<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tomar AS</submitter><funding>The Eye Cancer Foundation</funding><funding>The Paul T. Finger Fund</funding><funding>The John and Myrna Daniels Charitable Trust</funding><pagination>1409-1416</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12703232</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>109(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>To determine the unique clinical characteristics and treatment outcomes of diffuse infiltrating retinoblastoma (DIR).&lt;h4>Methods&lt;/h4>This international, multicentre, registry-based retrospective case series analysed pooled data from January 2001 to December 2013, including 132 eyes from 132 patients with DIR.&lt;h4>Results&lt;/h4>Among 2854 eyes with retinoblastoma, 132 (4.6%; 95% CI, 3.9 to 5.5) had DIR. The median age at diagnosis for DIR patients was 24 months (IQR, 15-33), with no bilateral cases of DIR. The American Joint Committee on Cancer staging showed 4.5% cT2 and 95.5% cT3 categories, with no cT1 or cT4 cases. Clinical features associated with DIR included secondary glaucoma (67%), retinal detachment (38%), diffuse vitreous seeds (37%), anterior segment involvement </pubmed_abstract><journal>The British journal of ophthalmology</journal><pubmed_title>Diffuse infiltrating retinoblastoma: a multicentre, international, data-sharing study.</pubmed_title><pmcid>PMC12703232</pmcid><funding_grant_id>N/A</funding_grant_id><pubmed_authors>Mallipatna A</pubmed_authors><pubmed_authors>Kivela TT</pubmed_authors><pubmed_authors>Carreras E</pubmed_authors><pubmed_authors>Yarovoy A</pubmed_authors><pubmed_authors>Brennan RC</pubmed_authors><pubmed_authors>Berry JL</pubmed_authors><pubmed_authors>Catala-Mora J</pubmed_authors><pubmed_authors>Volodin D</pubmed_authors><pubmed_authors>Esparza-Aguiar E</pubmed_authors><pubmed_authors>Tomar AS</pubmed_authors><pubmed_authors>Ushakova TL</pubmed_authors><pubmed_authors>Fandino A</pubmed_authors><pubmed_authors>Essuman VA</pubmed_authors><pubmed_authors>Moorthy S</pubmed_authors><pubmed_authors>Long QB</pubmed_authors><pubmed_authors>Sharwood P</pubmed_authors><pubmed_authors>Semenova E</pubmed_authors><pubmed_authors>Ganesan S</pubmed_authors><pubmed_authors>Yugay OV</pubmed_authors><pubmed_authors>Ramirez-Ortiz MA</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Yam JC</pubmed_authors><pubmed_authors>Zhao J</pubmed_authors><pubmed_authors>Kotova E</pubmed_authors><pubmed_authors>Jubran R</pubmed_authors><pubmed_authors>Khetan V</pubmed_authors><pubmed_authors>Schaiquevich P</pubmed_authors><pubmed_authors>Gallie B</pubmed_authors><pubmed_authors>Burges M</pubmed_authors><pubmed_authors>Lam CP</pubmed_authors><pubmed_authors>Nummi K</pubmed_authors><pubmed_authors>Yousef YA</pubmed_authors><pubmed_authors>Yarovaya V</pubmed_authors><pubmed_authors>Polyakov VG</pubmed_authors><pubmed_authors>Wilson MW</pubmed_authors><pubmed_authors>Lau WW</pubmed_authors><pubmed_authors>AJCC OOTF</pubmed_authors><pubmed_authors>Renner LA</pubmed_authors><pubmed_authors>Finger PT</pubmed_authors><pubmed_authors>Chantada G</pubmed_authors><pubmed_authors>Correa-Llano G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Diffuse infiltrating retinoblastoma: a multicentre, international, data-sharing study.</name><description>&lt;h4>Background&lt;/h4>To determine the unique clinical characteristics and treatment outcomes of diffuse infiltrating retinoblastoma (DIR).&lt;h4>Methods&lt;/h4>This international, multicentre, registry-based retrospective case series analysed pooled data from January 2001 to December 2013, including 132 eyes from 132 patients with DIR.&lt;h4>Results&lt;/h4>Among 2854 eyes with retinoblastoma, 132 (4.6%; 95% CI, 3.9 to 5.5) had DIR. The median age at diagnosis for DIR patients was 24 months (IQR, 15-33), with no bilateral cases of DIR. The American Joint Committee on Cancer staging showed 4.5% cT2 and 95.5% cT3 categories, with no cT1 or cT4 cases. Clinical features associated with DIR included secondary glaucoma (67%), retinal detachment (38%), diffuse vitreous seeds (37%), anterior segment involvement </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-06T02:24:51.907Z</modification><creation>2026-05-24T03:12:50.928Z</creation></dates><accession>S-EPMC12703232</accession><cross_references><pubmed>40738737</pubmed><doi>10.1136/bjo-2024-326778</doi></cross_references></HashMap>