Treatment for recurrent medulloblastoma with intrathecal liposomal cytarabine and systemic metronomic combination therapy

被引:11
|
作者
Nygaard, Randi [2 ]
Kivivuori, Sanna-Maria [1 ,3 ]
机构
[1] Univ Helsinki, Childrens Hosp, Div Hematol Oncol & Stem Cell Transplantat, Helsinki 00029, Finland
[2] St Olavs Univ Hosp, Dept Pediat, Trondheim, Norway
[3] Univ Helsinki, Cent Hosp, Helsinki 00029, Finland
关键词
antiangiogenic therapy; liposomal cytarabine; medulloblastoma; metronomic therapy; recurrence; HIGH-DOSE CHEMOTHERAPY; SOLID TUMORS; CHILDREN; RADIOTHERAPY; FEASIBILITY; LEUKEMIA; SAFETY; TRIAL;
D O I
10.1097/CAD.0b013e32834ee315
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis of recurrent medulloblastoma is dismal, with a median survival of less than 1 year. Our patient was initially diagnosed with high-risk medulloblastoma when he was 14 years old. He had a recurrence 18 months after the end of therapy. Recurrence treatment consisted of 13 intrathecal applications of liposomal cytarabine over an 18-month period, and oral metronomic antiangiogenic therapy with thalidomide, celecoxib, and etoposide. Side effects from the intrathecal treatment were most likely related to arachnoiditis despite prolonged prophylaxis with steroids. He also developed partial hearing loss. Neutropenia was the main side effect of the metronomic therapy. He remains alive, with a good quality of life and without evidence of disease 34 months from the start of recurrence therapy. This combination of local antineoplastic and systemic antiangiogenic therapy seems to be promising for recurrent medulloblastoma. However, more patients and standardized protocols are needed to verify the benefit of this combination therapy and to define the correct duration of treatment. Anti-Cancer Drugs 23: 342-346 (C) 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:342 / 346
页数:5
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