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Isolated limb infusion with hyperthermia and chemotherapy for advanced limb malignancy: factors influencing toxicity

机译:单独肢体输注热疗和化学疗法治疗晚期肢体恶性肿瘤:影响毒性的因素

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Background: The isolated limb infusion (ILI) technique is a simpler and less invasive alternative to isolated limb perfusion, which allows regional administration of high-dose chemotherapy to patients with advanced melanoma and other malignancies restricted to a limb. Methods: Patients from two institutions, treated by ILI between 1998 and 2009 for extensive disease restricted to a limb, were included. The cohort included 31 patients with melanoma who presented with in-transit metastases or an extensive primary lesion, one patient with squamous cell carcinoma and another with epithelioid sarcoma not suitable for local surgical treatment. Results: A complete response was achieved in 26.3% of patients and a partial response in 52.6%. Toxicity was assessed according to the Wieberdink limb toxicity scale. Grade II toxicity was noted in 39.5% of patients, grade III in 50% and grade IV in 10.5%. Toxicity was correlated with the results of a number of clinical and laboratory tests. The toxicity of melphalan and actinomycin D was dose-dependent. For melphalan, the relationship between toxicity and mean dose was as follows: grade II - 34.7 mg; grades III and IV - 47.5 mg (P = 0.012). The relationship between toxicity and maximum serum creatine phosphokinase (CPK) was as follows: grade II -431.5 U/L; grades III and IV - 3228 U/L (P = 0.010). Conclusion: Toxicity after ILI is dose-dependent and serum CPK correlates with toxicity.
机译:背景:孤立肢体灌注(ILI)技术是孤立肢体灌注的一种更简单,侵入性更小的替代方法,它允许对晚期黑色素瘤和其他局限于肢体的恶性肿瘤患者进行大剂量化疗。方法:纳入了1998年至2009年间由ILI治疗的两家机构因肢体广泛疾病而接受治疗的患者。该队列包括31例黑色素瘤患者,这些患者表现为转移性转移或广泛的原发性病变,一名患有鳞状细胞癌,另一名患有不适合局部手术治疗的上皮样肉瘤。结果:26.3%的患者获得了完全缓解,52.6%的患者获得了部分缓解。根据Wieberdink肢体毒性量表评估毒性。观察到39.5%的患者为II级毒性,50%的为III级,10.5%的为IV级。毒性与许多临床和实验室测试的结果相关。美法仑和放线菌素D的毒性是剂量依赖性的。对于美法仑,毒性与平均剂量之间的关系如下:II级-34.7 mg; III和IV级-47.5毫克(P = 0.012)。毒性与最大血清肌酸磷酸激酶(CPK)之间的关系如下:II级-431.5 U / L; III和IV级-3228 U / L(P = 0.010)。结论:ILI后的毒性是剂量依赖性的,血清CPK与毒性相关。

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