Peripheral NK cells identified as the predictor of response in extensive-stage small cell lung cancer patients treated with first-line immunotherapy plus chemotherapy

被引:2
作者
Cui, Yanan [1 ,2 ,3 ,4 ,5 ]
Chen, Yanping [1 ,2 ,3 ,4 ]
Zhao, Peiyan [6 ]
Li, Shuang [7 ]
Cheng, Ying [5 ]
Ren, Xiubao [1 ,2 ,3 ,4 ]
机构
[1] Tianjin Med Univ, Canc Inst & Hosp, Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[2] Tianjins Clin Res Ctr Canc, Tianjin, Peoples R China
[3] Key Lab Canc Prevent & Therapy, Tianjin, Peoples R China
[4] Key Lab Canc Immunol & Biotherapy, Tianjin, Peoples R China
[5] Jilin Canc Hosp, Div Thorac Oncol, Changchun, Peoples R China
[6] Jilin Canc Hosp, Translat Oncol Res Lab, Changchun, Peoples R China
[7] Jilin Canc Hosp, Big Data Ctr Clin, Changchun, Peoples R China
基金
中国国家自然科学基金;
关键词
Extensive-stage small-cell lung cancer; Natural killer cells; Immunotherapy; Biomarker; ETOPOSIDE; SURVIVAL;
D O I
10.1007/s12094-024-03479-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeAlthough immunotherapy improves outcomes in extensive-stage small-cell lung cancer (ES-SCLC), the search for biomarkers predicting treatment success is crucial. Natural killer (NK) cells are potential indicators in various cancers, however, their precise role in ES-SCLC prognosis remains unclear. MethodsIn this retrospective study, 33 patients with ES-SCLC treated with first-line immuno-chemotherapy were enrolled. The peripheral NK cell percentage and its longitudinal dynamics were analyzed using flow cytometry. Progression-free survival (PFS) and overall survival (OS) were calculated as hazard ratio (HR) and compared statistically. ResultsThe median PFS was better in the group with normal baseline NK cell levels than the low group (7.0 vs. 4.6 months; HR = 0.17; 95% CI 0.07-0.41; P < 0.0001), but there was no association with OS (14.9 vs. 10.3 months; HR = 0.55; 95% CI 0.23-1.31; P = 0.171). Furthermore, the NK cell% for 95.0% of patients increased after immunochemotherapy in the clinical response group (P = 0.0047), which led to a better median PFS (6.3 vs. 2.1 months; HR = 0.23; 95% CI 0.05-0.98; P < 0.0001) and OS (14.9 vs. 5.9 months; HR = 0.20; 95% CI 0.04-1.02; P < 0.0001). Similar trends were observed with NK cell% changes up to disease progression, improving PFS (6.5 vs. 4.3; HR = 0.41; 95% CI 0.12-0.92; P = 0.0049) and OS (17.4 vs. 9.7; HR = 0.42; 95% CI 0.17-1.02; P < 0.0001). ConclusionIn patients with ES-SCLC, the percentage and changes in peripheral NK cells can predict the response to combined immunotherapy and chemotherapy.
引用
收藏
页码:2522 / 2530
页数:9
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