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Tumour flare reaction in cancer treatments: a comprehensive literature review

机译:癌症治疗中的肿瘤火光反应:综合文献综述

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摘要

In the past decade, tumour flare reaction (TFR) was considered as a new side effect associated with immunomodulatory agents (IMiDs) and as a condition of chronic lymphocytic leukaemia (CLL). However, this phenomenon is also observed with immune checkpoint inhibitors in solid tumours. It is still poorly understood and its incidence is underestimated. TFR has been associated with morbidity, therefore, early recognition and management of patients with TFR is critical. An exhaustive literature research between 1985 and 2016 was performed using PubMed; American Society of Clinical Oncology and American Society of Hematology abstracts reporting TFR or pseudoprogression were identified. The incidence of TFR in CLL ranged from 28 to 58%. Tumour response in patients treated beyond progression was reported in 9.7% with ipilimumab, 10% with nivolumab, 6.7 and 12% with pembrolizumab, and in renal cell carcinoma 69% with nivolumab. Rare life-threatening or fatal cases were reported; symptoms were usually mild. Studies showed that treating patients beyond progression yielded tumour responses, considering TFR as predictive of response. Treatment with immunomodulatory agents is associated with TFR, often misinterpreted as progression. Therefore, the identification of appropriate clinical benefit criteria and the use of immune-related response criteria in prospective trials for a better understanding are compulsory. Copyright (C) 2019 The Author(s). Published by Wolters Kluwer Health, Inc.
机译:在过去的十年中,肿瘤闪光反应(TFR)被认为是与免疫调节剂(IMID)相关的新副作用,以及慢性淋巴细胞白血病(CLL)的条件。然而,在实体瘤中的免疫检查点抑制剂也观察到这种现象。它仍然明白,其发病率低估了。 TFR已经与发病率有关,因此,TFR患者的早期识别和管理是至关重要的。 1985年至2016年间的详尽文献研究是使用PUBMED进行的;鉴定了美国临床肿瘤学会和美国血液学会摘要报告TFR或假冒竞争。 TFR在CLL中的发病率范围为28%至58%。患者肿瘤反应以普通率为9.7%的患者,IPILIMIMAB为9.7%,含有彭洛米布的肺炎虫,6.7%和12%,肾细胞癌69%用Nivolumab。据报道罕见的生命危及生命或致命病例;症状通常是温和的。研究表明,将患者视为进展产生肿瘤反应,考虑到TFR作为预测反应的预测。用免疫调节剂处理与TFR相关,通常误解为进展。因此,鉴定适当的临床益处标准和使用免疫相关响应标准的前瞻性试验,以更好地理解是强制性的。版权所有(c)2019提交人。由Wolters Kluwer Health,Inc。出版

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