Kawakami Chihiro, Inoue Akiko, Takitani Kimitaka, Tsuji Motomu, Wakai Kimiko, Tamai Hiroshi
Department of Pediatrics, Osaka Medical College, Takatsuki, Osaka, Japan;
Department of Pathology, Osaka Medical College, Takatsuki, Osaka, Japan;
Clin Pract. 2012 May 7;2(2):e49. doi: 10.4081/cp.2012.e49. eCollection 2012 Mar 30.
We herein report a female child with choroid plexus carcinoma treated with standard dose of imatinib at disease recurrence. This patient failed initial twice-surgical resections, central nervous system (CNS) irradiation, and adjuvant chemotherapies and high-dose thiotepa and melphalan with auto peripheral blood stem cell rescue. Finally, imatinib treatment was undergone as a palliative setting, however the tumor did not reduce and the patient died of tumor bleedings. We consider that the reasons for the failure are as follows: i) adequate CNS level of imatinib were not obtained because of the blood brain barrier, ii) the lack of platelet-derived growth factor receptor beta expression in our case may have a crucial role.
我们在此报告一名患有脉络丛癌的女童,在疾病复发时接受了标准剂量的伊马替尼治疗。该患者初次手术切除两次、中枢神经系统(CNS)放疗、辅助化疗以及高剂量噻替派和马法兰联合自体外周血干细胞救援均失败。最后,在姑息治疗的情况下接受了伊马替尼治疗,但肿瘤并未缩小,患者死于肿瘤出血。我们认为失败的原因如下:i)由于血脑屏障,未获得足够的伊马替尼中枢神经系统水平;ii)在我们的病例中缺乏血小板衍生生长因子受体β表达可能起关键作用。