Department of Surgical Oncology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
J Surg Oncol. 2014 Mar;109(4):338-47. doi: 10.1002/jso.23552. Epub 2014 Jan 9.
Indications for treatment of melanoma in-transit metastases (ITMs) confined to the limb with isolated limb perfusion (ILP) are not well defined. This study reports the Groningen regional therapeutic perfusion experience with melphalan (M-ILP) and TNF-melphalan (TM-ILP) for ITMs, and reviews of the melanoma TNF-melphalan ILP literature. Between 1991 and 2012, 60 patients were treated with ILP. Patients with "small" ITMs received M-ILP (10-13 mg melphalan/L limb volume) and patients with "bulky" disease TM-ILP (1-4 mg TNF); 19 M-ILPs and 41 TM-ILPs were performed, 26 Stage IIIB, 31 Stage IIIB and 1 stage IV disease. Overall response after 57 ILPs was 90%; CR 27 (45%), PR 27 (45%), no response 3 (5%); after 9 M-ILPs CR 6 (32%) and 41 TM-ILPs CR 21 (51%, P = 0.124). For younger patients (<65 years) CR was 69% and for elderly patients 29% (P = 0.003). For low volume disease (<5 ITMs) CR was 75% and for high volume disease (≥5 ITMs) 41% (P = 0.038). After median follow-up of 15 months (range, 1-144) there was local recurrence or disease progression in 36 patients (60%). Positive lymph node status was associated with local progression, absence of CR and Stage IIIC disease; these were independent prognostic factors for progression to systemic disease. M-ILP is an effective regional treatment for melanoma ITMs, whereas for bulky disease TM-ILP should be the first choice. In-field progression-free survival after ILP is determined by the biological behavior of the ITMs and the patient's immune system.
对于局限于肢体的转移性黑色素瘤(ITM)经隔离肢体灌注(ILP)治疗的适应证尚不确定。本研究报告了格罗宁根地区采用美法仑(M-ILP)和 TNF-美法仑(TM-ILP)治疗 ITM 的治疗经验,并对黑色素瘤 TNF-美法仑 ILP 文献进行了复习。1991 年至 2012 年,60 例患者接受了 ILP 治疗。“小”ITM 患者接受 M-ILP(10-13mg 美法仑/L 肢体体积),“大”疾病患者接受 TM-ILP(1-4mg TNF);共进行了 19 例 M-ILP 和 41 例 TM-ILP,其中 26 例为 IIIB 期,31 例为 IIIB 期和 1 例 IV 期疾病。57 例 ILP 后的总体缓解率为 90%;完全缓解(CR)27(45%),部分缓解(PR)27(45%),无反应 3(5%);9 例 M-ILP 后 CR 为 6(32%),41 例 TM-ILP 后 CR 为 21(51%,P=0.124)。年轻患者(<65 岁)CR 为 69%,老年患者为 29%(P=0.003)。低体积疾病(<5 个 ITM)CR 为 75%,高体积疾病(≥5 个 ITM)CR 为 41%(P=0.038)。中位随访 15 个月(范围,1-144)后,36 例(60%)患者出现局部复发或疾病进展。阳性淋巴结状态与局部进展、无 CR 和 IIIIC 期疾病相关;这些是疾病进展为系统性疾病的独立预后因素。M-ILP 是治疗黑色素瘤 ITM 的有效局部治疗方法,而对于大体积疾病,TM-ILP 应作为首选。ILP 后的肿瘤内无进展生存由 ITM 的生物学行为和患者的免疫系统决定。