TreatmentCyclophosphamide / Etoposide / Fluorouracil / Vincristine


Journal of Neuro-Oncology, Volume 80, Number 3 / December, 2006, Pages 277-284, Published online: 29 June 2006, DOI: 10.1007/s11060-006-9185-2


Abstract

Effectiveness of novel combination chemotherapy, consisting of 5-fluorouracil, vincristine, cyclophosphamide and etoposide, in the treatment of low-grade gliomas in children

Mee Jeong Lee1, 6, Young Shin Ra2, Jun Bum Park2, Hyun Woo Goo3, Seung Do Ahn4, Shin Kwang Khang5, Joon Sup Song1, Yoon Jung Kim1 and Thad T. Ghim1, 7, * 

1Department of Pediatrics, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. 2Department of Neurosurgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. 3Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. 4Department of Therapeutic Radiology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. 5Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. 6Department of Pediatrics, Dankook University College of Medicine, Cheonan, Korea. 7Department of Pediatrics, Center for Ped. Hematology/Oncology, National Cancer Center, 809 Madu 1-dong, Ilsan-gu, Goyang-si, Gyeonggi-do, Korea. -- *Correspondence: Thad T. Ghim, Email: tghim@ncc.re.kr. -- Received: 15 February 2006  Accepted: 21 April 2006  Published online: 29 June 2006.


Low-grade gliomas (LGG), which account for about 30% of brain tumors in children, are usually treated with surgical excision and/or radiotherapy. 
For patients who have significant residual tumor after resection or relapse after radiation, the proper chemotherapy regimen has not yet been identified. 
Thirteen children diagnosed with LGG outside the cerebellum between January 1999 and December 2004, all of whom had significant residual tumor after surgical resection, relapsed after radiation or showed visual deterioration, were treated for 18 months with a multi-drug regimen of vincristine, etoposide, cyclophosphamide and 5-fluorouracil. 
Of the 7 patients who completed chemotherapy, 1 showed complete response (CR), 5 showed partial response (PR), and 1 had stable disease (SD). 
In 5 patients, chemotherapy was prematurely discontinued; 4 of these patients showed tumor progression and 1 had SD. 
One patient is still undergoing treatment. 
The side effects of chemotherapy were manageable. 
The median time to tumor response was 34 months (range, 2–82 months). 
The progression free survival was 67.3%. 
Pediatric LGG patients with residual tumor after surgery or who undergo relapse(s) may be successfully treated using our combination chemotherapy regimen.

Keywords: Brain tumor, Chemotherapy, Children, Low-grade glioma


© 2006 Springer
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