Department of Medical Oncology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Pediatr Blood Cancer. 2010 Dec 15;55(7):1431-2. doi: 10.1002/pbc.22755.
Desmoplastic small round cell tumor (DSRCT) is a rare and aggressive neoplasm that mostly occurs in young males. No curative treatment options currently exist for this type of tumor and long-term survival remains poor. In vitro rapamycin induces apoptotic death of JN-DSRCT-1 cells, a possible model for desmoplastic small round cell tumors in which the EWS gene is fused to the WT1 gene. We therefore demonstrate the prolonged activity of temsirolimus, an mTOR-inhibitor, in a patient with DSRCT.
促结缔组织增生性小圆细胞肿瘤(DSRCT)是一种罕见且侵袭性的肿瘤,主要发生在年轻男性中。目前针对这种类型的肿瘤还没有治愈的选择,长期生存仍然较差。体外雷帕霉素诱导 JN-DSRCT-1 细胞凋亡死亡,这可能是一种促结缔组织增生性小圆细胞肿瘤的模型,其中 EWS 基因与 WT1 基因融合。因此,我们证明了 mTOR 抑制剂替西罗莫司在 DSRCT 患者中的长期疗效。