Hu Da-Hai, Wong Wan-Ching, Zhou Jia-Xin, Luo Ji, Cai Song-Wang, Zhou Hong, Tang Hui
Department of General Surgery, The First Affiliated Hospital of Jinan University, Guangzhou 510632, China.
International School, Jinan University, Guangzhou, Guangdong 510632, China.
J Oncol. 2022 Jul 9;2022:1001796. doi: 10.1155/2022/1001796. eCollection 2022.
To determine if the use of the Proton Pump Inhibitors (PPI) impacts the clinical efficacy of Immune Checkpoint Inhibitors (ICIs) in Non-Small Cell Lung Cancer (NSCLC), a meta-analysis was conducted.
Eleven studies from PubMed, EMBASE, Cochrane Library, Web of Science, and other databases up to May 2022, were selected. The pertinent clinical outcomes were assessed by applying the Progression-free survival (PFS), Overall Survival (OS), Hazard Ratio (HR), and 95% Confidence Interval (CI).
This study included eleven articles containing 7,893 NSCLC patients. The result indicated that PPI use was dramatically related to poor OS (HR: 1.30 [1.10-1.54]), and poor PFS (HR: 1.25 [1.09-1.42]) in case of patients treated with ICIs. With regard to the subgroup analysis, PPI use was dramatically associated with poor OS (Europe: HR = 1.48 [1.26, 1.74], Worldwide: HR = 1.54 [1.24, 1.91]), and poor PFS (Europe: HR = 1.36 [1.18, 1.57], Worldwide: HR = 1.34 [1.16, 1.55]) in patients from Europe and multi-center studies across the world, poor OS in patients with age less than or equal to 65 (HR = 1.56 [1.14, 2.15]), poor PFS in patients aged more than 65 (HR = 1.36 [1.18, 1.57]), poor OS for patients receiving with PD-1 (HR = 1.37 [1.04, 1.79]), poor PFS for patients receiving with PD-L1 (HR = 1.33 [1.19, 1.49]), and poor OS (-30: HR = 1.89 [1.29, 2.78], ±30: HR = 1.44 [1.27, 1.64]) and poor PFS (-30: HR = 1.51 [1.11, 2.05], ±30: HR = 1.32 [1.20, 1.45]) for patients who received PPI at 30 days before and/or after starting the ICIs treatment.
Our meta-analysis indicated that PPI combined with ICIs in the treatment of NSCLC patients could result in poor OS and PFS. PPI use should be extremely cautious in clinical practices to avoid the impact on the efficacy of the ICIs.
为了确定质子泵抑制剂(PPI)的使用是否会影响免疫检查点抑制剂(ICI)在非小细胞肺癌(NSCLC)中的临床疗效,进行了一项荟萃分析。
选取了截至2022年5月来自PubMed、EMBASE、Cochrane图书馆、科学网和其他数据库的11项研究。通过应用无进展生存期(PFS)、总生存期(OS)、风险比(HR)和95%置信区间(CI)来评估相关临床结果。
本研究纳入了11篇文章,共7893例NSCLC患者。结果表明,在接受ICI治疗的患者中,使用PPI与较差的总生存期(HR:1.30 [1.10 - 1.54])和较差的无进展生存期(HR:1.25 [1.09 - 1.42])显著相关。在亚组分析中,在欧洲患者和全球多中心研究中,使用PPI与较差的总生存期(欧洲:HR = 1.48 [1.26, 1.74],全球:HR = 1.54 [1.24, 1.91])和较差的无进展生存期(欧洲:HR = 1.36 [1.18, 1.57],全球:HR = 1.34 [1.16, 1.55])显著相关;年龄小于或等于65岁的患者总生存期较差(HR = 1.56 [1.14, 2.15]),年龄大于65岁的患者无进展生存期较差(HR = 1.36 [1.18, 1.57]);接受PD - 1治疗的患者总生存期较差(HR = 1.37 [1.04, 1.79]),接受PD - L1治疗的患者无进展生存期较差(HR = 1.33 [1.19, 1.49]);在开始ICI治疗前30天内和/或开始ICI治疗后30天内使用PPI的患者总生存期较差(-30:HR = 1.89 [1.29, 2.78],±30:HR = 1.44 [1.27, 1.64])和无进展生存期较差(-30:HR = 1.51 [1.11, 2.05],±30:HR = 1.32 [1.20, 1.45])。
我们的荟萃分析表明,PPI与ICI联合用于治疗NSCLC患者可能会导致较差的总生存期和无进展生存期。在临床实践中使用PPI时应极其谨慎,以避免影响ICI的疗效。