Association of lymphocyte subsets percentage with prognosis for recurrent or metastatic nasopharyngeal carcinoma patients receiving PD-L1 inhibitors

鼻咽癌 医学 肿瘤科 内科学 免疫疗法 淋巴细胞 淋巴细胞亚群 免疫学 免疫系统 CD8型 癌症 放射治疗
作者
Jiayu Diao,Zhigong Wei,Yiyan Pei,Junyou Ge,Qing Yan,Youneng Wei,Ye Chen,Xingchen Peng
出处
期刊:Cancer Immunology, Immunotherapy [Springer Science+Business Media]
卷期号:74 (4)
标识
DOI:10.1007/s00262-024-03885-1
摘要

Immune checkpoint inhibitors (ICIs), particularly PD-1/PD-L1 inhibitors, have demonstrated significant survival benefits in treating recurrent or metastatic nasopharyngeal carcinoma (R/M-NPC). While baseline peripheral blood lymphocyte subsets have been identified as prognostic biomarkers in various cancers treated with ICIs, their relevance in R/M-NPC has not been extensively studied. This post hoc analysis used data from 153 R/M-NPC patients treated with PD-L1 inhibitor monotherapy in the phase 2 trial KL167-2-05-CTP. The lymphocyte subsets, including total T cells, CD4/CD8 ratio, helper T cells, suppressor cytotoxic T cells, NK cells, and B cells, were tested by flow cytometry. These subsets were grouped using optimal cutoff values identified by the Maximally Selected Log-rank Statistic. Overall survival (OS) and progression-free survival (PFS) were assessed using Kaplan–Meier and Cox regression analysis, and logistic regression analysis evaluated the associations with objective response rate (ORR) and disease control rate (DCR). Patients with lower NK cell percentages showed significantly longer OS (26.3 vs. 12.1 months, p < 0.001) and PFS (5.5 vs. 3.7 months, p < 0.001) compared to those with higher NK cell percentages. No significant differences in OS or PFS were observed for other lymphocyte subsets. High NK cell percentages were identified as risk factors for shorter OS (HR, 2.49) and PFS (HR, 1.62). There were no significant differences in ORR and DCR between high and low lymphocyte subsets. Lower baseline NK cell percentages are associated with improved OS and PFS in R/M-NPC patients undergoing PD-L1 inhibitor therapy.
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