TY - JOUR
T1 - Are Risk Factors for Growth of Choroidal Nevi Associated With Malignant Transformation? Assessment With a Validated Genomic Biomarker
AU - Harbour, J. William
AU - Paez-Escamilla, Manuel
AU - Cai, Louis
AU - Walter, Scott D.
AU - Augsburger, James J.
AU - Correa, Zelia M.
N1 - Funding Information:
Funding/Support: This work was supported by grants from the National Cancer Institute to Dr Harbour (R01 CA125970, Research to Prevent Blindness, Inc Senior Scientific Investigator Award, Melanoma Research Foundation, Melanoma Research Alliance, Ocular Melanoma Foundation, and the Sylvester Comprehensive Cancer Center), and to the Bascom Palmer Eye Institute (NIH Core Grant P30EY014801, Research to Prevent Blindness Unrestricted Grant, and Department of Defense Grant #W81XWH-09-1-0675). Financial Disclosures: J. William Harbour is the inventor of intellectual property related to the gene expression profile technology used in the study and intellectual property related to the discovery of BAP1 mutations in uveal melanoma. He is also a paid consultant for Castle Biosciences, which licensed this intellectual property, and he receives royalties from its commercialization. He is a member of the scientific advisory board for Aura Biosciences and Immunocore, Ltd. The following authors have no financial disclosures: Manuel Paez-Escamilla, Louis Cai, Scott D. Walter, James J. Augsburger, and Zelia M. Correa. All authors attest that they meet the current ICMJE criteria for authorship.
Funding Information:
Funding/Support: This work was supported by grants from the National Cancer Institute to Dr Harbour ( R01 CA125970 , Research to Prevent Blindness, Inc Senior Scientific Investigator Award, Melanoma Research Foundation, Melanoma Research Alliance, Ocular Melanoma Foundation, and the Sylvester Comprehensive Cancer Center), and to the Bascom Palmer Eye Institute ( NIH Core Grant P30EY014801 , Research to Prevent Blindness Unrestricted Grant, and Department of Defense Grant # W81XWH-09-1-0675 ). Financial Disclosures: J. William Harbour is the inventor of intellectual property related to the gene expression profile technology used in the study and intellectual property related to the discovery of BAP1 mutations in uveal melanoma. He is also a paid consultant for Castle Biosciences, which licensed this intellectual property, and he receives royalties from its commercialization. He is a member of the scientific advisory board for Aura Biosciences and Immunocore, Ltd. The following authors have no financial disclosures: Manuel Paez-Escamilla, Louis Cai, Scott D. Walter, James J. Augsburger, and Zelia M. Correa. All authors attest that they meet the current ICMJE criteria for authorship.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2019/1
Y1 - 2019/1
N2 - Purpose: To test the hypothesis that widely used clinical risk factors for growth of choroidal nevi are associated with malignant transformation. Methods: Fine needle biopsy for assignment of gene expression profile (class 1 or class 2) was performed in 207 choroidal melanocytic tumors < 3.5 mm in thickness. The class 2 profile was employed as a validated biomarker for malignant transformation. The following data were collected: patient age and sex, tumor diameter and thickness, distance of posterior tumor margin from the optic disc, and the presence or absence of serous retinal detachment, orange lipofuscin pigment, drusen, retinal pigment epithelial fibrosis, retinal pigment epithelial atrophy, visual symptoms, and documented tumor growth. Results: Clinical features associated with the class 2 profile included patient age > 60 years and tumor thickness > 2.25 mm (Fisher exact test, P =.002 for both). Documented growth was not associated with the class 2 profile (P =.5). The odds ratio of a tumor having the class 2 profile was 2.8 (95% confidence interval 1.3–5.9) for patient age > 60 years and 3.5 (95% confidence interval 1.4–8.8) for tumor thickness > 2.25 mm. For patients with both risk factors, the “number needed to treat” to identify 1 patient with a class 2 tumor was 4.3 (P =.0002). No other clinical feature or combination of features was associated with the class 2 profile. Conclusions: None of the widely used choroidal nevus risk factors for tumor growth, nor documented growth itself, is pathognomonic of malignant transformation as defined by class 2 gene expression profile. Patient age and tumor thickness may be helpful for identifying small choroidal melanocytic tumors that are more likely to have the class 2 profile. Observation for growth prior to treatment continues to be reasonable for most patients with suspicious choroidal nevi. NOTE: Publication of this article is sponsored by the American Ophthalmological Society.
AB - Purpose: To test the hypothesis that widely used clinical risk factors for growth of choroidal nevi are associated with malignant transformation. Methods: Fine needle biopsy for assignment of gene expression profile (class 1 or class 2) was performed in 207 choroidal melanocytic tumors < 3.5 mm in thickness. The class 2 profile was employed as a validated biomarker for malignant transformation. The following data were collected: patient age and sex, tumor diameter and thickness, distance of posterior tumor margin from the optic disc, and the presence or absence of serous retinal detachment, orange lipofuscin pigment, drusen, retinal pigment epithelial fibrosis, retinal pigment epithelial atrophy, visual symptoms, and documented tumor growth. Results: Clinical features associated with the class 2 profile included patient age > 60 years and tumor thickness > 2.25 mm (Fisher exact test, P =.002 for both). Documented growth was not associated with the class 2 profile (P =.5). The odds ratio of a tumor having the class 2 profile was 2.8 (95% confidence interval 1.3–5.9) for patient age > 60 years and 3.5 (95% confidence interval 1.4–8.8) for tumor thickness > 2.25 mm. For patients with both risk factors, the “number needed to treat” to identify 1 patient with a class 2 tumor was 4.3 (P =.0002). No other clinical feature or combination of features was associated with the class 2 profile. Conclusions: None of the widely used choroidal nevus risk factors for tumor growth, nor documented growth itself, is pathognomonic of malignant transformation as defined by class 2 gene expression profile. Patient age and tumor thickness may be helpful for identifying small choroidal melanocytic tumors that are more likely to have the class 2 profile. Observation for growth prior to treatment continues to be reasonable for most patients with suspicious choroidal nevi. NOTE: Publication of this article is sponsored by the American Ophthalmological Society.
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U2 - 10.1016/j.ajo.2018.08.045
DO - 10.1016/j.ajo.2018.08.045
M3 - Article
C2 - 30195895
AN - SCOPUS:85054596607
SN - 0002-9394
VL - 197
SP - 168
EP - 179
JO - American Journal of Ophthalmology
JF - American Journal of Ophthalmology
ER -