Literature DB >> 8906023

Chemoreduction in the initial management of intraocular retinoblastoma.

C L Shields1, P De Potter, B P Himelstein, J A Shields, A T Meadows, J M Maris.   

Abstract

BACKGROUND: Chemoreduction is a method of reducing tumor volume to allow for more focused, less damaging therapeutic measures.
OBJECTIVE: To determine whether chemoreduction could be used to decrease the size of retinoblastoma so that enucleation or external beam radiotherapy could be avoided and more conservative modalities employed.
METHODS: A prospective pilot study was performed to assess the effectiveness of a 2-month chemoreduction regimen of vincristine sulfate, etoposide, and carboplatin in patients with retinoblastoma. The study included 20 patients with 54 tumors in 31 eyes.
RESULTS: At the initial examination, the mean tumor base was 12 mm and the thickness, 7 mm. Vitreous seeds were present in 14 eyes (45%). A secondary retinal detachment was present in 24 eyes (77%) and, when present, involved a mean of 71% of the retina. In 11 eyes (36%) the retina was totally detached with serous subretinal fluid. After 2 months of chemoreduction, all 54 tumors showed regression in size, and 48 (89%) showed evidence of calcification. The mean tumor base was 8 mm and the thickness, 4 mm. Overall, there was a mean 35% decrease in base and 49% decrease in thickness of the tumor at the end of the treatment period. A complete response was found in 25 tumors (46%) and a partial response in 29 (54%). The subretinal fluid had resolved completely in 50% of the cases (12/24 eyes), and, in the 11 eyes with total retinal detachment, the subretinal fluid had completely resolved, leaving flat retina, in 6 eyes (54%). The vitreous seeds demonstrated some degree of regression in all cases, and in 5 eyes there was 90% to 100% calcification of the seeds. Short-term systemic toxic effects were mild (transient bone marrow suppression). Enucleation was avoided in all cases; external beam radiotherapy was necessary in 9 eyes because of diffuse vitreous seeds. The remaining 22 eyes were treated with local methods after chemoreduction.
CONCLUSION: Tumor shrinkage with chemoreduction may allow treatment with less invasive measures, such as cryotherapy, laser photocoagulation, thermotherapy, or plaque radiotherapy, thereby avoiding enucleation and external beam radiotherapy.

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Year:  1996        PMID: 8906023     DOI: 10.1001/archopht.1996.01100140530002

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN: 0003-9950


  59 in total

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4.  Retinoblastoma treated with primary chemotherapy alone: the significance of tumour size, location, and age.

Authors:  Dan S Gombos; Alison Kelly; Pietro G Coen; Judith E Kingston; John L Hungerford
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5.  Systemic carboplatin for retinoblastoma: change in tumour size over time.

Authors:  D H Abramson; S D Lawrence; K L Beaverson; T C Lee; I S Rollins; I J Dunkel
Journal:  Br J Ophthalmol       Date:  2005-12       Impact factor: 4.638

Review 6.  Current treatment and management of retinoblastoma.

Authors:  Dan S Gombos; And Patricia Chevez-Barrios
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7.  Chemoreduction for retinoblastoma: analysis of tumor control and risks for recurrence in 457 tumors.

Authors:  Carol L Shields; Arman Mashayekhi; Jacqueline Cater; Abdallah Shelil; Anna T Meadows; Jerry A Shields
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8.  Proliferative Vitreoretinopathy in Treated Retinoblastoma.

Authors:  Cindy S Hwang; Pia R Mendoza; Jill R Wells; Hans E Grossniklaus; G Baker Hubbard
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Review 9.  Factors in improved survival from paediatric cancer.

Authors:  J W Taub
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10.  Tumor Environment of Retinoblastoma, Intraocular Cancer.

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