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达布拉非尼和曲美替尼联合治疗晚期黑色素瘤相关噬血细胞性淋巴组织细胞增生症:两例报告

Hemophagocytic lymphohistiocytosis in advanced melanoma treated with dabrafenib and trametinib combination: two cases.

机构信息

Department of Dermatology and INSERM U1058 Pathogenesis and control of chronic infections, University of Montpellier.

Department of Medical Pharmacology and Toxicology, Regional Center of Pharmacovigilance, University Hospital of Montpellier, Montpellier, France.

出版信息

Melanoma Res. 2020 Oct;30(5):519-523. doi: 10.1097/CMR.0000000000000690.

Abstract

Hemophagocytic lymphohistiocytosis (HLH) has been only rarely reported in patients with BRAF-mutated advanced melanoma treated with targeted therapies and never with first-line dabrafenib/trametinib combination thus far. Two patients treated with first-line dabrafenib and trametinib combination therapy for metastatic melanoma presented with sudden occurrence of fever, cytopenia, rhabdomyolysis, hepatic cytolysis, hypertriglyceridemia and very high ferritin levels after few weeks of treatment, associated with concomitant epstein-barr virus (EBV) reactivation in one patient. In both cases, drug-induced HLH was primarily considered owing to a high H-score and the absence of other etiology. Patients rapidly improved after treatment discontinuation associated with oral steroids in one patient and did not relapse after subsequent treatment resumption with a concurrent anti-BRAF/anti-MEK combination. In metastatic melanoma HLH may occur either spontaneously in the absence of any treatment as a paraneoplastic condition, related to an intercurrent infection or drug-induced mainly with various immunotherapy or with dabrafenib and trametinib following immunotherapy. However, such observations are scarce and these are the first cases of HLH occurring during first-line treatment with dabrafenib and trametinib in advanced melanoma to our knowledge. Pathomechanisms remain to be elucidated since triggering factors may encompass the treatment itself but also other significant actors including viral reactivation along with the underlying disease. The liability of treatment should be considered in cases of HLH occurring in patients with advanced melanoma successfully treated with a combined targeted therapy. A rechallenge with a concurrent anti-BRAF/anti-MEK can be proposed in this setting.

摘要

噬血细胞性淋巴组织细胞增生症(HLH)仅在接受靶向治疗的 BRAF 突变型晚期黑色素瘤患者中很少见,迄今为止从未与一线达布拉非尼/曲美替尼联合治疗相关。两名接受一线达布拉非尼和曲美替尼联合治疗转移性黑色素瘤的患者在治疗数周后突然出现发热、血细胞减少、横纹肌溶解、肝细胞溶解、高甘油三酯血症和极高铁蛋白水平,其中一名患者同时伴有 EBV 再激活。在这两种情况下,药物诱导的 HLH 主要考虑是由于高 H 评分和没有其他病因。在一名患者中,停用药物并联合口服类固醇治疗后,患者迅速改善,在随后恢复治疗并联合抗 BRAF/抗 MEK 联合治疗后没有复发。在转移性黑色素瘤中,HLH 可能在没有任何治疗的情况下作为副肿瘤疾病自发发生,与并发感染或药物诱导有关,主要与各种免疫治疗或免疫治疗后达布拉非尼和曲美替尼有关。然而,这种观察结果很少,据我们所知,这是首例在晚期黑色素瘤中使用达布拉非尼和曲美替尼一线治疗期间发生 HLH 的病例。发病机制仍有待阐明,因为触发因素可能包括治疗本身,还可能包括其他重要因素,包括病毒再激活以及潜在疾病。在成功接受联合靶向治疗的晚期黑色素瘤患者中出现 HLH 时应考虑治疗的风险。在这种情况下,可以提出同时使用抗 BRAF/抗 MEK 进行再挑战。

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