Detection and oncological effect of circulating tumour cells in patients with variant urothelial carcinoma histology treated with radical cystectomy

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Detection and oncological effect of circulating tumour cells in patients with variant urothelial carcinoma histology treated with radical cystectomy. / Soave, Armin; Riethdorf, Sabine; Dahlem, Roland; Minner, Sarah; Weisbach, Lars; Engel, Oliver; Fisch, Margit; Pantel, Klaus; Rink, Michael.

in: BJU INT, Jahrgang 119, Nr. 6, 06.2017, S. 854-861.

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@article{18fcbad128224e03aceded56769cd51b,
title = "Detection and oncological effect of circulating tumour cells in patients with variant urothelial carcinoma histology treated with radical cystectomy",
abstract = "OBJECTIVES: To investigate for the presence of circulating tumour cells (CTC) in patients with variant urothelial carcinoma of the bladder (UCB) histology treated with radical cystectomy (RC), and to determine their impact on oncological outcomes.PATIENTS AND METHODS: We prospectively collected data of 188 patients with UCB treated with RC without neoadjuvant chemotherapy. Pathological specimens were meticulously reviewed for pure and variant UCB histology. Preoperatively collected blood samples (7.5 mL) were analysed for CTC using the CellSearch{\textregistered} system (Janssen, Raritan, NJ, USA).RESULTS: Variant UCB histology was found in 47 patients (25.0%), most frequently of squamous cell differentiation (16.5%). CTC were present in 30 patients (21.3%) and 12 patients (25.5%) with pure and variant UCB histology, respectively. At a median follow-up of 25 months, the presence of CTC and non-squamous cell differentiation were associated with reduced recurrence-free survival (RFS) and cancer-specific survival (pairwise P ≤ 0.016). Patients without CTC had better RFS, independent of UCB histology, than patients with CTC with any UCB histology (pairwise P < 0.05). In multivariable analyses, the presence of CTC, but not variant UCB histology, was an independent predictor for disease recurrence [hazard ratio (HR) 3.45; P < 0.001] and cancer-specific mortality (HR 2.62; P = 0.002).CONCLUSION: CTC are detectable in about a quarter of patients with pure or variant UCB histology before RC, and represent an independent predictor for outcomes, when adjusting for histological subtype. In addition, our prospective data confirm the unfavourable influence of non-squamous cell-differentiated UCB on outcomes.",
keywords = "Aged, Carcinoma, Transitional Cell/pathology, Cystectomy/methods, Female, Humans, Male, Middle Aged, Neoplastic Cells, Circulating, Predictive Value of Tests, Prospective Studies, Treatment Outcome, Urinary Bladder Neoplasms/pathology",
author = "Armin Soave and Sabine Riethdorf and Roland Dahlem and Sarah Minner and Lars Weisbach and Oliver Engel and Margit Fisch and Klaus Pantel and Michael Rink",
note = "{\textcopyright} 2017 The Authors BJU International {\textcopyright} 2017 BJU International Published by John Wiley & Sons Ltd.",
year = "2017",
month = jun,
doi = "10.1111/bju.13782",
language = "English",
volume = "119",
pages = "854--861",
journal = "BJU INT",
issn = "1464-4096",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Detection and oncological effect of circulating tumour cells in patients with variant urothelial carcinoma histology treated with radical cystectomy

AU - Soave, Armin

AU - Riethdorf, Sabine

AU - Dahlem, Roland

AU - Minner, Sarah

AU - Weisbach, Lars

AU - Engel, Oliver

AU - Fisch, Margit

AU - Pantel, Klaus

AU - Rink, Michael

N1 - © 2017 The Authors BJU International © 2017 BJU International Published by John Wiley & Sons Ltd.

PY - 2017/6

Y1 - 2017/6

N2 - OBJECTIVES: To investigate for the presence of circulating tumour cells (CTC) in patients with variant urothelial carcinoma of the bladder (UCB) histology treated with radical cystectomy (RC), and to determine their impact on oncological outcomes.PATIENTS AND METHODS: We prospectively collected data of 188 patients with UCB treated with RC without neoadjuvant chemotherapy. Pathological specimens were meticulously reviewed for pure and variant UCB histology. Preoperatively collected blood samples (7.5 mL) were analysed for CTC using the CellSearch® system (Janssen, Raritan, NJ, USA).RESULTS: Variant UCB histology was found in 47 patients (25.0%), most frequently of squamous cell differentiation (16.5%). CTC were present in 30 patients (21.3%) and 12 patients (25.5%) with pure and variant UCB histology, respectively. At a median follow-up of 25 months, the presence of CTC and non-squamous cell differentiation were associated with reduced recurrence-free survival (RFS) and cancer-specific survival (pairwise P ≤ 0.016). Patients without CTC had better RFS, independent of UCB histology, than patients with CTC with any UCB histology (pairwise P < 0.05). In multivariable analyses, the presence of CTC, but not variant UCB histology, was an independent predictor for disease recurrence [hazard ratio (HR) 3.45; P < 0.001] and cancer-specific mortality (HR 2.62; P = 0.002).CONCLUSION: CTC are detectable in about a quarter of patients with pure or variant UCB histology before RC, and represent an independent predictor for outcomes, when adjusting for histological subtype. In addition, our prospective data confirm the unfavourable influence of non-squamous cell-differentiated UCB on outcomes.

AB - OBJECTIVES: To investigate for the presence of circulating tumour cells (CTC) in patients with variant urothelial carcinoma of the bladder (UCB) histology treated with radical cystectomy (RC), and to determine their impact on oncological outcomes.PATIENTS AND METHODS: We prospectively collected data of 188 patients with UCB treated with RC without neoadjuvant chemotherapy. Pathological specimens were meticulously reviewed for pure and variant UCB histology. Preoperatively collected blood samples (7.5 mL) were analysed for CTC using the CellSearch® system (Janssen, Raritan, NJ, USA).RESULTS: Variant UCB histology was found in 47 patients (25.0%), most frequently of squamous cell differentiation (16.5%). CTC were present in 30 patients (21.3%) and 12 patients (25.5%) with pure and variant UCB histology, respectively. At a median follow-up of 25 months, the presence of CTC and non-squamous cell differentiation were associated with reduced recurrence-free survival (RFS) and cancer-specific survival (pairwise P ≤ 0.016). Patients without CTC had better RFS, independent of UCB histology, than patients with CTC with any UCB histology (pairwise P < 0.05). In multivariable analyses, the presence of CTC, but not variant UCB histology, was an independent predictor for disease recurrence [hazard ratio (HR) 3.45; P < 0.001] and cancer-specific mortality (HR 2.62; P = 0.002).CONCLUSION: CTC are detectable in about a quarter of patients with pure or variant UCB histology before RC, and represent an independent predictor for outcomes, when adjusting for histological subtype. In addition, our prospective data confirm the unfavourable influence of non-squamous cell-differentiated UCB on outcomes.

KW - Aged

KW - Carcinoma, Transitional Cell/pathology

KW - Cystectomy/methods

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Neoplastic Cells, Circulating

KW - Predictive Value of Tests

KW - Prospective Studies

KW - Treatment Outcome

KW - Urinary Bladder Neoplasms/pathology

U2 - 10.1111/bju.13782

DO - 10.1111/bju.13782

M3 - SCORING: Journal article

C2 - 28182321

VL - 119

SP - 854

EP - 861

JO - BJU INT

JF - BJU INT

SN - 1464-4096

IS - 6

ER -