The Toxic versus Therapeutic Interactions of Tyrosine Kinase Inhibitors and Radiation Therapy

G. Sokol
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Abstract

Introduction: Progress in both the development of Tyrosine Kinase Inhibitors (TKIs) and modern radiation therapy (RT) have opened new horizons for the safe and effective treatments of cancer. Combination therapies of TKIs and radiation therapy have been evaluated with variable sequencing and dosing of both agents. Radiation therapy induces cellular damage to cancer and normal tissue DNA by the production of direct and indirect ionization leading to a cascade of biological events. These ultimately lead to potential loss of cellular reproductive capacity, cell death or impotency. Repair mechanisms of RT-induced cell damage require repair pathways dependent on TK. TKIs are key regulators of cellular function and signaling proteins that catalyze phosphorylation reactions of tyrosine molecules. The purpose of this study was to briefly review the basic biology of RT and TKIs and to review the modern literature pertaining to the toxic and therapeutic effects of their combination in the treatment of cancer based on preclinical and clinical data. Methods: A retrospective review of the basic biology of RT and TKIs with the aim of identifying their combined toxicity and benefit in the treatment of cancer wa performed. A systematic search of the standard published radiotherapeutic, radiobiology, chemotherapy and radiotherapy texts, PubMed, Google Scholar, and Clinical Key using the search terms; TKI, RT and combination TKI and RT from 1985-2020 was employed. Data were abstracted from 220 entries from the literature published in English. Issues of toxicity and therapeutic efficacy were defined to evaluate the safe and effective use of combined modality therapy (CMT). Results: Few randomized studies were available for high-level recommendations. The combined treatment of cancer with TKIs and RT may have benefit for palliation, progression free survival, and potential survival under well-defined circumstances. Any benefit of combined therapy is accompanied by significant potential for enhanced radiation toxicity in addition to the baseline potential toxicities of both agents. Conclusion: The data reviewed suggest potential benefit from the CMT of TKIs and RT but at a significant risk of toxicity, which may include severe, hematological, cardiac, gastrointestinal, pulmonary and central nervous system toxicity. Further randomized prospective studies are necessary to define their safe and effective combined therapies.
酪氨酸激酶抑制剂和放射治疗的毒性与治疗相互作用
简介:酪氨酸激酶抑制剂(TKIs)的发展和现代放射治疗(RT)的进展为安全有效地治疗癌症开辟了新的视野。TKIs和放射治疗的联合治疗已经通过两种药物的不同排序和剂量进行了评估。放射治疗通过产生直接和间接电离导致一系列生物事件,从而诱导癌细胞和正常组织DNA的细胞损伤。这些最终导致细胞生殖能力的潜在丧失,细胞死亡或阳痿。rt诱导细胞损伤的修复机制需要依赖TK的修复途径。tki是细胞功能和信号蛋白的关键调节因子,催化酪氨酸分子的磷酸化反应。本研究的目的是简要回顾RT和TKIs的基础生物学,并根据临床前和临床数据回顾有关它们联合治疗癌症的毒性和治疗效果的现代文献。方法:回顾性回顾RT和TKIs的基础生物学,目的是确定它们在治疗癌症方面的综合毒性和益处。系统搜索标准出版的放射治疗、放射生物学、化疗和放疗文本、PubMed、Google Scholar和临床关键使用搜索词;采用1985-2020年的TKI、RT及TKI与RT的组合。数据摘自220篇已发表的英文文献。定义了毒性和治疗效果的问题,以评估联合治疗(CMT)的安全性和有效性。结果:很少有随机研究可用于高水平推荐。在明确的情况下,TKIs和RT联合治疗癌症可能有利于缓解、无进展生存和潜在生存。除了两种药物的基线潜在毒性外,联合治疗的任何益处都伴随着显著的放射毒性增强的潜力。结论:回顾的数据表明,TKIs和RT的CMT有潜在的益处,但有显著的毒性风险,可能包括严重的血液、心脏、胃肠道、肺和中枢神经系统毒性。需要进一步的随机前瞻性研究来确定其安全有效的联合治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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