Circulating tumor DNA posttreatment measurements and clinical correlates in retinoblastoma Journal Article


Authors: Abramson, D. H.; Robbins, M. A.; Gobin, Y. P.; Dunkel, I. J.; Francis, J. H.
Article Title: Circulating tumor DNA posttreatment measurements and clinical correlates in retinoblastoma
Abstract: Importance: Plasma measurements of RB1 circulating tumor DNA (ctDNA) after completion of treatment may be associated with the development of metastases in patients with retinoblastoma. Objective: To determine if the absence of previously detectable plasma ctDNA is associated with metastasis-free survival in patients with a minimum of 1 year follow-up after treatment of retinoblastoma. Design, Setting, and Participants: This cohort study was conducted from June 2019 to September 2023. Patients with retinoblastoma who had measurable ctDNA levels at diagnosis and had repeated ctDNA measurements after ocular treatment (enucleation or intra-arterial chemotherapy) with a minimum of 1 year of follow-up (mean [SD], 28.2 [10.3] months) were included in the study. Patients were recruited from a single-center, tertiary cancer hospital. Exposure: Memorial Sloan Kettering's New York State-approved gene test, which interrogates 129 known cancer genes (called ACCESS), was performed on plasma samples before and after ocular treatments. All exons of the RB1 gene are included in the test and listed as ctDNA in this article. Main Outcomes and Measures: Plasma ctDNA level before treatment, after completion of ocular treatment, and development or absence of metastases. Results: A total of 24 patients (mean [SD] age, 20.7 [17.1] months; 15 female [62.5%]) were included in the study. None of the 23 patients who had a measurable ctDNA level and then no detectable ctDNA level after completion of ocular treatment developed metastases with a minimum of 1 year of follow-up. One patient had persistent measurable ctDNA after initial treatment and developed metastases. Conclusion and Relevance: Patients with retinoblastoma who had a measurable ctDNA level at diagnosis did not develop metastases if the plasma ctDNA level became unrecordable after ocular treatment; 1 patient who had persistent measurable ctDNA after treatment did develop metastasis. © 2024 American Medical Association. All rights reserved.
Keywords: adult; young adult; genetics; cohort studies; cohort analysis; retinoblastoma; retina tumor; retinal neoplasms; tumor marker; humans; human; female; circulating tumor dna; biomarkers, tumor
Journal Title: JAMA Ophthalmology
Volume: 142
Issue: 3
ISSN: 2168-6165
Publisher: American Medical Association  
Date Published: 2024-03-01
Start Page: 257
End Page: 261
Language: English
DOI: 10.1001/jamaophthalmol.2023.6516
PUBMED: 38300595
PROVIDER: scopus
PMCID: PMC10835605
DOI/URL:
Notes: Article -- MSK Cancer Center Support Grant (P30 CA008748) acknowledged in PDF -- MSK corresponding author is David Abramson) -- Source: Scopus
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MSK Authors
  1. Ira J Dunkel
    371 Dunkel
  2. Jasmine Helen Francis
    256 Francis
  3. David H Abramson
    389 Abramson