Division of Integrated Oncology, Institute of Biomedical Research and Innovation, Kobe, Japan.
Department of Pulmonary Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Cancer. 2018 Feb 1;124(3):606-616. doi: 10.1002/cncr.31128. Epub 2017 Dec 4.
Cachexia, described as weight loss (mainly in lean body mass [LBM]) and anorexia, is common in patients with advanced cancer. This study examined the efficacy and safety of anamorelin (ONO-7643), a novel selective ghrelin receptor agonist, in Japanese cancer patients with cachexia.
This double-blind clinical trial (ONO-7643-04) enrolled 174 patients with unresectable stage III/IV non-small cell lung cancer (NSCLC) and cachexia in Japan. Patients were randomized to daily oral anamorelin (100 mg) or a placebo for 12 weeks. The primary endpoint was the change from the baseline LBM (measured with dual-energy x-ray absorptiometry) over 12 weeks. The secondary endpoints were changes in appetite, body weight, quality of life, handgrip strength (HGS), and 6-minute walk test (6MWT) results.
The least squares mean change (plus or minus the standard error) in LBM from the baseline over 12 weeks was 1.38 ± 0.18 and -0.17 ± 0.17 kg in the anamorelin and placebo groups, respectively (P < .0001). Changes from the baseline in LBM, body weight, and anorexia symptoms showed significant differences between the 2 treatment groups at all time points. Anamorelin increased prealbumin at weeks 3 and 9. No changes in HGS or 6MWT were detected between the groups. Twelve weeks' treatment with anamorelin was safe and well tolerated in NSCLC patients.
Anamorelin significantly increased LBM and improved anorexia symptoms and the nutritional state, but not motor function, in Japanese patients with advanced NSCLC. Because no effective treatment for cancer cachexia is currently available, anamorelin can be a beneficial treatment option. Cancer 2018;124:606-16. © 2017 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
恶病质是一种常见于晚期癌症患者的病症,表现为体重下降(主要是去脂体重 [LBM])和厌食。本研究评估了新型选择性胃饥饿素受体激动剂 anamorelin(ONO-7643)在日本癌症恶病质患者中的疗效和安全性。
这项双盲临床试验(ONO-7643-04)纳入了 174 例日本不可切除的 III/IV 期非小细胞肺癌(NSCLC)合并恶病质患者。患者随机接受每日口服 anamorelin(100mg)或安慰剂治疗 12 周。主要终点为 12 周时基线去脂体重(通过双能 X 射线吸收法测量)的变化。次要终点为食欲、体重、生活质量、握力(HGS)和 6 分钟步行试验(6MWT)结果的变化。
12 周时,去脂体重的最小二乘均数变化(±标准误差)在 anamorelin 组和安慰剂组分别为 1.38±0.18kg 和-0.17±0.17kg(P<0.0001)。两组患者在所有时间点的去脂体重、体重和厌食症状的变化均有显著差异。anamorelin 在第 3 周和第 9 周时升高了前白蛋白。两组患者的 HGS 或 6MWT 均无变化。12 周的 anamorelin 治疗在 NSCLC 患者中安全且耐受良好。
anamorelin 可显著增加去脂体重,改善晚期 NSCLC 患者的厌食症状和营养状况,但对运动功能无影响。由于目前尚无有效的癌症恶病质治疗方法,anamorelin 可能成为一种有益的治疗选择。癌症 2018;124:606-16。© 2017 美国癌症协会。Wiley Periodicals, Inc. 版权所有。这是一篇在知识共享署名-非商业性使用-禁止演绎 4.0 国际许可协议下发布的开放获取文章,在遵守许可协议的前提下,您可以自由复制、传播和展示作品,包括创建衍生作品。