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dc.contributor.authorOzbay, Mehmet Fatih
dc.contributor.authorHarputluoglu, Hakan
dc.contributor.authorKaraca, Mustafa
dc.contributor.authorTekin, Omer
dc.contributor.authorSendur, Mehmet Ali Nahit
dc.contributor.authorKaplan, Muhammed Ali
dc.contributor.authorSahin, Berksoy
dc.date.accessioned2025-01-12T18:54:45Z
dc.date.available2025-01-12T18:54:45Z
dc.date.issued2024
dc.identifier.issn2072-6694
dc.identifier.urihttps://doi.org/10.3390/cancers16223880
dc.identifier.urihttp://hdl.handle.net/11446/4966
dc.description.abstractBackground and Aims: During liver transplantation, hepatocellular carcinoma (HCC) recurrence remains a critical challenge for patient survival. Targeted therapies, such as sorafenib and regorafenib, have been utilized to manage relapsed HCC in this unique setting. This study aimed to assess the efficacy of Sorafenib and Regorafenib in patients with HCC who experienced recurrence after liver transplantation. We focused on survival outcomes, treatment responses, and the management of side effects in this patient group. Methods: We conducted a retrospective analysis of 73 patients who experienced HCC recurrence post-liver transplantation between 2012 and 2022 across 11 oncology centers in Turkey. Patients were categorized according to Child-Pugh classification and treated with sorafenib as first-line therapy and Regorafenib in case of progression. Survival rates were analyzed using the Kaplan-Meier method, and risk factors were evaluated using Cox regression analysis. Results: Of the 73 patients included in the study, 62 were male (84.9%), and 11 were female (15.1%), with a mean age of 61.5 +/- 10.9 years. All patients received sorafenib as first-line treatment. Among patients who experienced progression with sorafenib or discontinued treatment due to toxicity, 45.2% (n = 33) continued treatment with regorafenib. The median progression-free survival (PFS1) time with sorafenib was 5.6 months, and the one-year survival rate was 24.3%. The median progression-free survival (PFS2) time with regorafenib, which was administered as second-line treatment, was also calculated as 5.9 months. Overall survival (OS) duration was determined as 35.9 months. The most common side effects associated with both drugs included fatigue, hand and foot syndrome, and hypertension. Significantly better survival outcomes were shown in the Child-Pugh A group compared to other patients. Conclusions: These results suggest that Sorafenib and Regorafenib treatments offer a survival advantage in patients with relapsed HCC post-transplantation. However, individualized treatment strategies and close follow-up are crucial for optimizing outcomes. Further studies are needed to refine therapeutic protocols and enhance the care of this specific patient group.en_US
dc.language.isoengen_US
dc.publisherMdpien_US
dc.relation.ispartofCancersen_US
dc.identifier.doi10.3390/cancers16223880
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjecthepatocellular carcinoma (HCC)en_US
dc.subjectliver transplantationen_US
dc.subjectsorafeniben_US
dc.subjectregorafeniben_US
dc.subjectpost-transplant recurrenceen_US
dc.subjectCarcinomaen_US
dc.subjectSurvivalen_US
dc.subjectTherapyen_US
dc.titleSequential Use of Sorafenib and Regorafenib in Hepatocellular Cancer Recurrence After Liver Transplantation: Treatment Strategies and Outcomesen_US
dc.typearticleen_US
dc.departmentDBÜen_US
dc.identifier.issue22en_US
dc.identifier.volume16en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Ozbay, Mehmet Fatih] Kirsehir Training & Res Hosp, Dept Med Oncol, TR-40200 Kirsehir, Turkiye; [Harputluoglu, Hakan; Tekin, Omer] Inonu Univ, Fac Med, Dept Med Oncol, TR-44000 Malatya, Turkiye; [Karaca, Mustafa; Goksu, Sema Sezgin; Tatli, Ali Murat] Akdeniz Univ, Fac Med, Dept Med Oncol, TR-07070 Antalya, Turkiye; [Sendur, Mehmet Ali Nahit; Erol, Cihan] Ankara Bilkent City Hosp, Dept Med Oncol, Republ Turkey Minist Hlth, TR-06800 Ankara, Turkiye; [Kaplan, Muhammed Ali; Kalkan, Ziya] Dicle Univ, Fac Med, Dept Med Oncol, TR-21280 Diyarbakir, Turkiye; [Sahin, Berksoy; Bayram, Ertugrul] Cukurova Univ, Fac Med, Dept Med Oncol, TR-01330 Adana, Turkiye; [Geredeli, Caglayan; Selvi, Oguzhan] Hlth Sci Univ, Okmeydani Training & Res Hosp, Dept Med Oncol, TR-34098 Istanbul, Turkiye; [Teker, Fatih] Gaziantep Univ, Fac Med, Dept Med Oncol, TR-27410 Gaziantep, Turkiye; [Tural, Deniz; Gulturk, Ilkay] Bakirkoy Sadi Konuk Training & Res Hosp, Dept Med Oncol, TR-34147 Istanbul, Turkiye; [Saglam, Sezer] Demiroglu Bilim Univ, Gayrettepe Florence Nightingale Hosp, Dept Med Oncol, TR-34394 Istanbul, Turkiye; [Cil, Timucin] Univ Hlth Sci, Adana City Training & Res Hosp, Dept Med Oncol, Adana Fac Med, TR-01230 Adana, Turkiye; [Bilici, Ahmet] Istanbul Meden_US
dc.authoridcil, timucin/0000-0002-5033-1479
dc.authoridSendur, Mehmet/0000-0001-7021-6139
dc.authoridBayram, Ertugrul/0000-0001-8713-7613
dc.identifier.pmid39594835en_US
dc.identifier.scopus2-s2.0-85211074455en_US
dc.identifier.wosWOS:001364175500001en_US
dc.authorwosidTatlı, Ali/D-9111-2018
dc.authorwosidEROL, CİHAN/GWU-8797-2022
dc.authorwosidBayram, Ertugrul/JVZ-1992-2024
dc.authorwosidSendur, Mehmet/H-7555-2014
dc.authorwosidcil, timucin/HJZ-1735-2023
dc.authorscopusid24338750300
dc.authorscopusid10144082400
dc.authorscopusid20435967600
dc.authorscopusid57202248741
dc.authorscopusid57219456490
dc.authorscopusid57243378400
dc.authorscopusid7103169998


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