El-Hamamsy Manal, Elwakil Hesham, Saad Amr S, Shawki May A
Clinical Pharmacy, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Oncol Res. 2016 Oct 27;24(6):521-528. doi: 10.3727/096504016X14719078133528.
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.
据报道,他汀类药物具有潜在的放射增敏作用,但尚未在临床试验中进行评估。本研究的目的是评估辛伐他汀联合全脑放射治疗(WBRT)对脑转移瘤(BM)患者的疗效和安全性。对50例埃及BM患者进行了一项前瞻性随机、对照、开放标签的试点研究,这些患者被随机分配接受30 Gy的WBRT(对照组:25例患者)或在WBRT期间接受30 Gy的WBRT加80 mg/天的辛伐他汀(辛伐他汀组:25例患者)。主要结局是WBRT后4周的放射学反应。次要结局是1年无进展生存期(PFS)、1年总生存期(OS)以及使用欧洲癌症研究与治疗组织生活质量问卷C30(EORTC QLQ-C30)及其脑模块(BN-20)在基线、WBRT后和WBRT后4周评估的健康相关生活质量(HRQL)。辛伐他汀的添加是可耐受的。21例患者因死亡(n = 16)、未遵守随访(n = 4)和临床恶化(n = 1)未接受放射学反应评估。对照组和辛伐他汀组的缓解率分别为60%和78.6%(p = 0.427),1年PFS率分别为5.2%和17.7%(p = 0.392),1年OS率分别为12%和8%(p = 0.880)。两组在HRQL量表方面未发现显著差异。每天添加80 mg辛伐他汀并未改善接受WBRT的BM患者的临床结局。