Asakawa M, Maekawa T, Umeda M, Sakamoto W, Senju M, Iseki T, Nakatani T, Tanaka H, Horii A, Yamamoto K
Department of Urology, Osaka City University Medical School.
Hinyokika Kiyo. 1989 Aug;35(8):1451-5.
A clinical trial using human lymphoblastoid interferon (HLBI) was done on patients with advanced renal cell carcinoma to compare the efficacy of monotherapy with that of combined administration with a 5-fluorouracil (FU) agent. A total of 24 patients with definitely diagnosed advanced renal cell carcinoma were enrolled in either of the HLBI treatments. Principally, the daily intramuscular injection of 3 million units of HLBI was done for 4 consecutive days and thereafter followed by twice of weekly injections. The combined agent used in the present study was 300 or 600 mg of 5-fluorouracil agent given orally. The efficacy of HLBI was evaluated according to direct assessment standard of chemotherapy to a solid tumor expelled by the committee of Japanese health and welfare ministry. Of 11 patients who received monotherapy, 3 had a partial response rate of 27.3 percent. While only one of 13 patients having received combined HLBI administration with oral 5-FU tablets showed a partial response with a response rate of 7.7 percent. A total of 4 patients partially responded to either HLBI treatment with a subsequent response of 16.7 percent. Partial response implied reduction of lung metastatic foci in 3 patients and primary lesion in one patient. There was observed untoward fever-up in all patients with HLBI injections which was relieved with acquired tachyphylaxis owing to repeated injections. Otherwise minimal adverse effects were temporary elevation of liver transaminase in 4 and leucopenia in 2 patients during the HLBI treatment both of which eventually returned to the normal level without discontinuation of HLBI therapy.(ABSTRACT TRUNCATED AT 250 WORDS)
一项使用人淋巴母细胞干扰素(HLBI)的临床试验在晚期肾细胞癌患者中进行,以比较单药治疗与联合5-氟尿嘧啶(FU)药物给药的疗效。共有24例确诊为晚期肾细胞癌的患者参与了HLBI治疗中的任一种。原则上,每天肌肉注射300万单位的HLBI,连续注射4天,之后每周注射两次。本研究中使用的联合药物是口服300或600毫克的5-氟尿嘧啶药物。根据日本厚生省委员会制定的实体瘤化疗直接评估标准对HLBI的疗效进行评估。在接受单药治疗的11例患者中,3例部分缓解率为27.3%。而在接受HLBI与口服5-FU片剂联合给药的13例患者中,只有1例出现部分缓解,缓解率为7.7%。共有4例患者对HLBI治疗中的任一种出现部分缓解,随后的缓解率为16.7%。部分缓解意味着3例患者肺部转移灶缩小,1例患者原发灶缩小。在所有接受HLBI注射的患者中均观察到发热现象,由于反复注射产生快速耐受而缓解。此外,在HLBI治疗期间,有4例患者出现肝转氨酶暂时升高,2例患者出现白细胞减少,这些不良反应均为轻微,最终均在未中断HLBI治疗的情况下恢复至正常水平。(摘要截断于250字)