4.4 Review

Increased visceral to subcutaneous fat ratio is associated with decreased overall survival in patients with metastatic melanoma receiving anti-angiogenic therapy

Journal

SURGICAL ONCOLOGY-OXFORD
Volume 24, Issue 4, Pages 353-358

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.suronc.2015.09.002

Keywords

Melanoma; Visceral fat; Anti-angiogenic therapy; Abdominal fat

Funding

  1. NCI NIH HHS [UM1 CA186712] Funding Source: Medline

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Background: Body fat distribution is an emerging prognostic indicator in patients treated with anti-angiogenic (AA) therapy. We sought to evaluate the association of visceral and subcutaneous fat with progression free survival (PFS) and overall survival (OS) in patients with metastatic melanoma treated with AA therapy. Methods: Stage IV melanoma patients received bevacizumab +/- interferon-alpha. Total abdominal fat, visceral fat area (VFA) and subcutaneous fat area (SFA) were measured at L3-L4 on CT images (cm(2)). PFS and OS were estimated by the Kaplan-Meier method. Cox proportional hazards model was used to assess the association of fat and clinical variables with PFS and OS. Prediction accuracy was evaluated using receiver operating characteristic curve with area under the curve (AUC). Results: Forty-two patients were evaluated. Median VFA/SFA and body mass index (BMI) were used to group patients into high and low cohorts. PFS and OS were significantly decreased in patients with high VFA/SFA versus low (PFS, p = 0.009; OS, p = 0.007), but not for BMI (PFS, p = 0.774; OS, p = 0.881). VFA/SFA, LDH and liver metastasis (LM) were predictors of PFS and OS on multivariate analysis. A prognostic score combining VFA/SFA, LDH, and presence or absence of LM had a higher accuracy for predicting PFS at 3 months (AUC 0.759) and OS at 24 months (AUC 0.846) than LDH and LM alone (PFS, AUC 0.705; OS, AUC 0.786). Conclusion: Increased VFA/SFA is associated with decreased PFS and OS in patients with metastatic melanoma treated with AA therapy, indicating body fat distribution is an important prognostic factor. (C) 2015 Elsevier Ltd. All rights reserved.

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