Dewhirst M W, Prescott D M, Clegg S, Samulski T V, Page R L, Thrall D E, Leopold K, Rosner G, Acker J C, Oleson J R
Duke University Medical Center, Division of Radiation Oncology, Durham, North Carolina.
Int J Hyperthermia. 1990 Nov-Dec;6(6):971-83. doi: 10.3109/02656739009140980.
Hydralazine is an antihypertensive drug which theoretically could increase tumour temperatures during hyperthermia via reduction in tumour blood flow from a vascular 'steal' phenomenon. Doses that are therapeutically effective in reducing blood pressure in hypertensive patients would probably cause postural hypotension and other side-effects in normotensive patients beyond the hyperthermia treatment session, however. This study was designed to evaluate whether hydralazine, when administered at a safe dose for normotensive patients (0.125 mg/kg, i.v.) would be effective in increasing tumour temperatures during hyperthermia. The working hypothesis was that hydralazine at a dose of 0.125 mg/kg would be effective in raising tumour temperatures during hyperthermia treatment with minimal change in blood pressure. Fourteen human and five canine subjects were given hydralazine (0.125 mg/kg, i.v.) at the midpoint of a hyperthermia session. Temperatures and blood pressures were monitored before and after drug administration. Although hydralazine resulted in slight reduction in blood pressure, it was ineffective in increasing tumour temperatures in human patients (average maximum rise in median temperature was 0.26 +/- 0.32 degrees C). In canine subjects the same dose of hydralazine was effective in reducing blood pressure in four of five subjects studied (mean maximum drop was 22.7 +/- 4.1 mmHg) and the median temperature rose 0.8 +/- 0.7 degrees C. In the canine subjects the greater the decrease in blood pressure, the greater the increase in temperature. These results suggest that a rise in tumour temperature induced by hydralazine is dependent on creating a drop in blood pressure. Future studies in this laboratory will include tumour blood flow manipulation with antihypertensives which have a shorter half-life and a titratable effect. Using this approach, hypotension, which seems to be required to raise tumour temperature, will be more controllable in terms of magnitude and duration.
肼屈嗪是一种降压药,理论上它可能通过血管“窃血”现象减少肿瘤血流,从而在热疗期间提高肿瘤温度。然而,对高血压患者有治疗效果的降压剂量,在热疗疗程之外可能会导致血压正常的患者出现体位性低血压和其他副作用。本研究旨在评估以对血压正常患者安全的剂量(静脉注射0.125mg/kg)给予肼屈嗪,在热疗期间是否能有效提高肿瘤温度。工作假设是,0.125mg/kg剂量的肼屈嗪在热疗期间能有效提高肿瘤温度,同时使血压变化最小。14名人类受试者和5只犬类受试者在热疗疗程的中点接受静脉注射肼屈嗪(0.125mg/kg)。在给药前后监测体温和血压。尽管肼屈嗪导致血压略有下降,但它对提高人类患者的肿瘤温度无效(中位温度平均最大升高为0.26±0.32℃)。在犬类受试者中,相同剂量的肼屈嗪对所研究的5只犬中的4只有效降低血压(平均最大降幅为22.7±4.1mmHg),中位温度升高0.8±0.7℃。在犬类受试者中,血压下降越大,温度升高越大。这些结果表明,肼屈嗪引起的肿瘤温度升高依赖于血压下降。本实验室未来的研究将包括使用半衰期较短且有可滴定效应的抗高血压药物来控制肿瘤血流。采用这种方法,提高肿瘤温度所需的低血压在幅度和持续时间方面将更可控。