Isolated Limb Perfusion for In-Transit Melanoma Metastases: Melphalan or TNF-Melphalan Perfusion?

被引:25
|
作者
Hoekstra, Harald J. [1 ]
Veerman, Kelly [1 ]
Van Ginkel, Robert J. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Surg Oncol, NL-9700 RB Groningen, Netherlands
关键词
in-transit metastases; regional chemotherapy; melphalan; melanoma; perfusion; TNF alpha; TUMOR-NECROSIS-FACTOR; SOFT-TISSUE SARCOMAS; GAMMA IFN-GAMMA; FACTOR-ALPHA; INTERFERON-GAMMA; CUTANEOUS MELANOMA; EXTREMITY MELANOMA; IMPROVED SURVIVAL; REGIONAL THERAPY; STAGE-III;
D O I
10.1002/jso.23552
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. J. Surg. Oncol. 2014 109:338-347. (c) 2014 Wiley Periodicals, Inc.
引用
收藏
页码:338 / 347
页数:10
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