Maráz Anikó, Csejtei András, Kocsis Judit, Szűcs Miklós, Kahán Zsuzsanna, Bodoky György, Dank Magdolna, Mangel László, Révész János, Varga Zoltán, Géczi Lajos
Department of Oncotherapy, University of Szeged, Korányi fasor 12, Szeged, 6720, Hungary.
Markusovszky Teaching Hospital, Markusovszky str. 5, Szombathely, Hungary.
Pathol Oncol Res. 2019 Jan;25(1):149-156. doi: 10.1007/s12253-017-0317-0. Epub 2017 Oct 13.
Everolimus is indicated for adults with metastatic renal cell carcinoma (mRCC) after failure of vascular endothelial growth factor receptor-tyrosine kinase inhibitors (TKI). Currently, the therapeutic applicability of EVE has been changing. Multicenter evaluation of efficacy and safety of everolimus in daily routine and definition of patient characteristics with favorable outcome. Data of 165 patients from 9 oncology institutes in Hungary were analyzed retrospectively. Everolimus therapy was used after one TKI in 10 mg starting dose. Physical and laboratory examinations and imaging tests were performed monthly and every 3 months, respectively. Median progression-free survival (PFS) was 5.4 months. Median overall survival (OS) was 16.2 months. PFS and OS results were more favorable in patients with ECOG 0-1 (p = 0.033, p = 0.008) and after >9 months of TKI therapy (p = 0.019, p = 0.045). Survival was longer in nonanemic patients with ECOG 0-1 than in anemic patients with ECOG 2-3, 30.9 and 7.7 months, respectively (p = 0.029). Dose reduction and treatment delay was required in 6.2% and 8.9% of patients, respectively. Common adverse events were exanthema, edema, stomatitis, anemia, and abnormal kidney functions and glucose levels. Results of this study show that everolimus is safe and efficacious in a real-world setting. Everyday practice showed that nonanemic patients with good performance status receiving TKI therapy for >9 months are favorable candidates for this treatment. Despite the efficiency of novel, registered drugs, everolimus still plays an important role during and after second-line therapy for mRCC when availability of modern remedies is limited.
依维莫司适用于血管内皮生长因子受体酪氨酸激酶抑制剂(TKI)治疗失败后的转移性肾细胞癌(mRCC)成人患者。目前,依维莫司的治疗适用性一直在变化。对依维莫司在日常临床中的疗效和安全性进行多中心评估,并确定预后良好的患者特征。回顾性分析了匈牙利9家肿瘤研究所的165例患者的数据。依维莫司治疗在一种TKI治疗失败后使用,起始剂量为10mg。分别每月进行体格检查和实验室检查,每3个月进行影像学检查。中位无进展生存期(PFS)为5.4个月。中位总生存期(OS)为16.2个月。ECOG 0-1患者的PFS和OS结果更优(p = 0.033,p = 0.008),且在TKI治疗>9个月后(p = 0.019,p = 0.045)。ECOG 0-1的非贫血患者的生存期长于ECOG 2-3的贫血患者,分别为30.9个月和7.7个月(p = 0.029)。分别有6.2%和8.9%的患者需要减量和延迟治疗。常见的不良事件有皮疹、水肿、口腔炎、贫血以及肾功能和血糖异常。本研究结果表明,依维莫司在实际临床环境中是安全有效的。日常临床实践表明,体能状态良好的非贫血患者接受TKI治疗>9个月是该治疗的适宜人选。尽管有新型的已注册药物,但在现代治疗手段可及性有限时,依维莫司在mRCC二线治疗期间及之后仍发挥着重要作用。