Feasibility and Efficacy of Repeated Chemotherapy for Progressive Pediatric Low-Grade Gliomas

被引:27
作者
Scheinemann, Katrin [1 ,2 ]
Bartels, Ute [1 ]
Tsangaris, Elena [1 ]
Hawkins, Cynthia [3 ]
Huang, Annie [1 ]
Dirks, Peter [4 ]
Fried, Iris [1 ]
Bouffet, Eric [1 ]
Tabori, Uri [1 ]
机构
[1] Hosp Sick Children, Div Hematol Oncol, Toronto, ON M5G 1X8, Canada
[2] McMaster Childrens Hosp, Div Hematol Oncol, Hamilton, ON, Canada
[3] Hosp Sick Children, Div Pathol, Toronto, ON M5G 1X8, Canada
[4] Hosp Sick Children, Div Neurosurg, Toronto, ON M5G 1X8, Canada
关键词
chemotherapy; children; grade glioma; low recurrence; outcome; CENTRAL-NERVOUS-SYSTEM; BRAIN-TUMORS; RADIATION-THERAPY; ORAL ETOPOSIDE; ONCOLOGY-GROUP; CHILDREN; CHILDHOOD; RECURRENT; VINCRISTINE; CARBOPLATIN;
D O I
10.1002/pbc.22917
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Chemotherapy is widely accepted as first-line therapy for pediatric low-grade gliomas (LGG). Treatment modalities for further progression are not clearly established. The aim of the study was to determine the feasibility and long-term outcome of repeated chemotherapy for children with recurrent LGG. Methods. The study group consisted of patients who received a second line of chemotherapy at progression of their LGG. We compared toxicity, progression-free survival (PFS), and overall survival(OS) of patients treated with chemotherapy at the time of initial diagnosis and patients who received another treatment with chemotherapy at further progression. Results. Between 1985 and 2009, 118 patients received chemotherapy as primary treatment for LGG, 38 had repeated chemotherapy at further progression. Chemotherapy was tolerated extremely well. Ninety-two percent of patients completed their second line protocol and toxicity was comparable between initial and second line chemotherapy. Five-year OS and PFS were 86 +/- 6% and 37 +/- 8%, respectively, which were similar to first-line chemotherapy (P = 0.14). Repeated chemotherapy courses were not associated with worsening of visual, neuroendocrine, or other long-term organ sequelae. Conclusion. This study demonstrates high feasibility and low mortality of repeated chemotherapy treatment for progressive LGG. The chronic nature of LGG concerning tumor progression justifies consideration of nontoxic second-line treatment regimens at the time of recurrence. Prospective studies focusing on toxicity and long-term outcome are needed to substantiate this approach. Pediatr Blood Cancer 2011;57:84-88. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:84 / 88
页数:5
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