Sahdev Indira, James-Herry Angelica, Scimeca Philip, Parker Robert
Division of Pediatric Hematology/Oncology and Stem Cell Transplantation, Schneider Children's Hospital, Manhasset, New York 11040, USA.
J Pediatr Hematol Oncol. 2003 Jun;25(6):491-4. doi: 10.1097/00043426-200306000-00013.
We report identical twin boys who each had stage IV rhabdoid tumor of the left kidney at the age of 5 months and 2 years, respectively. The 5-month-old boy, despite receiving chemotherapy, died of progressive disease at the age of 12 months. Following resection of the tumor, his twin brother was treated with 6 cycles of combination chemotherapy consisting of cisplatinum, doxorubicin, vincristine, cyclophosphamide, and actinomycin-D alternating with ifosfamide and etoposide. After complete regression of lung and brain metastases, he received high-dose thiotepa, etoposide, and cyclophosphamide, followed by autologous peripheral stem cell rescue. The patient is presently alive and free of disease 6 years posttransplant. High-dose chemotherapy followed by autologous stem cell transplant may be an effective front-line therapeutic approach for patients with metastatic rhabdoid tumor of the kidney.
我们报告了一对同卵双胞胎男孩,他们分别在5个月和2岁时患有左肾IV期横纹肌肉瘤。5个月大的男孩尽管接受了化疗,但在12个月时因病情进展而死亡。肿瘤切除后,他的双胞胎兄弟接受了6个周期的联合化疗,化疗方案为顺铂、阿霉素、长春新碱、环磷酰胺和放线菌素-D,与异环磷酰胺和依托泊苷交替使用。肺和脑转移灶完全消退后,他接受了大剂量的噻替派、依托泊苷和环磷酰胺治疗,随后进行了自体外周干细胞救援。该患者目前在移植后6年仍存活且无疾病。大剂量化疗后进行自体干细胞移植可能是肾转移性横纹肌肉瘤患者有效的一线治疗方法。