dc.contributor.author | Demirci, Nebi Serkan | |
dc.contributor.author | Bedir, Sahin | |
dc.contributor.author | DEĞERLİ, Ezgi | |
dc.contributor.author | Derin, Sumeyra | |
dc.contributor.author | DEMİRELLİ, Fuat Hulusi | |
dc.contributor.author | ŞENGÜL SAMANCI, Nilay | |
dc.contributor.author | ÇELİK, Emir | |
dc.contributor.author | Bagcilar, Omer | |
dc.contributor.author | Erol, Burak Caglar | |
dc.contributor.author | Bicki, Ela | |
dc.contributor.author | ORUÇ, Kerem | |
dc.date.accessioned | 2021-03-02T16:31:46Z | |
dc.date.available | 2021-03-02T16:31:46Z | |
dc.date.issued | 2020 | |
dc.identifier.citation | ŞENGÜL SAMANCI N., ÇELİK E., Bagcilar O., Erol B. C. , Bicki E., ORUÇ K., Bedir S., DEĞERLİ E., Derin S., Demirci N. S. , et al., "Loss of skeletal muscle area and fat-free mass during dabrafenib/trametinib and vemurafenib/cobimetinib treatments in patients with BRAF-mutant metastatic malignant melanoma", MELANOMA RESEARCH, cilt.30, sa.5, ss.477-483, 2020 | |
dc.identifier.issn | 0960-8931 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_028e2a26-a474-4b9c-b7c2-2b72daba1bd7 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/3102 | |
dc.identifier.uri | https://doi.org/10.1097/cmr.0000000000000678 | |
dc.description.abstract | This study aimed to assess whether dabrafenib/trametinib and vemurafenib/cobimetinib treatments are associated with a change in skeletal muscle area (SMA) and total fat-free mass (FFM) assessed by computed tomography (CT), and to compare the efficacy and safety profile of these treatments in patients with metastatic melanoma. Thirty-one patients treated with B-Raf proto-oncogene, serine/threonine kinase/MAPK extracellular receptor kinase inhibitors were included between 2016 and 2019. Eighteen patients received dabrafenib/trametinib and remaining patients received vemurafenib/cobimetinib. CT scans were performed at baseline and at 4-6 months of follow-up to measure cross-sectional areas of SMA. FFM and skeletal muscle index (SMI) values were calculated. Of the patients, including 18 treated with dabrafenib/trametinib (58.1%) and 13 with vemurafenib/cobimetinib (41.9%); 58.1% were male, 41.9% were female and median age was 52 years. A significant decrease in SMA was observed after dabrafenib/trametinib and vemurafenib/cobimetinib treatments (P = 0.003 andP = 0.002, respectively). A significant decrease in FFM values was observed after dabrafenib/trametinib and vemurafenib/cobimetinib treatments (P = 0.003 andP = 0.002, respectively). Dose-limiting toxicity (DLT) was observed in 35.9% of the patients with sarcopenia. No significant difference was seen between the dabrafenib/trametinib and vemurafenib/cobimetinib groups in median progression-free survival (PFS) (11.9 vs. 7.3 months, respectively,P = 0.28) and in median overall survival (OS) (25.46 vs. 13.7 months, respectively,P = 0.41). Baseline sarcopenia was not significantly associated with PFS or OS (P = 0.172 andP = 0.326, respectively). We found a significant decrease in SMI values determined at 4-6 months compared to the values before treatment both in dabrafenib/trametinib and vemurafenib/cobimetinib groups. DLT was similar with both treatments. Baseline sarcopenia was not significantly associated with PFS or OS. | |
dc.language.iso | eng | |
dc.subject | Dermatoloji | |
dc.subject | İç Hastalıkları | |
dc.subject | Onkoloji | |
dc.subject | Tıbbi Ekoloji ve Hidroklimatoloji | |
dc.subject | ONKOLOJİ | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.subject | DERMATOLOJİ | |
dc.subject | TIP, ARAŞTIRMA VE DENEYSEL | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.title | Loss of skeletal muscle area and fat-free mass during dabrafenib/trametinib and vemurafenib/cobimetinib treatments in patients with BRAF-mutant metastatic malignant melanoma | |
dc.type | Makale | |
dc.relation.journal | MELANOMA RESEARCH | |
dc.contributor.department | İstanbul Üniversitesi-Cerrahpaşa , Cerrahpaşa Tıp Fakültesi , Dahili Tıp Bilimleri Bölümü | |
dc.identifier.volume | 30 | |
dc.identifier.issue | 5 | |
dc.identifier.startpage | 477 | |
dc.identifier.endpage | 483 | |
dc.contributor.firstauthorID | 2287396 | |