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1.
Ophthalmic Genet ; 44(2): 119-126, 2023 04.
Article in English | MEDLINE | ID: mdl-35848346

ABSTRACT

PURPOSE: We present an epidemiologic analysis of retinoblastoma (RB) and uveal melanoma (UM) in Jordan to aid national strategies for improved ocular cancer surveillance and control. METHODS: A retrospective cohort of all Jordanian patients with RB and UM diagnosed over 10 years (2011-2020). Outcome measures included incidence, demographics, and outcomes. RESULTS: Retinoblastoma (n = 124) was more common than UM (n = 82); there was no sex predilection for either group. The median age at diagnosis of RB was 15 months(Six and 28 months for bilateral and unilateral cases, respectively), and the mean age-adjusted incidence was 8.2 cases per-million-children per year for children aged five years or less(one per 15,620 newborn per year). Fifty-one(41%) had bilateral disease, and 18(15%) had familial disease. Ninety-six(55%) eyes were group D or E(78% were T3/T4), and the five-year survival rate was 96%.For UM, the median age at diagnosis was 45 years with an incidence of 1.39 new cases per year per one million population. All(100%) had nonfamilial unilateral disease. Seventy-three(89%) had the tumor in the choroid, and 48(58%) had an advanced tumor that had invaded the sclera or the orbit (T3/T4) tumor. Sixty-two(76%) were treated by I-125 radioactive plaque, with globe salvage in 59(95%); the five-year survival rate was 85%. CONCLUSION: In Jordan, RB is more common and has better survival than UM. RB in Jordan and Western countries is equal in terms of incidence, globe salvage, and survival. UM is less common, with lower age at diagnosis (that was associated with better survival) in Jordan than in Western countries.


Subject(s)
Retinal Neoplasms , Retinoblastoma , Uveal Neoplasms , Infant, Newborn , Humans , Middle Aged , Child , Retinoblastoma/diagnosis , Jordan/epidemiology , Iodine Radioisotopes , Incidence , Retrospective Studies , Uveal Neoplasms/epidemiology , Retinal Neoplasms/diagnosis
2.
Brachytherapy ; 11(3): 230-6, 2012.
Article in English | MEDLINE | ID: mdl-22226079

ABSTRACT

INTRODUCTION: Retinoblastoma and uveal melanoma are the most common ocular tumors in children and adults, respectively. Enucleation and external beam radiation therapy are integral in the management of ocular tumors. However, these tumors could also be treated effectively by plaque therapy, which has the potential of preserving the globe and maintaining vision. METHODS AND MATERIALS: We reviewed our experience with the introduction of this technique to our center. Furthermore, we highlighted the critical role of a specialized multidisciplinary team in the successful implementation of this procedure. DISCUSSION: This review represents a detailed report addressing the practical steps for successfully establishing plaque therapy in developing countries. RESULTS: Plaque therapy was successfully implemented at our center in 1.5 years. Integration with an advanced cancer center is crucial for the correct transfer of this complex technology. CONCLUSION: Complex brachytherapy procedures could be successfully established and implemented in developing countries.


Subject(s)
Brachytherapy/methods , Developing Countries , Melanoma/rehabilitation , Retinal Neoplasms/radiotherapy , Retinoblastoma/radiotherapy , Uveal Neoplasms/rehabilitation , Brachytherapy/instrumentation , Humans , Patient Care , Patient Safety , Practice Guidelines as Topic , Radiation Dosage , Time Factors
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