Ruthenium plaque radiotherapy in the current era of retinoblastoma treatment.


Journal

Ophthalmic genetics
ISSN: 1744-5094
Titre abrégé: Ophthalmic Genet
Pays: England
ID NLM: 9436057

Informations de publication

Date de publication:
12 2022
Historique:
pubmed: 2 11 2022
medline: 27 1 2023
entrez: 1 11 2022
Statut: ppublish

Résumé

Two major treatment modalities for retinoblastoma, intraarterial chemotherapy (IAC) and intravitreal chemotherapy (IVitC), have superseded external beam radiotherapy for eye salvage. In this new setting our objectives were to evaluate the indications for plaque radiotherapy, complications, and recurrence rates. Retrospective detailed review of patient's charts was performed for all subjects treated with plaque radiotherapy for retinoblastoma between January 2015 and December 2020. A total of 12 eyes of 12 patients were included. Mean age at plaque insertion was 45 months (median 29, range 17-150). The treatment dose was 40 Gy to the tumor apex. The indication for plaque radiotherapy was salvage therapy in 11 eyes (92%) and primary treatment in one eye (8%). At last follow-up from plaque insertion (mean 36 months, range 3-67), four (33%) patients had visual acuity better than 0.5 LogMAR and four (33%) had visual acuity worse than 1.0 LogMAR. Radiation-related complications were: one (8%) vitreous haemorrhage, two (16%) non-proliferative radiation retinopathy and one (8%) cataract. Recurrence was detected in four (33%) patients at a mean of 7.8 months (median 5, range 1-20) post-plaque. Globe salvage rate was 75%, as three eyes required enucleation, one to treat recurrence of the tumor treated with plaque and two to treat recurrence of other tumors. In the current era of retinoblastoma management, a role for plaque radiotherapy remains for salvage or primary treatment in eyes with localised active tumor, providing tumor control in 66%. Close observation is recommended to both detect recurrence and radiation-related complications.

Sections du résumé

BACKGROUND
Two major treatment modalities for retinoblastoma, intraarterial chemotherapy (IAC) and intravitreal chemotherapy (IVitC), have superseded external beam radiotherapy for eye salvage. In this new setting our objectives were to evaluate the indications for plaque radiotherapy, complications, and recurrence rates.
METHODS
Retrospective detailed review of patient's charts was performed for all subjects treated with plaque radiotherapy for retinoblastoma between January 2015 and December 2020.
RESULTS
A total of 12 eyes of 12 patients were included. Mean age at plaque insertion was 45 months (median 29, range 17-150). The treatment dose was 40 Gy to the tumor apex. The indication for plaque radiotherapy was salvage therapy in 11 eyes (92%) and primary treatment in one eye (8%). At last follow-up from plaque insertion (mean 36 months, range 3-67), four (33%) patients had visual acuity better than 0.5 LogMAR and four (33%) had visual acuity worse than 1.0 LogMAR. Radiation-related complications were: one (8%) vitreous haemorrhage, two (16%) non-proliferative radiation retinopathy and one (8%) cataract. Recurrence was detected in four (33%) patients at a mean of 7.8 months (median 5, range 1-20) post-plaque. Globe salvage rate was 75%, as three eyes required enucleation, one to treat recurrence of the tumor treated with plaque and two to treat recurrence of other tumors.
CONCLUSIONS
In the current era of retinoblastoma management, a role for plaque radiotherapy remains for salvage or primary treatment in eyes with localised active tumor, providing tumor control in 66%. Close observation is recommended to both detect recurrence and radiation-related complications.

Identifiants

pubmed: 36317817
doi: 10.1080/13816810.2022.2141795
doi:

Substances chimiques

Ruthenium 7UI0TKC3U5

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

756-761

Auteurs

Guy S Negretti (GS)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Ocular Oncology Service, Moorfields Eye Hospital, London, UK.

Hibba Quhill (H)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Ocular Oncology Service, Moorfields Eye Hospital, London, UK.

Catriona Duncan (C)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Department of Paediatric Oncology, Hospital for Sick Children, London, UK.

Tanzina Chowdhury (T)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Department of Paediatric Oncology, Hospital for Sick Children, London, UK.

Ian Stoker (I)

Department of Radiation Physics, St. Bartholomew's Hospital, London, UK.

M Ashwin Reddy (MA)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Ocular Oncology Service, Moorfields Eye Hospital, London, UK.
Queen Mary University of London, London, UK.

Mandeep S Sagoo (MS)

The London Retinoblastoma Service, The Royal London Hospital, London, UK.
Ocular Oncology Service, Moorfields Eye Hospital, London, UK.
NIHR Biomedical Research Centre for Ophthalmology, Moorfields Eye Hospital and University College London Institute of Ophthalmology, London, UK.

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