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Neoadjuvant
chemotherapy with temozolamide plus ifosfamide, carboplatin and etoposide in
pediatric patients with high grade astrocytomas. Phase II study
E.
Lopez Aguilar, S. Delgado-Huerta, A. C. Sepulveda-Vildosola, V.
Wanzke-Del-angel, H. Rodriguez-Jimenez
Hospital
de Pediatria CMN SXXI IMSS, Mexico, Mexico
Central
Nervous System tumors are the second most frequent malignancy in pediatric
oncology, and its survival has been poor.
Temozolamide (Schering Plough) has been used in adults with some success in
astrocytomas.
Our objective was to determine tumoral response to a chemotherapeutic regimen
consisting on: temozolamide, carboplatin, ifosfamide and etoposide in pediatric
patients with high-grade astrocytomas and to calculate overall survival and
toxic effects.
We included patients less than 16 years of age with newly diagnosed astrocytoma
between January 2001 and January 2002.
Every patient had normal renal and hepatic function tests and had a calculated
expectancy of life greater than 16 weeks.
After informed consent of their parents or tutors, every patient received
hyperhidratation, antiemetic treatment and MESNA followed by temozolamide
(200mg/m2 for 5 days), carboplatin (400 mg/m2 on day 1), ifosfamide (2 gm/m2 3
days) and etoposide (100 mg/m2 3 days) every 4 weeks for 4 courses.
They all then received radiotherapy (5,500 cGy).
We included 7 patients, 5 of which were boys (M:F 2.5:1).
Mean age was 10 years.
Four were located to the brain stem and 3 were supratentorial.
Six of them were anaplasic and 1 glioblastoma multiforme.
Overall tumor reduction was 44%, with 1 complete response, 1 partial response
and 2 stable diseases after the first 4 courses of chemotherapy.
Three patients died: 2 corresponding to the brain stem and 1 supratentorial.
Overall survival was 52% at 24 months.
There was no significant toxicity during the study.
Temozolamide in combination with other proven chemotherapeutic regimens such as
ICE seems to be useful and secure in the treatment of high grade astrocytomas in
children.
© Copyright 2003
American Society of Clinical Oncology All rights
reserved worldwide
Source: http://www.asco.org/ac/1,1003,_12-002489-00_18-002003-00_19-00100274-00_29-00A,00.asp?cat=CNS+Tumors&parent=
Central+Nervous+System+Tumors&returnpid=2325&SubCat_ID=4
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