CC BY 4.0 · World J Nucl Med 2023; 22(04): 257-260
DOI: 10.1055/s-0043-1774419
Original Article

How Radioactive Iodine Treatment Affects the Retina

1   Ophthalmology Clinic, Beyoglu Eye Training and Research Hospital, Health of Sciences University, Turkey
,
2   Nuclear Medicine Clinic, Bagcilar Training and Research Hospital, Health of Sciences University, Turkey
,
3   Nuclear Medicine Clinic, Sisli Hamidiye Etfal Training and Research Hospital, Health of Sciences University, Turkey
› Author Affiliations
 

Abstract

Objective The aim of this study was to quantitatively assess the macular and retinal nerve fiber layer thicknesses in patients with hyperthyroidism and thyroid cancer undergoing radioactive iodine (RAI) therapy.

Study Design This prospective study was conducted in accordance with the principles of the Declaration of Helsinki and approved by the Bagcilar Training and Research Hospital Clinical Research Ethics Committee. Written informed consent was obtained from the patients following a detailed explanation of the study objectives and protocol. Patient selection was randomized. Patients scheduled for RAI treatment in the Nuclear Medicine Clinic were referred to the ophthalmology clinic, respectively. Patients without additional ocular pathology were included in the study.

Methods All patients had received RAI therapy using Iodine-131 for hyperthyroidism or thyroid cancer. A complete ophthalmological examination and measurement of macular and retinal nerve fiber layer thickness using optical coherence tomography were performed on all patients before and at the first and sixth months and in first year after RAI treatment. The results were prospectively evaluated.

Results The study included 80 eyes of 40 patients. The hyperthyroid group was group 1, and the thyroid cancer group was group 2. There were 25 patients in group 1 and 15 patients in group 2. The mean age was 43.76 ± 11.85 years (range: 22–65 years) in group 1 and 39.87 ± 9.13 years (range: 30–58 years) in group 2. There was no significant difference between the two groups regarding age and sex (p > 0.05). In both groups, no significant difference was found in the macular thickness and retinal nerve fiber layer thicknesses values obtained in both eyes before and after the RAI treatment.

Conclusion As a result of our study, we observed that RAI intake did not harm the retinal layer.


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Introduction

Radioactive iodine (RAI) is a safe, effective, noninvasive, and simple ablation treatment recommended for patients diagnosed with hyperthyroidism or papillary and follicular thyroid carcinoma.[1] [2] This treatment eliminates residual normal or tumoral thyroid cells and allows post-treatment screening to reveal previously unidentified or additional disease foci.[3] [4] [5] [6] Although it is a repeatable and generally well-tolerated treatment, RAI can also accumulate in extrathyroidal tissues, such as gastric mucosa, intestine, choroid plexus, salivary glands, sweat glands, and lacrimal glands, and may be associated with complications such as transient neck pain and edema, as well as dysfunctions in the pulmonary, gastrointestinal, and hematopoietic systems, and damages to salivary glands, nasolacrimal apparatus, and gonads, along with the potential risk of secondary malignancies.[7] [8] [9] [10] [11] [12] While these complications are rarely life-threatening, they can negatively impact the patient's quality of life.

There have been several studies on the effects of RAI treatment on the lacrimal gland, which are related to the accumulation of iodine in the eye. However, there is currently a lack of known studies on its effects on the retina, which could be expected to be affected due to choroidal plexus involvement. This study aimed to conduct a quantitative assessment of the macular and retinal nerve fiber layer thicknesses (RNFLT) before and after RAI treatment in patients with hyperthyroidism and thyroid cancer, utilizing optical coherence tomography (OCT).


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Patients and Methods

This prospective study adhered to the principles outlined in the Declaration of Helsinki, and the study protocol received approval from the Bioethical Commission of The Health Sciences University Bagcilar Research and Training Hospital. Patients were enrolled in the study after providing written informed consent. The patient selection process was randomized. Specifically, patients scheduled for RAI treatment in the Nuclear Medicine Clinic were referred to the ophthalmology clinic. Only patients without any additional ocular pathology were included in the study. Exclusion criteria for all patients encompassed a history of significant ocular surface disease or ocular inflammation, thyroid eye disease, diabetes mellitus, and ocular surgery within the past year.

