胶质母细胞瘤的中位生存期为2年,有必要进行一项试验,将这两种简单药物添加到目前使用替莫唑胺的标准治疗方案中。