Deferral of Treatment for Small Choroidal Melanoma and the Risk of Metastasis: An Investigation Using the Liverpool Uveal Melanoma Prognosticator Online (LUMPO).

choroidal melanoma metastatic death monosomy 3 non-metastatic death treatment

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
22 Apr 2024
Historique:
received: 25 03 2024
revised: 12 04 2024
accepted: 14 04 2024
medline: 27 4 2024
pubmed: 27 4 2024
entrez: 27 4 2024
Statut: epublish

Résumé

We estimated metastatic-death risk when the treatment of small choroidal melanomas is deferred until growth is observed. In 24 patients with choroidal melanoma (median diameter 5.85 mm), the exponential growth rate estimated by a mixed-effects model was 4.3% per year. Using the Liverpool Uveal Melanoma Prognosticator Online v.3 (LUMPO3), we measured changes in 15-year metastatic and non-metastatic death risks according to whether the tumor is treated immediately or after observing growth 4 or 12 months later, considering age, sex, and metastasis predictors. In 40-year-old females with 10 mm, disomy 3 and monosomy 3 choroidal melanomas (prevalence 16%), the 15-year absolute risks of metastatic death are 4.2% and 76.6%, respectively, increasing after a 4-month delay by 0.0% and 0.2% and by 3.0% and 2.3% with tumor growth rates of 5.0% and 20.0%, respectively. With 12-month delays, these risks increase by 0.0% and 0.5% and by 1.0% and 7.1%, respectively. Increases in metastatic-death risk are less with smaller tumors and with a higher risk of non-metastatic death. Deferring treatment of choroidal melanomas until documentation of growth may delay iatrogenic visual loss by months or years and is associated with minimal increase in metastatic mortality, at least with small tumors with usual growth rates of up to 40% per year.

Sections du résumé

BACKGROUND BACKGROUND
We estimated metastatic-death risk when the treatment of small choroidal melanomas is deferred until growth is observed.
METHODS METHODS
In 24 patients with choroidal melanoma (median diameter 5.85 mm), the exponential growth rate estimated by a mixed-effects model was 4.3% per year. Using the Liverpool Uveal Melanoma Prognosticator Online v.3 (LUMPO3), we measured changes in 15-year metastatic and non-metastatic death risks according to whether the tumor is treated immediately or after observing growth 4 or 12 months later, considering age, sex, and metastasis predictors.
RESULTS RESULTS
In 40-year-old females with 10 mm, disomy 3 and monosomy 3 choroidal melanomas (prevalence 16%), the 15-year absolute risks of metastatic death are 4.2% and 76.6%, respectively, increasing after a 4-month delay by 0.0% and 0.2% and by 3.0% and 2.3% with tumor growth rates of 5.0% and 20.0%, respectively. With 12-month delays, these risks increase by 0.0% and 0.5% and by 1.0% and 7.1%, respectively. Increases in metastatic-death risk are less with smaller tumors and with a higher risk of non-metastatic death.
CONCLUSIONS CONCLUSIONS
Deferring treatment of choroidal melanomas until documentation of growth may delay iatrogenic visual loss by months or years and is associated with minimal increase in metastatic mortality, at least with small tumors with usual growth rates of up to 40% per year.

Identifiants

pubmed: 38672688
pii: cancers16081607
doi: 10.3390/cancers16081607
pii:
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Bertil Damato (B)

Ocular Oncology Service, St. Erik Eye Hospital, 17164 Stockholm, Sweden.
Department of Clinical Neuroscience, Division of Eye and Vision, Karolinska Institutet, 17177 Solna, Sweden.
Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool L7 8XT, UK.
Ocular Oncology Service, Moorfields Eye Hospital, London EC1V 2PD, UK.

Antonio Eleuteri (A)

NHS Digital Services, Liverpool University Hospitals NHS Foundation Trust, Kilby House, Liverpool Innovation Park, Liverpool L7 9NJ, UK.

Azzam Taktak (A)

Clinical Engineering, University Hospitals Bristol and Weston NHS Foundation Trust, Bristol BS2 8HW, UK.

Rumana Hussain (R)

Ocular Oncology Service, Liverpool University Hospitals NHS Foundation Trust, Liverpool L7 8XP, UK.

Maria Fili (M)

Ocular Oncology Service, St. Erik Eye Hospital, 17164 Stockholm, Sweden.
Department of Clinical Neuroscience, Division of Eye and Vision, Karolinska Institutet, 17177 Solna, Sweden.

Gustav Stålhammar (G)

Ocular Oncology Service, St. Erik Eye Hospital, 17164 Stockholm, Sweden.
Department of Clinical Neuroscience, Division of Eye and Vision, Karolinska Institutet, 17177 Solna, Sweden.

Heinrich Heimann (H)

Ocular Oncology Service, Liverpool University Hospitals NHS Foundation Trust, Liverpool L7 8XP, UK.

Sarah E Coupland (SE)

Department of Eye and Vision Science, University of Liverpool, Liverpool L7 8XT, UK.

Classifications MeSH