Kato T, Tamakawa Y, Unno K
Gan To Kagaku Ryoho. 1984 Apr;11(4):798-805.
Mitomycin C microcapsules (MMC-mc), which were developed as a novel drug carrier, have proved to exert a potential therapeutic effect due to both microinfarction and sustained drug action (chemo-embolization), when infused into a tumor supplying arteries. Experimental studies have demonstrated that chemo-embolization with MMC-mc produces a definitely marked and extensive cytotoxicity in target tissues as compared with traditional arterial chemotherapy, embolization or combination of both. Sixty-seven patients with advanced hepatoma were treated with intra-arterial MMC-mc during the period from 1978 to 1982. Since the majority of patients were in far advanced stages, 56 patients received only single or two infusions of an average dose of 20 mg MMC-mc. Objective tumor reduction greater than 25% in area was observed in 22 (40%) of measurable 55 tumors. Elevated serum alpha-fetoprotein in 26 patients improved in 22 (85%). Relative survival rates of 59 patients without distant metastasis were 64% at 3 months, 49% at 6 months and 26% at 12 months. Side effects such as bone marrow depression, decreased liver function, fever, anorexia, pain and infection were experienced in 9 to 39%, but the majority of them were mild and controllable. Our preliminary experience suggests that MMC-mc can be effectively used in treatment of liver tumors as a palliative but also as a preoperative measure. Further clinical trials including controlled study may well demonstrate the advantages of MMC-mc.
丝裂霉素C微胶囊(MMC-mc)作为一种新型药物载体而被研发,当注入肿瘤供血动脉时,已证明其因微梗死和持续的药物作用(化学栓塞)而发挥潜在治疗效果。实验研究表明,与传统动脉化疗、栓塞或两者联合相比,MMC-mc化学栓塞在靶组织中产生明显且广泛的细胞毒性。1978年至1982年期间,67例晚期肝癌患者接受了动脉内MMC-mc治疗。由于大多数患者处于晚期,56例患者仅接受了单次或两次平均剂量为20mg的MMC-mc输注。在可测量的55个肿瘤中,22个(40%)观察到客观肿瘤面积缩小超过25%。26例血清甲胎蛋白升高的患者中,22例(85%)有所改善。59例无远处转移患者的相对生存率在3个月时为64%,6个月时为49%,12个月时为26%。9%至39%的患者出现骨髓抑制、肝功能下降、发热、厌食、疼痛和感染等副作用,但大多数副作用较轻且可控。我们的初步经验表明,MMC-mc可有效用于治疗肝肿瘤,作为一种姑息性治疗手段,也可作为术前措施。包括对照研究在内的进一步临床试验很可能会证明MMC-mc的优势。