Eggermont A M, Schraffordt Koops H, Liénard D, Kroon B B, van Geel A N, Hoekstra H J, Lejeune F J
Department of Surgical Oncology, University Hospital Rotterdam-Daniel den Hoed Cancer Center, The Netherlands.
J Clin Oncol. 1996 Oct;14(10):2653-65. doi: 10.1200/JCO.1996.14.10.2653.
To determine the efficacy of isolated limb perfusion (ILP) with tumor necrosis factor-alpha (TNF) in combination with interferon-gamma (IFN) and melphalan as induction therapy to render tumors resectable and avoid amputation in patients with nonresectable extremity soft tissue sarcomas (STS).
Among 55 patients with 30 primary and 25 recurrent sarcomas, there were 48 high-grade and seven grade 1 sarcomas (very large, recurrent, or multiple). The composition of this series of patients is unusual: 13 patients (24%) had multifocal primary sarcomas or multiple recurrent tumors; tumors were very large (median, 18 cm); and nine patients (16%) had known systemic metastases. IFN was administered subcutaneously on the 2 days before ILP with TNF, IFN, and melphalan. A delayed marginal resection of the tumor remnant was usually performed 2 to 3 months after ILP.
A major tumor response was seen in 87% of patients and rendered the sarcomas resectable in most cases. Clinical response rates were as follows: 10 (18%) completes responses (CRs), 35 (64%) partial responses (PRs), and 10 (18%) no change (NC). Final outcome was defined as follows by clinical and pathologic response: 20 (36%) CRs, 28 (51%) PRs, and seven (13%) NC. Limb salvage was achieved in 84% (follow-up duration, 20+ to 50+ months). In 39 patients, resection of the tumor remnant (n = 31) or of two to eight tumors (n = 8) after ILP was performed; local recurrence developed in five (13%). When no resection was performed (multiple tumors or systemic metastases), local recurrences were frequent (five of 16), but limb salvage was often achieved as patients died of systemic disease. Regional toxicity was limited and systemic toxicity minimal to moderate with no toxic deaths. Histology showed hemorrhagic necrosis; angiographies showed selective destruction of tumor-associated vessels.
ILP with TNF, IFN, and melphalan is a safe and highly effective induction biochemotherapy procedure that can achieve limb salvage in patients with nonresectable extremity STS. TNF is an active anticancer drug in humans in the setting of ILP.
确定采用肿瘤坏死因子-α(TNF)联合干扰素-γ(IFN)及美法仑进行离体肢体灌注(ILP)作为诱导治疗,使不可切除的肢体软组织肉瘤(STS)患者的肿瘤可切除并避免截肢的疗效。
55例患者中,有30例原发性肉瘤和25例复发性肉瘤,其中48例为高级别肉瘤,7例为1级肉瘤(肿瘤非常大、复发或多发)。该系列患者的构成情况不常见:13例患者(24%)有多灶性原发性肉瘤或多个复发性肿瘤;肿瘤非常大(中位数为18 cm);9例患者(16%)已知有全身转移。在进行ILP联合TNF、IFN及美法仑治疗前2天皮下注射IFN。通常在ILP后2至3个月对肿瘤残余灶进行延迟边缘性切除。
87%的患者出现主要肿瘤反应,且在大多数情况下使肉瘤可切除。临床缓解率如下:10例(18%)完全缓解(CR),35例(64%)部分缓解(PR),10例(18%)无变化(NC)。最终结局根据临床和病理反应定义如下:20例(36%)CR,28例(51%)PR,7例(13%)NC。84%的患者实现了保肢(随访时间为20多个月至50多个月)。39例患者在ILP后切除了肿瘤残余灶(n = 31)或2至8个肿瘤(n = 8);5例(13%)出现局部复发。当未进行切除时(多个肿瘤或全身转移),局部复发很常见(16例中有5例),但由于患者死于全身疾病,常能实现保肢。区域毒性有限,全身毒性为轻度至中度,无毒性死亡。组织学显示出血性坏死;血管造影显示肿瘤相关血管被选择性破坏。
采用TNF、IFN及美法仑进行ILP是一种安全且高效的诱导生物化疗方法,可使不可切除的肢体STS患者实现保肢。在ILP情况下,TNF是一种对人类有效的抗癌药物。