TY - JOUR
T1 - A multicenter, open-label, single-arm study of anamorelin (ONO-7643) in patients with cancer cachexia and low body mass index
AU - Naito, Tateaki
AU - Uchino, Junji
AU - Kojima, Toru
AU - Matano, Yutaka
AU - Minato, Koichi
AU - Tanaka, Kentaro
AU - Mizukami, Takuro
AU - Atagi, Shinji
AU - Higashiguchi, Takashi
AU - Muro, Kei
AU - Takayama, Koichi
AU - Furuse, Junji
AU - Morishima, Eiichiro
AU - Takiguchi, Toru
AU - Tamura, Kazuo
N1 - Funding Information:
Qualified researchers may ask Ono Pharmaceutical Co, Ltd, to disclose individual patient-level data from clinical studies through the following website: https://www.clinicalstudydatarequest.com/. For more information on Ono Pharmaceutical's policy for the disclosure of clinical study data, please see the following website: https://www.ono.co.jp/eng/rd/policy.html. Tateaki Naito reports lecture fees and travel expenses from Ono Pharmaceutical, institutional research funds from Ono Pharmaceutical in relation to this work, and institutional research funds from Otsuka Pharmaceutical outside the submitted work. Junji Uchino, Toru Kojima, Yutaka Matano, Koichi Minato, Kentaro Tanaka, Takuro Mizukami, and Shinji Atagi report institutional research funds from Ono Pharmaceutical in relation to this work. Kentaro Tanaka reports institutional research funds from Ono Pharmaceutical in relation to this work and honoraria from AstraZeneca and Chugai outside the submitted work. Takuro Mizukami reports institutional research funds from Ono Pharmaceutical in relation to this work; institutional research funds from Taiho Pharmaceutical and Eli Lilly outside the submitted work; and honoraria from Taiho Pharmaceutical, Chugai, Bayer, Merck Serono, Takeda, Eli Lilly, Asahi Kasei, Otsuka Pharmaceutical, Bristol-Myers Squibb, and Ono Pharmaceutical outside the submitted work. Shinji Atagi reports institutional research funds from Ono Pharmaceutical in relation to this work; research grants from AstraZeneca, Eli Lilly, Ono Pharmaceutical, Taiho Pharmaceutical, Boehringer Ingelheim, Pfizer, Bristol-Myers Squibb, MSD, Chugai, Merck, and F. Hoffmann-La Roche outside the submitted work; honoraria from AstraZeneca, Eli Lilly, Ono Pharmaceutical, Taiho Pharmaceutical, Boehringer Ingelheim, Pfizer, Bristol-Myers Squibb, Hisamitsu, MSD, Chugai, Kyowa Hakko Kirin, Merck, Novartis Pharma, and Thermo Fisher Scientific outside the submitted work; and other financial or nonfinancial interests in F. Hoffmann-La Roche outside the submitted work. Takashi Higashiguchi reports consultancy fees and travel expenses from Ono Pharmaceutical outside the submitted work. Kei Muro reports consultancy fees, lecture fees, and travel expenses from Ono Pharmaceutical in relation to this work; institutional research funds from Solasia Pharma, Merck Serono, Daiichi Sankyo, Parexel International, Pfizer, MSD, Amgen, Sanofi, and Taiho Pharmaceutical outside the submitted work; consultancy fees from Amgen, Ono Pharmaceutical, and AstraZeneca outside the submitted work; and honoraria from Ono Pharmaceutical, Sanofi, Taiho Pharmaceutical, Chugai Pharma, Takeda, Eli Lily, Bristol-Myers Squibb, and Bayer outside the submitted work. Koichi Takayama reports consultancy fees, lecture fees, travel expenses, and institutional research funds from Ono Pharmaceutical in relation to this work; institutional research funds from Ono Pharmaceutical, Taiho Pharmaceutical Co, Eli Lilly, and Fukuda Lifetech Co outside the submitted work; lectures fees from Ono Pharmaceutical, AstraZeneca, MSD, Chugai-Roche, Eli Lilly, and Boehringer Ingelheim outside the submitted work; and travel expenses from Ono Pharmaceutical outside the submitted work. Junji Furuse reports consultancy fees, lecture fees, travel expenses, and institutional research funds from Ono Pharmaceutical in relation to this work; institutional research funds from Ono Pharmaceutical, MSD, Merck Bio, J-Pharma, Taiho Pharmaceutical, Takeda, Chugai Pharma, Astra Zeneca, Yakult Honsha, Eisai, Daiichi Sankyo, Mochida, Sanofi, Sumitomo Dainippon Bayer, Astellas, and Incyte Japan outside the submitted work; and honoraria or personal fees from Ono Pharmaceutical, Bayer, Eisai, Eli Lilly Japan, MSD, Yakult Honsha, Chugai Pharma, Novartis Pharma, Astra Zeneca, Pfizer, Takeda, Taiho Pharmaceutical, Sanofi, Mylan EPD, EA Pharma, Kyowa Hakko Kirin, Daiichi Sankyo, Teijin Pharma, Servier Japan, and Incyte Japan outside the submitted work. Eiichiro Morishima and Toru Takiguchi are employees of Ono Pharmaceutical. Kazuo Tamura reports consultancy fees, lecture fees, and travel expenses from Ono Pharmaceutical in relation to this work; consultancy fees from AC Medical outside the submitted work; and participation on advisory boards for Symbio and Eisai outside the submitted work. This work was funded by Ono Pharmaceutical Co, Ltd.
