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dc.contributor.authorAtcı, Muhammed Mustafa
dc.contributor.authorAkagündüz, Baran
dc.contributor.authorDemir, Metin
dc.contributor.authorDönmez Yılmaz, Binnur
dc.contributor.authorAkın Telli, Tuğba
dc.contributor.authorCan, Orçun
dc.contributor.authorÇil, İbrahim
dc.contributor.authorGöktaş Aydın, Sabin
dc.contributor.authorÖzyurt, Neslihan
dc.contributor.authorÖnder, Arif Hakan
dc.contributor.authorSelvi, Oğuzhan
dc.contributor.authorSakin, Abdullah
dc.date.accessioned2022-05-27T09:00:45Z
dc.date.available2022-05-27T09:00:45Z
dc.date.issued2022en_US
dc.identifier.citationAtcı, M. M., Akagündüz, B., Demir, M., Dönmez Yılmaz, B., Akın Telli, T., Can, O. ... Sakin, A. (2022). Effect of adjuvant chemotherapy in stage III cervical cancer patients treated with concurrent chemoradiation: A multicenter study. Oncology Research and Treatment, 45(5), 254-261. https://doi.org/10.1159/000521980en_US
dc.identifier.issn2296-5262
dc.identifier.urihttps://doi.org/10.1159/000521980
dc.identifier.urihttps://hdl.handle.net/20.500.12511/9473
dc.description.abstractINTRODUCTION: A significant proportion of cervical cancer (CC) patients are diagnosed at a locally advanced stage. Concurrent chemoradiotherapy (CCRT) is the cornerstone of treatment for patients with locally advanced CC. However, the role of adjuvant chemotherapy (AC) after CCRT is controversial. In this study, we analyzed the efficacy of AC after CCRT in stage III CC patients. METHODS: We performed a multicenter, retrospective analysis of 139 International Federation of Gynecology and Obstetrics stage III CC patients treated with CCRT of whom 45.3% received AC. Our goal was to determine the impact of AC on survival in these patients. RESULTS: Five-year progression-free survival (PFS) was 37.5% and 16% in patients receiving CCRT with and without AC, respectively (p = 0.008). Median PFS was 30.9 months (CI 95% 14.8-46.9) and 16.6 months (CI 95% 9.3-23.9) in patients receiving CCRT with and without AC, respectively. Five-year overall survival (OS) was 78.2% and 28.4% in patients receiving CCRT with and without AC, respectively (p < 0.001). Median OS was 132.2 months (CI 95, %66.5-197.8) and 34.9 months (CI 95% 23.1-46.7) in patients receiving CCRT with and without AC, respectively. CONCLUSION: Our study suggests that AC provides OS and PFS benefit in stage III CC patients. Larger studies are needed to identify subgroups of patients who would benefit from AC.en_US
dc.language.isoengen_US
dc.publisherNLM (Medline)en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAdjuvant Chemotherapyen_US
dc.subjectCervical Canceren_US
dc.subjectStage IIIen_US
dc.titleEffect of adjuvant chemotherapy in stage III cervical cancer patients treated with concurrent chemoradiation: A multicenter studyen_US
dc.typearticleen_US
dc.relation.ispartofOncology Research and Treatmenten_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, İç Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0002-0077-6971en_US
dc.identifier.volume45en_US
dc.identifier.issue5en_US
dc.identifier.startpage254en_US
dc.identifier.endpage261en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1159/000521980en_US
dc.institutionauthorGöktaş Aydın, Sabin
dc.identifier.wosqualityQ4en_US
dc.identifier.wos000833355100003en_US
dc.identifier.scopus2-s2.0-85129996780en_US
dc.identifier.pmid35034017en_US
dc.identifier.scopusqualityQ2en_US


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