Pretreatment pulmonary tumor necrosis is a promising prognostic imaging biomarker for first-line anti-PD-1/PD-L1 therapy in advanced lung squamous cell carcinoma: a multi-institutional, propensity score-matching cohort analysis

被引:0
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作者
Zhong, Qiaofeng [1 ,3 ,4 ]
Zhang, Longfeng [1 ]
Wu, Lin [5 ]
Zhao, Jun [6 ]
Sun, Jianguo [7 ]
Fang, Yong [8 ]
Zhou, Jin [9 ]
Chu, Qian [10 ]
Shen, Yihong [11 ]
Yang, Zhenzhou [12 ]
Chen, Lijin [13 ]
Huang, Meijuan [14 ,15 ]
Lin, Xiaoyan [16 ]
Liu, Zhenhua [17 ]
Shen, Peng [18 ]
Wang, Zhijie [19 ]
Wang, Xin [20 ]
Wang, Huijuan [21 ]
Han, Chengbo [22 ]
Liu, Anwen [23 ]
Zhang, Hongmei [24 ]
Ye, Feng [25 ]
Gao, Wen [26 ]
Wu, Fang [27 ]
Song, Zhengbo [28 ]
Chen, Shengchi [29 ]
Zhou, Chengzhi [30 ]
Huang, Dingzhi [31 ]
Zhang, Qiuyu [32 ]
Zheng, Xinlong [1 ]
Zheng, Xiaobin [1 ]
Miao, Qian [1 ]
Jiang, Kan [1 ]
Zou, Zihua [1 ]
Xu, Yiquan [1 ]
Wu, Shiwen [1 ]
Wang, Haibo [1 ]
Hong, Yaping [1 ]
Lu, Tao [33 ]
Li, Chao [34 ]
Huang, Cheng [1 ]
Chen, Chuanben [2 ]
Lin, Gen [1 ]
机构
[1] Fujian Med Univ, Fudan Univ, Fujian Canc Hosp, Dept Thorac Oncol,Clin Oncol Sch,Fujian Branch,Sha, Fuzhou 350014, Peoples R China
[2] Fujian Med Univ, Fudan Univ, Fujian Canc Hosp, Dept Radiat,Clin Oncol Sch,Fujian Branch,Shanghai, Fuma Rd 420, Fuzhou 350014, Peoples R China
[3] Fujian Prov Key Lab Translat Canc Med, Fuzhou, Peoples R China
[4] Fuzhou Univ, Interdisciplinary Inst Med Engn, Fuzhou, Peoples R China
[5] Cent South Univ, Affiliated Canc Hosp, Hunan Canc Hosp, Dept Thorac Oncol 2,Xiangya Sch Med, Changsha, Peoples R China
[6] Peking Univ Canc Hosp & Inst, Dept Thorac Oncol 1, Minist Educ Beijing, Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
[7] Army Med Univ, Xinqiao Hosp, Canc Inst, Chongqing, Peoples R China
[8] Zhejiang Univ, Sir Run Run Shaw Hosp, Dept Med Oncol, Zhejiang, Peoples R China
[9] Univ Elect Sci & Technol China, Sichuan Canc Hosp & Inst, Sichuan Canc Ctr, Sch Med, Chengdu, Sichuan, Peoples R China
[10] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Oncol, Wuhan, Peoples R China
[11] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Dept Resp Dis, Hangzhou, Peoples R China
[12] Chongqing Med Univ, Affiliated Hosp 2, Dept Canc Ctr, Chongqing, Peoples R China
[13] Fujian Med Univ, Affiliated Quanzhou Hosp 1, Dept Oncol, Quanzhou, Peoples R China
[14] Sichuan Univ, Canc Ctr, Dept Thorac Oncol, Chengdu, Peoples R China
[15] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
[16] Fujian Med Univ Union Hosp, Dept Oncol, Fuzhou, Peoples R China
[17] Fujian Med Univ, Fujian Prov Hosp, Prov Clin Coll, Dept Med Oncol, Fuzhou, Peoples R China
[18] Southern Med Univ, Nanfang Hosp, Dept Oncol, Guangzhou, Peoples R China
[19] Chinese Acad Med Sci & Peking Union Med Coll, Natl Clin Res Ctr Canc, Dept Med Oncol, State Key Lab Mol Oncol,Canc Hosp,Natl Canc Ctr, Beijing, Peoples R China
[20] Xiamen Univ, Zhongshan Hosp, Dept Oncol, Xiamen, Peoples R China
[21] Zhengzhou Univ, Affiliated Canc Hosp, Dept Resp Med, Zhengzhou, Peoples R China
[22] China Med Univ, Shengjing Hosp, Dept Oncol, Shenyang, Peoples R China
[23] Nanchang Univ, Affiliated Hosp 2, Dept Oncol, Nanchang, Peoples R China
[24] Air Force Mil Med Univ, Xijing Hosp, Dept Oncol, Xian, Shanxi, Peoples R China
[25] Fujian Med Univ, Xiamen Univ, Affiliated Hosp 1, Sch Med,Dept Med Oncol,Canc Hosp,Teaching Hosp, Xiamen, Peoples R China
[26] Nanjing Med Univ, Affiliated Hosp 1, Dept Med Oncol, Nanjing, Jiangsu, Peoples R China
[27] Cent South Univ, Xiangya Hosp 2, Dept Oncol, Changsha, Hunan, Peoples R China
[28] Univ Chinese Acad Sci, Canc Hosp, Dept Clin Trial, Hangzhou, Zhejiang, Peoples R China
[29] Fujian Med Univ, Nanping Hosp 1, Dept Oncol, Nanping, Peoples R China
[30] Guangzhou Med Univ, Affiliated Hosp 1, State Key Lab Resp Dis, Resp Med Dept,Natl Clin Res Ctr Resp Dis,Guangzhou, Guangzhou, Peoples R China
