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孤立肢体灌注术的分子层面

Molecular Aspects of the Isolated Limb Infusion Procedure.

作者信息

Teras Jüri, Carr Michael J, Zager Jonathan S, Kroon Hidde M

机构信息

Department of Surgical Oncology, North Estonia Medical Centre Foundation, 13419 Tallinn, Estonia.

Tallinn University of Technology, 12616 Tallinn, Estonia.

出版信息

Biomedicines. 2021 Feb 7;9(2):163. doi: 10.3390/biomedicines9020163.

Abstract

For decades, isolated limb infusion (ILI) and hyperthermic isolated limb perfusion (HILP) have been used to treat melanoma in-transit metastases and unresectable sarcoma confined to the limb utilizing the effect of loco-regional high-dose chemotherapy to the isolated limb. Both procedures are able to provide high response rates in patients with numerous or bulky lesions in whom other loco-regional treatments are becoming ineffective. In comparison to systemic therapies, on the other hand, ILI and HILP have the advantage of not being associated with systemic side-effects. Although in principle ILI and HILP are similar procedures, ILI is technically simpler to perform and differs from HILP in that it takes advantage of the hypoxic and acidotic environment that develops in the isolated limb, potentiating anti-tumour activity of the cytotoxic agents melphalan +/- actinomycin-D. Due to its simplicity, ILI can be used in both preclinical and clinical studies to test new cytotoxic regimens and combinations with the aim to overcome tumour resistance. In the future, administration of cytotoxic agents by ILI, in combination with systemic treatments such as BRAF/MEK/KIT inhibitors, immunotherapy (CTLA-4 blockade), and/or programmed death (PD-1) pathway inhibitors, has the potential to improve responses further by inducing increased tumour cell death while limiting the ability of the tumour to suppress the immune response.

摘要

几十年来,隔离肢体灌注(ILI)和热灌注隔离肢体(HILP)已被用于治疗肢体黑色素瘤的移行转移和局限于肢体的不可切除肉瘤,利用局部高剂量化疗对隔离肢体的作用。这两种方法都能在其他局部治疗无效的有大量或巨大病变的患者中提供高缓解率。另一方面,与全身治疗相比,ILI和HILP的优势在于不伴有全身副作用。虽然原则上ILI和HILP是相似的方法,但ILI在技术上操作更简单,与HILP的不同之处在于它利用了隔离肢体中形成的缺氧和酸中毒环境,增强了细胞毒性药物美法仑±放线菌素-D的抗肿瘤活性。由于其简单性,ILI可用于临床前和临床研究,以测试新的细胞毒性方案和联合用药,旨在克服肿瘤耐药性。未来,通过ILI给予细胞毒性药物,与BRAF/MEK/KIT抑制剂、免疫疗法(CTLA-4阻断)和/或程序性死亡(PD-1)通路抑制剂等全身治疗联合使用,有可能通过诱导更多肿瘤细胞死亡,同时限制肿瘤抑制免疫反应的能力,进一步提高缓解率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1d2/7915579/667627ac1004/biomedicines-09-00163-g001.jpg

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