Dergiler / Turkish Journal of Cancer / 2000 / Cilt: 30 - Sayı: 1

Radiotherapy in the management of optic pathway gliomas

Sayfa
31–35
DOI
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We conclude that postoperative radiotherapy is beneficial in patients with chiasmal involvement and with incomplete resections.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:A retrospective study was performed in 28 patients with optic pathway gliomas treated at our institution between 1975-1995.
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Temel Bulgular & Veri:The median age was 8 (range 1-55) years.
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Sonuç & Katkı:We conclude that postoperative radiotherapy is beneficial in patients with chiasmal involvement and with incomplete resections.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Optik sinir gliomu · Optik sinir neoplazmları · Kraniyal sinir neoplazmları

Özet

A retrospective study was performed in 28 patients with optic pathway gliomas treated at our institution between 1975-1995. The median age was 8 (range 1-55) years. The female-to-male ratio was 16:12. Seven patients (25%) had a history of neurofibromatosis. Twenty-two patients had histologic confirmation of the diagnosis and six patients were clinically diagnosed. Of the 22 surgically treated patients 12 (55%) had biopsy only and 10 (45%) underwent subtotal excision. Four patients showed tumor limited to optic nerve. Three patients had tumor located on chiasma only and nine patients were with tumors involving the chiasma and one or two optic nerves. More extensive involvement including involvement of hypothalamus and the third ventricle was recorded in 12 patients. Radiotherapy was applied with Co-60 unit or 6 MV photon beams and all patients received irradiation to local fields. The median dose was 5040 cGy in conventional fractions. The median follow-up time was 72 months. Ten-year overall survival and progression free survival were 93% and 84% respectively. The vision improved in 42% and remained stable in 58% of patients. We conclude that postoperative radiotherapy is beneficial in patients with chiasmal involvement and with incomplete resections.

Abstract

A retrospective study was performed in 28 patients with optic pathway gliomas treated at our institution between 1975-1995. The median age was 8 (range 1-55) years. The female-to-male ratio was 16:12. Seven patients (25%) had a history of neurofibromatosis. Twenty-two patients had histologic confirmation of the diagnosis and six patients were clinically diagnosed. Of the 22 surgically treated patients 12 (55%) had biopsy only and 10 (45%) underwent subtotal excision. Four patients showed tumor limited to optic nerve. Three patients had tumor located on chiasma only and nine patients were with tumors involving the chiasma and one or two optic nerves. More extensive involvement including involvement of hypothalamus and the third ventricle was recorded in 12 patients. Radiotherapy was applied with Co-60 unit or 6 MV photon beams and all patients received irradiation to local fields. The median dose was 5040 cGy in conventional fractions. The median follow-up time was 72 months. Ten-year overall survival and progression free survival were 93% and 84% respectively. The vision improved in 42% and remained stable in 58% of patients. We conclude that postoperative radiotherapy is beneficial in patients with chiasmal involvement and with incomplete resections.

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Bu Makaleye Atıf Yap

ZORLU, A. F., YILDIZ, F., GÜRKAYNAK, M., AKYOL, F., ATAHAN, İ. L. (2000). Radiotherapy in the management of optic pathway gliomas. Turkish Journal of Cancer, Cilt: 30 - Sayı: 1, 31–35. https://ajindex.com/articles/368432

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Kaynakça (14)

  1. Horwich A, Bloom HJG. Optic Gliomas: radiation therapy and prognosis. Int J Radiat Oncol Biol Phys 1985;11:1067-79
  2. Pierce S, Barnes PD, Loeffler JS, et al. Definitive radiation therapy in the management of symptomatic patients with optic glioma. Cancer 1990;65:45- 52
  3. Kovalic JJ, Grigsby P, Shepard MJ, et al. Radiation therapy for gliomas of the optic nerve and chiasm. Int J Radiat Oncol Biol Phys 1990;18:927-32
  4. Stern J, DiGiacinto CV, Housepian EM. Neurofibromatosis and optic glioma: clinical and morphological correlations. Neurosurg 1979;4:524-8
  5. Alvord EC, Lofton S. Gliomas of the optic nerve and chiasm. J Neurosurg 1988;68:85-98
  6. Flickinger JC, Torres J, Deutsch M. Management of low grade gliomas of the optic nerve and chiasm. Cancer 1988;61:635-42
  7. Hoyt VF, Baghdassarian SA. Optic glioma of childhood: natural history and rationale for conservative management. Br J Opthalmol 1969;53:793-8
  8. Regueiro CA, Ruiz M, Millan I, et al. Prognostic factors and results of radiation therapy in optic pathway tumors. Tumori 1996;82:4:353-9
  9. Rush JA, Younge BR, Campbell RJ, et al. Optic glioma: long term follow-up of 85 histopathologically verified cases. Opthalmology 1982;89:1213-9
  10. Tenny RT, Laws ER, Rush JA. The neurosurgical management of optic glioma: results in 104 patients. J Neurosurg 1982;57:452-8
  11. Wong JY, Uhl V, Wara WM, et al. A reanalysis of the University of California, San Fransisco experience. Cancer 1987;60:1847-55
  12. Erkal HS, Serin M, Çakmak A. Management of optic pathway and chiasmatic–hypothalamic gliomas in children with radiotherapy. Radiother Oncol 1997;45:1:11-5
  13. Chan MY, Foong AP, Helsey DM, et al. Potential prognostic factors of relapse free survival in childhood optic pathway glioma: a multivariate analysis. Pediatr Neurosurg 1998;29:1: 23-8
  14. Pierce SM, Barnes PD, Loeffler JS, et al. Definitive radiation therapy in the management of symptomatic patients with optic glioma: survival and long-term effects. Cancer 1990;65:45-52.