Radyasyonun Oküler Komplikasyonları
Özet
Radyoterapi (RT), intraoküler ve orbital tümörler ile belirli benign orbital hastalıkların tedavisinde göz ve görme fonksiyonunu koruma avantajı sunan kritik bir bileşendir. Ancak, gözün yüksek radyosensitivitesi nedeniyle tedavi sonrasında normal dokularda fonksiyon kayıpları ve çeşitli oküler komplikasyonlar gelişebilmektedir. Bu yan etkiler, ortaya çıkış zamanlarına göre akut (blefarit, konjonktivit, keratit) ve kalıcı vasküler hasara bağlı gelişen kronik geç etkiler (katarakt, kuru göz sendromu, retinopati ve optik nöropati) olarak sınıflandırılır. Özellikle posterior uveal melanom tedavisi sonrasında en sık görülen ve ciddi görme kaybına yol açan komplikasyonlar radyasyon retinopatisi ve radyasyona bağlı optik nöropatidir (RION). Toksisite riski; uygulanan toplam ve fraksiyon dozuna, hedef alanın büyüklüğüne ve lokalizasyonuna doğrudan bağlıdır. Bu komplikasyonların büyük oranda geri dönüşümsüz ve tedavi seçeneklerinin kısıtlı olması nedeniyle, risk altındaki organların tolerans doz limitlerinin altında tutulması, koruyucu gözlük/plak kullanımı ve tedavi portallarının hassas planlanması gibi önleyici stratejiler hayati önem taşımaktadır.
Radiotherapy (RT) is a critical component in treating intraocular and orbital tumors, as well as certain benign orbital diseases, offering the advantage of preserving the eye and visual function. However, due to the high radiosensitivity of the eye, treatment can lead to functional loss in normal tissues and various ocular complications. These side effects are classified as acute (blepharitis, conjunctivitis, keratitis) or chronic late effects (cataract, dry eye syndrome, retinopathy, and optic neuropathy) resulting from permanent vascular damage. Particularly following the treatment of posterior uveal melanoma, radiation retinopathy and radiation-induced optic neuropathy (RION) are the leading causes of severe, permanent visual impairment. The risk of toxicity is directly related to the total radiation dose, fraction dose, and the size and location of the target area. Since these complications are largely irreversible and treatment options remain limited, preventive strategies—such as keeping radiation doses below defined tolerance limits for organs at risk, using protective glasses or plaques, and meticulous treatment planning—are of vital importance.
Referanslar
Kadam SB , Shyama SK , Almeida VG. Evaluation of the in vivo genotoxic effects of gamma radiation on the peripheral blood leukocytes of head and neck cancer patients undergoing radiotherapy. Mutation research. Mutat Res; 2013;752(1–2): 42–46. doi:10.1016/J.MRGENTOX.2013.01.003
Virgili G, Gatta G, Ciccolallo L, et al. Survival in patients with uveal melanoma in Europe. Archives of ophthalmology (Chicago, Ill. : 1960). Arch Ophthalmol; 2008;126(10): 1413–1418. doi:10.1001/ARCHOPHT.126.10.1413
Singh AD, Topham A. Incidence of uveal melanoma in the United States: 1973-1997. Ophthalmology. Ophthalmology; 2003;110(5): 956–961. doi:10.1016/S0161-6420(03)00078-2
Van den Aardweg GJ, Kiliç E, Klein A de, Luyten GP. Dose fractionation effects in primary and metastatic human uveal melanoma cell lines. Investigative ophthalmology & visual science. Invest Ophthalmol Vis Sci; 2003;44(11): 4660–4664. doi:10.1167/IOVS.03-0151
Smitt MC, Donaldson SS . Radiation therapy for benign disease of the orbit. Seminars in radiation oncology. Semin Radiat Oncol; 1999;9(2): 189–193. doi:10.1016/S1053-4296(99)80008-3
Stannard C, Sauerwen W,Maree G,Leuona K. Radiotherapy for ocular tumours. Eye (London, England). Eye (Lond); 2013;27(2): 119–127. doi:10.1038/EYE.2012.241
Barabino S, Raghavan A, Loeffler J, et al. Radiotherapy-Induced Ocular Surface Disease.
