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癌症治疗中的肿瘤 flares 反应:全面文献综述。

Tumour flare reaction in cancer treatments: a comprehensive literature review.

机构信息

Oncology Department, Groupe Hospitalier Sud Ile-de-France, Melun, France.

出版信息

Anticancer Drugs. 2019 Oct;30(9):953-958. doi: 10.1097/CAD.0000000000000814.

Abstract

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.

摘要

在过去的十年中,肿瘤 flares 反应(TFR)被认为是一种与免疫调节药物(IMiDs)相关的新的副作用,也是慢性淋巴细胞白血病(CLL)的一种情况。然而,这种现象也在实体瘤的免疫检查点抑制剂中观察到。它仍然知之甚少,其发生率被低估。TFR 与发病率有关,因此,早期识别和管理 TFR 患者至关重要。我们使用 PubMed 进行了 1985 年至 2016 年的全面文献研究;确定了报告 TFR 或假性进展的美国临床肿瘤学会和美国血液学会摘要。CLL 中 TFR 的发生率为 28%至 58%。在接受治疗后进展的患者中,Ipilimumab 的肿瘤缓解率为 9.7%,nivolumab 为 10%,pembrolizumab 为 6.7%和 12%,而肾细胞癌的 nivolumab 为 69%。有罕见的危及生命或致命病例报告;症状通常较轻。研究表明,对进展后患者进行治疗可产生肿瘤反应,将 TFR 视为反应的预测指标。免疫调节药物的治疗与 TFR 相关,常被误解为进展。因此,在前瞻性试验中,必须确定适当的临床获益标准,并使用免疫相关反应标准,以更好地理解。

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