# Prospective implementation of an aqueous humor liquid biopsy platform informs clinical diagnosis and management of retinoblastoma and other intraocular lesions

**Authors:** Laura A. T. Kagami, Eirini Christodoulou, Venkata Yellapantula, Nerea Goni, David N. Buckley, Brianne Brown, Dolores Estrine, Cindy Fong, Rima Jubran, Dejerianne Ostrow, Mark Reid, Rachana Shah, Miao Sun, Dong Xu, Liya Xu, Jaclyn A. Biegel, Jesse L. Berry

PMC · DOI: 10.1038/s41698-025-01255-3 · NPJ Precision Oncology · 2026-01-12

## TL;DR

A new liquid biopsy platform called LBSeq4Kids helps diagnose and monitor eye cancers and other eye conditions by detecting genetic changes in cell-free DNA.

## Contribution

LBSeq4Kids is a clinically validated liquid biopsy platform that combines whole genome sequencing and targeted sequencing for diagnosing and monitoring intraocular malignancies.

## Key findings

- 94% of retinoblastoma samples at diagnosis showed copy number alterations.
- 83% of retinoblastoma samples had pathogenic variants detected by targeted sequencing.
- The platform detected ctDNA in 98% of active retinoblastoma cases but not in remission cases.

## Abstract

LBSeq4Kids is a clinically validated liquid biopsy platform combining low passage whole genome sequencing (LP-WGS) for copy number alterations (CNAs) and a custom cancer targeted sequencing panel (TSP) to detect sequence variants in cell-free DNA from the aqueous humor (AH) of the eye, cerebrospinal fluid, and plasma. We present LBSeq4Kids results from a prospective cohort of 60 ocular oncology patients, including 41 with retinoblastoma (RB),13 with non-malignant RB simulating lesions and six with other intraocular malignancies. Ninety-four percent of baseline RB samples obtained at diagnosis were positive for CNAs by LP-WGS and 83% were positive for pathogenic variants by TSP analysis. All samples obtained at clinical recurrence were positive for ctDNA whereas none of the eyes in remission had a positive finding. The presence of CNAs detected by serial sampling in patients being treated for RB was correlated with clinical disease status. None of the patients with RB-simulating lesions had a positive finding by LP-WGS. The sensitivity of the assay to detect ctDNA in the setting of active RB was 98%. LBSeq4Kids represents a groundbreaking improvement for intraocular malignancies and is highly effective in informing accurate diagnosis, risk stratification, response to therapy, and surveillance.

## Linked entities

- **Diseases:** retinoblastoma (MONDO:0008380)

## Full-text entities

- **Genes:** PAX5 (paired box 5) [NCBI Gene 5079] {aka ALL3, BSAP, PAX-5}, RB1 (RB transcriptional corepressor 1) [NCBI Gene 5925] {aka OSRC, PPP1R130, RB, p105-Rb, p110-RB1, pRb}, MYCN (MYCN proto-oncogene, bHLH transcription factor) [NCBI Gene 4613] {aka FGLDS1, MODED, MPAPA, MYCNsORF, MYCNsPEP, N-myc}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, BCOR (BCL6 corepressor) [NCBI Gene 54880] {aka ANOP2, MAA2, MCOPS2}, EWSR1 (EWS RNA binding protein 1) [NCBI Gene 2130] {aka EWS, EWS-FLI1}, THBS1 (thrombospondin 1) [NCBI Gene 7057] {aka THBS, THBS-1, TSP, TSP-1, TSP1}, NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}, IGF1R (insulin like growth factor 1 receptor) [NCBI Gene 3480] {aka CD221, IGFIR, IGFR, JTK13}, MSH6 (mutS homolog 6) [NCBI Gene 2956] {aka GTBP, GTMBP, HNPCC5, HSAP, LYNCH5, MMRCS3}, MDM4 (MDM4 regulator of p53) [NCBI Gene 4194] {aka BMFS6, HDMX, MDMX, MRP1}, FOXO1 (forkhead box O1) [NCBI Gene 2308] {aka FKH1, FKHR, FOXO1A}, ARID1A (AT-rich interaction domain 1A) [NCBI Gene 8289] {aka B120, BAF250, BAF250a, BM029, C1orf4, CSS2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}
- **Diseases:** leukemic infiltration (MESH:D017254), retinal detachment (MESH:D012163), brain, ocular, and other solid tumors (MESH:D001932), cataracts (MESH:D002386), masses (MESH:C536030), vision loss (MESH:D014786), Coat's disease (MESH:D058456), intraocular malignancies (MESH:C563596), hemorrhage (MESH:D006470), FEVR (MESH:D000080345), ocular (MESH:D015817), PFV (MESH:C565633), ocular disease (MESH:D005128), tumorigenic (MESH:D002471), intraocular leukemia (MESH:D007938), anaplasia (MESH:D000708), cotton wool spots (MESH:D008796), choroidal melanoma (MESH:D008545), bilateral disease (MESH:D006312), benign retinoma (MESH:D009369), B-ALL (MESH:D015456), retinal hamartoma (MESH:D012173), IIRC Group A (MESH:D012175), disease (MESH:D004194), optic nerve swelling (MESH:D000080344), vitreous hemorrhage (MESH:D014823), chronic myelogenous leukemia (MESH:D015464), white lesion (MESH:D014912), benign choroidal lesions (MESH:D015862), inflammation (MESH:D007249), intraocular disease (MESH:D064090), AH (MESH:C562390), lesions (MESH:D009059)
- **Chemicals:** VAF (-), melphalan (MESH:D008558)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.1221 C > A, A to E

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12868883/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12868883/full.md

## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12868883/full.md

---
Source: https://tomesphere.com/paper/PMC12868883