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A Randomized Controlled Open-Label Pilot Study of Simvastatin Addition to Whole-Brain Radiation Therapy in Patients With Brain Metastases

机译:辛伐他汀加全脑放疗对脑转移患者的随机对照开标签试验研究

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Statins have been reported to have a potential radiosensitizing effect that has not been evaluated in clinical trials. The aim of this study was to evaluate the efficacy and safety of simvastatin in addition to whole-brain radiation therapy (WBRT) in patients with brain metastases (BM). A prospective randomized, controlled, open-label pilot study was conducted on 50 Egyptian patients with BM who were randomly assigned to receive 30-Gy WBRT (control group: 25 patients) or 30 Gy WBRT + simvastatin 80 mg/day for the WBRT period (simvastatin group: 25 patients). The primary outcome was radiological response at 4 weeks after WBRT. Secondary outcomes were 1-year progression-free survival (PFS), 1-year overall survival (OS), and health-related quality of life (HRQL) that was assessed using the European Organization for the Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQ-C30) and its brain module (BN-20), at baseline, after WBRT, and 4 weeks after WBRT. The addition of simvastatin was tolerated. Twenty-one patients were not evaluated for radiological response because of death (n = 16), noncompliance to follow-up (n = 4), and clinical deterioration (n = 1). Response rates were 60% and 78.6% (p = 0.427), 1-year PFS rates were 5.2% and 17.7% (p = 0.392), and 1-year OS rates were 12% and 8% (p = 0.880) for the control group and simvastatin group, respectively. Nonsignificant differences were found between the two arms regarding HRQL scales. The addition of simvastatin 80 mg/day did not improve the clinical outcomes of patients with BM receiving WBRT.
机译:据报道他汀类药物具有潜在的放射增敏作用,尚未在临床试验中进行评估。这项研究的目的是评估辛伐他汀与全脑放射治疗(WBRT)以及脑转移瘤(BM)患者的疗效和安全性。在50名埃及BM患者中进行了一项前瞻性随机对照开放性试验研究,他们随机分配接受30 Gy WBRT(对照组:25名患者)或30 Gy WBRT +辛伐他汀80毫克/天,用于WBRT期间(辛伐他汀组:25例)。主要结果是WBRT后4周的放射学反应。次要结局为1年无进展生存期(PFS),1年总生存期(OS)和与健康相关的生活质量(HRQL),这些结果通过欧洲癌症研究和治疗生活质量组织进行评估基线,WBRT后和WBRT后4周,问卷C30(EORTC QLQ-C30)及其脑模块(BN-20)。耐受辛伐他汀的添加。由于死亡(n = 16),不依从随访(n = 4)和临床恶化(n = 1),未对21例患者进行放射学评估。缓解率分别为60%和78.6%(p = 0.427),1年PFS率为5.2%和17.7%(p = 0.392),并且1年OS率为12%和8%(p = 0.880)。对照组和辛伐他汀组。两组之间关于HRQL量表的差异无统计学意义。辛伐他汀80 mg /天的添加量并未改善接受WBRT的BM患者的临床结局。

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