Circulating tumor cells in patients with testicular germ cell tumors

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Circulating tumor cells in patients with testicular germ cell tumors. / Nastały, Paulina ; Ruf, Christian; Becker, Pascal; Bednarz-Knoll, Natalia; Stoupiec, Małgorzata ; Kavsur, Refik ; Isbarn, Hendrik; Matthies, Cord; Wagner, Walter; Höppner, Dirk; Fisch, Margit; Bokemeyer, Carsten; Ahyai, Sascha; Honecker, Friedemann; Riethdorf, Sabine; Pantel, Klaus.

In: CLIN CANCER RES, Vol. 20, No. 14, 15.07.2014, p. 3830-41.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Nastały, P, Ruf, C, Becker, P, Bednarz-Knoll, N, Stoupiec, M, Kavsur, R, Isbarn, H, Matthies, C, Wagner, W, Höppner, D, Fisch, M, Bokemeyer, C, Ahyai, S, Honecker, F, Riethdorf, S & Pantel, K 2014, 'Circulating tumor cells in patients with testicular germ cell tumors', CLIN CANCER RES, vol. 20, no. 14, pp. 3830-41. https://doi.org/10.1158/1078-0432.CCR-13-2819

APA

Nastały, P., Ruf, C., Becker, P., Bednarz-Knoll, N., Stoupiec, M., Kavsur, R., Isbarn, H., Matthies, C., Wagner, W., Höppner, D., Fisch, M., Bokemeyer, C., Ahyai, S., Honecker, F., Riethdorf, S., & Pantel, K. (2014). Circulating tumor cells in patients with testicular germ cell tumors. CLIN CANCER RES, 20(14), 3830-41. https://doi.org/10.1158/1078-0432.CCR-13-2819

Vancouver

Nastały P, Ruf C, Becker P, Bednarz-Knoll N, Stoupiec M, Kavsur R et al. Circulating tumor cells in patients with testicular germ cell tumors. CLIN CANCER RES. 2014 Jul 15;20(14):3830-41. https://doi.org/10.1158/1078-0432.CCR-13-2819

Bibtex

@article{073543c0f7574eaba1d740048f6aa013,
title = "Circulating tumor cells in patients with testicular germ cell tumors",
abstract = "PURPOSE: Germ cell tumors (GCTs) represent the most frequent malignancies among young men, but little is known about circulating tumor cells (CTCs) in these tumors. Considering their heterogeneity, CTCs were investigated using two independent assays targeting germ cell tumor and epithelial cell-specific markers, and results were correlated with disease stage, histology, and serum tumor markers.EXPERIMENTAL DESIGN: CTCs were enriched from peripheral blood (n = 143 patients) and testicular vein blood (TVB, n = 19 patients) using Ficoll density gradient centrifugation. For CTC detection, a combination of germ cell tumor (anti-SALL4, anti-OCT3/4) and epithelial cell-specific (anti-keratin, anti-EpCAM) antibodies was used. In parallel, 122 corresponding peripheral blood samples were analyzed using the CellSearch system.RESULTS: In total, CTCs were detected in 25 of 143 (17.5%) peripheral blood samples, whereas only 11.5% of patients were CTC-positive when considering exclusively the CellSearch assay. The presence of CTCs in peripheral blood correlated with clinical stage (P < 0.001) with 41% of CTC positivity in patients with metastasized tumors and 100% in patients with relapsed and chemotherapy-refractory disease. Histologically, CTC-positive patients suffered more frequently from nonseminomatous primary tumors (P < 0.001), with higher percentage of yolk sac (P < 0.001) and teratoma (P = 0.004) components. Furthermore, CTC detection was associated with elevated serum levels of α-fetoprotein (AFP; P = 0.025), β-human chorionic gonadotropin (βHCG; P = 0.002), and lactate dehydrogenase (LDH; P = 0.002). Incidence and numbers of CTCs in TVB were much higher than in peripheral blood.CONCLUSIONS: The inclusion of germ cell tumor-specific markers improves CTC detection in GCTs. CTCs occur frequently in patients with more aggressive disease, and there is a gradient of CTCs with decreasing numbers from the tumor-draining vein to the periphery.",
author = "Paulina Nasta{\l}y and Christian Ruf and Pascal Becker and Natalia Bednarz-Knoll and Ma{\l}gorzata Stoupiec and Refik Kavsur and Hendrik Isbarn and Cord Matthies and Walter Wagner and Dirk H{\"o}ppner and Margit Fisch and Carsten Bokemeyer and Sascha Ahyai and Friedemann Honecker and Sabine Riethdorf and Klaus Pantel",
note = "{\textcopyright}2014 American Association for Cancer Research.",
year = "2014",
month = jul,
day = "15",
doi = "10.1158/1078-0432.CCR-13-2819",
language = "English",
volume = "20",
pages = "3830--41",
journal = "CLIN CANCER RES",
issn = "1078-0432",
publisher = "American Association for Cancer Research Inc.",
number = "14",

}

RIS

TY - JOUR

T1 - Circulating tumor cells in patients with testicular germ cell tumors

AU - Nastały, Paulina

AU - Ruf, Christian

AU - Becker, Pascal

AU - Bednarz-Knoll, Natalia

AU - Stoupiec, Małgorzata

AU - Kavsur, Refik

AU - Isbarn, Hendrik

AU - Matthies, Cord

AU - Wagner, Walter

AU - Höppner, Dirk

AU - Fisch, Margit

AU - Bokemeyer, Carsten

AU - Ahyai, Sascha

AU - Honecker, Friedemann

AU - Riethdorf, Sabine

AU - Pantel, Klaus

N1 - ©2014 American Association for Cancer Research.

