Naldemedine for Opioid-Induced Constipation in Patients With Cancer: A Multicenter, Double-Blind, Randomized, Placebo-Controlled Trial

Author(s): Jun Hamano, MD, PhD1; Takahiro Higashibata, MD, PhD2; Takaomi Kessoku, MD, PhD3,4,5; Shinya Kajiura, MD, PhD6; Mami Hirakawa, MD, PhD7; Shunsuke Oyamada, PhD8; Keisuke Ariyoshi, MMedSci9; Takeshi Yamada, MD, PhD10; Yoshiyuki Yamamoto, MD, PhD11; Yasuyuki Takashima, MPharm10; Kosuke Doki, PhD12; Masato Homma, PhD12; Bryan J. Mathis, PhD, MS13; Tsumugi Jono, MD3,14; Tomoki Ogata, MD3; Kosuke Tanaka, MD3,4; Yuki Kasai, MD3; Michihiro Iwaki, MD, PhD3; Akiko Fuyuki, MD, PhD3,15; Atsushi Nakajima, MD, PhD3; Ryuji Hayashi, MD, PhD6; Takayuki Ando, MD, PhD16; Naoki Izawa, MD, PhD17; Yuko Kobayashi, MSc18; Yoshiki Horie, MD, PhD17; Tatsuya Morita, MD19,20
Source: https://doi.org/10.1200/JCO.24.003

Dr. Maen Hussein's Thoughts

This is another supportive care study that confirms the benefit of Naldemdine in preventing constipation induced by opioids.

PURPOSE

Opioid-induced constipation is the most frequent and non–self-limiting adverse effect of opioid analgesia, reducing adherence and interfering with pain relief. This clinical trial aimed to clarify the preventive effect of naldemedine versus placebo for constipation in patients with cancer starting regularly dosed strong opioids therapy.

METHODS

This multicenter, double-blinded, randomized, placebo-controlled, confirmatory trial was conducted between July 2021 and May 2023 at four academic hospitals in Japan (Japan Registry of Clinical Trials identifier: jRCTs031200397). Patients with cancer starting a first-time regularly dosed strong opioid for cancer pain and age 20+ years were included. Eligible patients were randomly assigned to the naldemedine (Symproic 0.2 mg) or placebo group in a 1:1 ratio for 14 days with protocol treatment. The primary end point was the proportion of patients with a Bowel Function Index (BFI) of <28.8 on day 14. The secondary end points included frequency of spontaneous bowel movements (SBM), quality of life (QOL), and frequency of opioid-induced nausea and vomiting (OINV).

RESULTS

Of the 103 patients assessed for eligibility, 99 received either naldemedine (n = 49) or placebo (n = 50). A BFI of <28.8 on day 14 was significantly more likely to occur in the naldemedine group (64.6%; 95% CI, 51.1 to 78.1) versus placebo (17.0%; 95% CI, 6.3 to 27.8), and the difference between groups was 47.6% (95% CI, 30.3 to 64.8; P < .0001). The frequency of SBM, QOL, and the severity of OINV were nominally significant in the naldemedine group than in the control group.

CONCLUSION

Naldemedine prevented constipation and improved constipation-related QOL, with possible preventive effect on OINV in patients with cancer starting regularly dosed opioids therapy.

Author Affiliations

1Department of Palliative and Supportive Care, Institute of Medicine, University of Tsukuba, Tsukuba, Japan; 2Department of Palliative and Supportive Care, University of Tsukuba Hospital, Tsukuba, Japan; 3Department of Gastroenterology and Hepatology, Yokohama City University Graduate School of Medicine, Yokohama, Japan; 4Department of Gastroenterology, International University Health and Welfare Graduate School of Medicine, Narita, Japan; 5Department of Palliative Medicine and Gastroenterology, International University Health and Welfare Narita Hospital, Narita, Japan; 6Department of Clinical Oncology, University of Toyama, Toyama, Japan; 7Department of Palliative Medicine, St. Marianna University School of Medicine, Kawasaki, Japan; 8Department of Biostatistics, JORTC Data Center, Tokyo, Japan; 9Department of Data Management, JORTC Data Center, Tokyo, Japan; 10Tsukuba Clinical Research & Development Organization (T-CReDO), University of Tsukuba, Tsukuba, Japan; 11Department of Gastroenterology, Institute of Medicine, University of Tsukuba, Tsukuba, Japan; 12Department of Pharmaceutical Sciences, Institute of Medicine, University of Tsukuba, Tsukuba, Japan; 13Department of Cardiovascular Surgery, Institute of Medicine, University of Tsukuba, Tsukuba, Japan; 14Department of Gastroenterology, Yokohama Sakae Kyosai Hospital, Yokohama, Japan; 15Department of Palliative Care, Shinyurigaoka General Hospital, Kawasaki, Japan; 16Third Department of Internal Medicine, University of Toyama, Toyama, Japan; 17Department of Clinical Oncology, St. Marianna University School of Medicine, Kawasaki, Japan; 18Department of Pharmacy, St. Marianna University Hospital, Kawasaki, Japan; 19Department of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu, Japan; 20Research Association for Community Health, Hamamatsu, Japan;

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