Myeloablative chemotherapy and autologous stem cell transplantation in patients with relapsed or progressed central nervous system germ cell tumors: results of Korean Society of Pediatric Neuro-Oncology (KSPNO) S-053 study

被引:23
作者
Baek, Hee Jo [1 ]
Park, Hyeon Jin [2 ]
Sung, Ki Woong [3 ]
Lee, Soo Hyun [3 ]
Han, Jung Woo [4 ]
Koh, Kyung Nam [5 ]
Im, Ho Joon [5 ]
Kang, Hyoung Jin [6 ]
Park, Kyung Duk [6 ]
机构
[1] Chonnam Natl Univ, Hwasun Hosp, Sch Med, Dept Pediat, Kwangju, South Korea
[2] Natl Canc Ctr, Ctr Pediat Oncol, Goyang, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pediat, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Severance Hosp, Dept Pediat, Seoul, South Korea
[5] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pediat, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Canc Res Inst, Dept Pediat, Seoul, South Korea
关键词
Central nervous system germ cell tumor; High-dose chemotherapy; Autologous stem cell transplantation; HIGH-DOSE CHEMOTHERAPY; MALIGNANT BRAIN-TUMORS; RADIATION-THERAPY; HIGH-RISK; INTRACRANIAL GERMINOMA; CNS GERMINOMA; RESCUE; RECURRENT; CHILDREN; CYCLOPHOSPHAMIDE;
D O I
10.1007/s11060-013-1188-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study evaluated the feasibility and effectiveness of myeloablative high-dose chemotherapy and autologous stem cell transplantation in patients with relapsed or progressed central nervous system germ cell tumors (CNS-GCTs). Eleven patients with non-germinomatous germ cell tumors and nine patients with germinomas were enrolled. Patients received between two and eight cycles of conventional chemotherapy prior to HDCT/autoSCT with or without radiotherapy. Overall, 16 patients proceeded to the first HDCT/autoSCT, and nine proceeded to the second HDCT/autoSCT. CTE (carboplatin-thiotepa-etoposide) and cyclophosphamide-melphalan (CM) regimens were used for the first and second HDCT, respectively. Toxicities during HDCT/autoSCT were acceptable, and there were no treatment-related deaths. Twelve patients experienced relapse or progression; however, four patients with germinomas remain alive after subsequent RT. Therefore, a total of 12 patients (four NGGCTs and eight germinomas) remain alive with a median follow-up of 47 months (range 22-90) after relapse or progression. The probability of 3-year overall survival was 59.1 +/- A 11.2 % (36.4 +/- A 14.5 % for NGGCTs vs. 88.9 +/- A 10.5 % for germinomas, P = 0.028). RT, particularly craniospinal RT, was associated with a better tumor response prior to HDCT/autoSCT and a better final outcome. In conclusion, HDCT/autoSCT was feasible, and survival rates were encouraging. Further study with a larger cohort of patients is needed to elucidate the role of HDCT/autoSCT in the treatment of relapsed or progressed CNS-GCTs.
引用
收藏
页码:329 / 338
页数:10
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