Improved risk stratification by circulating tumor cell counts in pancreatic cancer

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Improved risk stratification by circulating tumor cell counts in pancreatic cancer. / Effenberger, Katharina E; Schroeder, Cornelia; Hanssen, Annkathrin; Wolter, Stefan; Eulenburg, Christine; Tachezy, Michael; Gebauer, Florian; Izbicki, Jakob R; Pantel, Klaus; Bockhorn, Maximilian.

In: CLIN CANCER RES, Vol. 24, No. 12, 15.06.2018, p. 2844-2850.

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

Harvard

Effenberger, KE, Schroeder, C, Hanssen, A, Wolter, S, Eulenburg, C, Tachezy, M, Gebauer, F, Izbicki, JR, Pantel, K & Bockhorn, M 2018, 'Improved risk stratification by circulating tumor cell counts in pancreatic cancer', CLIN CANCER RES, vol. 24, no. 12, pp. 2844-2850. https://doi.org/10.1158/1078-0432.CCR-18-0120

APA

Effenberger, K. E., Schroeder, C., Hanssen, A., Wolter, S., Eulenburg, C., Tachezy, M., Gebauer, F., Izbicki, J. R., Pantel, K., & Bockhorn, M. (2018). Improved risk stratification by circulating tumor cell counts in pancreatic cancer. CLIN CANCER RES, 24(12), 2844-2850. https://doi.org/10.1158/1078-0432.CCR-18-0120

Vancouver

Bibtex

@article{4ee1424eff77437dbca61f57fa89dc60,
title = "Improved risk stratification by circulating tumor cell counts in pancreatic cancer",
abstract = "Purpose: Pancreatic cancer is one of the most devastating diseases with a 5-year survival rate of 3% to 5%. Here, we investigated whether circulating tumor cells (CTC) may predict metastatic spread and survival in pancreatic cancer patients.Experimental Design: In a prospective study, we enrolled 69 pancreatic cancer patients. In peripheral blood, CTCs were identified by MACS enrichment (anti-cytokeratin/anti-EpCam) and subsequent automated analysis after combined anti-cytokeratin/anti-CD45/DAPI staining. CTC results were correlated to established clinicopathologic risk factors, detection of disseminated tumor cells (DTC) in bone marrow, and clinical outcome (follow-up time: 48 months).Results: Median patient survival was 11 months (0-48 months). Thirty-eight patients were male and 31 were female, and the majority received gemcitabine (58/69). CTCs were present in 23 of 69 patients (33.3%) ranging from 1 to 19 cells (17 with >1 CTC). Although clinicopathologic parameters and DTC status did not correlate with CTC incidence, progression-free survival (PFS) and overall survival (OS) were significantly reduced in CTC-positive patients in univariate (P = 0.009, PFS; P = 0.030, OS, both log rank) and multivariate analysis [HR = 4.543; confidence interval (CI), 1.549-13.329; P = 0.006, PFS; HR = 2.093; CI, 1.081-4.050; P = 0.028, OS, both Cox regression). Also within patients receiving chemotherapy, PFS was significantly reduced in CTC-positive patients in univariate (P = 0.013) and multivariate (HR = 4.203; CI, 1.416-12.471; P = 0.010) analysis.Conclusions: CTCs affect the outcome of patients with pancreatic cancer independent from other risk factors, including patients receiving (adjuvant) cytotoxic therapy. CTC stratification may allow a better upfront identification of patients with a longer lifespan who might profit from new adjuvant therapies. Clin Cancer Res; 24(12); 2844-50. {\textcopyright}2018 AACR.",
keywords = "Journal Article",
author = "Effenberger, {Katharina E} and Cornelia Schroeder and Annkathrin Hanssen and Stefan Wolter and Christine Eulenburg and Michael Tachezy and Florian Gebauer and Izbicki, {Jakob R} and Klaus Pantel and Maximilian Bockhorn",
note = "Copyright {\textcopyright}2018, American Association for Cancer Research.",
year = "2018",
month = jun,
day = "15",
doi = "10.1158/1078-0432.CCR-18-0120",
language = "English",
volume = "24",
pages = "2844--2850",
journal = "CLIN CANCER RES",
issn = "1078-0432",
publisher = "American Association for Cancer Research Inc.",
number = "12",

}

RIS

TY - JOUR

T1 - Improved risk stratification by circulating tumor cell counts in pancreatic cancer

AU - Effenberger, Katharina E

AU - Schroeder, Cornelia

AU - Hanssen, Annkathrin

AU - Wolter, Stefan

AU - Eulenburg, Christine

AU - Tachezy, Michael

AU - Gebauer, Florian

AU - Izbicki, Jakob R

AU - Pantel, Klaus

AU - Bockhorn, Maximilian

N1 - Copyright ©2018, American Association for Cancer Research.

