9 results on '"Stübs F"'
Search Results
2. Correlation of referring cytology and in-house cytology in detection of early cervical neoplasia
- Author
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Schulmeyer, CE, additional, Stübs, F, additional, Gaß, P, additional, Renner, SK, additional, Mehlhorn, G, additional, Geppert, C, additional, Adler, W, additional, Beckmann, MW, additional, and Koch, MC, additional
- Published
- 2018
- Full Text
- View/download PDF
3. Colposcopic accuracy in detection of early cervical neoplasia
- Author
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Koch, M, additional, Stübs, F, additional, Schulmeyer, C, additional, Kehl, S, additional, Gass, P, additional, Renner, SK, additional, Adler, W, additional, Geppert, C, additional, Beckmann, MW, additional, and Mehlhorn, G, additional
- Published
- 2018
- Full Text
- View/download PDF
4. Accuracy of colposcopy-directed biopsy in detecting early cervical neoplasia
- Author
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Stübs, F, additional, Mehlhorn, G, additional, Gass, P, additional, Schulmeyer, C, additional, Renner, S, additional, Geppert, C, additional, Adler, W, additional, Beckmann, MW, additional, and Koch, M, additional
- Published
- 2018
- Full Text
- View/download PDF
5. Cerebroplacental versus Umbilicocerebral Ratio-Analyzing the Predictive Value Regarding Adverse Perinatal Outcomes in Low- and High-Risk Fetuses at Term.
- Author
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Stumpfe FM, Mayr A, Schneider MO, Kehl S, Stübs F, Antoniadis S, Titzmann A, Pontones CA, Bayer CM, Beckmann MW, and Faschingbauer F
- Subjects
- Female, Pregnancy, Infant, Newborn, Humans, Infant, Birth Weight, Retrospective Studies, Gestational Age, Fetus, Cesarean Section
- Abstract
Background and Objectives : The aim of this study was to investigate the prediction of adverse perinatal outcomes using the cerebroplacental (CPR) and umbilicocerebral (UCR) ratios in different cohorts of singleton pregnancies. Materials and Methods : In this retrospective cohort study, we established our own Multiple of Median (MoM) for CPR and UCR. The predictive value for both ratios was studied in the following outcome parameters: emergency cesarean delivery, operative intervention (OI), OI due to fetal distress, 5-min Apgar < 7, admission to neonatal intensive care unit, and composite adverse perinatal outcome. The performance of the ratios was assessed in the following cohorts: total cohort (delivery ≥ 37 + 0 weeks gestation, all birth weight centiles), low-risk cohort (delivery ≥ 37 + 0 weeks gestation, birth weight ≥ 10. centile), prolonged pregnancy cohort (delivery ≥ 41 + 0 weeks gestation, birth weight ≥ 10. centile) and small-for-gestational-age fetuses (delivery ≥ 37 + 0 weeks gestation, birth weight < 10. centile). The underlying reference values for MoM were estimated using quantile regression depending on gestational age. Prediction performance was evaluated using logistic regression models assessing the corresponding Brier score, combining discriminatory power and calibration. Results : Overall, 3326 cases were included. Across all cohorts, in the case of a significant association between a studied outcome parameter and CPR, there was an association with UCR, respectively. The Brier score showed only minimal differences for both ratios. Conclusions : Our study provides further evidence regarding predictive values of CPR and UCR. The results of our study suggest that reversal of CPR to UCR does not improve the prediction of adverse perinatal outcomes.
- Published
- 2023
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6. Genome-wide association study and functional follow-up identify 14q12 as a candidate risk locus for cervical cancer.
