Hartley-Asp B, Vukanovic J, Joseph I B, Strandgården K, Polacek J, Isaacs J T
Pharmacia & Upjohn, Lund, Sweden.
J Urol. 1997 Sep;158(3 Pt 1):902-7. doi: 10.1097/00005392-199709000-00069.
Escape from "castration inhibition," be it surgical or chemically induced, is still the major problem in prostate cancer treatment. New agents that can be given as adjuvant therapy are needed. Linomide has demonstrated both anti-tumor and anti-angiogenic activity with little toxicity in the Dunning R-3327 rat prostate tumor system. Therefore it was deemed essential to study the efficacy of this drug in the adjuvant situation.
Linomide, roquinimex, was administered 3 times a week i.p. alone or in conjunction with castration to rats bearing the Dunning R-3327 PAP rat prostate tumor and its effect on tumor growth analyzed. Similar experiments, in which Linomide 25 mg./kg./day was given in the drinking water were carried out in rats with the Dunning R-3327 G tumor. The effect of treatment on blood vessel density and blood flow in the tumor was also assessed using an image analysis system.
Linomide, 2.5 & 40 mg./kg., administered from the day after castration inhibited the regrowth of the Dunning R-3327 PAP tumors In addition, Linomide 40 mg./kg. administered after tumor regrowth occurred following castration(week 10) inhibited further tumor growth. Inhibition of tumor regrowth after castration was also found in the Dunning G tumor. When Linomide treatment was stopped regrowth of the tumors occurred, either in the same animal or on transplantation to new intact hosts, demonstrating that the tumor cells were still viable. Tumor blood vessel density was decreased both after castration and Linomide treatment alone, 40 and 32% respectively. On combination of castration and Linomide a 60% decrease in blood vessel density was found. This was significantly different from either of the two treatments given alone. The enhancement on combining castration and Linomide was confirmed by a further decrease in blood flow, from 19 and 22 to 12 ml. per minute/gm. tissue respectively.
Linomide, an anti-angiogenic drug, inhibits escape from "castration inhibition".
克服手术或化学诱导的“去势抑制”,仍是前列腺癌治疗中的主要问题。需要可作为辅助治疗的新药物。在邓宁R-3327大鼠前列腺肿瘤系统中,利诺米德已显示出抗肿瘤和抗血管生成活性,且毒性很小。因此,研究该药物在辅助治疗中的疗效被认为至关重要。
利诺米德(罗喹美克)每周腹腔注射3次,单独给药或与去势联合应用于携带邓宁R-3327 PAP大鼠前列腺肿瘤的大鼠,并分析其对肿瘤生长的影响。在携带邓宁R-3327 G肿瘤的大鼠中进行了类似实验,其中利诺米德以25毫克/千克/天的剂量加入饮用水中给药。还使用图像分析系统评估了治疗对肿瘤血管密度和血流的影响。
去势后第二天给予2.5毫克/千克和40毫克/千克的利诺米德可抑制邓宁R-3327 PAP肿瘤的再生长。此外,去势后(第10周)肿瘤再生长发生后给予40毫克/千克的利诺米德可抑制肿瘤进一步生长。在邓宁G肿瘤中也发现了去势后对肿瘤再生长的抑制作用。当停止利诺米德治疗时,肿瘤在同一动物体内或移植到新的完整宿主后均会再生长,表明肿瘤细胞仍然存活。去势和单独使用利诺米德治疗后,肿瘤血管密度分别降低了40%和32%。去势与利诺米德联合应用时,血管密度降低了60%。这与单独给予的两种治疗方法均有显著差异。联合去势和利诺米德后血流进一步降低,分别从每分钟19毫升和22毫升降至每分钟12毫升/克组织,证实了联合应用的增强效果。
抗血管生成药物利诺米德可抑制“去势抑制”的逃逸。