Man Shan, Bocci Guido, Francia Giulio, Green Shane K, Jothy Serge, Hanahan Douglas, Bohlen Peter, Hicklin Daniel J, Bergers Gabriele, Kerbel Robert S
Departments of Medical Biophysics, Sunnybrook and Women's College Health Sciences Centre, University of Toronto, 2075 Bayview Avenue, Toronto, Ontario, M4N 3M5 Canada.
Cancer Res. 2002 May 15;62(10):2731-5.
A number of recent preclinical studies have sparked interest in the concept of exploiting conventional chemotherapeutic drugs as antiangiogenics. Such antiangiogenic activity is achieved or optimized by metronomic-dosing protocols in which the drug is given at comparatively low doses using a frequent schedule of administration (e.g., once to three times per week) with no breaks, particularly when combined with an endothelial cell-specific antiangiogenic drug. The use of p.o. chemotherapeutic drugs is particularly suitable for this type of treatment strategy. We tested one such drug, cyclophosphamide (CTX), in a protocol wherein the drug was administered to mice at low doses, of approximately 10-40 mg/kg on a daily basis through the drinking water. CTX is typically given p.o. to patients, but it has almost always been injected when treating preclinical mouse tumor models. We found p.o. CTX to be a safe and convenient treatment with significant antitumor efficacy. Growth delays were observed for human orthotopic breast or ectopic colon cancer xenografts in nude or SCID mice. Established PC3 human prostate tumor xenografts could be induced to almost fully regress, remaining virtually nonpalpable for > or =2 months of continuous therapy, after which tumors began to grow progressively. These re-emergent tumors were not found to be drug resistant when tested in new hosts, using the same treatment protocol. Regression of spontaneously arising, late-stage pancreatic islet cell carcinomas in Rip Tag transgenic mice was also observed. The effects of continuous p.o. CTX treatment were enhanced significantly in an orthotopic, metastatic breast cancer xenograft model when used in combination with an antivascular endothelial growth factor receptor-2 blocking antibody. Maximum tolerated dose levels established for other mouse strains proved highly toxic to SCID mice, whereas daily p.o. low-dose regimens of CTX were well tolerated. Taken together, the results demonstrate the feasibility of delivering CTX in a p.o. metronomic chemotherapy regimen, which proved safe, reasonably efficacious, and potentially applicable to chronic treatment. Such a regimen may be particularly well suited for integration with antiangiogenic drugs.
近期的一些临床前研究激发了人们对利用传统化疗药物作为抗血管生成剂这一概念的兴趣。这种抗血管生成活性是通过节律性给药方案实现或优化的,即在该方案中,药物以相对低剂量、频繁给药(如每周1至3次)且不间断的方式给药,尤其是与内皮细胞特异性抗血管生成药物联合使用时。口服化疗药物特别适合这种治疗策略。我们在一项方案中测试了一种这样的药物,即环磷酰胺(CTX),该方案中通过饮用水以约10 - 40 mg/kg的低剂量每日给小鼠给药。CTX通常给患者口服,但在治疗临床前小鼠肿瘤模型时几乎总是注射给药。我们发现口服CTX是一种安全、方便的治疗方法,具有显著的抗肿瘤疗效。在裸鼠或SCID小鼠中观察到了人原位乳腺癌或异位结肠癌异种移植瘤的生长延迟。已建立的PC3人前列腺肿瘤异种移植瘤在连续治疗≥两个月后可被诱导几乎完全消退,在此期间几乎触诊不到,之后肿瘤开始逐渐生长。当在新宿主中使用相同治疗方案进行测试时,这些复发的肿瘤未发现耐药。在Rip Tag转基因小鼠中也观察到了自发产生的晚期胰岛细胞癌的消退。在原位转移性乳腺癌异种移植模型中,口服CTX连续治疗与抗血管内皮生长因子受体-2阻断抗体联合使用时,其效果显著增强。为其他小鼠品系确定的最大耐受剂量水平对SCID小鼠具有高度毒性,而CTX的每日口服低剂量方案耐受性良好。综上所述,结果表明在口服节律性化疗方案中给予CTX是可行的,该方案被证明是安全、相当有效的,并且可能适用于慢性治疗。这样的方案可能特别适合与抗血管生成药物联合使用。