Arterial Blood, Rather Than Venous Blood, is a Better Source for Circulating Melanoma Cells
Mizue Terai,
Zhaomei Mu,
David J. Eschelman,
Carin F. Gonsalves,
Ken Kageyama,
Inna Chervoneva,
Marlana Orloff,
Ryan Weight,
Michael J. Mastrangelo,
Massimo Cristofanilli,
Takami Sato
Affiliations
Mizue Terai
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Zhaomei Mu
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
David J. Eschelman
Department of Radiology, Division of Interventional Radiology, Thomas Jefferson University Hospital, Philadelphia, PA, USA
Carin F. Gonsalves
Department of Radiology, Division of Interventional Radiology, Thomas Jefferson University Hospital, Philadelphia, PA, USA
Ken Kageyama
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Inna Chervoneva
Department of Pharmacology and Experimental Therapeutics, Division of Biostatistics, Sidney Kimmel Medical College of Thomas Jefferson University, Philadelphia, PA, USA
Marlana Orloff
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Ryan Weight
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Michael J. Mastrangelo
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Massimo Cristofanilli
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Takami Sato
Department of Medical Oncology, Sidney Kimmel Medical College at Thomas Jefferson University, Philadelphia, PA, USA
Background: CTCs provide prognostic information and their application is under investigation in multiple tumor types. Of the multiple variables inherent in any such process, none is more important to outcome than the appropriateness of the sample source. To address this question, we investigated CTCs in paired peripheral venous and arterial blood specimens obtained from stage IV uveal melanoma patients. Methods: Blood specimens were obtained from both common femoral arteries and antecubital veins in 17 uveal melanoma patients with multiple hepatic metastases for CTC measurements. Finding: CTCs were detectable with greater frequency (100%) and in larger numbers (median 5, range 1 to 168) in all arterial blood specimens than in venous samples (52.9%; median 1, range 0 to 8). Patients with hepatic as well as extra-hepatic metastasis showed higher number of arterial CTCs, compared to patients with liver-only metastasis (p = 0.003). There was no significant association between the number of arterial CTCs and the tumor burden within the liver in patients who had liver-only metastases. Interpretation: Our data indicate that arterial blood specimens might be a better source of circulating uveal melanoma cells. Although less conveniently processed, perhaps arterial blood should be evaluated as sample source for measurement of CTCs.