The study comprised 80 eyes of 40 patients, consisting of 7 men and 33 women. The participants were divided into two groups: group 1, consisting of 25 patients with hyperthyroidism, and group 2, comprising 15 patients with thyroid cancer. The mean age was 43.76 ± 11.85 years (ranging from 22 to 65 years) for group 1 and 39.87 ± 9.13 years (ranging from 30 to 58 years) for group 2. Diagnosing hyperthyroidism was clinically confirmed through laboratory evaluations, thyroid scintigraphy, and RAI uptake values in all patients. For RAI therapy, all patients received Iodine-131, with group 1 receiving low-dose (up to 999 Mega Bequere—MBq) and group 2 receiving high-dose (3,700 MBq and higher) Iodine-131. The mean RAI dose in the hyperthyroid group was 603.1 MBq (ranging from 481 to 740 MBq); in the cancer group, it was 3,700 MBq (mean and total). All patients were prescribed a low iodine content diet 10 days before the therapy, and antithyroid medications were withdrawn 7 days before the therapy.[1] [2] RAI treatment was administered orally to all patients. Notably, all thyroid cancer patients and five hyperthyroid patients underwent surgery for their respective diseases (p = 0.0001).

In all patients, a complete ophthalmological examination and measurement of macular and RNFLT using OCT were performed before RAI treatment and at the first and sixth months and first year post-RAI treatment. The results were prospectively evaluated.

In this study, statistical analysis was conducted using the Number Cruncher Statistical System 2007 Statistical Software (Utah, United States) pocket program. The data were evaluated using descriptive statistics (mean, standard deviation), repeated variance analysis for multiple group comparisons, and the Newman–Keuls multiple comparison test for subgroup comparisons. Additionally, an independent t-test was employed to compare paired groups, while the chi-square and Fisher's exact tests were used to compare qualitative data. The results were evaluated at a significance level of p-value less than 0.05.

Imaging

OCT (Nidek RS-3000) was utilized to obtain cross-sectional retina measurements through dilated pupils. This instrument employed partial coherence interferometry technology, resulting in optical A-scans of the retina with an axial resolution of approximately 10 µm.[13] [14] [15] The peripapillary RNFL thickness was measured using the “fast RNFL thickness” scan protocol, which involved 256 sampling points along a circular scan path. Three scans were conducted, and the average value was used for analyses. The “fast macular scan” protocol was employed for macular thickness measurements to measure the distance between the internal limiting membrane and the retinal pigment epithelium. The macula center and 1-, 3-, and 6-mm rings in different segments (superior, inferior, nasal, and temporal) were measured, and an average of five scans were used for analysis. A single-experience operator performed all scans.


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Results

The age and sex characteristics of both groups were similar. In Group 1, only five patients underwent surgery, while all patients in Group 2 underwent surgery ([Table 1]).

Table 1

Characteristics of the two groups

Group 1 (n = 25)

Group 2 (n = 15)

p-Value

Age(years)

43.76 ± 11.85

39.87 ± 9.13

0.282

Sex

Female

19

76.00%

14

93.33%

0.162

Male

6

24.00%

1

6.67%

Operation

No

20

80.00%

0

0%

0.0001[a]

Yes

5

20.00%

15

100%

a p-Value < 0.05.


In both groups, no significant difference was observed in macular thickness and RNFLT values before and after RAI treatment. Since the results were nearly identical in both eyes, the right eye was used for the analysis. In Group 1, the pretreatment values were as follows: average macular center thickness was 223.84 ± 16.8 µm, average macular 6-mm ring area thickness was 252.72 ± 14.77 µm, and average RNFLT was 107.52 ± 7.47 µm. At the end of 6 months, these values were found to be 223.42 ± 13.18 µm, 250.66 ± 12.93 µm, and 105.48 ± 15.25 µm, respectively (p > 0.05 for all three tests).

In Group 2, the pretreatment values were as follows: average macular center thickness was 230.53 ± 14.72 µm, average macular 6-mm ring area thickness was 250.4 ± 14.09 µm, and average RNFLT was 109.27 ± 5.19 µm. At the end of 6 months, these values were found to be 229.4 ± 16.67 µm, 249.7 ± 12.28 µm, and 109.1 ± 4.51 µm, respectively (p > 0.05 for all three tests) ([Table 2]).