- Author
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Ramachandran D, Dennis J, Fachal L, Schürmann P, Bousset K, Hülse F, Mao Q, Wang Y, Jentschke M, Böhmer G, Strauß HG, Hirchenhain C, Schmidmayr M, Müller F, Runnebaum I, Hein A, Stübs F, Koch M, Ruebner M, Beckmann MW, Fasching PA, Luyten A, Dürst M, Hillemanns P, Easton DF, and Dörk T
- Subjects
- Female, Follow-Up Studies, Forkhead Transcription Factors genetics, Forkhead Transcription Factors metabolism, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Nerve Tissue Proteins genetics, Papillomaviridae genetics, Papillomaviridae metabolism, Polymorphism, Single Nucleotide genetics, Papillomavirus Infections complications, Papillomavirus Infections genetics, Uterine Cervical Neoplasms genetics
- Abstract
Cervical cancer is among the leading causes of cancer-related death in females worldwide. Infection by human papillomavirus (HPV) is an established risk factor for cancer development. However, genetic factors contributing to disease risk remain largely unknown. We report on a genome-wide association study (GWAS) on 375 German cervical cancer patients and 866 healthy controls, followed by a replication study comprising 658 patients with invasive cervical cancer, 1361 with cervical dysplasia and 841 healthy controls. Functional validation was performed for the top GWAS variant on chromosome 14q12 (rs225902, close to PRKD1). After bioinformatic annotation and in silico predictions, we performed transcript analysis in a cervical tissue series of 317 samples and demonstrate rs225902 as an expression quantitative trait locus (eQTL) for FOXG1 and two tightly co-regulated long non-coding RNAs at this genomic region, CTD-2251F13 (lnc-PRKD1-1) and CTD-2503I6 (lnc-FOXG1-6). We also show allele-specific effects of the 14q12 variants via luciferase assays. We propose a combined effect of genotype, HPV status and gene expression at this locus on cervical cancer progression. Taken together, this work uncovers a potential candidate locus with regulatory functions and contributes to the understanding of genetic susceptibility to cervical cancer., (© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.)
- Published
- 2022
- Full Text
- View/download PDF
7. [Revised German guidelines on the diagnosis and treatment of carcinoma of the uterine cervix-what's new for pathologists in 2021?]
- Author
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Horn LC, Beckmann MW, Follmann M, Koch MC, Nothacker M, Pöschel B, Stübs F, Schmidt D, and Höhn AK
- Subjects
- Female, Humans, Pathologists, Adenocarcinoma diagnosis, Carcinoma, Papillomavirus Infections diagnosis, Uterine Cervical Neoplasms diagnosis
- Abstract
In 2021, the 2015 German consensus guideline for the diagnosis and treatment of uterine cervical carcinoma was updated. The present article summarises the new recommendations for pathologists: the incorporation of the International Endocervical Adenocarcinoma Classification (IECC), which morphologically separates HPV-associated and non-HPV-associated adenocarcinomas, as well as the reporting of the prognostic relevant growth pattern of the adenocarcinoma of the endocervical subtype (Silva pattern). Histologically, multifocality has been defined as the presence of clearly invasive foci with a minimum distance between each focus of 0.2 cm. Because of its intratumoural heterogeneity, all carcinomas ≤ 2 cm in their largest dimension should be processed completely, and tumours > 2 cm should be processed with one block per centimetre of their greatest dimension. In cases of (radical) trachelectomy/hysterectomy, the distal vaginal resection margin and all parametrial tissue should be processed completely. Sentinel lymph nodes have to be processed completely by lamellation along its long axis in 0.2 cm intervals. Immunohistochemical ultrastaging is mandatory. Staging should be performed using the 2009 FIGO classification and 2017 TNM classification. Reporting the revised 2018 FIGO classification is optional. To date, molecular markers have not been relevant for prognostication and treatment decision making., (© 2022. The Author(s).)
- Published
- 2022
- Full Text
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8. Evaluation of Integrated HPV DNA as Individualized Biomarkers for the Detection of Recurrent CIN2/3 during Post-Treatment Surveillance.
