Department of Medical Oncology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Laboratory of Clinical and Analytical Chemistry, Ritsumeikan University College of Pharmaceutical Sciences, Shiga, Japan.
JAMA Netw Open. 2020 Apr 1;3(4):e202895. doi: 10.1001/jamanetworkopen.2020.2895.
Immunotherapy using immune checkpoint inhibitors has been remarkably effective for treating multiple cancer types, and the gut microbiome is a possible factor affecting immune checkpoint inhibitor efficacy. However, the association between the gut microbiome and immune status of the tumor microenvironment remains unclear. Short-chain fatty acids (SCFAs) are major end product metabolites produced by the gut microbiota and have wide-ranging impacts on host physiology.
To evaluate fecal and plasma SCFAs in patients with solid cancer tumors treated with programmed cell death-1 inhibitors (PD-1i).
DESIGN, SETTING, AND PARTICIPANTS: This was a prospective cohort biomarker study of patients with cancer who planned therapy with PD-1i at Kyoto University Hospital between July 2016 and February 2019. Data were analyzed from October 2019 to February 2020.
Patients who were treated with nivolumab or pembrolizumab were classified into 2 groups based on their treatment response using Response Evaluation Criteria in Solid Tumors version 1.1: responders who achieved an objective response and nonresponders. Dietary information in terms of intake frequency was obtained. Concentrations of SCFAs in fecal and plasma samples collected before PD-1i administration were measured using ultra-high-performance liquid chromatography coupled with tandem mass spectrometry.
The concentration of SCFAs and progression-free survival.
Among 52 patients enrolled, the median (range) patient age was 67 (27-84) years, and 23 (44%) were women. Median (range) duration of follow-up of the survivors after administration of PD-1i was 2.0 (0.4-4.1) years. The overall response rate was 28.8%. High concentrations of some SCFAs were associated with longer progression-free survival. These included fecal acetic acid (hazard ratio [HR], 0.29; 95% CI, 0.15-0.54), propionic acid (HR, 0.08; 95% CI, 0.03-0.20), butyric acid (HR, 0.31; 95% CI, 0.16-0.60), valeric acid (HR, 0.53; 95% CI, 0.29-0.98), and plasma isovaleric acid (HR, 0.38; 95% CI, 0.14-0.99).
Results of this study suggest that fecal SCFA concentrations may associated with PD-1i efficacy; thus, SCFAs may be the link between the gut microbiota and PD-1i efficacy. Because fecal examinations are completely noninvasive, they may be applicable for routine monitoring of patients.
免疫检查点抑制剂的免疫疗法在治疗多种癌症类型方面已取得显著成效,而肠道微生物组可能是影响免疫检查点抑制剂疗效的一个因素。然而,肠道微生物组与肿瘤微环境免疫状态之间的联系仍不清楚。短链脂肪酸(SCFAs)是肠道微生物群产生的主要终产物代谢物,对宿主生理学有广泛的影响。
评估接受程序性细胞死亡蛋白-1 抑制剂(PD-1i)治疗的实体瘤患者的粪便和血浆 SCFAs。
设计、地点和参与者:这是一项在京都大学医院接受 PD-1i 治疗的癌症患者的前瞻性队列生物标志物研究,时间为 2016 年 7 月至 2019 年 2 月。数据分析于 2019 年 10 月至 2020 年 2 月进行。
根据使用实体瘤反应评价标准 1.1 对接受纳武单抗或帕博丽珠单抗治疗的患者进行反应评估:达到客观缓解的应答者和未达到客观缓解的应答者。以摄入频率的形式获得饮食信息。使用超高效液相色谱-串联质谱法测量 PD-1i 给药前采集的粪便和血浆样本中 SCFAs 的浓度。
SCFA 浓度和无进展生存期。
在纳入的 52 名患者中,中位(范围)患者年龄为 67(27-84)岁,23 名(44%)为女性。PD-1i 给药后幸存者的中位(范围)随访时间为 2.0(0.4-4.1)年。总体缓解率为 28.8%。一些 SCFAs 的高浓度与无进展生存期延长相关。这些包括粪便乙酸(HR,0.29;95%CI,0.15-0.54)、丙酸(HR,0.08;95%CI,0.03-0.20)、丁酸(HR,0.31;95%CI,0.16-0.60)、戊酸(HR,0.53;95%CI,0.29-0.98)和血浆异戊酸(HR,0.38;95%CI,0.14-0.99)。
本研究结果表明,粪便 SCFA 浓度可能与 PD-1i 疗效相关;因此,SCFAs 可能是肠道微生物组与 PD-1i 疗效之间的联系。由于粪便检查是完全无创的,因此它们可能适用于患者的常规监测。