Wondergem J, Stephens L C, Strebel F R, Baba H, Ohno S, Siddik Z H, Newman R A, Bull J M
University of Texas Medical School, Department of Internal Medicine, Houston.
Cancer Res. 1991 Jul 1;51(13):3559-67.
Thermal enhancement of Adriamycin-mediated antitumor activity and normal tissue toxicities by whole body hyperthermia were compared using a F344 rat model. Antitumor activity was studied using a tumor growth delay assay. Acute normal tissue toxicities (i.e., leukopenia and thrombocytopenia) and late normal tissue toxicities (i.e., myocardial and kidney injury) were evaluated by functional/physiological assays and by morphological techniques. Whole body hyperthermia (120 min at 41.5 degrees C) enhanced both Adriamycin-mediated antitumor activity and toxic side effects. The thermal enhancement ratio calculated for antitumor activity was 1.6. Thermal enhancement ratios estimated for "acute" hematological changes were 1.3, whereas those estimated for "late" damage (based on morphological cardiac and renal lesions) varied between 2.4 and 4.3. Thus, while whole body hyperthermia enhances Adriamycin-mediated antitumor effect, normal tissue toxicity is also increased, and the potential therapeutic gain of the combined modality treatment is eroded.
使用F344大鼠模型比较了全身热疗对阿霉素介导的抗肿瘤活性和正常组织毒性的热增强作用。使用肿瘤生长延迟试验研究抗肿瘤活性。通过功能/生理试验和形态学技术评估急性正常组织毒性(即白细胞减少和血小板减少)和晚期正常组织毒性(即心肌和肾脏损伤)。全身热疗(41.5℃,120分钟)增强了阿霉素介导的抗肿瘤活性和毒副作用。计算得出的抗肿瘤活性热增强比为1.6。“急性”血液学变化的热增强比为1.3,而“晚期”损伤(基于心脏和肾脏形态学病变)的热增强比在2.4至4.3之间变化。因此,虽然全身热疗增强了阿霉素介导的抗肿瘤作用,但正常组织毒性也增加了,联合治疗的潜在治疗获益被削弱。