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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/s00381-006-0243-z</subfield>
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   <subfield code="a">Astrocytic tumors in children: treatment results from a single institution</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ali Varan, Canan Akyüz, Nejat Akalan, Lale Atahan, Figen Söylemezoglu, Ugur Selek, Bilgehan Yalçin, Tezer Kutluk, Münevver Büyükpamukçu]</subfield>
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   <subfield code="a">Objective: The aims of this study are to evaluate the patients with astrocytomas and to investigate survival rates and prognosis. Patients and methods: Five hundred fourteen patients diagnosed with brain tumor between 1972 and 2003 were retrospectively analyzed. Three different chemotherapy regimens were used according to years. CCNU-based protocols were used in the early years; COPP (cyclophosphamide, oncovin, procarbazine, prednisolone) and CDDP+VP16 (cisplatinum + etoposide) were the other protocols used in the following years. Radiotherapy was used after 3years of age according to protocols. Results: Ninety-eight (19%) out of 514 patients have astrocytic histopathology. The histopathologic distribution was as follows: low grade, 55 patients; high grade, 43 patients. COPP regimen was given to 24 patients, CCNU-based regimen to 13, and CDDP+VP16 to 10 patients. We did not use any chemotherapy in 51 patients. Overall survival (OS) and event free-survival rates were 59.2 and 45.7% in whole group. OS rates were 93.3 and 22.4% for low-grade and high-grade histopathology, respectively (p=0.0001). OS for CCNU, CDDP+VP16, and COPP were 35.9, 22.8, and 30.4%, respectively. Conclusion: Low-grade astrocytomas are highly responsive to the surgery, and they do not need any further treatment unless the patient has relapse or recurrence. Still, the treatment of the high-grade tumors is a problem, and it needs new treatment approaches.</subfield>
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   <subfield code="a">Springer-Verlag, 2006</subfield>
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   <subfield code="a">Astrocytic tumors</subfield>
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   <subfield code="a">Children</subfield>
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   <subfield code="a">Treatment</subfield>
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   <subfield code="a">Varan</subfield>
   <subfield code="D">Ali</subfield>
   <subfield code="u">Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="a">Akyüz</subfield>
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   <subfield code="u">Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="a">Akalan</subfield>
   <subfield code="D">Nejat</subfield>
   <subfield code="u">Department of Neurosurgery, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="a">Atahan</subfield>
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   <subfield code="u">Department of Radiation Oncology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="a">Söylemezoglu</subfield>
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   <subfield code="u">Department of Pathology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="u">Department of Radiation Oncology, Faculty of Medicine, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="u">Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="a">Kutluk</subfield>
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   <subfield code="u">Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="u">Department of Pediatric Oncology, Institute of Oncology, Hacettepe University, 06100, Ankara, Turkey</subfield>
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   <subfield code="t">Child's Nervous System</subfield>
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   <subfield code="g">23/3(2007-03-01), 315-319</subfield>
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