Department of Respiratory Medicine, Saitama Cardiovascular and Respiratory Center, 1696 Itai, Kumagaya, Saitama, 360-0197, Japan.
Department of Respiratory Medicine, Saitama Cardiovascular and Respiratory Center, 1696 Itai, Kumagaya, Saitama, 360-0197, Japan.
Respir Investig. 2024 Nov;62(6):951-959. doi: 10.1016/j.resinv.2024.08.013. Epub 2024 Aug 25.
Proton pump inhibitors (PPIs) are reported to decrease the efficacy of immune checkpoint inhibitors (ICIs), but there are few reports on the association between ICI efficacy and antacids other than PPIs, and simultaneous examination of the effects of antacids, corticosteroids, and non-steroidal anti-inflammatory drugs (NSAIDs) on ICI therapy.
We conducted a retrospective study of 381 patients with non-small cell lung cancer who received ICI therapy from January 1, 2016 to December 31, 2022. The primary endpoint was overall survival (OS) and the secondary endpoint was progression-free survival (PFS). Antacids included histamine type 2 receptor antagonists (H2RAs), PPIs, and potassium-competitive acid blockers (P-CABs).
Antacids were administered to 218 patients, including 168 with PPIs, 37 with P-CABs, and 13 with H2RAs. Patients with antacids had worse median PFS and OS than those without antacids (PFS, 2.9 vs. 6.2 months; OS, 12.3 vs. 24.0 months), and those with PPIs, P-CABs, or H2RAs had similar results. However, there were no significant differences between patients with and without antacids when stratified by corticosteroid and NSAID use. Multivariate analyses showed that corticosteroids and NSAIDs administered for cancer-associated symptoms were related to poor prognosis, but antacids including PPIs, P-CABs, or H2RAs were not related.
Antacids were not related to ICI efficacy when NSAIDs or corticosteroids were taken into consideration. This may be because the most frequent reason for administering NSAIDs and corticosteroids was cancer-associated symptoms, which are a poor prognostic factor, and most of the patients treated with these medications also received antacids.
质子泵抑制剂(PPIs)被报道会降低免疫检查点抑制剂(ICI)的疗效,但关于除 PPIs 以外的抗酸剂与 ICI 疗效之间的关系的报告较少,同时检查抗酸剂、皮质类固醇和非甾体抗炎药(NSAIDs)对 ICI 治疗的影响的研究也较少。
我们对 2016 年 1 月 1 日至 2022 年 12 月 31 日期间接受 ICI 治疗的 381 例非小细胞肺癌患者进行了回顾性研究。主要终点是总生存期(OS),次要终点是无进展生存期(PFS)。抗酸剂包括 H2 受体拮抗剂(H2RAs)、PPIs 和钾竞争酸阻滞剂(P-CABs)。
218 例患者使用了抗酸剂,其中 168 例使用了 PPIs,37 例使用了 P-CABs,13 例使用了 H2RAs。使用抗酸剂的患者的中位 PFS 和 OS 均劣于未使用抗酸剂的患者(PFS,2.9 个月 vs. 6.2 个月;OS,12.3 个月 vs. 24.0 个月),且使用 PPIs、P-CABs 或 H2RAs 的患者也得到了类似的结果。然而,当按皮质类固醇和 NSAID 使用情况分层时,使用抗酸剂的患者和未使用抗酸剂的患者之间无显著差异。多变量分析显示,用于治疗癌症相关症状的皮质类固醇和 NSAIDs 与不良预后相关,但包括 PPIs、P-CABs 或 H2RAs 在内的抗酸剂与不良预后无关。
在考虑到 NSAIDs 或皮质类固醇的情况下,抗酸剂与 ICI 疗效无关。这可能是因为使用 NSAIDs 和皮质类固醇的最常见原因是癌症相关症状,这是一个预后不良的因素,而且大多数接受这些药物治疗的患者也同时使用了抗酸剂。