Funding Information:
We thank all the patients and their families, investigators, and site staff who participated in the current study. We also thank Nicholas D. Smith (EMC KK) for medical writing support, which was funded by Ono Pharmaceutical Co, Ltd.
Publisher Copyright:
© 2022 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society.
PY - 2022/5/15
Y1 - 2022/5/15
N2 - Background: Cancer cachexia is a syndrome characterized by anorexia and decreased body weight. This study evaluated the efficacy and safety of anamorelin, an orally active, selective ghrelin receptor agonist, in patients with cancer cachexia and a low body mass index (BMI). Methods: This multicenter, open-label, single-arm study enrolled Japanese patients with non–small cell lung cancer or gastrointestinal cancer with cancer cachexia (BMI < 20 kg/m2, involuntary weight loss > 2% in the last 6 months, and anorexia). Patients were administered 100 mg of anamorelin once daily for up to 24 weeks. The primary end point was a composite clinical response (CCR) at 9 weeks, which was defined as an increase in body weight of ≥5% from the baseline, an increase of ≥2 points in the score of the 5-item Anorexia Symptom Scale of the Functional Assessment of Anorexia/Cachexia Therapy, and being alive. Results: One hundred two patients were eligible and enrolled. The means and standard deviations for age and BMI were 71.0 ± 8.2 years and 17.47 ± 1.48 kg/m2, respectively. The CCR rate at 9 weeks was 25.9% (95% confidence interval [CI], 18.3%-35.3%), which met the primary end point with a lower 95% CI exceeding the prespecified minimum of 8%. Improvements in body weight and anorexia were durable and were accompanied by improvements in patients' global impression of change for appetite/eating-related symptoms and overall condition. Adverse drug reactions occurred in 37 of 101 treated patients (36.6%), with the most common being glycosylated hemoglobin increases, constipation, and peripheral edema. Conclusions: Anamorelin improved body weight and anorexia-related symptoms in patients with cancer cachexia and a low BMI with durable efficacy and favorable safety and tolerability. Lay Summary: Anamorelin is a drug that stimulates appetite and promotes weight gain. This clinical trial was aimed at determining its efficacy and safety in Japanese cancer patients with a low body mass index and cachexia, a syndrome associated with anorexia and weight loss. Anamorelin was found to improve body weight and anorexia-related symptoms in these patients, and these effects were durable for up to 24 weeks. Moreover, anamorelin was generally well tolerated. These findings suggest that anamorelin is a valuable treatment option for patients with cancer cachexia and a low body mass index.
AB - Background: Cancer cachexia is a syndrome characterized by anorexia and decreased body weight. This study evaluated the efficacy and safety of anamorelin, an orally active, selective ghrelin receptor agonist, in patients with cancer cachexia and a low body mass index (BMI). Methods: This multicenter, open-label, single-arm study enrolled Japanese patients with non–small cell lung cancer or gastrointestinal cancer with cancer cachexia (BMI < 20 kg/m2, involuntary weight loss > 2% in the last 6 months, and anorexia). Patients were administered 100 mg of anamorelin once daily for up to 24 weeks. The primary end point was a composite clinical response (CCR) at 9 weeks, which was defined as an increase in body weight of ≥5% from the baseline, an increase of ≥2 points in the score of the 5-item Anorexia Symptom Scale of the Functional Assessment of Anorexia/Cachexia Therapy, and being alive. Results: One hundred two patients were eligible and enrolled. The means and standard deviations for age and BMI were 71.0 ± 8.2 years and 17.47 ± 1.48 kg/m2, respectively. The CCR rate at 9 weeks was 25.9% (95% confidence interval [CI], 18.3%-35.3%), which met the primary end point with a lower 95% CI exceeding the prespecified minimum of 8%. Improvements in body weight and anorexia were durable and were accompanied by improvements in patients' global impression of change for appetite/eating-related symptoms and overall condition. Adverse drug reactions occurred in 37 of 101 treated patients (36.6%), with the most common being glycosylated hemoglobin increases, constipation, and peripheral edema. Conclusions: Anamorelin improved body weight and anorexia-related symptoms in patients with cancer cachexia and a low BMI with durable efficacy and favorable safety and tolerability. Lay Summary: Anamorelin is a drug that stimulates appetite and promotes weight gain. This clinical trial was aimed at determining its efficacy and safety in Japanese cancer patients with a low body mass index and cachexia, a syndrome associated with anorexia and weight loss. Anamorelin was found to improve body weight and anorexia-related symptoms in these patients, and these effects were durable for up to 24 weeks. Moreover, anamorelin was generally well tolerated. These findings suggest that anamorelin is a valuable treatment option for patients with cancer cachexia and a low body mass index.
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U2 - 10.1002/cncr.34154
DO - 10.1002/cncr.34154
M3 - Article
C2 - 35195274
AN - SCOPUS:85125091380
SN - 0008-543X
VL - 128
SP - 2025
EP - 2035
JO - Cancer
JF - Cancer
IS - 10
ER -