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Comparison of First-Line Chemotherapeutics and Validation of the Eortc Prognostic Index in Malignant Pleural Mesothelioma: Retrospective Single-Centre Experience

dc.authorscopusid 57215653678
dc.authorscopusid 57190280701
dc.authorscopusid 55274300100
dc.authorscopusid 55328081200
dc.authorscopusid 57869936800
dc.authorscopusid 24339272800
dc.authorwosid Ebinç, Senar/Hnp-6891-2023
dc.contributor.author Sezgin, Yasin
dc.contributor.author Karhan, Ogur
dc.contributor.author Ileri, Serdar
dc.contributor.author Ebinc, Senar
dc.contributor.author Tunc, Sezai
dc.contributor.author Urakci, Zuhat
dc.date.accessioned 2025-05-10T17:23:16Z
dc.date.available 2025-05-10T17:23:16Z
dc.date.issued 2024
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Sezgin, Yasin; Urakci, Zuhat] Van Yuzuncu Yil Univ, Dept Med Oncol, Van, Turkiye; [Karhan, Ogur] Harran Univ, Dept Med Oncol, Sanliurfa, Turkiye; [Ileri, Serdar; Ebinc, Senar] Gazi Yasargil Training & Res Hosp, Dept Med Oncol, Diyarbakir, Turkiye; [Tunc, Sezai] Dicle Univ Hosp, Dept Med Oncol, Diyarbakir, Turkiye en_US
dc.description.abstract Objective: To evaluate the efficiency of pemetrexed cisplatin in comparison with gemcitabine cisplatin and to validate the EORTC (European Organisation for Research and Treatment of Cancer) prognostic score in combination chemotherapy treatment for malignant pleural mesothelioma. Study Design: An observational study. Place and Duration of the Study: Department of Oncology, Dicle University Hospital, Diyarbakir, Turkiye, from October 2000 to Methodology: Malignant pleural mesothelioma (MPM) patients with EORTC score 0- were recruited. Factors affecting the prognosis of the disease and the effectiveness of first-line treatment were retrospectively analysed. EORTC prognostic score was calculated with a cut-off and survival analyses were used by the Kaplan-Meier method. Log-rank and univariable Cox regression tests were used to search for prognostic factors' impact on survival. Results: Patients who received gemcitabine cisplatin treatment had a median progression-free survival (PFS) of 9 months, while those who received pemetrexed cisplatin therapy had a median PFS of 7 months. Median overall survival (OS) was 17 months in the gemcitabine cisplatin group and 18 months in the pemetrexed cisplatin group (p = 0.051). When the low-risk group was compared with the high-risk group, the median OS was found to be statistically significant (p = 0.009). Conclusion: The EORTC prognostic score, which is used for prognostic prediction in the period when pemetrexed is not utilised in the treatment of MPM, accurately predicts prognosis subsequent to the administration of pemetrexed in treatment. In the context of first-line treatment, cisplatin in combination with gemcitabine and cisplatin in combination with pemetrexed demonstrated comparable efficacy with respect to both overall survival and progression-free survival. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.29271/jcpsp.2024.08.904
dc.identifier.endpage 909 en_US
dc.identifier.issn 1022-386X
dc.identifier.issn 1681-7168
dc.identifier.issue 8 en_US
dc.identifier.pmid 39113507
dc.identifier.scopus 2-s2.0-85200939412
dc.identifier.scopusquality Q2
dc.identifier.startpage 904 en_US
dc.identifier.uri https://doi.org/10.29271/jcpsp.2024.08.904
dc.identifier.uri https://hdl.handle.net/20.500.14720/10815
dc.identifier.volume 34 en_US
dc.identifier.wos WOS:001291236800008
dc.identifier.wosquality Q4
dc.language.iso en en_US
dc.publisher Coll Physicians & Surgeons Pakistan en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Chemotherapy en_US
dc.subject Mesothelioma en_US
dc.subject Prognosis en_US
dc.subject Gemcitabine en_US
dc.subject Progression-Free Survival en_US
dc.title Comparison of First-Line Chemotherapeutics and Validation of the Eortc Prognostic Index in Malignant Pleural Mesothelioma: Retrospective Single-Centre Experience en_US
dc.type Article en_US

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