Taguchi T, Kondo M, Tanikawa K, Nakamura H, Okawa T, Ogawa N
1st Dept. of Internal Medicine, Kyoto Prefectural University of Medicine.
Gan To Kagaku Ryoho. 1993 Oct;20(13):2027-35.
In the present comparative study, we examined an intra-arterial chemotherapy combined with PJ-203 in 60 patients with liver cancer metastasized from gastrointestinal cancer, using an intra-arterial chemotherapy alone as the control. Sixty patients who had been registered by telephone contact were allocated to groups either treated with the intra-arterial chemotherapy alone or with PJ-203 combined, 30 patients each. Mitomycin C was used as the anticancer drug and given at the dose of 8mg/m2 per time. The dose of PJ-203 was 600 +/- 300 mg as degradable starch microspheres. A significantly higher response rate (CR + PR/complete cases) of 54.5% (p = 0.021) was noted in the PJ-203 combined group, as compared to 20.0% for the control group. The 50% survival duration was 282 and 214 days for the PJ-203 combined group and control group, respectively, with no significant difference being noted between the two groups. Principal adverse reactions such as pain, gastrointestinal symptoms and fever were statistically more frequent (p < 0.01) in the PJ-203 combined group than in the control group. Among the abnormal laboratory values, the incidence of decreased leukocytes was significantly lower (p = 0.022) in the PJ-203 combined group than in the control group. One of the patients concomitantly treated with PJ-203 died of drug-induced hepatitis, which was probably attributed to mitomycin C. However, overall utility assessment was significantly better (p = 0.002) in the PJ-203 combined group.
在本比较研究中,我们对60例胃肠道癌肝转移患者采用单纯动脉内化疗作为对照,研究动脉内化疗联合PJ - 203的疗效。通过电话联系登记的60例患者被分为单纯动脉内化疗组或联合PJ - 203组,每组30例。丝裂霉素C用作抗癌药物,每次剂量为8mg/m²。PJ - 203作为可降解淀粉微球的剂量为600±300mg。与对照组20.0%相比,PJ - 203联合组的缓解率(CR + PR/总病例数)显著更高,为54.5%(p = 0.021)。PJ - 203联合组和对照组的50%生存时间分别为282天和214天,两组之间无显著差异。PJ - 203联合组中疼痛、胃肠道症状和发热等主要不良反应在统计学上比对照组更频繁(p < 0.01)。在实验室异常值中,PJ - 203联合组白细胞减少的发生率显著低于对照组(p = 0.022)。1例同时接受PJ - 203治疗的患者死于药物性肝炎,这可能归因于丝裂霉素C。然而,PJ - 203联合组的总体效用评估显著更好(p = 0.002)。