Optical Coherence Tomography (OCT) in Retinoblastoma Management: Experience of the Portuguese National Reference Center

Authors

  • Margarida Q. Dias Departamento de Oftalmologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal https://orcid.org/0000-0003-4125-4245
  • Joana Providência Departamento de Oftalmologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal; Faculdade Medicina, Universidade de Coimbra, Coimbra, Portugal https://orcid.org/0000-0003-1312-7978
  • Madalena Monteiro Departamento de Oftalmologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal
  • Guilherme Castela Departamento de Oftalmologia, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal; Faculdade Medicina, Universidade de Coimbra, Coimbra, Portugal https://orcid.org/0000-0003-0568-8265

DOI:

https://doi.org/10.48560/rspo.28264

Keywords:

Disease Management, Retinoblastoma, Tomography, Optical Coherence

Abstract

INTRODUCTION: Patients under 5 years old with retinoblastoma require close monitoring under anesthesia to ensure early detection of new tumors. They undergo monthly observations after diagnosis and during the first 6 months after treatment, then observations are gradually spaced in time until the age of five. Optical coherence tomography (OCT) is a relatively new exam in monitoring retinoblastoma patients. The advantages include pre-clinical diagnosis of new tumors when located in the posterior pole and evaluation of retinal layers in eyes submitted to intraarterial chemotherapy. We aimed to review the role of handheld OCT in evaluating eyes affected by retinoblastoma and to report our experience using this device.

METHODS: The observational case series included children with retinoblastoma followed at Centro Hospitalar e Universitário de Coimbra from January 2022 to August 2022 who underwent an OCT session during their routine observations under anesthesia. We collected data regarding patients’ age at presentation, family history, RB1 mutation status and International Intraocular Retinoblastoma Classification. The OCT images were analyzed for primary tumor characterization, relapse tumors and associated findings, and correlated to the fundus image on Retcam®.

RESULTS: We included 23 eyes of 19 children that had a total of 44 OCT exams. The median number of OCT scans per eye was 2 (range 1-6). The mean age at presentation of retinoblastoma was 9.37 months old. After reviewing the images, we were able to identify all 4 types of tumor remnants in our series. One patient had a new relapsed tumor that was detected primarily with OCT and treatment was initiated accordingly. In nine eyes, it was impossible to scan the primary tumor due to peripheral localization in the fundus due to advanced stages.

CONCLUSION: Hand-held OCT allows direct visualization of the retina and ensures a closer follow-up of young children with retinoblastoma, leading to the earlier diagnosis of relapses and the ability to treat them with less aggressive options, which may preserve more vision. The use and experience with OCT are increasing in all specialized centers that treat retinoblastoma. Hence, its usefulness will continue to grow and, in the future, there will be more clues to help diagnose retinoblastoma even sooner.

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References

Kivela T. The epidemiological challenge of the most frequent eye cancer: retinoblastoma, an issue of birth and death. Br J Ophthalmol. 2009;93:1129-31. doi: 10.1136/bjo.2008.150292

Jenkinson H. Retinoblastoma: diagnosis and management- the UK perspective. Arch Dis Child. 2015;100:1070-5. doi: 10.1136/archdischild-2014-306208

Yun J, Li Y, Xu CT, Pan BR. Epidemiology and Rb1 gene of retinoblastoma. Int J Ophthalmol. 2011;4:103-9. doi: 10.3980/j. issn.2222-3959.2011.01.24

Dimaras H, Corson TW, Cobrinik D, White A, Zhao J, Munier FL, et al. Retinoblastoma. Nat Rev Dis Primers. 2015;1:15021. doi: 10.1038/nrdp.2015.21

Medina CA, Plesec T, Singh AD. Optical coherence tomog- raphy imaging of ocular and periocular tumours. Br J Oph- thalmol. 2014;98 Suppl 2:ii40-46. doi: 10.1136/bjophthal- mol-2013-304299

Panozzo G, Parolini B, Gusson E, Mercanti A, Pinackatt S, Bertoldo G, et al. Diabetic macular edema: an OCT- based classification. Semin Ophthalmol. 2004;19:13-20. doi: 10.1080/08820530490519934