Table 2

Comparison between beginning and end-of-treatment macular center thickness, macular 6-mm ring area thickness, and RNFLT for the two groups

Group 1 (n = 25)

Group 2 (n = 15)

p-Value

Macular CT Pre-t

223.84 ± 16.80

230.53 ± 14.72

0.075

Macular CT 1 month

224.00 ± 14.98

228.57 ± 18.27

0.228

Macular CT 6 month

223.42 ± 13.18

229.40 ± 16.67

0.080

p-Value

0.815

0.272

RNFLT Pre-t

107.52 ± 7.47

109.27 ± 5.19

0.263

RNFLT 1 month

107.80 ± 7.29

108.63 ± 5.68

0.594

RNFLT 6 month

105.48 ± 15.25

109.10 ± 4.51

0.210

p-Value

0.325

0.855

Macular 6-mm T Pre-t

252.72 ± 14.77

250.40 ± 14.09

0.491

Macular 6-mm T 1 month

250.60 ± 12.91

250.27 ± 12.66

0.911

Macular 6-mm T 6 month

250.66 ± 12.93

249.70 ± 12.28

0.744

p-Value

0.055

0.657

Abbreviations: Macular 6-mm T, macular 6-mm ring area thickness; Macular CT, macular center thickness; Pre-t, pretreatment; RNFLT, retinal nerve fiber layer thicknesses.



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Discussion

To our knowledge, no other study has addressed macular and retinal nerve fiber layer thicknesses in patients with hyperthyroidism and thyroid cancer undergoing RAI therapy. However, some studies focus on the adverse effects of radioiodine therapy for differentiated thyroid carcinoma and hyperthyroidism in the eye. These studies have reported side effects, particularly related to the lacrimal system.[7] [16] [17] Additionally, there are studies on the adverse effects of iodine brachytherapy (IBT) applied in uveal melanomas.[18] [19] [20] [21] Furthermore, a study on radiation retinopathy may develop due to Iodine-131, which provides only the results of the fundoscopic examination.[22]

For this reason, we aimed to investigate whether RAI treatment affects the posterior segment of the eye.

Ocular complications, such as cataracts, vitreous hemorrhage, and persistent retinal detachment, were observed frequently, particularly in the early period after IBT of large uveal melanomas. These occurrences indicate that limiting radiation damage to the retina and optic nerve remains challenging.[23] [24] The primary options to address this issue involve shielding these tissues through plaque design and seed positioning or considering alternative treatment modalities that do not involve irradiation.[25] [26]

A more posterior tumor location can lead to increased complications such as maculopathy and optic neuropathy due to iodine accumulation in the posterior segment. Conversely, it may also give rise to anterior segment complications like cataracts. This observation aligns with the low radiation tolerance of the lens, which can be exceeded when a thick tumor, even a posterior one, is irradiated with an iodine plaque. The association between tumor height and largest basal diameter with maculopathy and optic neuropathy was found to be weak.[27] [28] Moreover, maculopathy and optic neuropathy are partly linked to tumor height and tumor distance from these ocular structures, suggesting that these factors hold potential as dose determinants per macula and optic nerve head.[26]

In a study conducted by Kaçar Güveli et al, no retinopathy was observed in any of the patients who received 9,250 to 37,000 MBq Iodine-131 treatment for differentiated thyroid cancer, as assessed through dilated fundus examination of 40 eyes from 20 patients.[22] In our study, unlike this previous study, we evaluated the retina not only with slit-lamp examination but also with OCT, allowing for a more sensitive examination.

Our study revealed no significant side effects related to the accumulation of systemically administered RAI in the retina. We found no significant difference in macular thickness, and RNFLT measured at the beginning and the end of the treatment in both groups.

A limitation of our study is that we did not consider the RAI dose accumulated by the tissues. If the exact accumulation of RAI in the tissues is determined, and a dose–response relationship can be established accordingly, it could significantly contribute to the existing literature.


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Conclusion

This result indicates that RAI therapy, utilized in treating thyroid cancer and hyperthyroidism, does not harm the retina. However, further extensive studies are required to obtain more precise data regarding the potential risk of retinal damage.


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Conflict of Interest

None declared.

Authors' Contribution

Ceren Gürez was involved in patient selection, data collection, and writing. Aynur Özen and Özgül Ekmekçioğlu helped in patient selection and data collection.


Ethical Approval

The study was reviewed and approved by the Bagcilar Training and Research Hospital Ethics Committee with the 2014-319 registration number by principles of the Declaration of Helsinki and, written informed consent was obtained from all patients.


