Herr H W, Warrel R P, Burchenal J H
Urology. 1986 Dec;28(6):508-11. doi: 10.1016/0090-4295(86)90154-8.
Both alpha-difluoromethyl ornithine (DFMO) and methylglyoxal bis (guanylhydrazone) (MGBG) inhibit sequential enzymatic reactions in the pathway of polyamine biosynthesis. Since polyamines may be important factors in proliferation of cancer cells and DFMO combined with MGBG has shown synergistic cytotoxicity in an experimental prostatic tumor, we evaluated these agents in phase I clinical trial involving 5 patients with advanced, hormone-resistant prostatic cancer. Toxic reaction to combined DFMO and MGBG was dose-related and included nausea, fatigue, and diarrhea especially with the higher doses of MGBG. No therapeutic responses of significance were seen, but toxicity precluded adequate evaluation. Future Phase II studies of combined DFMO and MGBG should employ low, nontoxic doses of MGBG combined with evaluation of polyamine levels and inhibition of polyamine enzymatic activity to minimize toxicity.
α-二氟甲基鸟氨酸(DFMO)和甲基乙二醛双(脒腙)(MGBG)均可抑制多胺生物合成途径中的连续酶促反应。由于多胺可能是癌细胞增殖的重要因素,且DFMO与MGBG联合使用在实验性前列腺肿瘤中已显示出协同细胞毒性,因此我们在一项I期临床试验中对5例晚期激素抵抗性前列腺癌患者评估了这些药物。DFMO与MGBG联合使用的毒性反应与剂量相关,包括恶心、疲劳和腹泻,尤其是在使用较高剂量MGBG时。未观察到明显的治疗反应,但毒性妨碍了充分评估。未来DFMO与MGBG联合使用的II期研究应采用低剂量、无毒的MGBG,并结合多胺水平评估和多胺酶活性抑制,以尽量减少毒性。