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Dive into the research topics where Josef Chovanec is active.

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Featured researches published by Josef Chovanec.


Gynecologic Oncology | 2015

A novel diagnostic index combining HE4, CA125 and age may improve triage of women with suspected ovarian cancer — An international multicenter study in women with an ovarian mass

Mona Aarenstrup Karlsen; Estrid Høgdall; Ib Jarle Christensen; Christer Borgfeldt; Grigorios Kalapotharakos; Lenka Zdrazilova-Dubska; Josef Chovanec; C.A.R. Lok; Anna Stiekema; Irene Mutz-Dehbalaie; Adam N. Rosenthal; Elizabeth K. Moore; Beth A. Schodin; Walfrido W. Sumpaico; Karin Sundfeldt; Björg Kristjansdottir; Ignacio Zapardiel; Claus Høgdall

AIM To develop and validate a biomarker-based index to optimize referral and diagnosis of patients with suspected ovarian cancer. Furthermore, to compare this new index with the Risk of Malignancy Index (RMI) and Risk of Ovarian Malignancy Algorithm (ROMA). PATIENTS AND METHODS A training study, consisting of patients with benign ovarian disease (n=809) and ovarian cancer (n=246), was used to develop the Copenhagen Index (CPH-I) utilizing the variables serum HE4, serum CA125 and patient age. Eight international studies provided the validation population; comprising 1060 patients with benign ovarian masses and 550 patients with ovarian cancer. RESULTS Overall, 2665 patients were included. CPH-I was highly significant in discriminating benign from malignant ovarian disease. At the defined cut-off of 0.070 for CPH-I the sensitivity and specificity were 95.0% and 78.4% respectively in the training cohort and 82.0% and 88.4% in the validation cohort. Comparison of CPH-I, ROMA and RMI demonstrated area-under-curve (AUC) at 0.960, 0.954 and 0.959 respectively in the training study and 0.951, 0.953 and 0.935 respectively in the validation study. Using a sensitivity of 95.0%, the specificities for CPH-I, ROMA and RMI in the training cohort were 78.4%, 71.7% and 81.5% respectively, and in the validation cohort 67.3%, 70.7% and 69.5% respectively. CONCLUSION All three indices perform well at the clinically relevant sensitivity of 95%, but CPH-I, unlike RMI and ROMA, is independent of ultrasound and menopausal status, and may provide a simple index to optimize referral of women with suspected ovarian cancer.


European Journal of Obstetrics & Gynecology and Reproductive Biology | 2011

A common variation in the cannabinoid 1 receptor (CNR1) gene is associated with pre-eclampsia in the Central European population.

Julie Bienertova-Vasku; Petr Bienert; Zuzana Dostálová; Josef Chovanec; Anna Vasku; Vladimir Vasku

OBJECTIVE Recently it has been proposed that tightly regulated levels of endogenous cannabinoids play a fundamental role in early placental development. The aim of this study was to investigate associations of three single-nucleotide polymorphisms (SNPs) in the cannabinoid 1 receptor (CNR1) gene (rs1049353, rs12720071 and rs806368) and their inferred haplotypes with pre-eclampsia, a severe pregnancy-associated condition characterized by abnormal development and remodeling of spiral decidual arteries. STUDY DESIGN The case-control study comprised a total of 115 pre-eclamptic women and 145 healthy pregnant controls, all originating from the Central-European Czech population. Using PCR-based methods, we tested rs1049353, rs12720071 and rs806368 in the CNR1 gene and haplotypes were constructed. RESULTS Statistically significant difference in genotype distributions of rs806368 (p(g)<10(-3)) was observed when comparing the cases and the controls; the cases presenting with significantly lower proportion of CC homozygotes. In multivariate modeling, the rs806368 served as a predictor for pre-eclampsia development (β=0.15; p=0.04). Haplotype analysis revealed presence of four common haplotypes; the CAA haplotype being less frequent in pre-eclamptic cases compared to the controls (p<0.008). Analysis of regression models confirmed the independent prediction role of AAC haplotype for pre-eclampsia onset (β=-0.18; p=0.03). CONCLUSION This is the first study focusing on the relationship between SNPs in the CNR1 gene and pre-eclampsia risk. Although limited by a relatively small sample size, the study indicates that rs806368 in the CNR1 gene may act as a susceptibility marker for pre-eclampsia in humans.


