皮肤病学中的血浆癌治疗

Q1 Medicine
Georg Daeschlein , Claudia Sicher , Sebastian von Podewils , Rico Rutkowski , Michael Jünger
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引用次数: 0

摘要

皮肤科癌症治疗的主要主题是黑色素瘤(MM),基底细胞癌(BCC),鳞状细胞癌(SCC)和转移性皮肤肿瘤。因此,由于致命的结果,IV期MM是至关重要的。尽管目前免疫疗法在治疗上取得了一些实质性进展,但当疾病在治疗中进展或肿瘤基本表现出难治性时,替代疗法是有保证的。国家指南目前推荐ipilumumab, vemurafenib, dabrafenib和高剂量IL-2作为IV期黑色素瘤的一线药物,但没有数据指导非常常见的皮肤和皮下转移的管理。治疗方案包括病灶内电化疗和卡介苗-谷氨酰胺、离体肢体灌注/输注、干扰素-α、局部咪喹莫特、冷冻疗法、放射、干扰素治疗和瘤内白介素-2注射。最近的发展包括抗程序性细胞死亡1受体药物(PD-1,纳武单抗和派姆单抗),抗程序性死亡配体1药物,溶瘤疫苗(talimogene laherparepevec),过继T细胞治疗和树突状细胞疫苗。对于BCC和SCC,主要是侵袭性变异是新疗法的兴趣。第三种实体是不同来源的转移性肿瘤,暴露于单一到现场消毒。与传统药物化疗相比,冷等离子体(CAP)的反应方式不同且复杂得多,现代抗代谢物和免疫疗法与迄今为止的常规治疗相比,剂量选择有限,以避免更强的毒性,因此与CAP联合治疗疗效更好,副作用更少。通过这种方法,可以在体外显示足素、达卡霉素、紫杉醇和博来霉素的大量附加效应。在博来霉素(全身性)存在的情况下,将CAP与化疗一起应用于鳞状细胞癌和光化性角化病时,也可以实现类似的增强作用。这是CAP首次在人类中显示出有效的抗癌功效。在转移性肿瘤中,CAP被证明可以减缓肿瘤生长,击败微生物重复感染,支持疼痛缓解,从而提高生活质量。此外,与标准治疗相比,CAP证明了一些患者明显更好的预后和更好的耐受性。常规化疗和物理支持化疗与CAP的结合在治疗黑色素瘤和鳞状细胞癌等人类癌症方面非常有益,因为化疗药物的肿瘤缩小程度提高,药物毒性降低,从而显着提高了生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Plasma Cancer Therapy In Dermatology

Main topics in cancer treatment in dermatology are melanoma (MM), basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and metastatic skin tumors. Thereof stage IV MM because of fatal outcome is uf utmost importance. Despite some substantial therapeutic progress now in this entity by immunologic treatments alternatives are warranted when disease is progressing under therapy or the tumor basically appears refractory. National guidelines currently recommend ipilumumab, vemurafenib, dabrafenib, and high-dose IL-2 as first line agents for Stage IV melanoma but no data exists to guide management of cutaneous and subcutaneous metastases which are very common. Therapeutic options include intralesional electrochemotherapy and Bacillus Calmette-Guérin, isolated limb perfusion/infusion, interferon-α, topical imiquimod, cryotherapy, radiation, interferon therapy, and intratumoral interleukin-2 injections. Recent developments include anti-programmed cell death 1 receptor agents (PD-1, nivolumab and pembrolizumab), anti-programmed death-ligand 1 agents, and oncolytic vaccines (talimogene laherparepevec), adoptive T cell therapy and dendritic cell vaccines. Regarding BCC and SCC mainly the aggressive variants are of interest for new therapies. A third entity are metastatic tumors of different origin exposing single to field canzerization. Since Cold Plasma (CAP) reacts by different and substantially more complex modes compared to classic drug chemotherapy and also modern antimetabolite and immune therapies like hitherto conventional treatment suffers from limited dosage options to avoid stronger toxicity, combined treatment with CAP offers better efficacy with less adverse effects. By this way substantial add on effects can be shown in vitro for fotemustin, dacarbacin, paclitaxel, and bleomycin. Similar potentiation can be achieved when electrochemotherapy is applied together with CAP in the presence of bleomycin (systemic) and with the squamous cell carcinoma and the actinic keratosis for the first time CAP was also shown to exert effective anticancer efficacy in humans. In metastatic tumors CAP was shown to decelerate tumor growth, defeat microbial superinfection, support pain relief and therewith increasing quality of life. Additionally for some patients CAP proved significantly better outcome together with better tolerability compared with standard treatment. The combination of conventional and physically supported chemotherapy with CAP appears highly beneficial in therapy of human cancer like melanoma and squamous cell carcinoma by enhanced tumor reduction and less drug toxicity of chemotherapeutics thus improving markedly quality of life.

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Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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