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转移性黑色素瘤对BRAF/MEK双重抑制快速反应导致肝出血和骨转移:一例报告

Hemorrhage of liver and bone metastases as a result of rapid response to dual BRAF/MEK inhibition in metastatic melanoma: a case report.

作者信息

Loyson Tine, Werbrouck Emilie, Punie Kevin, Bonne Lawrence, Vandecaveye Vincent, Bechter Oliver

机构信息

Department of Medical Oncology, General Hospital Sint-Jozef Malle, Malle.

Department of Medical Oncology, General Hospital Klina Brasschaat, Brasschaat.

出版信息

Melanoma Res. 2018 Apr;28(2):147-150. doi: 10.1097/CMR.0000000000000419.

Abstract

Combination therapy using a BRAF and MEK inhibitor significantly improves both progression-free and overall survival in patients with BRAF V600-mutated stage IV melanoma. Dual MAPK inhibition achieves an objective response in the majority of patients. We present a case of a woman with BRAF V600E-mutated malignant melanoma and rapidly progressing liver, bone, and lymph node metastases. The patient commenced dabrafenib and trametinib with clinical and biochemical signs of response after 2 days. On day 3 she developed grade 3 liver hemorrhage, which was successfully embolized. Her anemia responded appropriately to transfusions and stabilized after interventional resolution of the hemorrhagic event. Subsequently she developed a pathological fracture of the right proximal humerus. MRI showed cystic bone metastases with stigmata of bleeding. To our knowledge, this is the first case report of a patient with hemorrhage of both liver and bone metastases of a melanoma. As the patient responded rapidly to dabrafenib and trametinib we hypothesize that the hemorrhage may be due to rapid tumor necrosis and bleeding of affected tumor supplying blood vessels. Our case demonstrates the importance of considering tumoral bleeding as a side effect of BRAF and MEK inhibition in responding melanoma patients. Mechanical intervention can be effective in resolving this treatment-related adverse event.

摘要

使用BRAF和MEK抑制剂的联合疗法可显著提高BRAF V600突变的IV期黑色素瘤患者的无进展生存期和总生存期。双重MAPK抑制在大多数患者中实现了客观缓解。我们报告了一例患有BRAF V600E突变恶性黑色素瘤且肝、骨和淋巴结转移迅速进展的女性病例。患者开始使用达拉非尼和曲美替尼,2天后出现临床和生化反应迹象。第3天,她发生了3级肝出血,经成功栓塞治疗。她的贫血对输血反应良好,在出血事件经介入治疗缓解后病情稳定。随后,她出现了右肱骨近端病理性骨折。MRI显示囊性骨转移并伴有出血迹象。据我们所知,这是首例黑色素瘤肝转移和骨转移均发生出血的病例报告。由于患者对达拉非尼和曲美替尼反应迅速,我们推测出血可能是由于肿瘤快速坏死以及受影响肿瘤供血血管出血所致。我们的病例证明了在有反应的黑色素瘤患者中,将肿瘤出血视为BRAF和MEK抑制的副作用的重要性。机械干预可有效解决这种与治疗相关的不良事件。

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