AIM To examine how tumour location affects ocular morbidity after ophthalmic plaque radiotherapy for uveal melanoma.
METHODS 69 eyes were irradiated and followed for a mean 42 months. There were 23 anterior uveal melanomas and 46 were posterior to the equator. Anterior and posterior tumours had similar basal dimensions. Their mean apical heights were 4.8 mm (anterior) and 3.5 mm (posterior) which received a mean 88 Gy and 83.4 Gy respectively.
RESULTS Only one patient (4%) plaqued for an anterior uveal melanoma developed secondary retinopathy (cystoid macular oedema). In contrast, 24 (52%) of the posterior choroidal melanoma patients developed retinopathy (p value <0.0001). Cataract developed in 18 (86%) eyes with phakic anterior tumour compared with seven (17%) eyes with posterior tumours (p value <0.0000). No posterior nasal tumours lost more than two lines of vision though 45% developed retinopathy.
CONCLUSION While plaque radiation of anterior melanomas is more likely to cause reversible vision loss secondary to cataract, treatment of posterior tumours is more likely to be associated with irreversible loss because of retinopathy. Nasal location is also protective against severe loss of vision.
- optic neuropathy
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Enucleation and radiotherapy are the most commonly used treatments for choroidal melanoma.1 2 High energy cobalt-60 ophthalmic plaques have been replaced by the lower energy ruthenium-106 (106Ru) and iodine-125 (125I).3-7 Most recently, palladium-103 (103Pd) has become available.8-11 Though all four radionuclides can be used successfully to treat choroidal melanoma, they differ in their distribution of radiation.1 12
Tumour, and therefore plaque location, affects the distribution of intraocular radiation. Since the plaque is centred over the tumour during treatment, the radiation dose distribution shifts along with the plaque (Fig 1). Treatment of anterior tumours results in a higher dose to the lens, and irradiation of posterior tumours increases the dose to the macula. This study examines tumour location as a risk factor for ocular complications of plaque radiotherapy.
Patients and methods
I report on 69 patients with uveal melanoma. The methods of diagnosis, informed consent, treatment, and follow up have been described.8 9 The basal dimensions of the tumours were determined by ophthalmoscopy, transillumination, fluorescein angiography, and B scan ultrasonography. A scan was also used to measure tumour height. B scan ultrasonography was also used to determine tumour location. Fundus photography with fluorescein angiography was used to evaluate patterns of tumour circulation, focal leakage, cystoid macular oedema (CMO), and radiation retinopathy.
In a manner similar to the COMS protocol, we calculated the103Pd seeds as isotropic point sources. No attenuation was attributed to the gold plaque. “Back scatter”, as has been noted with 125I plaque radiotherapy, has not been measured with103Pd and was not used in COMS calculations.1
Our surgical techniques of tumour localisation and episcleral plaque insertion have been described.1 All patients received one103Pd brachytherapy session over 5–7 days. Plaque radiotherapy started at insertion and was continued until the prescribed dose was delivered to the tumour's apex. Anterior tumours were treated to an average apex dose of 88 Gy, while the posterior group was calculated to receive 83.4 Gy (5% less).
The tumour's base was centred either at or anterior to the equator in 23 eyes, and posterior to the equator in 46. The average tumour size for the anterior tumour group was 10.5 × 9 mm (base) and 4.8 mm in apical height. Similarly, the posterior tumours averaged 10.3 × 9 mm in basal dimension, but they were on average slightly shorter at 3.5 mm in height and therefore received slightly less radiation.
No patients in the anterior tumour group developed, posterior pole haemorrhages cotton wool spots, vascular sheathing, or optic neuropathy. One patient (4%) plaqued for a 15 × 15 × 8.4 mm anterior uveal melanoma developed CMO. In contrast, 24 (52%) of the posterior choroidal melanomas developed some form of secondary retinopathy. This difference was statistically significant (p= <0.0001) Though 45% of the posterior nasal tumours developed retinopathy none lost more than two lines of vision.
Eighteen of the 21 phakic patients (85%) plaqued for anterior uveal melanomas developed a secondary cataract. All but one of the cataract surgeries were performed within the first 3 years of follow up. Eleven of 21 (52%) had predominantly posterior subcapsular cataracts. Eleven patients had cataract surgery, 10 were improved by visual rehabilitation. Overall, four (17.4%) of the 23 anterior uveal melanoma patients lost three or more lines of vision at their last follow up examination (mean follow up 3.8 years).
In contrast, only seven (17%) of the 42 phakic patients with posterior choroidal melanomas developed a significant cataract. This difference was statistically significant (p value <0.0000). Five have undergone surgery (all within the first 2 years of follow up). In contrast to the anterior tumours, four (80%) of those patients lost three or more lines of vision despite cataract surgery. Twenty four of 46 (52%) have developed some form of posterior segment complication (radiation or tumour related retinopathy, radiation optic neuropathy, cystoid macular oedema, secondary retinal detachment, vitreous haemorrhage). Overall, 48% of the 46 patients with posterior choroidal melanoma lost three or more lines of vision at their last follow up examination (mean 3.3 years).
One patient from each group required a small prism correction for diplopia, iris neovascularisation occurred twice (solely in the anterior tumour group). No eyelash loss, severe dry eye, or keratopathy was associated with ophthalmic plaque radiation therapy in either group.
Ocular radiation distribution affects the type and incidence of complications.1 Treatment of large tumours increases the amount of radiation delivered to all ocular structures resulting in a higher complication rate.1 12 13 Charged particle irradiation (proton) typically delivers 70% of the dose to the anterior segment with a resultant increase in adnexal and anterior segment complications.1 14 15 In contrast, the gold of low energy eye plaques protects adnexal structures and is therefore associated with a lower incidence of dry eye and neovascular glaucoma.1
In our study, we found that shifting the targeted zone toward the anterior segment all but eliminated the incidence of posterior segment complications while increasing the incidence of cataract (Table 1) Similarly, treatment of tumours located in the posterior nasal quadrant resulted in moving the radiation away from the macula giving less profound vision loss. No clinically significant eyelash loss, keratopathy, or dry eye was found in either group.
The visual prognosis for patients treated with ophthalmic plaque radiotherapy is good for anterior and nasal uveal melanomas and poor for most posterior temporal melanomas. These findings are particularly striking in that the anterior uveal tumours were larger (mean 4.8 versus 3.5 mm in height) and received a higher radiation dose (a mean 88 versus 83.4 Gy). Both of these facts might have, but didn't, skew the results towards more, not fewer, complications after radiation of anterior uveal melanomas (Table 1).
This study has demonstrated that changing the distribution of radiation dose within the eye, affecting the incidence and location secondary complications. Therefore, techniques focused on decreasing the amount of radiation to normal ocular structures will decrease radiation associated complications.10 16-22 It is hoped that this study has revealed information that may be helpful for patient education and informed consent.
Supported (in part) by the EyeCare Foundation, Inc, New York City, New York, USA (http://www.eyecarefoundation.org).
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