TY - JOUR
T1 - Anamorelin (ONO-7643) for the treatment of patients with non–small cell lung cancer and cachexia
T2 - Results from a randomized, double-blind, placebo-controlled, multicenter study of Japanese patients (ONO-7643-04)
AU - Katakami, Nobuyuki
AU - Uchino, Junji
AU - Yokoyama, Takuma
AU - Naito, Tateaki
AU - Kondo, Masashi
AU - Yamada, Kouzo
AU - Kitajima, Hiromoto
AU - Yoshimori, Kozo
AU - Sato, Kazuhiro
AU - Saito, Hiroshi
AU - Aoe, Keisuke
AU - Tsuji, Tetsuya
AU - Takiguchi, Yuichi
AU - Takayama, Koichi
AU - Komura, Naoyuki
AU - Takiguchi, Toru
AU - Eguchi, Kenji
N1 - Funding Information:
Nobuyuki Katakami reports personal fees from AstraZeneca, Eli Lilly, Pfizer, Boehringer Ingelheim, Ono, Taiho, and Novartis Pharma KK and grants from MSD, Astellas, AstraZeneca, Eisai, Amgen, Shionogi, Daiichi Sankyo, Chugai, Eli Lilly, Boehringer Ingelheim, Bristol-Myers Squibb, Maruishi, and Merck Serono outside the submitted work. Tateaki Naito reports personal fees from Ono during the conduct of the study. Masashi Kondo reports personal fees from Ono, Chugai, Pfizer, Novartis, Eli Lilly, Taiho, and AstraZeneca and grants from Eli Lilly outside the submitted work. Hiroshi Saito reports personal fees from Ono during the conduct of the study; grants from Taiho and Merck Serono outside the submitted work; and personal fees from Pfizer, AstraZeneca, and Kyowa Hakko Kirin outside the submitted work. Yuichi Takiguchi reports grants and personal fees from Ono, AstraZeneca, Taiho, Nippon Boehringer Ingelheim, and Chugai outside the submitted work. Koichi Takayama reports personal fees from Ono during the conduct of the study and personal fees from AstraZeneca, Eli Lilly, Chugai, and Ono outside the submitted work. Naoyuki Komura and Toru Takiguchi are employees of Ono. Kenji Eguchi reports grants from Ono outside the submitted work.
Publisher Copyright:
© 2017 American Cancer Society
PY - 2018/2/1
Y1 - 2018/2/1
N2 - BACKGROUND: 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. METHODS: 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. 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. CONCLUSIONS: 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.
AB - BACKGROUND: 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. METHODS: 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. 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. CONCLUSIONS: 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.
KW - anamorelin (ONO-7643)
KW - cachexia
KW - lean body mass
KW - non–small cell lung cancer
KW - randomized controlled trial
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UR - http://www.scopus.com/inward/citedby.url?scp=85037640798&partnerID=8YFLogxK
U2 - 10.1002/cncr.31128
DO - 10.1002/cncr.31128
M3 - Article
C2 - 29205286
AN - SCOPUS:85037640798
SN - 0008-543X
VL - 124
SP - 606
EP - 616
JO - Cancer
JF - Cancer
IS - 3
ER -