Prognostic value of PD-L1 expression on immune cells or tumor cells for locally advanced esophageal squamous cell carcinoma in patients treated with neoadjuvant chemoradiotherapy

被引:3
|
作者
Huang, Ta-Chen [1 ,2 ]
Liang, Cher-Wei [4 ]
Li, Yu-, I [4 ]
Guo, Jhe-Cyuan [2 ,5 ]
Lin, Chia-Chi [2 ]
Chen, Ya-Jhen [1 ]
Cheng, Ann-Lii [1 ,2 ,3 ,5 ]
Hsu, Chih-Hung [1 ,2 ,5 ]
机构
[1] Natl Taiwan Univ, Grad Inst Oncol, Coll Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[4] Fu Jen Catholic Univ Hosp, Dept Pathol, New Taipei, Taiwan
[5] Natl Taiwan Univ, Canc Ctr, Coll Med, Taipei, Taiwan
关键词
Esophageal squamous cell carcinoma; PD-L1; Immune cells; Neoadjuvant chemoradiotherapy; Prognosis; DEATH-LIGAND; 1; PREOPERATIVE CHEMORADIOTHERAPY; MESENCHYMAL TRANSITION; LUNG-CANCER; HOST-CELLS; MICROENVIRONMENT; SURVIVAL; B7-H1;
D O I
10.1007/s00432-021-03772-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Programmed death-ligand 1 (PD-L1) expression may influence the prognosis of patients with localized esophageal cancer. The current study compared the prognostic value of PD-L1 expression between tumor cells and immune cells. Methods Archival esophageal tumor tissue samples were collected from patients who received paclitaxel and cisplatin-based neoadjuvant chemoradiotherapy (CRT) for locally advanced esophageal squamous cell carcinoma (ESCC) in three prospective phase II trials. PD-L1 expression on tumor and immune cells was examined immunohistochemically by using the SP142 antibody and scored by two independent pathologists. The association of PD-L1 expression with patient's outcomes was analyzed using a log-rank test and Cox regression multivariate analysis. Results A total of 100 patients were included. PD-L1 expression on tumor cells was positive (>= 1%, TC-positive) in 55 patients; PD-L1 expression on immune cells was high (>= 5%, IC-high) in 30 patients. TC-positive status was associated with poor overall survival (OS) (HR: 1.63, P = 0.035), whereas IC-high status was associated with improved OS (HR: 0.44, P = 0.0024). Multivariate analysis revealed that TC-positive, IC-high, and performance status were independent prognostic factors for progression-free survival and that IC-high and performance status were independent factors for OS. Furthermore, the combination of IC-high and TC-negative status was associated with the optimal OS, whereas that of TC-positive and IC-low status was associated with the worst OS. Conclusion PD-L1 expression on tumor and immune cells may have different prognostic value for patients with locally advanced ESCC receiving neoadjuvant CRT. A combination of these two indexes may further improve the prognostic prediction.
引用
收藏
页码:1803 / 1811
页数:9
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