Asakura Masanori, Yamamoto Haruko, Asai Kuniya, Hanatani Akihisa, Hirata Ken-ichi, Hirayakma Atsushi, Kimura Kazuo, Kobayashi Youichi, Momomura Shin-ichi, Nakagawa Yoshihisa, Nishi Yutaro, Saito Yoshihiko, Satoh Yasuhiro, Yamada Takahisa, Yamashina Akira, Yasuda Satoshi, Yoshikawa Tsutomu, Kada Akiko, Uesaka Hiroyuki, Kitakaze Masafumi
Department of Clinical Medicine and Development, National Cerebral and Cardiovascular Center, Suita, Japan.
Cardiovasc Drugs Ther. 2015 Apr;29(2):179-85. doi: 10.1007/s10557-014-6565-2.
Aldosterone is one of the major factors to cause organ damage during an acute phase of heart failure (HF), and many reports have demonstrated that patients with acute decompensated HF (ADHF) have high blood aldosterone concentrations, and the high aldosterone concentrations predict poor prognosis in patients with HF. These findings suggest that eplerenone, an antagonist of aldosterone receptors may provide a new concept and strategy for the treatment of ADHF, protecting the heart and other organs during chronic phases, depending on the restoration of hemodynamic abnormalities.
EARLIER is an event-driven clinical trial with an estimated enrolment of 300 patients hospitalized with ADHF with reduced left ventricular ejection fraction. ADHF includes ischemic or non-ischemic HF, and patients can be enrolled within 72 h after the visit to the hospital. We randomize the patients taking standard therapies for ADHF to the eplerenone and placebo groups. Eplerenone, either 25 or 50 mg, is administered for 6 months in the eplerenone group, and the corresponding placebo is administered in the placebo group on top of the standard care. We set the primary endpoint as the incidence of the composite endpoint (cardiac death or first re-hospitalization due to cardiac disease) 6 months after the enrollment, and also check the quality of life, i.e., exercise capacity and safety features of eplerenone.
EARLIER is a clinical trial of eplerenone targeting ADHF and also the first multicenter investigator-initiated phase III trial in the cardiovascular field in Japan, funded by the Japanese government.
醛固酮是导致心力衰竭(HF)急性期器官损伤的主要因素之一,许多报告表明,急性失代偿性心力衰竭(ADHF)患者的血醛固酮浓度较高,且高醛固酮浓度预示着HF患者预后不良。这些发现表明,醛固酮受体拮抗剂依普利酮可能为ADHF的治疗提供新的理念和策略,在慢性期保护心脏和其他器官,这取决于血流动力学异常的恢复情况。
EARLIER是一项事件驱动的临床试验,预计招募300例因ADHF住院且左心室射血分数降低的患者。ADHF包括缺血性或非缺血性HF,患者可在入院72小时内入组。我们将接受ADHF标准治疗的患者随机分为依普利酮组和安慰剂组。依普利酮组给予25或50mg依普利酮治疗6个月,安慰剂组在标准治疗基础上给予相应安慰剂。我们将主要终点设定为入组6个月后复合终点(心源性死亡或因心脏病首次再次住院)的发生率,并同时检查依普利酮的生活质量,即运动能力和安全性。
EARLIER是一项针对ADHF的依普利酮临床试验,也是日本心血管领域首个由多中心研究者发起的III期试验,由日本政府资助。