June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Electroretinogram monitoring of retinal toxicity of ophthalmic artery chemosurgery for retinoblastoma: Six year experience
Author Affiliations & Notes
  • Jasmine Francis
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
  • David Abramson
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Department of Ophthalmology, Weill Cornell Medical College of New York Presbyterian, New York, NY
  • Pierre Gobin
    Department of Neurosurgery, Weill Cornell Medical College of New York Presbyterian, New York, NY
  • Brian Marr
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Department of Ophthalmology, Weill Cornell Medical College of New York Presbyterian, New York, NY
  • Ira Dunkel
    Department of Pediatrics, Memorial Sloan Kettering, New York, NY
  • Elyn Riedel
    Department of Epidemiology and Biostatistics, Memorial Sloan Kettering, New York, NY
  • Scott Brodie
    Ophthalmic Oncology, Memorial Sloan Kettering Cancer Center, New York, NY
    Department of Ophthalmology, Mount Sinai School of Medicine, New York, NY
  • Footnotes
    Commercial Relationships Jasmine Francis, None; David Abramson, None; Pierre Gobin, None; Brian Marr, None; Ira Dunkel, None; Elyn Riedel, None; Scott Brodie, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 3979. doi:
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      Jasmine Francis, David Abramson, Pierre Gobin, Brian Marr, Ira Dunkel, Elyn Riedel, Scott Brodie; Electroretinogram monitoring of retinal toxicity of ophthalmic artery chemosurgery for retinoblastoma: Six year experience. Invest. Ophthalmol. Vis. Sci. 2013;54(15):3979.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract
 
Purpose
 

The effectiveness of ophthalmic artery chemosurgery (OAC) for retinoblastoma derives from the very high local tissue concentrations achieved in the distribution of the ophthalmic artery, before the drug is safely diluted in the systemic venous circulation. We have recorded electroretinogram (ERG) responses before and after OAC to monitor retinal function as a gauge of local toxicity, and we herein report these results.

 
Methods
 

Prospective review of 6-year experience of retinoblastoma patients receiving OAC. This study recorded the ERG 30 Hz flicker amplitude response changes from baseline, at 3 and 12 months following treatment completion. Inclusion criteria consisted of eyes treated with OAC with ERG measurements a. before OAC, and b. 3 months after the last OAC treatment +/- 1 month, and if available, c. 12 months after last OAC treatment +/- 2 months. Both univariate and multivariate linear regression models were performed, with generalized estimating equations to correct for correlations within patients. Independent numerical variables included maximum and cumulative doses of melphalan, topotecan and carboplatin.

 
Results
 

ERG data were available for 103 eyes of 81 patients; a total of 270 recordings were analyzed. Results from the univariate and multivariate regressive analysis are shown in figures 1 and 2, respectively.

 
Conclusions
 

Melphalan has the strongest, and carboplatin the weakest association to change in ERG response. By univariate analysis, both melphalan and topotecan appear to be associated with changes in ERG amplitude at both 3 and 12 months; but for the most part, these changes are minimal and likely clinically insignificant. By multivariate analysis, maximum and cumulative melphalan have a modest, temporary effect on the ERG amplitude change, which is apparent at 3 months but no longer evident at 12 months after completing treatment. By multivariate analysis, topotecan and carboplatin do not appear to adversely effect the change in ERG response.

 
 
Univariate regression analysis
 
Univariate regression analysis
 
 
Multivariate regression analysis
 
Multivariate regression analysis
 
Keywords: 703 retinoblastoma • 744 tumors • 503 drug toxicity/drug effects  
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