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A prospective randomized study of regional extremity perfusion in patients with malignant melanoma.

机译:恶性黑色素瘤患者区域性肢端灌注的前瞻性随机研究。

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One hundred seven patients presenting with malignant melanoma of the extremities were included in a prospective randomized study, which was conducted to evaluate the effectiveness of adjuvant hyperthermic regional cytostatic perfusion. In a control group (A, N = 54) the tumors were excised widely and the regional lymph nodes were dissected. The patients in the second group (B, N = 53) received additional hyperthermic (42 C) perfusion with melphalan. The mean follow-up observation period was 554 days. We chose the disease-free survival time as the criterion for success. The study could be discontinued prematurely, since the intermediate evaluation revealed a highly significant difference between the groups (p = 0.0001). We observed 21 local recurrences in the control group and four recurrences in the perfusion group. The retrospective breakdown by clinical stages also showed significant differences. The recurrence rate in the control group was 27.8% in Stage I, 31.6% in Stage II, and 58.8% in Stage III. In the perfusion group we observed recurrences equaling 5.6% in Stage I, 5.5% in Stage II, and 12.5% in Stage III. The differences between the groups based on the target-criterion of disease-free survival represent significance levels of p = 0.09 in Stage I, p = 0.03 in Stage II, and p = 0.003 in Stage III. We feel that on the evidence provided by our study, shown in the above results, the adjuvant application of regional hyperthermic cytostatic perfusion has proven itself to be superior to conventional procedures alone.
机译:一项前瞻性随机研究包括了一百四十七名四肢恶性黑色素瘤患者,以评估辅助性高热区域细胞抑制性灌注的有效性。在对照组(A,N = 54)中,广泛切除肿瘤并解剖区域淋巴结。第二组(B,N = 53)的患者接受了美法仑的额外热灌注(42 C)。平均随访观察期为554天。我们选择无病生存时间作为成功的标准。该研究可能会过早终止,因为中间评估显示两组之间存在显着差异(p = 0.0001)。我们在对照组中观察到21例局部复发,在灌注组中观察到4例复发。临床分期的回顾性分类也显示出显着差异。对照组的复发率在I期为27.8%,在II期为31.6%,在III期为58.8%。在灌注组中,我们观察到复发率在第一阶段为5.6%,在第二阶段为5.5%,在第三阶段为12.5%。基于无病生存目标指标的组之间的差异表示显着性水平在第一阶段为p = 0.09,在第二阶段为p = 0.03,在第三阶段为p = 0.003。我们认为,根据我们的研究提供的证据(如上结果所示),区域性高温细胞抑制性灌注的辅助应用已证明其本身优于常规程序。

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