Kusama K, Ekimoto H, Ishii T, Okamoto K, Takahashi K
Research Laboratories, Nippon Kayaku Co., Ltd., Tokyo, Japan.
Gan To Kagaku Ryoho. 1991 May;18(6):959-63.
Antitumor activity by long term administration of low dose etoposide (ETP) was investigated in mice. In a spontaneous metastasis system, intraperitoneal consecutive administration of ETP at 2 mg/kg/day inhibited the number of metastatic nodules of Lewis lung carcinoma in the lung and showed a greater activity than 5-fluorouracil (5-FU) at the dose of 5 mg/kg/day. Alternative administration of ETP and 5-FU also exhibited the anti-metastatic activity, but mean survival time of mice was similar in all of these groups. Mean survival time of ETP-treated mice was prolonged when administration interval was shortened. Also in an artificial metastasis system, ETP inhibited metastasis of Lewis lung carcinoma in the lung. ETP showed antitumor activity against Colon adenocarcinoma 38 as 5-FU, when drugs were administered orally for long term, and the activity did not declined during the experimental period. These results suggest that long term administration of low dose ETP is clinically useful for post-operative and maintenance chemotherapy.
研究了长期给予低剂量依托泊苷(ETP)对小鼠的抗肿瘤活性。在自发转移模型中,以2mg/kg/天的剂量腹腔连续给予ETP可抑制Lewis肺癌肺转移结节的数量,且比5mg/kg/天剂量的5-氟尿嘧啶(5-FU)表现出更强的活性。交替给予ETP和5-FU也表现出抗转移活性,但所有这些组中小鼠的平均生存时间相似。当给药间隔缩短时,ETP治疗组小鼠的平均生存时间延长。在人工转移模型中,ETP也抑制了Lewis肺癌在肺中的转移。当长期口服给药时,ETP对结肠腺癌38表现出与5-FU相同的抗肿瘤活性,且在实验期间活性未下降。这些结果表明,长期给予低剂量ETP在临床术后及维持化疗中具有应用价值。