  • References

  • 1 Silberstein EB, Alavi A, Balon HR. et al. The SNMMI practice guideline for therapy of thyroid disease with 131I 3.0.131 . J Nucl Med 2012; 53 (10) 1633-1651
  • 2 Cooper DS, Doherty GM, Haugen BR. et al; American Thyroid Association (ATA) Guidelines Taskforce on Thyroid Nodules and Differentiated Thyroid Cancer. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid 2009; 19 (11) 1167-1214
  • 3 Pacini F, Schlumberger M, Dralle H, Elisei R, Smit JW, Wiersinga W. European Thyroid Cancer Taskforce. European consensus for the management of patients with differentiated thyroid carcinoma of the follicular epithelium. Eur J Endocrinol 2006; 154 (06) 787-803
  • 4 Van Nostrand D. The benefits and risks of I-131 therapy in patients with well-differentiated thyroid cancer.131 . Thyroid 2009; 19 (12) 1381-1391
  • 5 Haugen BR. Patients with differentiated thyroid carcinoma benefit from radioiodine remnant ablation. J Clin Endocrinol Metab 2004; 89 (08) 3665-3667
  • 6 Sawka AM, Thephamongkhol K, Brouwers M, Thabane L, Browman G, Gerstein HC. Clinical review 170: a systematic review and metaanalysis of the effectiveness of radioactive iodine remnant ablation for well-differentiated thyroid cancer. J Clin Endocrinol Metab 2004; 89 (08) 3668-3676
  • 7 Fard-Esfahani A, Emami-Ardekani A, Fallahi B. et al. Adverse effects of radioactive iodine-131 treatment for differentiated thyroid carcinoma. Nucl Med Commun 2014; 35 (08) 808-817
  • 8 Isgoren S, Daglioz Gorur G, Demir H, Berk F. Radioiodine therapy in Graves' disease: is it possible to predict outcome before therapy?. Nucl Med Commun 2012; 33 (08) 859-863
  • 9 Tuttle RM, Becker DV, Hurley JR. Radioiodine treatment of thyroid diseases. In: Sandler MP, Coleman RE, Patton JA, Wackers FJ, Gottschalk A. eds. Diagnostic nuclear medicine. Philadelphia: Lippincott Williams & Wilkins; 2003: 653-670
  • 10 Bakheet SM, Hammami MM, Hemidan A, Powe JE, Bajaafar F. Radioiodine secretion in tears. J Nucl Med 1998; 39 (08) 1452-1454
  • 11 Zettinig G, Karanikas G, Hanselmayer G, Havlik E, Dudczak R. Radioactive contamination of contact lenses during radioiodine therapy. Nucl Med Commun 2000; 21 (10) 955-957
  • 12 Aydogan F, Ayhan Tuzcu E, Aydogan A. et al. Effect of radioactive iodine therapy on lacrimal gland functions in patients with hyperthyroidism. Clin Nucl Med 2014; 39 (04) 315-318
  • 13 Hee MR, Izatt JA, Swanson EA. et al. Optical coherence tomography of the human retina. Arch Ophthalmol 1995; 113 (03) 325-332
  • 14 Schuman JS, Pedut-Kloizman T, Hertzmark E. et al. Reproducibility of nerve fiber layer thickness measurements using optical coherence tomography. Ophthalmology 1996; 103 (11) 1889-1898
  • 15 Paunescu LA, Schuman JS, Price LL. et al. Reproducibility of nerve fiber thickness, macular thickness, and optic nerve head measurements using Stratus OCT. Invest Ophthalmol Vis Sci 2004; 45: 1716-1724
  • 16 Clement SC, Peeters RP, Ronckers CM. et al. Intermediate and long-term adverse effects of radioiodine therapy for differentiated thyroid carcinoma–a systematic review. Cancer Treat Rev. S0305–7372(15)00165–6
  • 17 Dreger S, Pfinder M, Christianson L, Lhachimi SK, Zeeb H. The effects of iodine blocking following nuclear accidents on thyroid cancer, hypothyroidism, and benign thyroid nodules: design of a systematic review. Syst Rev 2015; 4: 126
  • 18 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Plaque radiotherapy of uveal melanoma with predominant ciliary body involvement. Arch Ophthalmol 1999; 117 (02) 170-177
  • 19 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Radiation retinopathy following plaque radiotherapy for posterior uveal melanoma. Arch Ophthalmol 1999; 117 (05) 609-614
  • 20 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Radiation complications and tumor control after plaque radiotherapy of choroidal melanoma with macular involvement. Am J Ophthalmol 1999; 127 (05) 579-589
  • 21 Puusaari I, Heikkonen J, Kivelä T. Ocular complications after iodine brachytherapy for large uveal melanomas. Ophthalmology 2004; 111 (09) 1768-1777
  • 22 Kaçar Güveli T, Özkan S, Öner Tamam M. et al. The effect of high dose radioiodine therapy on formation of radiation retinopathy during thyroid cancer treatment. Mol Imaging Radionucl Ther 2014; 23 (03) 84-88
  • 23 Hykin PG, Shields CL, Shields JA, Arevalo JF. The efficacy of focal laser therapy in radiation-induced macular edema. Ophthalmology 1998; 105 (08) 1425-1429
  • 24 Kinyoun JL, Chittum ME, Wells CG. Photocoagulation treatment of radiation retinopathy. Am J Ophthalmol 1988; 105 (05) 470-478
  • 25 Astrahan MA, Luxton G, Jozsef G, Liggett PE, Petrovich Z. Optimization of 125I ophthalmic plaque brachytherapy. Med Phys 1990; 17 (06) 1053-1057
  • 26 Bechrakis NE, Bornfeld N, Zöller I, Foerster MH. Iodine 125 plaque brachytherapy versus transscleral tumor resection in the treatment of large uveal melanomas. Ophthalmology 2002; 109 (10) 1855-1861
  • 27 Henk JM, Whitelocke RA, Warrington AP, Bessell EM. Radiation dose to the lens and cataract formation. Int J Radiat Oncol Biol Phys 1993; 25 (05) 815-820
  • 28 Finger PT. Tumour location affects the incidence of cataract and retinopathy after ophthalmic plaque radiation therapy. Br J Ophthalmol 2000; 84 (09) 1068-1070

