Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka, Japan
Medical Information Center, Kyushu University, Fukuoka, Japan.
BMJ Open. 2022 Jun 8;12(6):e061674. doi: 10.1136/bmjopen-2022-061674.
Immunotherapy is the fourth leading therapy for lung cancer following surgery, chemotherapy and radiotherapy. Recently, several studies have reported about the potential association between the gut microbiome and therapeutic response to immunotherapy. Nevertheless, the specific composition of the gut microbiome or combination of gut microbes that truly predict the efficacy of immunotherapy is not definitive.
The present multicentre, prospective, observational study aims to discover the specific composition of the gut microbiome or combination of gut microbes predicting the therapeutic response to immunotherapy in lung cancer using artificial intelligence. The main inclusion criteria are as follows: (1) pathologically or cytologically confirmed metastatic or postoperative recurrent lung cancer including non-small cell lung cancer and small cell lung cancer; (2) age≥20 years at the time of informed consent; (3) planned treatment with immunotherapy including combination therapy and monotherapy, as the first-line immunotherapy; and (4) ability to provide faecal samples. In total, 400 patients will be enrolled prospectively. Enrolment will begin in 2021, and the final analyses will be completed by 2024.
The study protocol was approved by the institutional review board of each participating centre in 2021 (Kyushu Cancer Center, IRB approved No. 2021-13, 8 June 2021 and Kyushu Medical Center, IRB approved No. 21-076, 31 August 2021). Study results will be disseminated through peer-reviewed journals and national and international conferences.
UMIN000046428.
免疫疗法是继手术、化疗和放疗之后肺癌的第四大主要疗法。最近,有几项研究报告了肠道微生物组与免疫治疗反应之间的潜在关联。然而,真正预测免疫治疗疗效的肠道微生物组的具体组成或肠道微生物组合尚不确定。
本项多中心、前瞻性、观察性研究旨在使用人工智能发现预测肺癌免疫治疗疗效的肠道微生物组的具体组成或肠道微生物组合。主要纳入标准如下:(1)经病理或细胞学证实的转移性或术后复发性肺癌,包括非小细胞肺癌和小细胞肺癌;(2)在获得知情同意时年龄≥20 岁;(3)计划接受免疫治疗,包括联合治疗和单药治疗,作为一线免疫治疗;(4)能够提供粪便样本。总共将前瞻性纳入 400 例患者。招募工作将于 2021 年开始,最终分析将于 2024 年完成。
本研究方案于 2021 年获得各参与中心的机构审查委员会批准(九州癌症中心,IRB 批准编号 2021-13,2021 年 6 月 8 日和九州医疗中心,IRB 批准编号 21-076,2021 年 8 月 31 日)。研究结果将通过同行评议的期刊和国内外会议进行传播。
UMIN000046428。