PY - 2018/6/15

Y1 - 2018/6/15

N2 - Purpose: Pancreatic cancer is one of the most devastating diseases with a 5-year survival rate of 3% to 5%. Here, we investigated whether circulating tumor cells (CTC) may predict metastatic spread and survival in pancreatic cancer patients.Experimental Design: In a prospective study, we enrolled 69 pancreatic cancer patients. In peripheral blood, CTCs were identified by MACS enrichment (anti-cytokeratin/anti-EpCam) and subsequent automated analysis after combined anti-cytokeratin/anti-CD45/DAPI staining. CTC results were correlated to established clinicopathologic risk factors, detection of disseminated tumor cells (DTC) in bone marrow, and clinical outcome (follow-up time: 48 months).Results: Median patient survival was 11 months (0-48 months). Thirty-eight patients were male and 31 were female, and the majority received gemcitabine (58/69). CTCs were present in 23 of 69 patients (33.3%) ranging from 1 to 19 cells (17 with >1 CTC). Although clinicopathologic parameters and DTC status did not correlate with CTC incidence, progression-free survival (PFS) and overall survival (OS) were significantly reduced in CTC-positive patients in univariate (P = 0.009, PFS; P = 0.030, OS, both log rank) and multivariate analysis [HR = 4.543; confidence interval (CI), 1.549-13.329; P = 0.006, PFS; HR = 2.093; CI, 1.081-4.050; P = 0.028, OS, both Cox regression). Also within patients receiving chemotherapy, PFS was significantly reduced in CTC-positive patients in univariate (P = 0.013) and multivariate (HR = 4.203; CI, 1.416-12.471; P = 0.010) analysis.Conclusions: CTCs affect the outcome of patients with pancreatic cancer independent from other risk factors, including patients receiving (adjuvant) cytotoxic therapy. CTC stratification may allow a better upfront identification of patients with a longer lifespan who might profit from new adjuvant therapies. Clin Cancer Res; 24(12); 2844-50. ©2018 AACR.

AB - Purpose: Pancreatic cancer is one of the most devastating diseases with a 5-year survival rate of 3% to 5%. Here, we investigated whether circulating tumor cells (CTC) may predict metastatic spread and survival in pancreatic cancer patients.Experimental Design: In a prospective study, we enrolled 69 pancreatic cancer patients. In peripheral blood, CTCs were identified by MACS enrichment (anti-cytokeratin/anti-EpCam) and subsequent automated analysis after combined anti-cytokeratin/anti-CD45/DAPI staining. CTC results were correlated to established clinicopathologic risk factors, detection of disseminated tumor cells (DTC) in bone marrow, and clinical outcome (follow-up time: 48 months).Results: Median patient survival was 11 months (0-48 months). Thirty-eight patients were male and 31 were female, and the majority received gemcitabine (58/69). CTCs were present in 23 of 69 patients (33.3%) ranging from 1 to 19 cells (17 with >1 CTC). Although clinicopathologic parameters and DTC status did not correlate with CTC incidence, progression-free survival (PFS) and overall survival (OS) were significantly reduced in CTC-positive patients in univariate (P = 0.009, PFS; P = 0.030, OS, both log rank) and multivariate analysis [HR = 4.543; confidence interval (CI), 1.549-13.329; P = 0.006, PFS; HR = 2.093; CI, 1.081-4.050; P = 0.028, OS, both Cox regression). Also within patients receiving chemotherapy, PFS was significantly reduced in CTC-positive patients in univariate (P = 0.013) and multivariate (HR = 4.203; CI, 1.416-12.471; P = 0.010) analysis.Conclusions: CTCs affect the outcome of patients with pancreatic cancer independent from other risk factors, including patients receiving (adjuvant) cytotoxic therapy. CTC stratification may allow a better upfront identification of patients with a longer lifespan who might profit from new adjuvant therapies. Clin Cancer Res; 24(12); 2844-50. ©2018 AACR.

KW - Journal Article

U2 - 10.1158/1078-0432.CCR-18-0120

DO - 10.1158/1078-0432.CCR-18-0120

M3 - SCORING: Journal article

C2 - 29559560

VL - 24

SP - 2844

EP - 2850

JO - CLIN CANCER RES

JF - CLIN CANCER RES

SN - 1078-0432

IS - 12

ER -