[31] Tianjin Med Univ, Canc Inst & Hosp, Dept Thorac Oncol, Tianjin, Peoples R China
[32] Fujian Med Univ, Inst Immunotherapy, Fuzhou, Peoples R China
[33] Fujian Med Univ, Fujian Canc Hosp, Dept Radiol, Fujian Branch,Shanghai Canc Ctr,Clin Oncol Sch, Fuzhou, Peoples R China
[34] Fujian Med Univ, Fujian Canc Hosp, Dept Pathol, Fujian Branch,Shanghai Canc Ctr,Clin Oncol Sch, Fuzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
anti-PD-1/PD-L1; inhibitor; lung squamous cell carcinoma; prognostic biomarker; propensity score-matching; pulmonary tumor necrosis; NEOADJUVANT CHEMOTHERAPY; MUTATIONAL BURDEN; CANCER; HYPOXIA; CT; DETERMINANTS; DISEASE; IMPACT;
D O I
10.1177/17588359241266188
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Tumor necrosis (TN) is a common feature in lung squamous cell carcinoma (LSCC), which could provide useful predictive and prognostic information.Objectives: This study aimed to investigate the effect of pretreatment pulmonary TN (PTN) on the prognosis of first-line anti-programmed cell death 1 (PD-1)/PD ligand 1 (PD-L1) inhibitor in advanced LSCC.Design: We conducted a retrospective study to analyze the association between the presence of PTN and clinical outcomes in advanced LSCC patients treated with anti-PD-1/PD-L1 inhibitors.Methods: Data from 240 eligible patients were collected from 27 hospitals across China between 2016 and 2020. The presence of PTN was assessed using contrast-enhanced chest computed tomography (CT) imaging at baseline. We utilized the Cox proportional-hazards regression model to analyze the association between PTN and clinical outcomes. In addition, to account for potential confounding factors and ensure comparability between groups, we employed propensity score-matching (PSM) analysis.Results: In the overall patient cohort, the presence of PTN was 39.6%. The median follow-up duration was 20.3 months. The positive PTN group exhibited a notably inferior median progression-free survival (PFS; 6.5 months vs 8.6 months, p = 0.012) compared to the negative PTN group. Within the Cox proportional-hazards regression model, PTN emerged as an independent predictor of unfavorable PFS (hazard ratio (HR) = 1.354, 95% confidence interval (CI): 1.002-1.830, p = 0.049). After PSM, the median PFS for the positive PTN group (6.5 months vs 8.0 months, p = 0.027) remained worse than that of the negative PTN group. Multivariate analyses also further underscored that the presence of PTN independently posed a risk for shorter PFS (HR = 1.494, 95% CI: 1.056-2.112, p = 0.023). However, no statistically significant difference in overall survival was observed between the two groups.Conclusion: Our study suggests that the presence of PTN on baseline contrast-enhanced chest CT is a potential negative prognostic imaging biomarker for the outcome of anti-PD-1/PD-L1 inhibitor therapy in advanced LSCC. Further studies are warranted to validate these findings and explore the underlying mechanisms. Predicting anti-PD-1/PD-L1 inhibitor treatment outcomes: pulmonary tumor necrosis in lung squamous cell carcinomaOur study focused on lung squamous cell carcinoma (LSCC) patients receiving first-line anti-PD-1/PD-L1 therapy. We explored the impact of a feature called pretreatment pulmonary tumor necrosis (PTN) on their prognosis. PTN was identified in 39.6% of patients using baseline chest CT scans. Results revealed that patients with PTN had a shorter time without disease progression (median PFS of 6.5 months compared to 8.6 months) and a higher risk of unfavorable outcomes. This suggests that PTN may serve as a negative prognostic imaging marker for anti-PD-1/PD-L1 therapy in advanced LSCC. Further research is needed to confirm and understand these findings better.
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页数:15
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