Sugimachi K, Maehara Y, Akazawa K, Kondo Y, Kunii Y, Kitamura M, Yamaoka H, Takahashi Y, Kito T, Katou M
Department of Surgery II, Kyushu University, Fukuoka, Japan.
Cancer Chemother Pharmacol. 1994;33(5):366-70. doi: 10.1007/BF00686264.
We studied the effects on survival time of postoperative immuno-chemotherapy, including the streptococcal preparation OK-432, in patients with gastric cancer and synchronous peritoneal dissemination. The patients were prospectively randomized and a valid statistical assessment could be made for 109. Patients randomized to group B received therapy that is widely used in Japan to treat patients with gastric cancer: mitomycin C (MMC) and UFT, a combination of tegafur and uracil in a molar ratio of 1:4, for 1 year. Patients randomized to group A received the same drugs as were given to group B patients plus OK-432 i.p. for 7 days, beginning on postoperative day 0, and OK-432 by intradermal injection for 1 year, at 2-week intervals. There were no differences between the two groups in any known prognostic factor or in the dose of any drug administered except for OK-432. There was no difference in the toxicity rate between the groups. In this negative trial, there was no improvement in survival time with the addition of OK-432 to MMC and UFT for patients with gastric cancer and peritoneal dissemination.
我们研究了术后免疫化疗(包括链球菌制剂OK-432)对胃癌伴同步腹膜播散患者生存时间的影响。患者被前瞻性随机分组,109例患者可进行有效统计评估。随机分为B组的患者接受日本广泛用于治疗胃癌患者的疗法:丝裂霉素C(MMC)和UFT(替加氟与尿嘧啶以1:4摩尔比的组合),为期1年。随机分为A组的患者接受与B组患者相同的药物,再加上术后第0天开始腹腔注射OK-432共7天,之后皮内注射OK-432共1年,每隔2周注射一次。除OK-432外,两组在任何已知预后因素或所给任何药物剂量方面均无差异。两组之间的毒性率无差异。在这项阴性试验中,对于胃癌和腹膜播散患者,在MMC和UFT基础上加用OK-432并未改善生存时间。