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首页> 外文期刊>Annals of surgical oncology >Hyperthermic isolated limb perfusion with low-dose tumor necrosis factor-alpha and melphalan for bulky in-transit melanoma metastases.
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Hyperthermic isolated limb perfusion with low-dose tumor necrosis factor-alpha and melphalan for bulky in-transit melanoma metastases.

机译:高剂量孤立性肢体灌注用低剂量肿瘤坏死因子-α和美法仑治疗大体积的转运黑色素瘤转移。

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BACKGROUND: Melphalan (L-PAM) hyperthermic isolated limb perfusion (HILP) is currently considered the standard treatment for patients with in-transit metastases from cutaneous melanoma. We here report on the results of L-PAM and low-dose tumor necrosis factor (TNF)alpha HILP in patients with bulky disease. METHODS: Twenty patients underwent TNFalpha (1 mg) and L-PAM (10 mg/L) HILP. Perfusion was performed for 90 minutes, and systemic leakage was strictly monitored. Locoregional toxicity was evaluated according to Wieberdink's criteria, whereas tumor response was evaluated with physical examination and ultrasound scan with or without fine-needle aspiration of any suspected recurrence. RESULTS: In all cases, systemic leakage was <5%. No postoperative deaths occurred, and locoregional toxicity was mild (grade 1 or 2) in 95% of patients. A complete tumor response was obtained in 14 patients (70%), and partial responses were obtained in 5 patients (25%). After a median follow-up of 18 months, six patients are alive and disease free, seven are alive with local or distant recurrence or both, and seven have died of disease. CONCLUSIONS: Low-dose TNFalpha HILP can achieve tumor responses comparable with those reported with higher doses of cytokine. Moreover, this drug regimen is associated with acceptable local toxicity, carries a smaller risk of systemic toxicity, and incurs lower costs.
机译:背景:Melphalan(L-PAM)高温离体肢体灌注(HILP)目前被认为是皮肤黑素瘤转移途中转移患者的标准治疗方法。我们在这里报告了L-PAM和大剂量疾病患者低剂量肿瘤坏死因子(TNF)alpha HILP的结果。方法:20例患者接受TNFα(1mg)和L-PAM(10mg / L)HILP治疗。进行灌注90分钟,并严格监测全身性渗漏。根据Wieberdink的标准评估局部毒性,同时通过体检和超声扫描评估是否有肿瘤复发,并通过或不进行细针抽吸进行评估。结果:在所有情况下,全身性渗漏均小于5%。 95%的患者未发生术后死亡,局部毒性轻微(1级或2级)。 14名患者(70%)获得了完整的肿瘤缓解,5名患者(25%)获得了部分缓解。在中位随访18个月后,有6名患者活着并且没有疾病,有7名患者活着局部或远处复发或两者兼有,还有7名患者死于疾病。结论:低剂量的TNFalpha HILP可以达到与较高剂量的细胞因子可比的肿瘤反应。而且,该药物方案与可接受的局部毒性有关,具有较小的全身毒性风险,并产生较低的成本。

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