Nathanson S D, Nelson L, Anaya P, Havstad S, Hetzel F W
Department of Surgery, Henry Ford Hospital, Detroit, MI 48202.
Clin Exp Metastasis. 1991 Jul-Aug;9(4):377-92. doi: 10.1007/BF01769357.
C57BL/6 mice with syngeneic B16-F10 melanomas were treated 7 days after tumor inoculation into the footpad with local hyperthermia (HT) of 43.5 degrees C for 90 min. A combination of local 30 Gy X-irradiation (XRT) given 2, 4 or 12 h after HT cured the primary tumor in 34/35 mice, with irreversible damage to normal foot tissues in most of the animals. When 7.5, 10 or 15 Gy XRT were delivered 4, 18 or 24 h after HT, there were only a small number of cures and also a much smaller incidence of irreversible normal tissue damage. HT alone resulted in a significant (P less than 0.001) increase in metastases to regional lymph nodes (RLN) and the lungs. The 'curative' doses of combined XRT and HT resulted in a significant (P less than 0.001) decrease in metastasis to RLN and to the lungs. Conversely, subcurative doses of combined therapy resulted in an increase in RLN and lung metastasis (P less than 0.001). Abdominal lymph node metastasis, not usually seen in control mice, is markedly increased after HT alone or in combination with subcurative XRT (P less than 0.001). The overall survival of mice treated with HT alone is decreased (P less than 0.0028). The survival of mice treated with HT followed 4, 18 or 24 h later with 10 Gy XRT is further decreased (P less than 0.0025). These data show that subcurative HT, or XRT plus HT, increases the incidence of spontaneous metastasis in this syngeneic mouse melanoma model. Curative doses prevent this effect on metastasis, but there is an unacceptable incidence of irreversible damage to the tumor-bearing foot. The cause(s) of this phenomenon are not known.
将同基因B16 - F10黑色素瘤接种到足垫的C57BL/6小鼠,在肿瘤接种7天后,用43.5摄氏度的局部热疗(HT)处理90分钟。在热疗后2、4或12小时给予局部30 Gy的X射线照射(XRT),可使34/35只小鼠的原发性肿瘤治愈,但大多数动物的正常足部组织受到不可逆损伤。当在热疗后4、18或24小时给予7.5、10或15 Gy的XRT时,只有少数治愈病例,且不可逆正常组织损伤的发生率也低得多。单独热疗导致区域淋巴结(RLN)和肺部转移显著增加(P<0.001)。联合XRT和热疗的“治愈”剂量导致RLN和肺部转移显著减少(P<0.001)。相反,联合治疗的亚治愈剂量导致RLN和肺部转移增加(P<0.001)。单独热疗或与亚治愈性XRT联合后,腹部淋巴结转移(通常在对照小鼠中未见)显著增加(P<0.001)。单独接受热疗的小鼠总体生存率降低(P<0.0028)。热疗后4、18或24小时接受10 Gy XRT治疗的小鼠生存率进一步降低(P<0.0025)。这些数据表明,亚治愈性热疗或XRT加HT会增加这种同基因小鼠黑色素瘤模型中自发转移的发生率。治愈剂量可防止对转移的这种影响,但对荷瘤足部有不可接受的不可逆损伤发生率。这种现象的原因尚不清楚。