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Episcleral plaque brachytherapy for retinoblastoma

Background The purpose of this study was to report our experience using episcleral plaque brachytherapy (EPBRT) to treat retinoblastoma and to demonstrate its applicability in multimodality treatment. Procedure We treated 26 tumors in 25 eyes from a group of 21 children with unilateral (n = 4) or bi...

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Published in:Pediatric blood & cancer 2004-08, Vol.43 (2), p.134-139
Main Authors: Merchant, Thomas E., Gould, Ciara J., Wilson, Matthew W., Hilton, Nathan E., Rodriguez-Galindo, Carlos, Haik, Barrett G.
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container_title Pediatric blood & cancer
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creator Merchant, Thomas E.
Gould, Ciara J.
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description Background The purpose of this study was to report our experience using episcleral plaque brachytherapy (EPBRT) to treat retinoblastoma and to demonstrate its applicability in multimodality treatment. Procedure We treated 26 tumors in 25 eyes from a group of 21 children with unilateral (n = 4) or bilateral (n = 17) retinoblastoma. The group comprised 8 girls and 13 boys; the median age was 25 months (range: 2–64 months) at the time of EPBRT. Iodine‐125 (125I) was used for all applications. The median dose was 44 Gy (range: 35–47.6 Gy). EPBRT was administered primarily at the time of relapse after primary chemotherapy or radiation therapy. Results For eyes treated with EPBRT, the eye preservation rate was 15/25 with a median follow‐up of 47 months (range: 2–198 months); the lesion control rate was 25/26 with a median follow‐up of 13 months (range: 1–140 months). The median time to additional whole‐eye treatment after EPBRT was 12 months (range: 2–105 months). Conclusions Similar to previously reported series, EPBRT shows a high rate of successful tumor control as a primary treatment for retinoblastoma, as well as a secondary therapy at the time of relapse. EPBRT also allows for a clinically significant delay in the time to additional measures for the affected eye. Therefore, EPBRT should be considered as a form of local ophthalmic therapy that avoids or delays the use of external‐beam radiotherapy, especially for patients primarily treated with chemotherapy who might require consolidation therapy.© 2004 Wiley‐Liss, Inc.
doi_str_mv 10.1002/pbc.20094
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Procedure We treated 26 tumors in 25 eyes from a group of 21 children with unilateral (n = 4) or bilateral (n = 17) retinoblastoma. The group comprised 8 girls and 13 boys; the median age was 25 months (range: 2–64 months) at the time of EPBRT. Iodine‐125 (125I) was used for all applications. The median dose was 44 Gy (range: 35–47.6 Gy). EPBRT was administered primarily at the time of relapse after primary chemotherapy or radiation therapy. Results For eyes treated with EPBRT, the eye preservation rate was 15/25 with a median follow‐up of 47 months (range: 2–198 months); the lesion control rate was 25/26 with a median follow‐up of 13 months (range: 1–140 months). The median time to additional whole‐eye treatment after EPBRT was 12 months (range: 2–105 months). Conclusions Similar to previously reported series, EPBRT shows a high rate of successful tumor control as a primary treatment for retinoblastoma, as well as a secondary therapy at the time of relapse. EPBRT also allows for a clinically significant delay in the time to additional measures for the affected eye. Therefore, EPBRT should be considered as a form of local ophthalmic therapy that avoids or delays the use of external‐beam radiotherapy, especially for patients primarily treated with chemotherapy who might require consolidation therapy.