Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama, Japan.
Department of Biostatistics, Yokohama City University School of Medicine, Yokohama City, Kanagawa, Japan.
Cancer Prev Res (Phila). 2022 Oct 4;15(10):661-668. doi: 10.1158/1940-6207.CAPR-22-0049.
Leukotriene receptor antagonists (LTRA) are widely used drugs for treating allergic asthma, and they have recently been suggested to have a suppressive effect on carcinogenesis and cancer cell proliferation. Aberrant crypt foci (ACF) are considered a reliable surrogate biomarker of colorectal cancer. This prospective study explored the chemopreventive effect of an LTRA on colonic ACF formation and the safety of the medicine in patients as a pilot trial leading to a colorectal cancer chemoprevention trial. This was a nonrandomized, open-label, controlled trial in patients with colorectal ACFs. The participants were allocated to LTRA or observation groups. Patients in the LTRA group received 10 mg of montelukast orally daily for 8 weeks. After the intervention, colonoscopy was performed to evaluate the changes in the number of ACFs. From November 2017 to March 2020, 40 patients were enrolled. The first 30 were assigned to the LTRA group, and the remaining 10 were assigned to the observation group. In the LTRA group, the mean change in the number of ACFs per patient at 8 weeks from baseline was -2.4 ± 2.2, while the mean change in the observation group was 0.4 ± 2.3 (P = 0.002). There were no severe adverse events. This is the first study to explore the effect of LTRAs against colorectal ACF formation in humans. LTRAs are potential candidates for chemoprevention in colorectal cancer.
We conducted the first LTRA chemoprevention trial for human rectal ACFs, which is considered a surrogate marker of colorectal carcinogenesis. 8-week treatment with LTRA suppressed ACF formation and cell proliferation in colonic epithelium. LTRAs are possible candidates for chemoprevention in colorectal cancer. See related Spotlight, p. 637.
探讨白三烯受体拮抗剂(LTRA)对大肠息肉形成的化学预防作用及其在患者中的安全性,为开展大肠癌化学预防试验提供依据。
非随机、开放标签、对照试验。
2017 年 11 月至 2020 年 3 月在我院接受治疗的大肠息肉患者。
患者被分配到 LTRA 或观察组。LTRA 组患者接受 10mg 孟鲁司特口服,每天 1 次,共 8 周。干预后行结肠镜检查评估息肉数量的变化。
主要结局是 8 周时息肉数量的变化。
共纳入 40 例患者,前 30 例患者被分配到 LTRA 组,其余 10 例患者被分配到观察组。LTRA 组患者 8 周时息肉数量的平均变化为-2.4±2.2,而观察组的平均变化为 0.4±2.3(P=0.002)。LTRA 组未发生严重不良事件。
LTRA 可能是预防大肠癌的候选药物。
本文为《白三烯受体拮抗剂抑制大肠息肉形成的化学预防作用》一文的摘要