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一项关于在脑转移瘤患者中添加辛伐他汀至全脑放射治疗的随机对照开放标签试点研究。

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

作者信息

El-Hamamsy Manal, Elwakil Hesham, Saad Amr S, Shawki May A

机构信息

Clinical Pharmacy, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.

出版信息

Oncol Res. 2016 Oct 27;24(6):521-528. doi: 10.3727/096504016X14719078133528.

DOI:10.3727/096504016X14719078133528
PMID:28281972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7838650/
Abstract

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.

摘要

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。

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