Literature DB >> 23937863

Retinoblastoma in Turkey: results from a tertiary care center in Ankara.

Kaan Gündüz, Kenan Köse, Rengin Aslihan Kurt, Elçin Süren, Nurdan Taçyildiz, Handan Dinçaslan, Emel Ünal, Esra Erden, Aylin Okçu Heper.   

Abstract

PURPOSE: To evaluate the presentation patterns and results of management of retinoblastoma at a tertiary care center in Ankara, Turkey, with special emphasis on globe conservation rate in unilateral and bilateral intraocular retinoblastoma.
METHODS: Patients were grouped according to the International Classification of Retinoblastoma. For intraocular retinoblastoma, group E and some group D eyes underwent primary enucleation. Secondary enucleation was performed after failure of chemoreduction, focal treatments, external beam radiotherapy (EBRT), and intra-arterial chemotherapy used in various combinations. For extraocular retinoblastoma cases, treatment consisted of enucleation/exenteration or orbital biopsy, high-dose chemotherapy, and EBRT to the orbit and metastatic sites.
RESULTS: During the study period from October 1998 to May 2010, 165 of 192 (85.9%) patients had intraocular disease and 27 (14.1%) patients had extraocular disease. In total, primary or secondary enucleation was performed in 70 of 94 eyes with unilateral retinoblastoma (74.5%) and in 34 of 142 eyes with bilateral retinoblastoma (23.9%). The overall globe conservation rate was 69.6%. Only one patient in the intraocular retinoblastoma group died of metastatic retinoblastoma to the central nervous system. Twenty of 27 patients (74.1%) with extraocular retinoblastoma were found to have metastasis to the central nervous system, bone, bone marrow, and/or lymph nodes. At a mean follow-up of 28.0 months (median: 12 months; range: 1 to 120 months), survival was 33.3% despite intensive treatment.
CONCLUSIONS: The overall risk of enucleation was 75% in eyes with unilateral retinoblastoma and 24% in eyes with bilateral retinoblastoma. Extraocular retinoblastoma carries a 75% risk of systemic metastasis and 67% risk of death. Copyright 2013, SLACK Incorporated.

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Year:  2013        PMID: 23937863     DOI: 10.3928/01913913-20130730-02

Source DB:  PubMed          Journal:  J Pediatr Ophthalmol Strabismus        ISSN: 0191-3913            Impact factor:   1.402


  6 in total

Review 1.  Determining the incidence of the hereditary form of retinoblastoma.

Authors:  Alan Edmund Stark
Journal:  Ann Transl Med       Date:  2016-05

2.  Ophthalmic artery chemosurgery for eyes with advanced retinoblastoma.

Authors:  David H Abramson; Armida W M Fabius; Jasmine H Francis; Brian P Marr; Ira J Dunkel; Scott E Brodie; Anna Escuder; Y Pierre Gobin
Journal:  Ophthalmic Genet       Date:  2017-01-17       Impact factor: 1.803

3.  Globe salvage treatment in group D and group E retinoblastoma.

Authors:  Ahmad Khaqan Hussain; Rachwani Anil Rahul; Rocha de Lossada Carlos; Zamorano Martín Francisco; García Lorente María; Pennisi Flavia; Bonzano Chiara; Borroni Davide
Journal:  Rom J Ophthalmol       Date:  2021 Jan-Mar

Review 4.  Risk definition and management strategies in retinoblastoma: current perspectives.

Authors:  Fariba Ghassemi; Alireza Khodabande
Journal:  Clin Ophthalmol       Date:  2015-06-08

Review 5.  Chemotherapy in Retinoblastoma: Current Approaches.

Authors:  Özge Yanık; Kaan Gündüz; Kıvılcım Yavuz; Nurdan Taçyıldız; Emel Ünal
Journal:  Turk J Ophthalmol       Date:  2015-12-05

6.  Intra-Arterial Chemotherapy (Ophthalmic Artery Chemosurgery) for Group D Retinoblastoma.

Authors:  David H Abramson; Anthony B Daniels; Brian P Marr; Jasmine H Francis; Scott E Brodie; Ira J Dunkel; Y Pierre Gobin
Journal:  PLoS One       Date:  2016-01-12       Impact factor: 3.240

  6 in total

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