Department of Medicine, Division of Hematology/Oncology, University of Virginia, Charlottesville, VA 22903, USA.
School of Medicine, University of Virginia, Charlottesville, VA 22903, USA.
Curr Oncol. 2024 Jan 3;31(1):260-273. doi: 10.3390/curroncol31010017.
Immune checkpoint inhibitors (ICI) have significantly improved outcomes in advanced non-small cell lung cancer (NSCLC). We evaluated the effect of opioid use on outcomes in patients receiving ICI either alone or with chemotherapy. We conducted a retrospective review of 209 patients with advanced NSCLC who received an ICI at the University of Virginia between 1 February 2015 and 1 January 2020. We performed univariate and multivariate analyses to evaluate the impact of opioid use on duration of therapy (DOT) and overall survival (OS). Patients with no or low opioid use (n = 172) had a median DOT of 12.2 months (95% CI: 6.9-17.4) compared to 1.9 months (95% CI: 1.8-2.0) for those with high opioid use (n = 37, HR 0.26 95% CI: 0.17-0.40, < 0.001). Patients with no or low opioid use had a median OS of 22.6 months (95% CI: 14.8-30.4) compared to 3.8 months (95% CI: 2.7-4.9) for those with high opioid use (HR 0.26 95% CI: 0.17-0.40 < 0.001). High opioid use was associated with a shorter DOT and worse OS. This difference remained significant when accounting for possible confounding variables. These data warrant investigation of possible mechanistic interactions between opioids, tumor progression, and ICIs, as well as prospective evaluation of opioid-sparing pain management strategies, where possible.
免疫检查点抑制剂(ICI)显著改善了晚期非小细胞肺癌(NSCLC)患者的预后。我们评估了阿片类药物使用对单独或联合化疗接受 ICI 治疗的患者结局的影响。我们对 209 例在弗吉尼亚大学接受 ICI 治疗的晚期 NSCLC 患者进行了回顾性研究,这些患者的治疗时间为 2015 年 2 月 1 日至 2020 年 1 月 1 日。我们进行了单因素和多因素分析,以评估阿片类药物使用对治疗持续时间(DOT)和总生存期(OS)的影响。无或低阿片类药物使用(n = 172)的患者中位 DOT 为 12.2 个月(95%CI:6.9-17.4),而高阿片类药物使用(n = 37)的患者中位 DOT 为 1.9 个月(95%CI:1.8-2.0)(HR 0.26,95%CI:0.17-0.40,<0.001)。无或低阿片类药物使用的患者中位 OS 为 22.6 个月(95%CI:14.8-30.4),而高阿片类药物使用的患者中位 OS 为 3.8 个月(95%CI:2.7-4.9)(HR 0.26,95%CI:0.17-0.40,<0.001)。高阿片类药物使用与 DOT 缩短和 OS 恶化相关。在考虑可能的混杂变量后,这种差异仍然显著。这些数据表明,有必要研究阿片类药物、肿瘤进展和 ICI 之间可能存在的机制相互作用,并尽可能对阿片类药物节约型疼痛管理策略进行前瞻性评估。