Vujaskovic Z, Poulson J M, Gaskin A A, Thrall D E, Page R L, Charles H C, MacFall J R, Brizel D M, Meyer R E, Prescott D M, Samulski T V, Dewhirst M W
Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Int J Radiat Oncol Biol Phys. 2000 Jan 1;46(1):179-85. doi: 10.1016/s0360-3016(99)00362-4.
The objectives of this study were to evaluate effects of hyperthermia on tumor oxygenation, extracellular pH (pHe), and blood flow in 13 dogs with spontaneous soft tissue sarcomas prior to and after local hyperthermia.
Tumor pO2 was measured using an Eppendorf polarographic device, pHe using interstitial electrodes, and blood flow using contrast-enhanced magnetic resonance imaging (MRI).
There was an overall improvement in tumor oxygenation observed as an increase in median pO2 and decrease in hypoxic fraction (% of pO2 measurements <5 mm Hg) at 24-h post hyperthermia. These changes were most pronounced when the median temperature (T50) during hyperthermia treatment was less than 44 degrees C. Tumors with T50 > 44 degrees C were characterized by a decrease in median PO2 and an increase in hypoxic fraction. Similar thermal dose-related changes were observed in tumor perfusion. Perfusion was significantly higher after hyperthermia. Increases in perfusion were most evident in tumors with T50 < 44 degrees C. With T50 > 44 degrees C, there was no change in perfusion after hyperthermia. On average, pHe values declined in all animals after hyperthermia, with the greatest reduction seen for larger T50 values.
This study suggests that hyperthermia has biphasic effects on tumor physiologic parameters. Lower temperatures tend to favor improved perfusion and oxygenation, whereas higher temperatures are more likely to cause vascular damage, thus leading to greater hypoxia. While it has long been recognized that such effects occur in rodent tumors, this is the first report to tie such changes to temperatures achieved during hyperthermia in the clinical setting. Furthermore, it suggests that the thermal threshold for vascular damage is higher in spontaneous tumors than in more rapidly growing rodent tumors.
本研究的目的是评估热疗对13只患有自发性软组织肉瘤的犬在局部热疗前后肿瘤氧合、细胞外pH值(pHe)和血流的影响。
使用Eppendorf极谱仪测量肿瘤pO2,使用间质电极测量pHe,使用对比增强磁共振成像(MRI)测量血流。
热疗后24小时观察到肿瘤氧合总体改善,表现为中位pO2增加和缺氧分数降低(pO2测量值<5 mmHg的百分比)。当热疗期间的中位温度(T50)低于44摄氏度时,这些变化最为明显。T50>44摄氏度的肿瘤表现为中位PO2降低和缺氧分数增加。在肿瘤灌注中观察到类似的热剂量相关变化。热疗后灌注显著更高。灌注增加在T50<44摄氏度的肿瘤中最为明显。当T50>44摄氏度时,热疗后灌注没有变化。平均而言,热疗后所有动物的pHe值均下降,T50值越大下降幅度越大。
本研究表明热疗对肿瘤生理参数有双相影响。较低温度倾向于促进灌注和氧合改善,而较高温度更可能导致血管损伤,从而导致更严重的缺氧。虽然长期以来人们已经认识到这种效应在啮齿动物肿瘤中会发生,但这是第一份将此类变化与临床环境中热疗期间达到的温度联系起来的报告。此外,这表明自发性肿瘤中血管损伤的热阈值高于生长更快的啮齿动物肿瘤。