Clinical factors and conventional MRI may independently predict progression-free survival and overall survival in adult pilocytic astrocytomas

[1] Louis DN(2016)The 2016 World Health Organization classification of tumors of the central nervous system: a summary Acta Neuropathol 131 803-820

[2] Perry A(2018)CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2011–2015 Neuro Oncol. 20 iv1-iv86

[3] Reifenberger G(2003)A population-based study of the incidence and survival rates in patients with pilocytic astrocytoma J Neurosurg 98 1170-1174

[4] Ostrom QT(2004)Pilocytic astrocytoma of the adult—clinical features, radiological features and management Br J Neurosurg 18 613-616

[5] Gittleman H(1985)Juvenile pilocytic astrocytoma of the cerebrum in adults. A distinctive neoplasm with favorable prognosis J Neurosurg. 63 382-386

[6] Truitt G(2015)Adult patients with supratentorial pilocytic astrocytoma: long-term follow-up of prospective multicenter clinical trial NCCTG-867251 (Alliance) Neurooncol Pract 2 199-204

[7] Boscia A(2012)Pilocytic astrocytoma survival in adults: analysis of the Surveillance, Epidemiology, and End Results Program of the National Cancer Institute J Neurooncol 108 187-193

[8] Kruchko C(2020)Clinical characteristics and prognostic factors of adult patients with pilocytic astrocytoma J Neurooncol 148 187-198

[9] Barnholtz-Sloan JS(2019)Characteristics, survival and incidence rates and trends of pilocytic astrocytoma in children in the United States; SEER-based analysis J Neurol Sci 400 148-152

[10] Burkhard C(2016)Low rates of recurrence and slow progression of pediatric pilocytic astrocytoma after gross-total resection: justification for reducing surveillance imaging J Neurosurg Pediatr 17 569-572

[1] Louis DN(2016)The 2016 World Health Organization classification of tumors of the central nervous system: a summary Acta Neuropathol 131 803-820

[2] Perry A(2018)CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2011–2015 Neuro Oncol. 20 iv1-iv86

[3] Reifenberger G(2003)A population-based study of the incidence and survival rates in patients with pilocytic astrocytoma J Neurosurg 98 1170-1174

[4] Ostrom QT(2004)Pilocytic astrocytoma of the adult—clinical features, radiological features and management Br J Neurosurg 18 613-616

[5] Gittleman H(1985)Juvenile pilocytic astrocytoma of the cerebrum in adults. A distinctive neoplasm with favorable prognosis J Neurosurg. 63 382-386

[6] Truitt G(2015)Adult patients with supratentorial pilocytic astrocytoma: long-term follow-up of prospective multicenter clinical trial NCCTG-867251 (Alliance) Neurooncol Pract 2 199-204

[7] Boscia A(2012)Pilocytic astrocytoma survival in adults: analysis of the Surveillance, Epidemiology, and End Results Program of the National Cancer Institute J Neurooncol 108 187-193

[8] Kruchko C(2020)Clinical characteristics and prognostic factors of adult patients with pilocytic astrocytoma J Neurooncol 148 187-198

[9] Barnholtz-Sloan JS(2019)Characteristics, survival and incidence rates and trends of pilocytic astrocytoma in children in the United States; SEER-based analysis J Neurol Sci 400 148-152

[10] Burkhard C(2016)Low rates of recurrence and slow progression of pediatric pilocytic astrocytoma after gross-total resection: justification for reducing surveillance imaging J Neurosurg Pediatr 17 569-572