TY - JOUR
T1 - Long-term outcome of centrally located low-grade glioma in children
AU - Terashima, Keita
AU - Chow, Kevin
AU - Jones, Jeremy
AU - Ahern, Charlotte
AU - Jo, Eunji
AU - Ellezam, Benjamin
AU - Paulino, Arnold C.
AU - Okcu, M. Fatih
AU - Su, Jack
AU - Adesina, Adekunle
AU - Mahajan, Anita
AU - Dauser, Robert
AU - Whitehead, William
AU - Lau, Ching
AU - Chintagumpala, Murali
PY - 2013/7/15
Y1 - 2013/7/15
N2 - BACKGROUND Optimal management of children with centrally located low-grade glioma (LGG) is unclear. Initial interventions in most children are chemotherapy in younger and radiation therapy (RT) in older children. A better understanding of the inherent risk factors along with the effects of interventions on long-term outcome can lead to reassessment of the current approaches to minimize long-term morbidity. METHODS To reassess the current treatment strategies of centrally located LGG, we compared the long-term survival and morbidity of different treatment regimens. Medical records of patients primarily treated at Texas Children's Cancer and Hematology Centers between 1987 and 2008 were reviewed. RESULTS Forty-seven patients with a median follow-up of 79 months were included in the analysis. The 5-year overall survival and progression-free survival (PFS) for all patients were 96% and 53%, respectively. The 5-year PFS for those treated initially with RT (12 patients; median age, 11 years [range, 3-15 years]) and with chemotherapy (28 patients; median age, 2 years [range 0-8 years]) were 76% and 37%, respectively (log-rank test P =.02). Among children who progressed after chemotherapy, the 5-year PFS after salvage RT was 55%. Patients diagnosed at a younger age (<5 years) were more likely to experience endocrine abnormalities (Fisher exact test; P<.00001). CONCLUSIONS Effective and durable tumor control was obtained with RT as initial treatment. In younger patients, chemotherapy can delay the use of RT; however, frequent progression and long-term morbidity are common. More effective and less toxic therapies are required in these patients, the majority of whom are long-term survivors.
AB - BACKGROUND Optimal management of children with centrally located low-grade glioma (LGG) is unclear. Initial interventions in most children are chemotherapy in younger and radiation therapy (RT) in older children. A better understanding of the inherent risk factors along with the effects of interventions on long-term outcome can lead to reassessment of the current approaches to minimize long-term morbidity. METHODS To reassess the current treatment strategies of centrally located LGG, we compared the long-term survival and morbidity of different treatment regimens. Medical records of patients primarily treated at Texas Children's Cancer and Hematology Centers between 1987 and 2008 were reviewed. RESULTS Forty-seven patients with a median follow-up of 79 months were included in the analysis. The 5-year overall survival and progression-free survival (PFS) for all patients were 96% and 53%, respectively. The 5-year PFS for those treated initially with RT (12 patients; median age, 11 years [range, 3-15 years]) and with chemotherapy (28 patients; median age, 2 years [range 0-8 years]) were 76% and 37%, respectively (log-rank test P =.02). Among children who progressed after chemotherapy, the 5-year PFS after salvage RT was 55%. Patients diagnosed at a younger age (<5 years) were more likely to experience endocrine abnormalities (Fisher exact test; P<.00001). CONCLUSIONS Effective and durable tumor control was obtained with RT as initial treatment. In younger patients, chemotherapy can delay the use of RT; however, frequent progression and long-term morbidity are common. More effective and less toxic therapies are required in these patients, the majority of whom are long-term survivors.
KW - BRAF-KIAA1549 fusion protein
KW - chemotherapy
KW - childhood cerebral astrocytoma
KW - childhood optic nerve glioma
KW - hypothalamic-chiasmatic neoplasms
KW - long-term effects
KW - pilocytic astrocytoma
KW - radiotherapy
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U2 - 10.1002/cncr.28110
DO - 10.1002/cncr.28110
M3 - Article
C2 - 23625612
AN - SCOPUS:84879661588
SN - 0008-543X
VL - 119
SP - 2630
EP - 2638
JO - Cancer
JF - Cancer
IS - 14
ER -