- Author
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Hoyer H, Mehlhorn G, Scheungraber C, Hagemann I, Hirchenhain C, Woelber L, Stolte C, Hampl M, Scherbring S, Denecke A, Bartels J, Ebert AD, Meneder S, Petzold A, Heller T, Heidtke KR, Schwarz E, Stübs F, Schütze S, Stange EL, Jaeger A, Martignoni F, Dellmann A, Rody A, Hillemanns P, Fehm T, Petry KU, Böhmer G, Schmalfeldt B, Wimberger P, Beckmann MW, Runnebaum IB, and Dürst M
- Abstract
Purpose: Post-treatment follow-up in women with cervical pre-cancers (CIN3) is mandatory due to relapse in up to 10% of patients. Standard follow-up based on hrHPV-DNA/cytology co-testing has high sensitivity but limited specificity. The aim of our prospective, multicenter, observational study was to test the hypothesis that an individualized viral-cellular-junction test (vcj-PCR) combined with cytology has a lower false positive rate for the prediction of recurrence compared to standard co-testing., Methods: Pre-surgical cervical swabs served for the identification of HPV16/18 DNA integration sites by next-generation-sequencing (NGS). Samples taken at 6, 12 and 24 months post-surgery were evaluated by cytology, hrHPV-DNA and the patients' individual HPV-integration sites (vcj-PCR on the basis of NGS)., Results: Integration sites were detected in 48 of 445 patients (10.8%), 39 of them had valid follow-up data. The false positive rate was 18.2% (95% CI 8.6-34.4%) for standard hrHPV/cytology at six months compared to 12.1% (95% CI 4.8-27.3%) for vcj-PCR/cytology, respectively (McNemar p = 0.50). Six patients developed recurrences (1 CIN2, 5 CIN3) during follow-up. Standard co-testing detected all, whereas vcj-PCR/cytology detected only five patients with recurrences. Data of 269 patients without evidence of HPV16/18 integration were subject to post-hoc analyses. Standard co-testing revealed a false positive rate of 15.7% (95% CI 11.7-20.7%) and predicted ten of fourteen recurrences at six months., Conclusions: Although highly specific on its own vcj-PCR could not detect all recurrent CIN2/3. Possible reasons for this unexpected result may be multifocal lesions, intratumoral heterogeneity with respect to HPV integration and/or incident CIN.
- Published
- 2021
- Full Text
- View/download PDF
9. Correlation between referral cytology and in-house colposcopy-guided cytology for detecting early cervical neoplasia.
- Author
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Schulmeyer CE, Stübs F, Gass P, Renner SK, Hartmann A, Strehl J, Mehlhorn G, Geppert C, Adler W, Beckmann MW, and Koch MC
- Subjects
- Adult, Colposcopy methods, Female, Humans, Pregnancy, Retrospective Studies, Uterine Cervical Neoplasms pathology, Uterine Cervical Dysplasia pathology, Cytological Techniques methods, Early Detection of Cancer methods, Uterine Cervical Neoplasms surgery
- Abstract
Purpose: The current cervical cancer screening program in Germany recommends that the results showing suspected HPV infection should be further examined in specialized colposcopy units. This study aimed to correlate externally documented Pap smear results with in-house colposcopy-guided Pap cytology results and compare colposcopy-guided biopsy and postoperative histopathology results., Methods: Clinical data were analyzed from 3627 examinations in 2844 patients who visited a university certified dysplasia unit from 2014 to 2017; 2212 patients underwent complete assessments, including Pap smear, colposcopy, HPV testing, colposcopy-guided biopsy, and/or surgery. The results were analyzed descriptively., Results: External and in-house Pap results were consistent in 1054 ofthe 2212 patients (47.65%). Referral cytology showed a higher grade than in-house in 456 (20.61%) and a lower grade in 702 (31.74%). Using the histopathological findings as the gold standard, overdiagnosis in the referral cytology was noted in 180 patients (13.19%), underdiagnosis in 263 (19.27%), and concordant findings in 922 (67.55%). For in-house cytology, overdiagnosis was found in 133 patients (10.74%), underdiagnosis in 192 (15.51%), and accurate diagnosis with congruent cytology and histopathology findings in 913 (73.75%)., Conclusions: The rate of detection of cervical abnormalities differs significantly depending on whether the examination is performed routinely or in specialized units. Colposcopy-guided Pap smears correlate significantly better with histology than referral cytology results without colposcopic guidance. More severe lesions were also detected more accurately.
- Published
- 2020
- Full Text
- View/download PDF
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