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. 2022 Apr 11;14(2):130–139. doi: 10.5114/jcb.2022.115379

Table 1.

Baseline characteristics of patients: tumor, treatment, and outcome

Patient characteristics (n = 212*) n/value %
Gender
Female 96 45.3
Male 116 54.7
Age at diagnosis
Median 63
Range 19-91
Tumor characteristics (n = 214*)
Laterality of affected eye
OD 103 48.1
OS 111 51.9
Tumor apical height (mm)
Mean ±SD 4.6 ±3.0
Median 3.3
Range 1-15
≤ 2.5 70 32.7
> 2-5 79 36.9
> 5-10 51 23.8
> 10 14 6.5
Basal diameter (mm)
Mean ±SD 11.5 ±3.2
Median 11.5
Range 2-21 -–
≤ 8 33 15.4
8-11 72 33.6
11-16 93 43.5
> 16 16 7.5
AJCC1 staging
Stage I 81 37.9
Stage IIA 60 28.0
Stage IIB 47 22.0
Stage IIIA 17 7.9
Stage IIIB 8 3.7
Stage IIIC 0 0.0
Stage IV 1 0.5
COMS2 staging
Small 90 42.1
Medium 81 37.9
Large 43 20.1
Genetic class
1A 119 55.6
1B 30 14.0
2 55 25.7
N.A. 10 4.7
Treatment characteristics (n = 214*)
Treatment dose (Gy)
At height > 5 mm 85.0
At height ≤ 5 mm 120.6
% of tumor volume receiving prescription dose
Mean ±SD 99.9% ±0.6%
Range 94.9-100%
% tumor + 2 mm margin volume receiving prescription dose
Mean ±SD 96.8% ±2.8%
Range 85.0-100%
Plaque repositioning
Number of plaques repositioned 33 15.4
Outcome characteristics (n = 180**)
Status
Alive without disease 150 83.3
Alive with uveal melanoma 8 4.4
Dead of other or unknown cause 8 4.4
Dead of uveal melanoma 14 7.8
Follow-up by ocular oncology
Mean (months) 37.3
Median (months) 30.8
Range (months) 12.2-96.3
Lost to follow-up 22
Local control rate 100.0
Distant metastasis 22 12.2
Site(s) of distant metastasis
Liver 22
Lung 2
Bone 3
Spleen 1
Radiation-related toxicities
Radiation retinopathy 85 47.2
Retinal vein occlusion 9 5.0
Serous retinal detachment 2 1.1
Vitreous hemorrhage 2 1.1
Optic neuropathy 1 0.6
Hypotony maculopathy 1 0.6
Radiation retinopathy (RR) factors (n = 85)
Median time to RR (months) 24
Treated with anti-VEGF or trial 45 52.9
CTCAE3 grade 1 33
CTCAE grade 2 13
CTCAE grade 3 18
CTCAE grade 4 21
CTCAE grade 5 0
1

8th edition of the American Joint Committee on Cancer, 2 Collaborative ocular melanoma study, 3 Common terminology criteria for adverse events, * One patient presented with two UMs: one OS and one OD treated at separate times. One patient presented with two UMs at separate times within OS, treated at separate times, ** 180 patients had at least 12 months follow-up, for which outcomes are reported