Oncotarget | 2017

Adjustment of serum HE4 to reduced glomerular filtration and its use in biomarker-based prediction of deep myometrial invasion in endometrial cancer

Josef Chovanec; Iveta Selingerová; Kristína Greplová; Sofie Leisby Antonsen; Monika Nalezinska; Claus Høgdall; Estrid Høgdall; Erik Søgaard-Andersen; Kirsten Marie Jochumsen; Pavel Fabian; Dalibor Valík; Lenka Zdrazilova-Dubska

Background We investigated the efficacy of circulating biomarkers together with histological grade and age to predict deep myometrial invasion (dMI) in endometrial cancer patients. Methods HE4ren was developed adjusting HE4 serum levels towards decreased glomerular filtration rate as quantified by the eGFR-EPI formula. Preoperative HE4, HE4ren, CA125, age, and grade were evaluated in the context of perioperative depth of myometrial invasion in endometrial cancer (EC) patients. Continuous and categorized models were developed by binary logistic regression for any-grade and for G1-or-G2 patients based on single-institution data from 120 EC patients and validated against multicentric data from 379 EC patients. Results In non-cancer individuals, serum HE4 levels increase log-linearly with reduced glomerular filtration of eGFR ≤ 90 ml/min/1.73 m2. HE4ren, adjusting HE4 serum levels to decreased eGFR, was calculated as follows: HE4ren = exp[ln(HE4) + 2.182 × (eGFR-90) × 10-2]. Serum HE4 but not HE4ren is correlated with age. Model with continuous HE4ren, age, and grade predicted dMI in G1-or-G2 EC patients with AUC = 0.833 and AUC = 0.715, respectively, in two validation sets. In a simplified categorical model for G1-or-G2 patients, risk factors were determined as grade 2, HE4ren ≥ 45 pmol/l, CA125 ≥ 35 U/ml, and age ≥ 60. Cumulation of weighted risk factors enabled classification of EC patients to low-risk or high-risk for dMI. Conclusions We have introduced the HE4ren formula, adjusting serum HE4 levels to reduced eGFR that enables quantification of time-dependent changes in HE4 production and elimination irrespective of age and renal function in women. Utilizing HE4ren improves performance of biomarker-based models for prediction of dMI in endometrial cancer patients.


Klinická onkologie : casopis Ceské a Slovenské onkologické spolecnosti | 2013

[Preinvasive lesions in gynaecology - uterine cervix].

Lucie Mouková; Richard Feranec; Josef Chovanec

Preinvasive lesion of the uterine cervix can give rise to cervical cancer. High-risk human papillomaviruses with high oncogenic potential are considered to be the main etiopathological factors with interaction of other risk factors (recurrent inflammation of the cervix, injury of the cervix, immunosuppressive conditions, sexual promiscuity, etc.). Early dia-gnosis of these changes at regular gynecological examinations and adequate treatment can prevent of malignant transformation. Organized cervical screening and implementation of nationwide vaccination against human papillomavirus promises to reduce the incidence of cervical cancer.


Neoplasma | 2011

Relationship of resistin levels with endometrial cancer risk

M. Hlavna; L. Kohut; Jolana Lipková; Julie Bienertova-Vasku; Zuzana Dostálová; Josef Chovanec; Anna Vasku


Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti | 2009

Leptin--2548 g/A polymorphism in endometrial cancer.

Josef Chovanec; Julie Bienertová Vašků; Zuzana Dostálová


Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti | 2013

Prognostic factors for cervical cancer

Lucie Mouková; Rudolf Nenutil; Pavel Fabian; Josef Chovanec


Klinická onkologie : casopis Ceské a Slovenské onkologické spolecnosti | 2013

Preinvasive Lesions in Gynecology - Vulva

Josef Chovanec; Lucie Mouková; Richard Feranec


Archive | 2006

Association of leptin and adiponectin polymorphisms with endometrial cancer

Josef Chovanec; Zuzana Dostálová; Julie Bienertová Vašků; Anna Vašků; Atanas-Ivan Belkov


Onkologie | 2017

Serózní tubární intraepiteliální karcinomy (STIC)

Gabriel Jelenek; Josef Chovanec

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