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首页> 外文期刊>Melanoma research >Loss of skeletal muscle area and fat-free mass during dabrafenib/trametinib and vemurafenib/cobimetinib treatments in patients with BRAF-mutant metastatic malignant melanoma
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Loss of skeletal muscle area and fat-free mass during dabrafenib/trametinib and vemurafenib/cobimetinib treatments in patients with BRAF-mutant metastatic malignant melanoma

机译:Dabrafenib / Trametinib和vemurafenib / Cobimetinib在Braf-突变体转移性恶性黑色素瘤患者中失去骨骼肌区域和无脂肪肿块

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摘要

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.
机译:None

著录项

  • 来源
    《Melanoma research 》 |2020年第5期| 共7页
  • 作者单位

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Radiol Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Radiol Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Internal Med Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

    Istanbul Univ Cerrahpasa Cerrahpasa Med Fac Dept Med Oncol TR-34130 Istanbul Turkey;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学 ;
  • 关键词

    BRAF mutant; dabrafenib; trametinib; melanoma; sarcopenia; vemurafenib; cobimetinib;

    机译:漂亮的突变体;Dunarafenib;Trantinib;黑色素瘤;Sarcopenia;vemurafenib;cobimetinib;

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