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J Clin Oncol ; 34(26): 3183-8, 2016 09 10.
Artículo en Inglés | MEDLINE | ID: mdl-27382102

RESUMEN

PURPOSE: Intraocular retinoblastoma is curable, but survivors with a heritable predisposition are at high risk for second malignancies. Because second malignancies are associated with high mortality, prognostic factors for second malignancy influence long-term overall survival. This study investigates the impact of all types of eye-preserving therapies on long-term survival in the complete German cohort of patients with heritable retinoblastoma. PATIENTS AND METHODS: Overall survival, disease staging using international scales, time period of diagnosis, and treatment type were analyzed in the 633 German children treated at the national reference center for heritable retinoblastoma. RESULTS: The 5-year overall survival of children diagnosed in Germany with heritable retinoblastoma between 1940 and 2008 was 93.2% (95% CI, 91.2% to 95.1%), but long-term mortality was increased compared with patients with nonheritable disease. Overall survival correlated with tumor staging, and 92% of patients were diagnosed with a favorable tumor stage (International Retinoblastoma Staging System stage 0 or I). Despite a 5-year overall survival of 97.4% (95% CI, 96.0% to 98.8%) in patients with stage 0 or I, only 79.5% (95% CI, 74.2% to 84.8%) of these patients survived 40 years after diagnosis. Long-term overall survival was reduced in children treated with eye-preserving radiotherapy compared with enucleation alone, and adding chemotherapy aggravated this effect. CONCLUSION: The benefits of preserving vision must be balanced with the impact of eye-preserving treatments on long-term survival in heritable retinoblastoma, and the genetic background of the patient influences choice of eye-preserving treatment. Germline RB1 genetic analysis is important to identify heritable retinoblastoma among unilateral retinoblastoma cases. Eye-preserving radiotherapy should be carefully considered in patients with germline RB1 mutations. Life-long oncologic follow-up is crucial for all retinoblastoma survivors, and less detrimental eye-preserving therapies must be developed.


Asunto(s)
Quimioradioterapia/efectos adversos , Enucleación del Ojo/efectos adversos , Tratamientos Conservadores del Órgano/efectos adversos , Neoplasias de la Retina/terapia , Retinoblastoma/terapia , Sobrevivientes , Biomarcadores de Tumor/genética , Quimioradioterapia/mortalidad , Niño , Preescolar , Análisis Mutacional de ADN , Enucleación del Ojo/mortalidad , Femenino , Predisposición Genética a la Enfermedad , Mutación de Línea Germinal , Alemania , Herencia , Humanos , Lactante , Recién Nacido , Estimación de Kaplan-Meier , Masculino , Estadificación de Neoplasias , Tratamientos Conservadores del Órgano/métodos , Tratamientos Conservadores del Órgano/mortalidad , Fenotipo , Modelos de Riesgos Proporcionales , Neoplasias de la Retina/diagnóstico , Neoplasias de la Retina/genética , Neoplasias de la Retina/mortalidad , Retinoblastoma/diagnóstico , Retinoblastoma/genética , Retinoblastoma/mortalidad , Proteínas de Unión a Retinoblastoma/genética , Estudios Retrospectivos , Factores de Riesgo , Factores de Tiempo , Resultado del Tratamiento , Ubiquitina-Proteína Ligasas/genética , Visión Ocular/efectos de los fármacos , Visión Ocular/efectos de la radiación
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