TY - JOUR
T1 - Visualization of circulating melanoma cells in peripheral blood of patients with primary uveal melanoma
AU - Ulmer, Anja
AU - Beutel, Julia
AU - Süsskind, Daniela
AU - Hilgers, Ralf Dieter
AU - Ziemssen, Focke
AU - Lüke, Matthias
AU - Röcken, Martin
AU - Rohrbach, Martin
AU - Fierlbeck, Gerhard
AU - Bartz-Schmidt, Karl Ulrich
AU - Grisanti, Salvatore
PY - 2008/7/15
Y1 - 2008/7/15
N2 - Purpose: In patients with uveal melanoma, tumor cell dissemination and subsequent formation of metastases are confined mainly to the hematogenous route. Here, we sought to isolate circulating melanoma cells in peripheral blood of patients with primary uveal melanoma and clinically localized disease. Experimental Design: Blood samples from 52 patients with clinically localized uveal melanoma and from 20 control individuals were prospectively collected before therapy of the primary tumor. Tumor cells expressing the melanoma-associated chondroitin sulfate proteoglycan were enriched by immunomagnetic cell sorting and visualized by immunocytologic staining. Results were compared with clinical data at presentation. Results: In 10 of 52 patients [19%; 95% confidence interval (95% CI), 10-33%], between 1 and 5 circulating melanoma cells were detected in 50 mL peripheral blood. No melanoma-associated chondroitin sulfate proteoglycan - positive cells were detected in any of the 20 controls examined. The presence of tumor cells in peripheral blood was associated with ciliary body invasion [odds ratio (OR), 20.0; 95% Cl, 3.0-131.7], advanced local tumor stage (OR, 6.7; 95% Cl, 1.8-25.4), and anterior tumor localization (OR, 4.0; 95% Cl, 1.2-12.7), all established factors for uveal melanoma progression. Conclusions: Immunomagnetic enrichment enables detection of intact melanoma cells in peripheral blood of patients with clinically localized ocular disease. Visualization and capturing of these cells provide a unique tool for characterizing potentially metastasizing tumor cells from a primary melanoma at an early stage of the disease.
AB - Purpose: In patients with uveal melanoma, tumor cell dissemination and subsequent formation of metastases are confined mainly to the hematogenous route. Here, we sought to isolate circulating melanoma cells in peripheral blood of patients with primary uveal melanoma and clinically localized disease. Experimental Design: Blood samples from 52 patients with clinically localized uveal melanoma and from 20 control individuals were prospectively collected before therapy of the primary tumor. Tumor cells expressing the melanoma-associated chondroitin sulfate proteoglycan were enriched by immunomagnetic cell sorting and visualized by immunocytologic staining. Results were compared with clinical data at presentation. Results: In 10 of 52 patients [19%; 95% confidence interval (95% CI), 10-33%], between 1 and 5 circulating melanoma cells were detected in 50 mL peripheral blood. No melanoma-associated chondroitin sulfate proteoglycan - positive cells were detected in any of the 20 controls examined. The presence of tumor cells in peripheral blood was associated with ciliary body invasion [odds ratio (OR), 20.0; 95% Cl, 3.0-131.7], advanced local tumor stage (OR, 6.7; 95% Cl, 1.8-25.4), and anterior tumor localization (OR, 4.0; 95% Cl, 1.2-12.7), all established factors for uveal melanoma progression. Conclusions: Immunomagnetic enrichment enables detection of intact melanoma cells in peripheral blood of patients with clinically localized ocular disease. Visualization and capturing of these cells provide a unique tool for characterizing potentially metastasizing tumor cells from a primary melanoma at an early stage of the disease.
UR - http://www.scopus.com/inward/record.url?scp=51649086229&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-08-0012
DO - 10.1158/1078-0432.CCR-08-0012
M3 - Journal articles
C2 - 18628461
AN - SCOPUS:51649086229
SN - 1078-0432
VL - 14
SP - 4469
EP - 4474
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 14
ER -