Hildebrandt B, Dräger J, Kerner T, Deja M, Löffel J, Stroszczynski C, Ahlers O, Felix R, Riess H, Wust P
Medizinische Klinik für Hämatologie und Onkologie, Universitätklinikum Charité, Berlin, Germany.
Int J Hyperthermia. 2004 May;20(3):317-33. doi: 10.1080/02656730310001637316.
This phase I/II study evaluated the feasibility, toxicity and response rates of von Ardenne's systemic cancer multistep therapy (sCMT) when applied as an adjunct to cytostatic therapy in patients with metastatic colorectal cancer. sCMT consists of whole-body hyperthermia (WBH) at 41.8-42.1 degrees C, hyperglycaemia and hyperoxaemia. All patients who entered the trial first received three monthly courses of chemotherapy (folinic acid, 50 mg, days 1-5; 5-fluorouracil, 425 mg/m2, days 1-5; mitomycin 8 mg/m2, day 1), followed by response evaluation according World Health Organization (WHO) criteria. Responders (partial/complete remission) were assigned to three further courses of chemotherapy, whereas non-responders (stable/progressive disease) were allocated to additional sCMT on day 1 of every subsequent chemotherapy course. The WBH procedure was administered under general anaesthesia employing the Iratherm-2000 radiant heat device. Of 28 patients enrolled, 19 received more than three treatment courses. Eight of these 19 patients had responded to chemotherapy (PR) and thus obtained three further courses of chemotherapy alone. In 10 of 19 patients who had not responded (SD, PD), three additional courses of chemotherapy were combined with sCMT (with 25 sCMT applications). One patient who did not respond to initial treatment declined sCMT and was continued with chemotherapy alone. It was found that sCMT was feasible, but associated with a specific spectrum of grade III/IV toxicity (skin 20%, pain 16%, peripheral nerves 8% of treatment courses). The fact that three patients who did not respond to initial chemotherapy achieved a PR after additional sCMT suggests that sCMT may enhance the effect of chemotherapy in patients with colorectal cancer.
这项I/II期研究评估了冯·阿登纳全身癌症多步骤疗法(sCMT)作为细胞毒性疗法辅助手段应用于转移性结直肠癌患者时的可行性、毒性及缓解率。sCMT包括41.8 - 42.1摄氏度的全身热疗(WBH)、高血糖和高氧血症。所有进入试验的患者首先接受三个月疗程的化疗(亚叶酸,50毫克,第1 - 5天;5 - 氟尿嘧啶,425毫克/平方米,第1 - 5天;丝裂霉素8毫克/平方米,第1天),随后根据世界卫生组织(WHO)标准进行疗效评估。缓解者(部分/完全缓解)接受另外三个疗程的化疗,而未缓解者(病情稳定/进展)在随后每个化疗疗程的第1天接受额外的sCMT治疗。WBH程序在全身麻醉下使用Iratherm - 2000辐射热装置进行。入组的28例患者中,19例接受了超过三个疗程的治疗。这19例患者中有8例对化疗有反应(PR),因此仅接受了另外三个疗程的化疗。在19例未缓解的患者(SD,PD)中,有10例将另外三个疗程的化疗与sCMT联合(共进行25次sCMT应用)。1例对初始治疗无反应的患者拒绝sCMT,继续单独接受化疗。结果发现,sCMT是可行的,但伴有特定的III/IV级毒性谱(皮肤毒性20%,疼痛16%,周围神经毒性占治疗疗程的8%)。3例对初始化疗无反应的患者在接受额外的sCMT后达到PR,这一事实表明sCMT可能增强结直肠癌患者化疗的效果。
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