© 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 1545-5009</identifier><identifier>EISSN: 1545-5017</identifier><identifier>DOI: 10.1002/pbc.20094</identifier><identifier>PMID: 15236279</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; brachytherapy ; Brachytherapy - methods ; Child, Preschool ; Combined Modality Therapy ; Female ; Humans ; Infant ; Iodine Radioisotopes - therapeutic use ; Male ; Medical sciences ; Ophthalmology ; pediatrics ; radiotherapy ; Retinal Neoplasms - mortality ; Retinal Neoplasms - radiotherapy ; Retinal Neoplasms - therapy ; retinoblastoma ; Retinoblastoma - mortality ; Retinoblastoma - radiotherapy ; Retinoblastoma - therapy ; Retinopathies ; Survival Rate ; Treatment Outcome ; Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus</subject><ispartof>Pediatric blood &amp; cancer, 2004-08, Vol.43 (2), p.134-139</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3894-1b7dbe5fd02036775a1420eaf37ca5b9806fd7d8de0cb00d4442522663a30b2f3</citedby><cites>FETCH-LOGICAL-c3894-1b7dbe5fd02036775a1420eaf37ca5b9806fd7d8de0cb00d4442522663a30b2f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,780,784,789,790,23930,23931,25140,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=15932219$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15236279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merchant, Thomas E.</creatorcontrib><creatorcontrib>Gould, Ciara J.</creatorcontrib><creatorcontrib>Wilson, Matthew W.</creatorcontrib><creatorcontrib>Hilton, Nathan E.</creatorcontrib><creatorcontrib>Rodriguez-Galindo, Carlos</creatorcontrib><creatorcontrib>Haik, Barrett G.</creatorcontrib><title>Episcleral plaque brachytherapy for retinoblastoma</title><title>Pediatric blood &amp; cancer</title><addtitle>Pediatr. Blood Cancer</addtitle><description>Background The purpose of this study was to report our experience using episcleral plaque brachytherapy (EPBRT) to treat retinoblastoma and to demonstrate its applicability in multimodality treatment. Procedure We treated 26 tumors in 25 eyes from a group of 21 children with unilateral (n = 4) or bilateral (n = 17) retinoblastoma. The group comprised 8 girls and 13 boys; the median age was 25 months (range: 2–64 months) at the time of EPBRT. Iodine‐125 (125I) was used for all applications. The median dose was 44 Gy (range: 35–47.6 Gy). EPBRT was administered primarily at the time of relapse after primary chemotherapy or radiation therapy. Results For eyes treated with EPBRT, the eye preservation rate was 15/25 with a median follow‐up of 47 months (range: 2–198 months); the lesion control rate was 25/26 with a median follow‐up of 13 months (range: 1–140 months). The median time to additional whole‐eye treatment after EPBRT was 12 months (range: 2–105 months). Conclusions Similar to previously reported series, EPBRT shows a high rate of successful tumor control as a primary treatment for retinoblastoma, as well as a secondary therapy at the time of relapse. EPBRT also allows for a clinically significant delay in the time to additional measures for the affected eye. 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Results For eyes treated with EPBRT, the eye preservation rate was 15/25 with a median follow‐up of 47 months (range: 2–198 months); the lesion control rate was 25/26 with a median follow‐up of 13 months (range: 1–140 months). The median time to additional whole‐eye treatment after EPBRT was 12 months (range: 2–105 months). Conclusions Similar to previously reported series, EPBRT shows a high rate of successful tumor control as a primary treatment for retinoblastoma, as well as a secondary therapy at the time of relapse. EPBRT also allows for a clinically significant delay in the time to additional measures for the affected eye. 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subjects Biological and medical sciences
brachytherapy
Brachytherapy - methods
Child, Preschool
Combined Modality Therapy
Female
Humans
Infant
Iodine Radioisotopes - therapeutic use
Male
Medical sciences
Ophthalmology
pediatrics
radiotherapy
Retinal Neoplasms - mortality
Retinal Neoplasms - radiotherapy
Retinal Neoplasms - therapy
retinoblastoma
Retinoblastoma - mortality
Retinoblastoma - radiotherapy
Retinoblastoma - therapy
Retinopathies
Survival Rate
Treatment Outcome
Tumors and pseudotumors of the eye, orbit, eyelid, lacrimal apparatus
title Episcleral plaque brachytherapy for retinoblastoma
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