Quellec G, Lee K, Dolejsi M, Garvin MK, Abramoff MD, Sonka M. Three-dimensional analysis of retinal layer texture: identification of fluid-filled regions in SD-OCT of the macu- la. IEEE Trans Med Imaging. 2010;29:1321-30. doi: 10.1109/ TMI.2010.2047023

Scott AW, Farsiu S, Enyedi LB, Wallace DK, Toth CA. Imaging the infant retina with a hand-held spectral-domain optical co- herence tomography device. Am J Ophthalmol. 2009;147:364- 73 e362. doi: 10.1016/j.ajo.2008.08.010

Rootman DB, Gonzalez E, Mallipatna A, Vandenhoven C, Hampton L, Dimaras H, et al. Hand-held high-resolution spectral domain optical coherence tomography in retinoblas- toma: clinical and morphologic considerations. Br J Ophthalmol. 2013;97:59-65. doi: 10.1136/bjophthalmol-2012-302133

Samara WA, Pointdujour-Lim R, Say EA, Shields CL. Foveal microanatomy documented by SD-OCT following treatment of advanced retinoblastoma. J AAPOS. 2015;19:368-72. doi: 10.1016/j.jaapos.2015.02.019

Yousef YA, Shroff M, Halliday W, Gallie BL, Heon E. Detection of optic nerve disease in retinoblastoma by use of spectral domain optical coherence tomography. J AAPOS. 2012;16:481- 3. doi: 10.1016/j.jaapos.2012.05.010

Soliman SE, VandenHoven C, MacKeen LD, Gallie BL. Secondary Prevention of Retinoblastoma Revisited: Laser Pho- tocoagulation of Invisible New Retinoblastoma. Ophthalmol- ogy. 2020;127:122-7. doi: 10.1016/j.ophtha.2019.08.011

Nadiarnykh O, McNeill-Badalova NA, Gaillard MC, Bosscha MI, Fabius AW, Verbraak FD, et al. Optical coherence tomog- raphy (OCT) to image active and inactive retinoblastomas as well as retinomas. Acta Ophthalmol. 2020;98:158-65. doi: 10.1111/aos.14214

Soliman SE, VandenHoven C, MacKeen LD, Heon E, Gallie BL. Optical Coherence Tomography-Guided Decisions in Ret- inoblastoma Management. Ophthalmology. 2017;124:859-72. doi: 10.1016/j.ophtha.2017.01.052

Welch RJ, Rao R, Gordon PS, Say EAT, Shields CL. Optical Coherence Tomography of Small Retinoblastoma. Asia Pac J Ophthalmol. 2018;7:301-6. doi: 10.22608/APO.2018189

Linn Murphree A. Intraocular retinoblastoma: the case for a new group classification. Ophthalmol Clin North Am.

;18:41-53, viii. doi: 10.1016/j.ohc.2004.11.003

Shields CL, Palamar M, Sharma P, Ramasubramanian A, Leahey A, Meadows AT,et al. Retinoblastoma regression pat- terns following chemoreduction and adjuvant therapy in 557 tumors. Arch Ophthalmol. 2009;127:282-90. doi: 10.1001/archophthalmol.2008.626

Castela G, Providencia J, Monteiro M, Silva S, Brito M, Sá J, et

al. Characterization of the Portuguese population diagnosed with retinoblastoma. Sci Rep. 2022;12:4378. doi: 10.1038/ s41598-022-08326-6

Rothschild PR, Levy D, Savignoni A, Lumbroso-Le Rouic L, Aerts I, Gauthier-Villars M, et al. Familial retinoblastoma: fundus screening schedule impact and guideline proposal. A retrospective study. Eye. 2011;25:1555-61. doi: 10.1038/ eye.2011.198

Maldonado RS, Izatt JA, Sarin N, Wallace DK, Freedman S, Cotten CM, et al. Optimizing hand-held spectral domain optical coherence tomography imaging for neonates, infants, and children. Invest Ophthalmol Vis Sci. 2010;51:2678-85. doi: 10.1167/iovs.09-4403

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Published

2023-06-29

How to Cite

Q. Dias, M., Providência, J., Monteiro, M., & Castela, G. (2023). Optical Coherence Tomography (OCT) in Retinoblastoma Management: Experience of the Portuguese National Reference Center. Revista Sociedade Portuguesa De Oftalmologia, 47(2), 125–131. https://doi.org/10.48560/rspo.28264

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