Address for correspondence

Ceren Gürez, MD
Kartaltepe Mah, Lavanta Sok, Umut Apt. No:1/13, Bakırköy, 34145, Istanbul
Turkey   

Publication History

Article published online:
04 December 2023

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  • References

  • 1 Silberstein EB, Alavi A, Balon HR. et al. The SNMMI practice guideline for therapy of thyroid disease with 131I 3.0.131 . J Nucl Med 2012; 53 (10) 1633-1651
  • 2 Cooper DS, Doherty GM, Haugen BR. et al; American Thyroid Association (ATA) Guidelines Taskforce on Thyroid Nodules and Differentiated Thyroid Cancer. Revised American Thyroid Association management guidelines for patients with thyroid nodules and differentiated thyroid cancer. Thyroid 2009; 19 (11) 1167-1214
  • 3 Pacini F, Schlumberger M, Dralle H, Elisei R, Smit JW, Wiersinga W. European Thyroid Cancer Taskforce. European consensus for the management of patients with differentiated thyroid carcinoma of the follicular epithelium. Eur J Endocrinol 2006; 154 (06) 787-803
  • 4 Van Nostrand D. The benefits and risks of I-131 therapy in patients with well-differentiated thyroid cancer.131 . Thyroid 2009; 19 (12) 1381-1391
  • 5 Haugen BR. Patients with differentiated thyroid carcinoma benefit from radioiodine remnant ablation. J Clin Endocrinol Metab 2004; 89 (08) 3665-3667
  • 6 Sawka AM, Thephamongkhol K, Brouwers M, Thabane L, Browman G, Gerstein HC. Clinical review 170: a systematic review and metaanalysis of the effectiveness of radioactive iodine remnant ablation for well-differentiated thyroid cancer. J Clin Endocrinol Metab 2004; 89 (08) 3668-3676
  • 7 Fard-Esfahani A, Emami-Ardekani A, Fallahi B. et al. Adverse effects of radioactive iodine-131 treatment for differentiated thyroid carcinoma. Nucl Med Commun 2014; 35 (08) 808-817
  • 8 Isgoren S, Daglioz Gorur G, Demir H, Berk F. Radioiodine therapy in Graves' disease: is it possible to predict outcome before therapy?. Nucl Med Commun 2012; 33 (08) 859-863
  • 9 Tuttle RM, Becker DV, Hurley JR. Radioiodine treatment of thyroid diseases. In: Sandler MP, Coleman RE, Patton JA, Wackers FJ, Gottschalk A. eds. Diagnostic nuclear medicine. Philadelphia: Lippincott Williams & Wilkins; 2003: 653-670
  • 10 Bakheet SM, Hammami MM, Hemidan A, Powe JE, Bajaafar F. Radioiodine secretion in tears. J Nucl Med 1998; 39 (08) 1452-1454
  • 11 Zettinig G, Karanikas G, Hanselmayer G, Havlik E, Dudczak R. Radioactive contamination of contact lenses during radioiodine therapy. Nucl Med Commun 2000; 21 (10) 955-957
  • 12 Aydogan F, Ayhan Tuzcu E, Aydogan A. et al. Effect of radioactive iodine therapy on lacrimal gland functions in patients with hyperthyroidism. Clin Nucl Med 2014; 39 (04) 315-318
  • 13 Hee MR, Izatt JA, Swanson EA. et al. Optical coherence tomography of the human retina. Arch Ophthalmol 1995; 113 (03) 325-332
