Teicher B A, Dupuis N P, Emi Y, Ikebe M, Kakeji Y, Menon K
Dana-Farber Cancer Institute, Boston, MA 02115, USA.
In Vivo. 1995 Jan-Feb;9(1):11-8.
Tissue oxygen tensions were measured in the rat 9L gliosarcoma under conditions of normal air breathing or carbogen breathing and after intravenous administration of a hemoglobin solution with air breathing or carbogen breathing. Administration of the hemoglobin decreased the level of hypoxia in the tumors. Treatment of the animals with the antiangiogenic combination of TNP-470 and minocycline also increased tumor oxygenation compared with untreated controls. Treatment with the antiangiogenic agents along with administration of the hemoglobin solution/carbogen breathing decreased the hypoxic fraction (% pO2 readings < or = 5 mmHg) from 71 % to 30%. Treatment of the tumor-bearing animals with BCNU or adriamycin modestly reduced hypoxia in the tumors, while treatment with fractionated radiation markedly increased hypoxia in the tumors. Tumor growth delay was used to assess the response of the subcutaneous tumor to the various treatment combinations. There was a strong correlation between increased therapeutic response and decreased tumor hypoxia. Tumor growth delay from BCNU increased from 5.3 days to 16.4 days with TNP-470/-minocycline/hemoglobin solution/carbogen. Similarly, the tumor growth delay from adriamycin increased from 3.9 days to 17.0 days with TNP-470/minocycline/hemoglobin solution/carbogen. Finally, the tumor growth delay from fractionated radiation increased from 4.8 days to 13.3 days with TNP-470/minocycline/hemoglobin solution/carbogen. When etanidazole was added to the complete radiation regimen, the tumor growth delay increased further to 20.5 days. These data show that the addition of non-toxic agents that increase tumor oxygenation to cytotoxic therapies can markedly increase therapeutic response.
在正常空气呼吸或卡波金呼吸条件下,以及静脉注射血红蛋白溶液后进行空气呼吸或卡波金呼吸时,测量大鼠9L胶质肉瘤中的组织氧张力。血红蛋白的给药降低了肿瘤中的缺氧水平。与未治疗的对照组相比,用TNP - 470和米诺环素的抗血管生成组合治疗动物也增加了肿瘤氧合。抗血管生成药物与血红蛋白溶液/卡波金呼吸联合给药可使缺氧分数(% pO2读数≤5 mmHg)从71%降至30%。用卡莫司汀(BCNU)或阿霉素治疗荷瘤动物可适度降低肿瘤中的缺氧,而分次放疗则显著增加肿瘤中的缺氧。肿瘤生长延迟用于评估皮下肿瘤对各种治疗组合的反应。治疗反应增加与肿瘤缺氧减少之间存在很强的相关性。卡莫司汀的肿瘤生长延迟从5.3天增加到16.4天(使用TNP - 470/米诺环素/血红蛋白溶液/卡波金)。同样,阿霉素的肿瘤生长延迟从3.9天增加到17.0天(使用TNP - 470/米诺环素/血红蛋白溶液/卡波金)。最后,分次放疗的肿瘤生长延迟从4.8天增加到13.3天(使用TNP - 470/米诺环素/血红蛋白溶液/卡波金)。当将乙磺唑添加到完整的放疗方案中时,肿瘤生长延迟进一步增加到20.5天。这些数据表明,将增加肿瘤氧合的无毒药物添加到细胞毒性疗法中可显著提高治疗反应。