Prognostic value of HPV-mRNA in sentinel lymph nodes of cervical cancer patients with pN0-status
Identifieur interne : 001950 ( Main/Exploration ); précédent : 001949; suivant : 001951Prognostic value of HPV-mRNA in sentinel lymph nodes of cervical cancer patients with pN0-status
Auteurs : Matthias Dürst [Allemagne] ; Heike Hoyer [Allemagne] ; Christoph Altgassen [Allemagne] ; Christiane Greinke [Allemagne] ; Norman H Fner [Allemagne] ; Alba Fishta [Allemagne] ; Mieczyslaw Gajda [Allemagne] ; Ute Mahnert [Allemagne] ; Peter Hillemanns [Allemagne] ; Thomas Dimpfl [Allemagne] ; Miriam Lenhard [Allemagne] ; K. Ulrich Petry [Allemagne] ; Ingo B. Runnebaum [Allemagne] ; Achim Schneider [Allemagne]Source :
- Oncotarget [ 1949-2553 ] ; 2015.
Abstract
Up to 15% of patients with cervical cancer and pN0-status develop recurrent-disease. This may be due to occult metastatic spread of tumor cells. We evaluated the use of human-papillomavirus-(HPV)-mRNA as a molecular marker for disseminated tumor cells to predict the risk of recurrence. For this prospective, multi-center prognostic study, 189 patients free of lymphnode metastases by conventional histopathology could be analyzed. All patients underwent complete lymphadenectomy. Of each sentinel node (SLN) a biopsy was taken for the detection of HPV-E6-E7-mRNA. Median follow-up time after surgery was 8.1 years. HPV-mRNA could be detected in SLN of 52 patients (27.5%). Recurrence was observed in 22 patients. Recurrence-free-survival was significantly longer for patients with HPV-negative SLN (log rank
Url:
PubMed: 26008982
PubMed Central: 4673218
Affiliations:
- Allemagne
- Basse-Saxe, Bavière, Berlin, District de Haute-Bavière, District de Kassel, Hesse (Land)
- Berlin, Cassel (Hesse), Hanovre, Munich
Links toward previous steps (curation, corpus...)
- to stream Pmc, to step Corpus: 000386
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- to stream Pmc, to step Checkpoint: 000F48
- to stream Ncbi, to step Merge: 007414
- to stream Ncbi, to step Curation: 007414
- to stream Ncbi, to step Checkpoint: 007414
- to stream Main, to step Merge: 001952
- to stream Main, to step Curation: 001950
Le document en format XML
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<front><div type="abstract" xml:lang="en"><p>Up to 15% of patients with cervical cancer and pN0-status develop recurrent-disease. This may be due to occult metastatic spread of tumor cells. We evaluated the use of human-papillomavirus-(HPV)-mRNA as a molecular marker for disseminated tumor cells to predict the risk of recurrence. For this prospective, multi-center prognostic study, 189 patients free of lymphnode metastases by conventional histopathology could be analyzed. All patients underwent complete lymphadenectomy. Of each sentinel node (SLN) a biopsy was taken for the detection of HPV-E6-E7-mRNA. Median follow-up time after surgery was 8.1 years. HPV-mRNA could be detected in SLN of 52 patients (27.5%). Recurrence was observed in 22 patients. Recurrence-free-survival was significantly longer for patients with HPV-negative SLN (log rank <italic>p</italic>
= 0.002). By Cox regression analysis the hazard ratio (95%CI) for disease-recurrence was 3.8 (1.5 – 9.3, <italic>p</italic>
= 0.004) for HPV-mRNA-positive compared to HPV-mRNA-negative patients. After adjustment for tumor size as the most influential covariate the HR was still 2.8 (1.1 – 7.0, <italic>p</italic>
= 0.030). In patients with cervical cancer and tumor-free lymph nodes by conventional histopathology HPV-mRNA-positive SLN were of prognostic value independent of tumor size. Particularly, patients with tumors larger than 20mm diameter could possibly benefit from further risk stratification using HPV-mRNA as a molecular marker.</p>
</div>
</front>
<back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Delgado, G" uniqKey="Delgado G">G Delgado</name>
</author>
<author><name sortKey="Bundy, Bn" uniqKey="Bundy B">BN Bundy</name>
</author>
<author><name sortKey="Fowler, Wc" uniqKey="Fowler W">WC Fowler</name>
</author>
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<li>Berlin</li>
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<name sortKey="H Fner, Norman" sort="H Fner, Norman" uniqKey="H Fner N" first="Norman" last="H Fner">Norman H Fner</name>
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