Literature DB >> 14522776

New retinoblastoma tumor formation in children initially treated with systemic carboplatin.

Thomas C Lee1, Naomi I Hayashi, Ira J Dunkel, Katherine Beaverson, Danielle Novetsky, David H Abramson.   

Abstract

PURPOSE: To determine the frequency and timing of new intraocular tumor formation in children with hereditary retinoblastoma initially treated with systemic carboplatin.
DESIGN: Retrospective, noncomparative case series. PARTICIPANTS: This study included 34 children (57 eyes) with hereditary bilateral retinoblastoma initially treated with systemic carboplatin at the Robert M. Ellsworth Ophthalmic Oncology Center at NewYork-Presbyterian Hospital from 1994 through 2000. MAIN OUTCOME MEASURES: New tumor formation after initial treatment with systemic carboplatin.
RESULTS: There were a total of 165 tumors in 57 eyes. There were 63 new tumors in 27 eyes (47%) after administration of systemic carboplatin, for a mean of 1.1 new tumors per eye. The mean patient age at time of new tumor presentation was 9 months, with 57% of new tumors developing within 4 months of carboplatin treatment. Kaplan-Meier analysis showed that children who were treated when younger than 6 months of age were more likely to have new tumors (60%) compared with those treated after 6 months of age (31%; P = 0.0182).
CONCLUSIONS: New intraocular tumors continue to develop after systemic carboplatin; most new tumors appeared within 4 months of treatment.

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Year:  2003        PMID: 14522776     DOI: 10.1016/S0161-6420(03)00669-9

Source DB:  PubMed          Journal:  Ophthalmology        ISSN: 0161-6420            Impact factor:   12.079


  10 in total

1.  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

2.  The National Registry of Retinoblastoma in Japan (1983-2014).

Authors: 
Journal:  Jpn J Ophthalmol       Date:  2018-05-30       Impact factor: 2.447

3.  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
Journal:  Trans Am Ophthalmol Soc       Date:  2004

4.  Prognostic factors and treatment outcomes of retinoblastoma in pediatric patients: a single-institution study.

Authors:  La-Ongsri Atchaneeyasakul; Chutima Wongsiwaroj; Mongkol Uiprasertkul; Kleebsabai Sanpakit; Kullathorn Thephamongkhol; Adisak Trinavarat
Journal:  Jpn J Ophthalmol       Date:  2009-01-30       Impact factor: 2.447

Review 5.  Current management strategies for intraocular retinoblastoma.

Authors:  Jonathan W Kim; David H Abramson; Ira J Dunkel
Journal:  Drugs       Date:  2007       Impact factor: 9.546

6.  Retinoblastoma major review with updates on Middle East management protocols.

Authors:  Ihab Saad Othman
Journal:  Saudi J Ophthalmol       Date:  2012-04

7.  Differential gene expression profile of retinoblastoma compared to normal retina.

Authors:  Arupa Ganguly; Carol L Shields
Journal:  Mol Vis       Date:  2010-07-13       Impact factor: 2.367

8.  Unusually very late-onset new growth of intraocular retinoblastoma: A case report and review of literature.

Authors:  Yeshigeta Gelaw; Shoeib Mohamed Shoukry; Ihab Saad Othman
Journal:  Am J Ophthalmol Case Rep       Date:  2016-12-28

Review 9.  Intra-arterial chemotherapy in retinoblastoma - A paradigm change.

Authors:  Fairooz P Manjandavida; Christina Stathopoulos; Jing Zhang; Santhosh G Honavar; Carol L Shields
Journal:  Indian J Ophthalmol       Date:  2019-06       Impact factor: 1.848

10.  Electroretinogram monitoring of dose-dependent toxicity after ophthalmic artery chemosurgery in retinoblastoma eyes: six year review.

Authors:  Jasmine H Francis; David H Abramson; Y Pierre Gobin; Brian P Marr; Ira J Dunkel; Elyn R Riedel; Scott E Brodie
Journal:  PLoS One       Date:  2014-01-20       Impact factor: 3.240

  10 in total

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