PY - 2014/7/15

Y1 - 2014/7/15

N2 - PURPOSE: Germ cell tumors (GCTs) represent the most frequent malignancies among young men, but little is known about circulating tumor cells (CTCs) in these tumors. Considering their heterogeneity, CTCs were investigated using two independent assays targeting germ cell tumor and epithelial cell-specific markers, and results were correlated with disease stage, histology, and serum tumor markers.EXPERIMENTAL DESIGN: CTCs were enriched from peripheral blood (n = 143 patients) and testicular vein blood (TVB, n = 19 patients) using Ficoll density gradient centrifugation. For CTC detection, a combination of germ cell tumor (anti-SALL4, anti-OCT3/4) and epithelial cell-specific (anti-keratin, anti-EpCAM) antibodies was used. In parallel, 122 corresponding peripheral blood samples were analyzed using the CellSearch system.RESULTS: In total, CTCs were detected in 25 of 143 (17.5%) peripheral blood samples, whereas only 11.5% of patients were CTC-positive when considering exclusively the CellSearch assay. The presence of CTCs in peripheral blood correlated with clinical stage (P < 0.001) with 41% of CTC positivity in patients with metastasized tumors and 100% in patients with relapsed and chemotherapy-refractory disease. Histologically, CTC-positive patients suffered more frequently from nonseminomatous primary tumors (P < 0.001), with higher percentage of yolk sac (P < 0.001) and teratoma (P = 0.004) components. Furthermore, CTC detection was associated with elevated serum levels of α-fetoprotein (AFP; P = 0.025), β-human chorionic gonadotropin (βHCG; P = 0.002), and lactate dehydrogenase (LDH; P = 0.002). Incidence and numbers of CTCs in TVB were much higher than in peripheral blood.CONCLUSIONS: The inclusion of germ cell tumor-specific markers improves CTC detection in GCTs. CTCs occur frequently in patients with more aggressive disease, and there is a gradient of CTCs with decreasing numbers from the tumor-draining vein to the periphery.

AB - PURPOSE: Germ cell tumors (GCTs) represent the most frequent malignancies among young men, but little is known about circulating tumor cells (CTCs) in these tumors. Considering their heterogeneity, CTCs were investigated using two independent assays targeting germ cell tumor and epithelial cell-specific markers, and results were correlated with disease stage, histology, and serum tumor markers.EXPERIMENTAL DESIGN: CTCs were enriched from peripheral blood (n = 143 patients) and testicular vein blood (TVB, n = 19 patients) using Ficoll density gradient centrifugation. For CTC detection, a combination of germ cell tumor (anti-SALL4, anti-OCT3/4) and epithelial cell-specific (anti-keratin, anti-EpCAM) antibodies was used. In parallel, 122 corresponding peripheral blood samples were analyzed using the CellSearch system.RESULTS: In total, CTCs were detected in 25 of 143 (17.5%) peripheral blood samples, whereas only 11.5% of patients were CTC-positive when considering exclusively the CellSearch assay. The presence of CTCs in peripheral blood correlated with clinical stage (P < 0.001) with 41% of CTC positivity in patients with metastasized tumors and 100% in patients with relapsed and chemotherapy-refractory disease. Histologically, CTC-positive patients suffered more frequently from nonseminomatous primary tumors (P < 0.001), with higher percentage of yolk sac (P < 0.001) and teratoma (P = 0.004) components. Furthermore, CTC detection was associated with elevated serum levels of α-fetoprotein (AFP; P = 0.025), β-human chorionic gonadotropin (βHCG; P = 0.002), and lactate dehydrogenase (LDH; P = 0.002). Incidence and numbers of CTCs in TVB were much higher than in peripheral blood.CONCLUSIONS: The inclusion of germ cell tumor-specific markers improves CTC detection in GCTs. CTCs occur frequently in patients with more aggressive disease, and there is a gradient of CTCs with decreasing numbers from the tumor-draining vein to the periphery.

U2 - 10.1158/1078-0432.CCR-13-2819

DO - 10.1158/1078-0432.CCR-13-2819

M3 - SCORING: Journal article

C2 - 24634372

VL - 20

SP - 3830

EP - 3841

JO - CLIN CANCER RES

JF - CLIN CANCER RES

SN - 1078-0432

IS - 14

ER -