Immune killer cells treatment for previously treated stage IV NSCLC patients

被引:0
作者
Tseng, Yen-Han [1 ,2 ]
Ho, Ching-Liang [3 ]
Chian, Chih-Feng [4 ]
Chiang, Chi-Lu [1 ,2 ]
Chao, Heng-Sheng [1 ,2 ]
Tsai, Chen-Liang [4 ]
Perng, Wann-Cherng [4 ]
Hsiao, Chin-Fu [5 ]
Chuang, Mei-Hsing [5 ]
Ko, Kai-Hsiung [6 ]
Cheng, Yun-Ching [7 ]
Chen, Shin-Jung [7 ]
Wang, Chia-Jen [7 ]
Chen, Yuh-Min [1 ,2 ]
机构
[1] Taipei Vet Gen Hosp, Dept Chest Med, 201,Sec 2,Shipai Rd, Taipei 11217, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Sch Med, Sec2,Linong St,112, Taipei 155, Taiwan
[3] Triserv Gen Hosp, Natl Def Med Ctr, Dept Med, Div Hematol & Oncol, 325 Chenggong Rd, Taipei 114, Taiwan
[4] Triserv Gen Hosp, Natl Def Med Ctr, Dept Internal Med, Div Pulm & Crit Care Med, 325 Sect 2,Cheng Kung Rd, Taipei City 114, Taiwan
[5] Inst Populat Hlth Sci, Natl Hlth Res Inst, 35 Keyan Rd, Zhunan 350, Miaoli County, Taiwan
[6] Triserv Gen Hosp, Natl Def Med Ctr, Dept Radiol, 325 Sec 2,Cheng Kung Rd, Taipei 114, Taiwan
[7] Ivy Life Sci Co Ltd, 76,Yuhe St, Taoyuan 330, Taiwan
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
关键词
Cell immunotherapy; Immune killer cells; Non-small cell lung cancer; Overall survival; Safety; LUNG-CANCER; CHEMOTHERAPY; AFATINIB; IMMUNOTHERAPY; ERLOTINIB;
D O I
10.1038/s41598-024-69587-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The 5-year survival is poor for stage IV non-small cell lung cancer (NSCLC). Recently, cell immunotherapy has emerged as a new treatment strategy. This study aimed to evaluate the efficacy and safety of Immune killer cells (IKC) in patients with stage IV NSCLC after the failure of prior chemotherapy. This study enrolled 26 patients with stage IV NSCLC who failed at least two lines of chemotherapy with or without targeted therapy. The IKC was given alone weekly for 24 weeks. The primary endpoint was progression-free survival (PFS). Secondary outcomes included overall survival (OS), pain intensity, quality of life (QOL), and safety. The median PFS for the intent-to-treat (ITT) population (i.e., all enrolled patients) was 3.8 month. In the per-protocol (PP) population (i.e., patients receiving > 12 IKC infusions), the median PFS was 5.6 months. Moreover, the ITT population showed a 1-year survival rate of 60.0%, while that for the PP population was 85.7%. Only 7 out of 200 AEs (3.5%) were related to the IKC infusion, and they were all rated as grade 1 in severity. The IKC infusion was well tolerated. This novel immunotherapy prolonged the PFS and improved the survival compared with historical data. It might be a potential treatment strategy for stage IV NSCLC patient who failed prior chemotherapy.
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页数:10
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