Klinik für Pneumologie, Kardiologie und Internistische Intensivmedizin, Florence-Nightingale-Krankenhaus, Kreuzbergstr. 79, 40489, Düsseldorf, Germany.
J Cancer Res Clin Oncol. 2023 Aug;149(9):5915-5919. doi: 10.1007/s00432-022-04567-0. Epub 2023 Jan 3.
The choice between immunotherapy with a checkpoint inhibitor (CPI) and chemo-/immunotherapy (CIT) in patients with NSCLC stage IV is often discussed. There are some data that the effect of CPI therapy is impaired by antimicrobial therapy (AMT). Little is known about the influence of AMT on CIT.
We retrospectively analysed 114 patients (age 68 ± 8.5 years) with NSCLC stage IV. Patients were treated according to the guidelines with either CPI alone (pembrolizumab, nivolumab, atezolizumab, cemiplimab) or CIT (Carboplatin/Pemetrexed/Pembrolizumab, Carboplatin/Paclitaxel/Pembrolizumab). We registered patients' characteristics including presence and timing of AMT. Group 1 consisted of 42 patients with AMT in the month before CPI or CIT, group 2 were 49 patients with AMT during CPI or CIT, and group 3 were 64 patients without AMT and CPI or CIT.
Group 1-3 showed comparable patients characteristics. Using cox-regression analysis, we found that AMT in the month before CPI resulted in a decreased progression-free survival (PFS) compared to patients with CPI and no AMT (14 ± 1.02 vs. 4 ± 1.02 months, p = 0.002, 95% CI 1.88-9). In patients, who were treated with CIT, there was no difference in PFS in those with or without AMT in the month before therapy (10 ± 2.5 vs. 6 ± 1.2 months, p = 0.7). Interestingly, AMT during CIT or CPI therapy showed no effect on PFS.
In a real-life setting, we found that AMT reduces PFS when given in the month before CIT therapy. AMT before or during CIT does not seem to influence PFS. As a consequence, AMT before start of therapy might be a factor that could lead to a preference of CIT instead of CPI in NSCLC stage IV patients.
在 IV 期非小细胞肺癌(NSCLC)患者中,免疫检查点抑制剂(CPI)与化疗/免疫治疗(CIT)的选择经常被讨论。有一些数据表明,抗菌治疗(AMT)会影响 CPI 治疗的效果。然而,关于 AMT 对 CIT 的影响知之甚少。
我们回顾性分析了 114 例 IV 期 NSCLC 患者(年龄 68±8.5 岁)。根据指南,患者接受了单独 CPI(pembrolizumab、nivolumab、atezolizumab、cemiplimab)或 CIT(卡铂/培美曲塞/帕博利珠单抗、卡铂/紫杉醇/帕博利珠单抗)治疗。我们登记了患者的特征,包括 AMT 的存在和时间。第 1 组包括 42 例在 CPI 或 CIT 前 1 个月接受 AMT 的患者,第 2 组包括 49 例在 CPI 或 CIT 期间接受 AMT 的患者,第 3 组包括 64 例未接受 AMT 和 CPI 或 CIT 的患者。
第 1-3 组患者特征相似。使用 cox 回归分析,我们发现与未接受 AMT 的 CPI 患者相比,CPI 前 1 个月接受 AMT 的患者无进展生存期(PFS)较短(14±1.02 个月 vs. 4±1.02 个月,p=0.002,95%CI 1.88-9)。在接受 CIT 治疗的患者中,治疗前 1 个月接受或未接受 AMT 的患者 PFS 无差异(10±2.5 个月 vs. 6±1.2 个月,p=0.7)。有趣的是,CIT 或 CPI 治疗期间的 AMT 对 PFS 没有影响。
在真实环境中,我们发现 AMT 会降低 CIT 治疗前 1 个月的 PFS。CIT 前或期间的 AMT 似乎不会影响 PFS。因此,治疗前的 AMT 可能是导致 IV 期 NSCLC 患者倾向于选择 CIT 而非 CPI 的一个因素。