Ko Sae Hee, Ueno Tomio, Yoshimoto Yasunori, Yoo Jin Soo, Abdel-Wahab Omar I, Abdel-Wahab Zeinab, Chu Edward, Pruitt Scott K, Friedman Henry S, Dewhirst Mark W, Tyler Douglas S
Department of Surgery, Duke University School of Medicine, Durham, North Carolina 27710, USA.
Clin Cancer Res. 2006 Jan 1;12(1):289-97. doi: 10.1158/1078-0432.CCR-05-0210.
Previous preclinical studies have shown that regional temozolomide therapy via isolated limb infusion is more effective than melphalan, the current drug of choice for regional chemotherapy for advanced extremity melanoma. The aim of this study was to determine whether hyperthermia could further augment the efficacy of temozolomide, an alkylating agent, against melanoma and improve its therapeutic index in a rat model of isolated limb infusion.
Athymic rats bearing s.c. human melanoma xenografts (DM6) in their hind limbs were randomized to a 15-minute isolated limb infusion procedure with or without temozolomide at room temperature, normothermic (37.5 degrees C), or hyperthermic (43 degrees C) conditions.
The concomitant administration of hyperthermia during an infusion with temozolomide led to the greatest increase in tumor growth delay, decreased proliferative index, and increased cell death. Isolated limb infusion treatment with a low dose (350 mg/kg) of temozolomide was ineffective at producing tumor growth delay (P = 0.07). Similarly, temozolomide infusion under normothermia yielded minimal tumor growth delay (P = 0.08). In contrast, the combination of hyperthermia plus temozolomide treatment produced marked tumor growth delay of 10.4 days (P = 0.02) with minimal toxicity. The addition of heat to temozolomide treatment yielded the smallest proliferative index (P = 0.001), while markedly increasing the level of apoptosis 48 hours after isolated limb infusion.
This study, the first to examine the interaction between hyperthermia and temozolomide, shows a strong, synergistic antitumor effect when hyperthermia is combined with temozolomide for regional treatment of melanoma confined to an extremity. The mechanism of this synergy seems to be through an augmentation, by hyperthermia, of the antiproliferative and proapoptotic effects of temozolomide.
先前的临床前研究表明,通过隔离肢体灌注进行的局部替莫唑胺治疗比美法仑更有效,美法仑是目前晚期肢体黑色素瘤局部化疗的首选药物。本研究的目的是确定热疗是否能进一步增强烷基化剂替莫唑胺对黑色素瘤的疗效,并在隔离肢体灌注大鼠模型中提高其治疗指数。
后肢皮下接种人黑色素瘤异种移植物(DM6)的无胸腺大鼠被随机分为两组,分别在室温、常温(37.5摄氏度)或热疗(43摄氏度)条件下进行15分钟的隔离肢体灌注,灌注过程中使用或不使用替莫唑胺。
在替莫唑胺灌注期间同时进行热疗导致肿瘤生长延迟增加最多,增殖指数降低,细胞死亡增加。低剂量(350mg/kg)替莫唑胺的隔离肢体灌注治疗在产生肿瘤生长延迟方面无效(P=0.07)。同样,常温下替莫唑胺灌注产生的肿瘤生长延迟最小(P=0.08)。相比之下,热疗加替莫唑胺治疗组合产生了显著的肿瘤生长延迟,为10.4天(P=0.02),且毒性最小。在替莫唑胺治疗中加入热疗产生了最小的增殖指数(P=0.001),同时在隔离肢体灌注48小时后显著增加了凋亡水平。
本研究首次考察了热疗与替莫唑胺之间的相互作用,结果表明,热疗与替莫唑胺联合用于局限于肢体的黑色素瘤局部治疗时,具有强大的协同抗肿瘤作用。这种协同作用的机制似乎是热疗增强了替莫唑胺的抗增殖和促凋亡作用。