Evidence map›Paper›PMID 42200737›Full record

ArticleIndian journal of ophthalmology2026

Cavitary retinoblastoma: Clinical features and treatment outcomes.

Nakul Verma, Rohan Kapoor, Vijitha S Vempuluru, P Vijay Anand Reddy, Vishal R Raval, Swathi Kaliki

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Article in Indian journal of ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Nakul VermaAnant Bajaj Retina Institute, Hyderabad, Telangana, India.
Rohan KapoorAnant Bajaj Retina Institute, Hyderabad, Telangana, India.
Vijitha S VempuluruThe Operation Eyesight Universal Institute for Eye Cancer, L V Prasad Eye Institute, Hyderabad, Telangana, India.
P Vijay Anand ReddyThe Operation Eyesight Universal Institute for Eye Cancer, L V Prasad Eye Institute, Hyderabad, Telangana, India.
Vishal R RavalAnant Bajaj Retina Institute, Hyderabad, Telangana, India.
Swathi KalikiThe Operation Eyesight Universal Institute for Eye Cancer, L V Prasad Eye Institute, Hyderabad, Telangana, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo describe clinical characteristics and treatment outcomes of children diagnosed with cavitary retinoblastoma (RB).

methodsRetrospective analysis of children treated for cavitary RB.

resultsOf the 40 patients (43 eyes) with cavitary RB, 14 (35%) were female and 26 (65%) were male. At diagnosis, the average age was 25 months (median, 24 months; range 3-84 months). In 3 cases (8%), bilateral cavitary RB was seen. The most prevalent presenting symptoms were leukocoria (n = 21, 53%) and strabismus (n = 6, 15%) with a mean duration of symptoms of 23 weeks (median, 16 weeks; range 0-104 weeks). As per the ICRB classification, 15 eyes (35%) were in group D, 12 eyes (28%) in group C, 10 eyes (23%) in group B, and 6 eyes (14%) in group E. Primary cavities, within the tumor, were seen in 14 eyes (33%), whereas secondary cavities were seen in 29 eyes (67%). Most of the eyes (n = 42, 98%) were treated with intravenous chemotherapy (IVC), and one eye (2%) received intra-arterial chemotherapy. In ten eyes (23%), the tumor recurred following IVC, and two cases exhibited a partial response to IVC. At the last follow-up (mean, 31 months), all eyes (100%) had local tumor control with no evidence of systemic metastasis or death. Regression of the cavities within the tumor was noted in 27 eyes (63%), while it remained stable in 16 eyes (37%).

conclusionCavitary RB (both primary and secondary) had a good initial response to standard chemotherapy with an overall excellent prognosis for globe salvage.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsRetinal NeoplasmsRetinoblastomaAntineoplastic AgentsChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleRetrospective StudiesTreatment OutcomeAntineoplastic AgentsCavitarycavityclinical featuresretinoblastomatreatment

Identifiers

PMID42200737
PMCPMC13271549

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