Department of Medical Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 71067Sun Yat-sen University Cancer Center, Guangzhou, China.
Department of Endoscopy, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 71067Sun Yat-sen University Cancer Center, Guangzhou, China.
Cancer Control. 2023 Jan-Dec;30:10732748221148912. doi: 10.1177/10732748221148912.
We aimed to investigate the determinant factors of anti-PD-1 therapy outcome in nasopharyngeal carcinoma (NPC).
In this retrospective study, we included 64 patients with recurrent/metastatic NPC. The association of patients' characteristics, C-reactive protein (CRP), neutrophil to lymphocyte ratio (NLR), and lactate dehydrogenase (LDH) with survival benefit of anti-PD-1 therapy were analyzed using Cox regression models and Kaplan-Meier analyses. Patients were divided based on the median value of CRP, NLR or LDH into different subgroups.
At a median follow-up time of 11.4 months (range: 1-28 months), median progression-free survival (PFS) and overall survival (OS) were 1.9 months (95% CI, .18-3.6) and 15 months (95% CI, 10.9-19.1) months, respectively. Pretreatment metastases numbers was significant predictor of PFS (HR = 1.99; 95% CI 1.10-3.63; = .024) and OS (HR = 2.77; 95% CI 1.36-5.61; = .005). Baseline LDH level was independent predictor of OS (HR = 7.01; 95% CI 3.09-15.88; < .001). Patients with LDH level >435 U/L at the baseline had significantly shorter PFS and OS compared to patients with LDH level ≤435 U/L (median PFS: 1.7 vs 3.5 months, = .040; median OS: 3.7 vs 18.5 months, < .001). Patients with non-durable clinical benefit (NDB) had significantly higher LDH level at the baseline compared to patients who achieved durable clinical benefit (DCB) ( = .025). Post-treatment levels of CRP, LDH, and NLR were decreased compared to baseline in patients with DCB ( = .030, = .088, and = .066, respectively), whereas, there was a significant increase in post-treatment level of LDH compared with baseline in patients with NDB ( = .024).
LDH level at the baseline was an independent predictor of OS and pretreatment metastases numbers was a significant predictor of PFS and OS.
我们旨在研究抗 PD-1 治疗鼻咽癌(NPC)的结果的决定因素。
在这项回顾性研究中,我们纳入了 64 例复发性/转移性 NPC 患者。使用 Cox 回归模型和 Kaplan-Meier 分析,分析了患者特征、C-反应蛋白(CRP)、中性粒细胞与淋巴细胞比值(NLR)和乳酸脱氢酶(LDH)与抗 PD-1 治疗生存获益的相关性。根据 CRP、NLR 或 LDH 的中位数将患者分为不同的亚组。
中位随访时间为 11.4 个月(范围:1-28 个月),中位无进展生存期(PFS)和总生存期(OS)分别为 1.9 个月(95%CI,0.18-3.6)和 15 个月(95%CI,10.9-19.1)个月。治疗前转移灶数量是 PFS(HR=1.99;95%CI 1.10-3.63; =.024)和 OS(HR=2.77;95%CI 1.36-5.61; =.005)的显著预测因子。基线 LDH 水平是 OS 的独立预测因子(HR=7.01;95%CI 3.09-15.88; <.001)。基线时 LDH 水平 >435U/L 的患者的 PFS 和 OS 明显短于 LDH 水平 ≤435U/L 的患者(中位 PFS:1.7 与 3.5 个月, =.040;中位 OS:3.7 与 18.5 个月, <.001)。非持久临床获益(NDB)患者的基线 LDH 水平明显高于持久临床获益(DCB)患者( =.025)。在 DCB 患者中,治疗后 CRP、LDH 和 NLR 水平与基线相比均有下降( =.030、 =.088 和 =.066),而在 NDB 患者中,治疗后 LDH 水平与基线相比显著升高( =.024)。
基线 LDH 水平是 OS 的独立预测因子,而治疗前转移灶数量是 PFS 和 OS 的显著预测因子。