TY - JOUR
T1 - The efficacy and safety of anamorelin among patients with diabetes
AU - Ando, Kenju
AU - Naito, Tateaki
AU - Hamauchi, Satoshi
AU - Miura, Keita
AU - Nishibori, Yuichiro
AU - Tonsho, Ayumi
AU - Matsuda, Suguru
AU - Morita, Meiko
AU - Sekikawa, Motoki
AU - Doshita, Kosei
AU - Kodama, Hiroaki
AU - Yabe, Michitoshi
AU - Morikawa, Noboru
AU - Iida, Yuko
AU - Mamesaya, Nobuaki
AU - Kobayashi, Haruki
AU - Ryo, Ko
AU - Wakuda, Kazushige
AU - Ono, Akira
AU - Kenmotsu, Hirotsugu
AU - Murakami, Haruyasu
AU - Yamazaki, Kentaro
AU - Takahashi, Toshiaki
N1 - Publisher Copyright:
© The Author(s) under exclusive licence to Japan Society of Clinical Oncology 2024.
PY - 2024/8
Y1 - 2024/8
N2 - Background: Anamorelin is a selective ghrelin receptor agonist approved for cancer cachexia in Japan. Little is known about predictors of anamorelin efficacy. This study aimed to assess the effect of diabetes on the efficacy and safety of anamorelin in patients with cancer cachexia. Methods: Medical records of patients with advanced non-small-cell lung, gastric, pancreatic, or colorectal cancer who received anamorelin between January 2021 and March 2023 were retrospectively reviewed. The diabetic (DM) group included patients with a confirmed diagnosis of type 2 diabetes mellitus, random plasma glucose of ≥ 200 mg/dL, or hemoglobin A1c of ≥ 6.5%. The maximum body weight gain and adverse events during anamorelin administration were compared between the DM and non-DM groups. Patients with a maximum body weight gain ≥ 0 kg were classified as the responders. Results: Of 103 eligible patients, 31 (30.1%) were assigned to the DM group. The DM group gained less weight (median of −0.53% vs. + 3.00%, p < 0.01) and had fewer responders (45.2% vs. 81.9%, p < 0.01) than the non-DM group. The odds ratio for non-response in the DM group was 6.55 (95% confidential interval 2.37–18.06, p < 0.01), adjusted by age and performance status. The DM group had a higher cumulative incidence of hyperglycaemic adverse events (72.2% vs. 6.3%, p < 0.01) and more discontinuations due to hyperglycaemic adverse events (25.8% vs. 4.2%, p < 0.01) than the non-DM group. Conclusions: Patients with diabetes and cancer cachexia are less likely to gain weight with anamorelin despite a high risk of hyperglycaemic adverse events.
AB - Background: Anamorelin is a selective ghrelin receptor agonist approved for cancer cachexia in Japan. Little is known about predictors of anamorelin efficacy. This study aimed to assess the effect of diabetes on the efficacy and safety of anamorelin in patients with cancer cachexia. Methods: Medical records of patients with advanced non-small-cell lung, gastric, pancreatic, or colorectal cancer who received anamorelin between January 2021 and March 2023 were retrospectively reviewed. The diabetic (DM) group included patients with a confirmed diagnosis of type 2 diabetes mellitus, random plasma glucose of ≥ 200 mg/dL, or hemoglobin A1c of ≥ 6.5%. The maximum body weight gain and adverse events during anamorelin administration were compared between the DM and non-DM groups. Patients with a maximum body weight gain ≥ 0 kg were classified as the responders. Results: Of 103 eligible patients, 31 (30.1%) were assigned to the DM group. The DM group gained less weight (median of −0.53% vs. + 3.00%, p < 0.01) and had fewer responders (45.2% vs. 81.9%, p < 0.01) than the non-DM group. The odds ratio for non-response in the DM group was 6.55 (95% confidential interval 2.37–18.06, p < 0.01), adjusted by age and performance status. The DM group had a higher cumulative incidence of hyperglycaemic adverse events (72.2% vs. 6.3%, p < 0.01) and more discontinuations due to hyperglycaemic adverse events (25.8% vs. 4.2%, p < 0.01) than the non-DM group. Conclusions: Patients with diabetes and cancer cachexia are less likely to gain weight with anamorelin despite a high risk of hyperglycaemic adverse events.
KW - Anamorelin
KW - Cancer cachexia
KW - Diabetes
KW - Hyperglycaemia
UR - https://www.scopus.com/pages/publications/85192444116
U2 - 10.1007/s10147-024-02546-8
DO - 10.1007/s10147-024-02546-8
M3 - Article
C2 - 38722487
AN - SCOPUS:85192444116
SN - 1341-9625
VL - 29
SP - 1115
EP - 1121
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 8
ER -