Nag S,Quiley JM,Earle JD, et al. The American Brachytherapy Society recommendations for brachytherapy of uveal melanomas. International journal of radiation oncology, biology, physics. Int J Radiat Oncol Biol Phys; 2003;56(2): 544–555. doi:10.1016/S0360-3016(03)00006-3
Smitt MC,Donaldson SS . Radiation therapy for benign disease of the orbit. Seminars in radiation oncology. Semin Radiat Oncol; 1999;9(2): 179–189. doi:10.1016/S1053-4296(99)80008-3
Conway RM,Chua WC,Qureshi C,Billson FA. Primary iris melanoma: diagnostic features and outcome of conservative surgical treatment. The British journal of ophthalmology. Br J Ophthalmol; 2001;85(7): 848–854. doi:10.1136/BJO.85.7.848
Tektas ZO,Bıcer A,Demirci G et al. Gamma knife stereotactic radiosurgery yields good long-term outcomes for low-volume uveal melanomas without intraocular complications. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. J Clin Neurosci; 2010;17(4): 441–445. doi:10.1016/J.JOCN.2009.08.004
Margo CE. The Collaborative Ocular Melanoma Study: an overview. Cancer control : journal of the Moffitt Cancer Center. Cancer Control; 2004;11(5): 304–309. doi:10.1177/107327480401100504
Bell D,Wilson MW . Choroidal melanoma: natural history and management options. Cancer control : journal of the Moffitt Cancer Center. Cancer Control; 2004;11(5): 296–303. doi:10.1177/107327480401100503
Bartalena L, Morcocci C, Manetti L, et al. Orbital radiotherapy for Graves’ ophthalmopathy. Thyroid : official journal of the American Thyroid Association. Thyroid; 1998;8(5): 439–441. doi:10.1089/THY.1998.8.439
Prummel MF, Terwee CB, Gerding MN, et al. A randomized controlled trial of orbital radiotherapy versus sham irradiation in patients with mild Graves’ ophthalmopathy. The Journal of clinical endocrinology and metabolism. J Clin Endocrinol Metab; 2004;89(1): 15–20. doi:10.1210/JC.2003-030809
Kahaly GJ, Rosler HP, Pitz S, Hommel G. Low- versus high-dose radiotherapy for Graves’ ophthalmopathy: a randomized, single blind trial. The Journal of clinical endocrinology and metabolism. J Clin Endocrinol Metab; 2000;85(1): 102–108. doi:10.1210/JCEM.85.1.6257
Lacka K, Manuszevska E, Korczowska I, Lackı JK. The effect of methylprednisolone pulse treatment on cytokine network in Graves ophthalmopathy. Current eye research. Curr Eye Res; 2007;32(3): 291–297. doi:10.1080/0271368060118669818. W S, G W. Radiation toxicity: a practical guide. Introduction. Cancer treatment and research. Cancer Treat Res; 2006;128: 3–5. https://pubmed.ncbi.nlm.nih.gov/16335011/
Batth SS, Sreeraman R, Dienes E, et al. Clinical-dosimetric relationship between lacrimal gland dose and ocular toxicity after intensity-modulated radiotherapy for sinonasal tumours. The British journal of radiology. Br J Radiol; 2013;86(1032). doi:10.1259/BJR.20130459
Nanda VGY , Peng W,Hwu P, et al. Melanoma and immunotherapy bridge 2015 : Naples, Italy. 1-5 December 2015. Journal of translational medicine. J Transl Med; 2016;14(1). doi:10.1186/S12967-016-0791-2
Jeganathan VSE, Wirth A, MacManus MP. Ocular risks from orbital and periorbital radiation therapy: A critical review. International Journal of Radiation Oncology Biology Physics. 2011;79(3): 650–659. doi:10.1016/j.ijrobp.2010.09.056
Haas A, Pinter O, Papaefthymiou G, et al. Incidence of radiation retinopathy after high-dosage single-fraction gamma knife radiosurgery for choroidal melanoma. Ophthalmology. Ophthalmology; 2002;109(5): 909–913. doi:10.1016/S0161-6420(02)01011-4
Seregard S, Pelayes DE, Singh AD. Radiation therapy: posterior segment complications. Developments in ophthalmology. Dev Ophthalmol; 2013;52: 114–123. doi:10.1159/000351088
Gündüz K, Shields CL, Shields JA , Cater J, Freire JE, Brady LW.Radiation retinopathy following plaque radiotherapy for posterior uveal melanoma. Archives of ophthalmology (Chicago, Ill. : 1960). Arch Ophthalmol; 1999;117(5): 609–614. doi:10.1001/ARCHOPHT.117.5.609
Zamber RW, Kinyoun JL. Radiation retinopathy. Western Journal of Medicine. BMJ Publishing Group; 1992;157(5): 530. /pmc/articles/PMC1022030/?report=abstract
