Abstract
Retinoblastoma was traditionally treated with enucleation and external-beam radiotherapy. However, in the past decade, systemic chemotherapy has become the primary globe-salvaging approach. This approach is generally combined with focal treatment, allowing for tumor consolidation following initial chemoreduction. A recently developed classification scheme may improve our ability to predict outcomes with this treatment modality. The Children’s Oncology Group has initiated a series of prospective multicenter trials to improve treatment outcomes with systemic chemotherapy.
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Gombos, D.S., Chevez-Barrios, P. Current treatment and management of retinoblastoma. Curr Oncol Rep 9, 453–458 (2007). https://doi.org/10.1007/s11912-007-0063-7
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DOI: https://doi.org/10.1007/s11912-007-0063-7