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首页> 外文期刊>Journal of Surgical Oncology >Australian multi-center experience outside of the Sydney Melanoma Unit of isolated limb infusion chemotherapy for melanoma
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Australian multi-center experience outside of the Sydney Melanoma Unit of isolated limb infusion chemotherapy for melanoma

机译:悉尼黑素瘤部门以外的澳大利亚多中心经验:黑色素瘤的独立肢体输液化疗

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Introduction Isolated limb infusion (ILI) is a minimally invasive alternative to isolated limb perfusion (ILP) for delivering high-dose regional chemotherapy to treat locally advanced limb melanoma. The current study aimed to evaluate the applicability of ILI in four Australian tertiary referral centers outside of its originating institution, the Sydney Melanoma Unit (SMU; currently known as the Melanoma Institute Australia). Methods Data of 131 patients, treated between 1992 and 2008 were collectively analyzed. The ILI procedures were based on the Sydney Melanoma Unit protocol using melphalan. Response was determined using the WHO criteria and toxicity was assessed using the Wieberdink scale. Results The median patient age was 74 years (range 28-100). Fifty-six percent were female. Overall response (OR) rate to ILI was 63% (CR 27%; PR 36%). Wieberdink toxicity grade III or higher was seen in 13%. No toxicity-related amputations occurred. Median follow-up was 24 months; median survival was 58 months. In patients with a complete response (CR), median survival was 101 months; in patients with a partial response (PR) this was 41 months (P-=-0.026). On univariate analysis a younger age, lower-limb procedures and a lower Breslow thickness of the primary melanoma were associated with a favorable response. On multivariate analysis Breslow thickness and lower-limb ILI remained significant predictors for response. Conclusion In this, to date, largest multi-center study of ILI for melanoma the results are comparable to other reports and demonstrate that ILI can be widely implemented and safely applied across tertiary referral centers.
机译:简介孤立肢体输注(ILI)是孤立肢体灌注(ILP)的微创替代方案,用于进行大剂量局部化疗以治疗局部晚期肢体黑色素瘤。当前的研究旨在评估ILI在其发起机构悉尼黑素瘤部门(SMU;现称为澳大利亚黑素瘤研究所)之外的四个澳大利亚三级转诊中心的适用性。方法对1992年至2008年收治的131例患者的资料进行汇总分析。 ILI程序基于使用美法仑的悉尼黑色素瘤病房规程。使用WHO标准确定反应,并使用Wieberdink量表评估毒性。结果患者中位年龄为74岁(范围28-100)。 56%为女性。对ILI的总体反应(OR)率为63%(CR 27%; PR 36%)。观察到Wieberdink毒性等级为III或更高,占13%。没有发生与毒性有关的截肢。中位随访时间为24个月。中位生存期为58个月。完全缓解(CR)患者的中位生存期为101个月;有部分反应(PR)的患者为41个月(P-=-0.026)。单因素分析显示,年龄较小,下肢手术和原发性黑色素瘤的Breslow厚度较低与良好的反应有关。在多变量分析中,Breslow厚度和下肢ILI仍是反应的重要预测指标。结论在迄今为止的最大规模的ILI黑色素瘤多中心研究中,结果可与其他报告相媲美,并证明ILI可以在三级转诊中心广泛实施和安全应用。

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