Viebahn M, Barricks ME, Osterioh MD. Synergism between diabetic and radiation retinopathy: case report and review. The British journal of ophthalmology. Br J Ophthalmol; 1991;75(10): 629–632. doi:10.1136/BJO.75.10.629
Missotten GS, Nothing IC, Schlingemann RO, et al. Vascular endothelial growth factor a in eyes with uveal melanoma. Archives of ophthalmology (Chicago, Ill. : 1960). Arch Ophthalmol; 2006;124(10): 1428–1434. doi:10.1001/ARCHOPHT.124.10.1428
Quivey JM, Char DH, Phillips TL, Weaver KA, Castro JR, Kroll SM. High intensity 125-iodine (125I) plaque treatment of uveal melanoma. International journal of radiation oncology, biology, physics. Int J Radiat Oncol Biol Phys; 1993;26(4): 613–618. doi:10.1016/0360-3016(93)90277-3
Detorakis ET, Engstrom R, Wallace R, Straatsma BR.Iris and anterior chamber angle neovascularization after iodine 125 brachytherapy for uveal melanoma. Ophthalmology. Ophthalmology; 2005;112(3): 505–510. doi:10.1016/J.OPHTHA.2004.09.028
Miguel D,Frutos-Baraja JM de, Lopez-Lara F, et al. Radiobiological doses, tumor, and treatment features influence on outcomes after epiescleral brachytherapy. A 20-year retrospective analysis from a single-institution: part II. Journal of contemporary brachytherapy. J Contemp Brachytherapy; 2018;10(4): 347–359. doi:10.5114/JCB.2018.77955
Finger PT, Chin KJ. Antivascular endothelial growth factor bevacizumab for radiation optic neuropathy: secondary to plaque radiotherapy. International journal of radiation oncology, biology, physics. Int J Radiat Oncol Biol Phys; 2012;82(2): 789–798. doi:10.1016/J.IJROBP.2010.11.075
Danesh-Meyer H V. Radiation-induced optic neuropathy. Journal of Clinical Neuroscience. Elsevier; 2008;15(2): 95–100. doi:10.1016/J.JOCN.2007.09.004
Taylor A, Jacques PF, Epstein EM. Relations among aging, antioxidant status, and cataract. The American journal of clinical nutrition. Am J Clin Nutr; 1995;62(6 Suppl). doi:10.1093/AJCN/62.6.1439S
Stewart FA, Akleyev AV, Hauer-Jensen M, et al. ICRP publication 118: ICRP statement on tissue reactions and early and late effects of radiation in normal tissues and organs--threshold doses for tissue reactions in a radiation protection context. Annals of the ICRP. Ann ICRP; 2012;41(1–2): 1–322. doi:10.1016/J.ICRP.2012.02.001
Merriam GR, Worgul BV. Experimental radiation cataract--its clinical relevance. Bulletin of the New York Academy of Medicine. Bull N Y Acad Med; 1983;59(4): 372–392. https://pubmed.ncbi.nlm.nih.gov/6575847/
Dayal Varma S, Kovtun S, Rajeev Hegde K. Role of UV Irradiation and Oxidative Stress in Cataract Formation. Medical Prevention by Nutritional Antioxidants and Metabolic Agonists. doi:10.1097/ICL.0b013e31821ec4f2
Incidence of cataract and outcomes after cataract surgery in the first 5 years after iodine 125 brachytherapy in the Collaborative Ocular Melanoma Study: COMS Report No. 27. Ophthalmology. Ophthalmology; 2007;114(7). doi:10.1016/J.OPHTHA.2006.10.039
The definition and classification of dry eye disease: report of the Definition and Classification Subcommittee of the International Dry Eye WorkShop (2007). The ocular surface. Ocul Surf; 2007;5(2): 75–92. doi:10.1016/S1542-0124(12)70081-2
Bessell EM, Henk JM, Whitelocke RA,Wright JE. Ocular morbidity after radiotherapy of orbital and conjunctival lymphoma. Eye (London, England). Eye (Lond); 1987;1 ( Pt 1)(1): 90–96. doi:10.1038/EYE.1987.14
Parsons JT, Bova FJ, Fitzgerald CR, Mendenhall WM, Million RR. Severe dry-eye syndrome following external beam irradiation. International journal of radiation oncology, biology, physics. Int J Radiat Oncol Biol Phys; 1994;30(4): 775–780. doi:10.1016/0360-3016(94)90348-4
Parsons JT, Bova FJ, Fitzgerald CR, et al. Radiation optic neuropathy after megavoltage external-beam irradiation: analysis of time-dose factors. International Journal of Radiation Oncology, Biology, Physics. 1994;30(4): 755–763. doi:10.1016/0360-3016(94)90346-8
Nakamura T, Suzuki S, Kato K, et al. Effect of protective glasses on radiation dose to eye lenses during whole breast irradiation. J Appl Clin Med Phys. 2020;21(11): 272–277. doi:10.1002/acm2.13073