  • 14 Schuman JS, Pedut-Kloizman T, Hertzmark E. et al. Reproducibility of nerve fiber layer thickness measurements using optical coherence tomography. Ophthalmology 1996; 103 (11) 1889-1898
  • 15 Paunescu LA, Schuman JS, Price LL. et al. Reproducibility of nerve fiber thickness, macular thickness, and optic nerve head measurements using Stratus OCT. Invest Ophthalmol Vis Sci 2004; 45: 1716-1724
  • 16 Clement SC, Peeters RP, Ronckers CM. et al. Intermediate and long-term adverse effects of radioiodine therapy for differentiated thyroid carcinoma–a systematic review. Cancer Treat Rev. S0305–7372(15)00165–6
  • 17 Dreger S, Pfinder M, Christianson L, Lhachimi SK, Zeeb H. The effects of iodine blocking following nuclear accidents on thyroid cancer, hypothyroidism, and benign thyroid nodules: design of a systematic review. Syst Rev 2015; 4: 126
  • 18 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Plaque radiotherapy of uveal melanoma with predominant ciliary body involvement. Arch Ophthalmol 1999; 117 (02) 170-177
  • 19 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Radiation retinopathy following plaque radiotherapy for posterior uveal melanoma. Arch Ophthalmol 1999; 117 (05) 609-614
  • 20 Gündüz K, Shields CL, Shields JA, Cater J, Freire JE, Brady LW. Radiation complications and tumor control after plaque radiotherapy of choroidal melanoma with macular involvement. Am J Ophthalmol 1999; 127 (05) 579-589
  • 21 Puusaari I, Heikkonen J, Kivelä T. Ocular complications after iodine brachytherapy for large uveal melanomas. Ophthalmology 2004; 111 (09) 1768-1777
  • 22 Kaçar Güveli T, Özkan S, Öner Tamam M. et al. The effect of high dose radioiodine therapy on formation of radiation retinopathy during thyroid cancer treatment. Mol Imaging Radionucl Ther 2014; 23 (03) 84-88
  • 23 Hykin PG, Shields CL, Shields JA, Arevalo JF. The efficacy of focal laser therapy in radiation-induced macular edema. Ophthalmology 1998; 105 (08) 1425-1429
  • 24 Kinyoun JL, Chittum ME, Wells CG. Photocoagulation treatment of radiation retinopathy. Am J Ophthalmol 1988; 105 (05) 470-478
  • 25 Astrahan MA, Luxton G, Jozsef G, Liggett PE, Petrovich Z. Optimization of 125I ophthalmic plaque brachytherapy. Med Phys 1990; 17 (06) 1053-1057
  • 26 Bechrakis NE, Bornfeld N, Zöller I, Foerster MH. Iodine 125 plaque brachytherapy versus transscleral tumor resection in the treatment of large uveal melanomas. Ophthalmology 2002; 109 (10) 1855-1861
  • 27 Henk JM, Whitelocke RA, Warrington AP, Bessell EM. Radiation dose to the lens and cataract formation. Int J Radiat Oncol Biol Phys 1993; 25 (05) 815-820
  • 28 Finger PT. Tumour location affects the incidence of cataract and retinopathy after ophthalmic plaque radiation therapy. Br J Ophthalmol 2000; 84 (09) 1068-1070