Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/24815
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dc.contributor.authorBasheska, Nelien_US
dc.contributor.authorProdanova, Irinaen_US
dc.contributor.authorKubelka-Sabit, Katerinaen_US
dc.contributor.authorVeljanovska, Slavicaen_US
dc.contributor.authorArsovski, Oliveren_US
dc.contributor.authorZografski, Georgeen_US
dc.date.accessioned2022-12-12T13:27:10Z-
dc.date.available2022-12-12T13:27:10Z-
dc.date.issued2008-05-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/24815-
dc.description.abstractBACKGROUND: The objective of this prospective study was to validate the prognostic criteria defined by the results of our previous study in an independent population of surgically treated cervical carcinoma patients. METHOD: The study group consisted of 340 patients who underwent abdominal hysterectomy with pelvic lymphadenectomy as primary therapy between 2000 and 2005. Based on the scores of the variables (blood vessel invasion, lymph node metastases, tumor diameter, degree of inflammatory reaction at the invasive front, and minimum thickness of uninvolved cervical stroma/parametrial extension) and calculated prognostic index (PI) values, the patients were divided into three prognostic groups. RESULTS: During the follow-up period (range, 1.6–89.7, mean, 39.7±22.2 months) recurrences were observed in 1% (1/97), 12.2% (16/131) and 23.2% (26/112) of the low-, intermediate-, or high-risk group patients, respectively. The 5-year disease-free survival (DFS) rates of the low, intermediate, and high-risk groups were 98.82%, 84.57%, and 74.01%, respectively. The differences in DFS rates were statistically significant (P<0.0001). In order to validate the model from our previous study, we have compared DFS rates between the groups. There was no difference in DFS rate between low-risk groups, in spite of the fact that majority of the patients in this study were not irradiated, while radiotherapy was administrated invariably to all the patients included in the original study. Similarly, DFS did not differ significantly between the intermediate-risk groups from both studies, which could be expected since radiotherapy was administrated to majority of the patients (125/131) in this study. In contrast, the high-risk group patients in this study had significantly higher DFS rate (74.01% vs. 44.24, P=0.0010), probably as the result of the adjuvant chemotherapy administrated to 69% of them. CONCLUSION: PI could be a sound and reliable basis for an appropriate planning of the following therapeutical strategy of the surgically treated cervical cancer patients.en_US
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.relation.ispartofVirchows Archiveen_US
dc.subjectuterine cervixen_US
dc.subjectinvasive carcinomaen_US
dc.subjectprognostic factorsen_US
dc.subjectprognostic indexen_US
dc.subjectprognostic groupen_US
dc.subjectdisease-free survivalen_US
dc.titleThe implementation of prognostic index and risk grouping in surgically treated cervical carcinoma patients: A prospective validation study.en_US
dc.typeProceeding articleen_US
dc.relation.conference3rd Intercontinental Congress of Pathology, May 17-22, 2008, Barcelona, Spainen_US
dc.identifier.doi10.1007/s00428-008-0613-x-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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