Rastrelli Marco, Campana Luca Giovanni, Valpione Sara, Tropea Saveria, Zanon Antonio, Rossi Carlo Riccardo
a Melanoma and Sarcoma Unit, Veneto Institute of Oncology , Padua .
b Melanoma and Oesophageal Cancer Unit, Veneto Institute of Oncology , Padua , and.
Int J Hyperthermia. 2016;32(2):165-72. doi: 10.3109/02656736.2015.1101170. Epub 2015 Nov 25.
Hyperthermic isolated limb perfusion (HILP) is a locoregional treatment aimed at avoiding amputation in patients with advanced extremity soft tissue sarcomas (STS). Over the last 25 years, HILP procedure has been implemented to maximise its therapeutic ratio.
A retrospective analysis including 117 patients who underwent HILP from 1989 to 2013 was performed. Three different drug schedules were applied: 1) doxorubicin (n = 47), 2) high dose (3-4 mg) tumour necrosis factor-alpha (TNF-α) plus doxorubicin (n = 30), 3) low dose (1 mg) TNF-α plus melphalan (L-PAM) (n = 40). Tumour response was evaluated by MRI or CT and surgical specimens. Toxicity and local progression-free survival (LPFS) were also evaluated.
In total 92 (78.6%) patients had primary, 25 (21.4%) had recurrent and 17 (14.5%) had metastatic disease. The subjects in the three groups were homogeneous for clinical-pathological features. Pathological response was complete in 55 patients (47%), partial in 35 (29.9%), regardless of drug schedule (p = 0.501) and tumour presentation (p = 0.094). Wieberdink III-V toxicity was registered in 19.1%, 20% and 2.5% of patients, respectively (p < 0.051). Twenty-eight patients (23.9%) received adjuvant radiotherapy with no relevant toxicity. Five-year LPFS was 81.6% and 74.2% in patients with primary or recurrent disease, respectively (p = 0.652). After a median follow-up of 36.5 months, the limb sparing rate was 77.8%.
HILP performed with different drugs was equally active, either in primary, recurrent or metastatic STS, providing effective limb sparing and durable local control. Low dose TNF-α plus L-PAM had the most favourable toxicity profile. Adjuvant radiotherapy was not associated with relevant toxicity.
热灌注隔离肢体疗法(HILP)是一种局部区域治疗方法,旨在避免晚期肢体软组织肉瘤(STS)患者截肢。在过去25年中,已实施HILP程序以最大化其治疗比率。
对1989年至2013年接受HILP的117例患者进行回顾性分析。应用了三种不同的药物方案:1)阿霉素(n = 47),2)高剂量(3 - 4毫克)肿瘤坏死因子-α(TNF-α)加阿霉素(n = 30),3)低剂量(1毫克)TNF-α加美法仑(L-PAM)(n = 40)。通过MRI或CT以及手术标本评估肿瘤反应。还评估了毒性和局部无进展生存期(LPFS)。
总共92例(78.6%)患者为原发性疾病,25例(21.4%)为复发性疾病,17例(14.5%)为转移性疾病。三组患者的临床病理特征相似。55例患者(47%)病理反应完全,35例(29.9%)部分缓解,与药物方案(p = 0.501)和肿瘤表现(p = 0.094)无关。分别有19.1%、20%和2.5%的患者出现Wieberdink III - V级毒性(p < 0.051)。28例患者(23.9%)接受辅助放疗,无相关毒性。原发性或复发性疾病患者的5年LPFS分别为81.6%和74.2%(p = 0.652)。中位随访36.5个月后,保肢率为77.8%。
使用不同药物进行的HILP在原发性、复发性或转移性STS中同样有效,可有效保肢并实现持久的局部控制。低剂量TNF-α加L-PAM的毒性特征最有利。辅助放疗与相关毒性无关。