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Prognostic Significance of Tumor-Infiltrating Lymphocytes in Patients With Pancreatic Ductal Adenocarcinoma Treated With Neoadjuvant Chemotherapy.

Authors :
Nejati R
Goldstein JB
Halperin DM
Wang H
Hejazi N
Rashid A
Katz MH
Lee JE
Fleming JB
Rodriguez-Canales J
Blando J
Wistuba II
Maitra A
Wolff RA
Varadhachary GR
Wang H
Source :
Pancreas [Pancreas] 2017 Oct; Vol. 46 (9), pp. 1180-1187.
Publication Year :
2017

Abstract

Objectives: The aim of this study was to examine tumor-infiltrating lymphocytes (TILs) and their prognostic value in patients with pancreatic ductal adenocarcinoma (PDAC) after neoadjuvant therapy.<br />Methods: Intratumoral CD4, CD8, and FOXP3 lymphocytes were examined by immunohistochemistry using a computer-assisted quantitative analysis in 136 PDAC patients who received neoadjuvant therapy and pancreaticoduodenectomy. The results were correlated with clinicopathological parameters and survival.<br />Results: High CD4 TILs in treated PDAC were associated with high CD8 TILs (P = 0.003), differentiation (P = 0.04), and a lower frequency of recurrence (P = 0.02). Patients with high CD4 TILs had longer disease-free survival and overall survival (OS) than did patients with low CD4 TILs (P < 0.01). The median OS of patients with a high CD8/FOXP3 lymphocyte ratio (39.5 [standard deviation, 6.1] months) was longer than that of patients with a low CD8/FOXP3 lymphocyte ratio (28.3 [standard deviation, 2.3] months; P = 0.01). In multivariate analysis, high CD4 TILs were an independent prognostic factor for disease-free survival (hazard ratio, 0.49; 95% confidence interval, 0.30-0.81; P = 0.005) and OS (hazard ratio, 0.54; 95% confidence interval, 0.33-0.89; P = 0.02).<br />Conclusions: High level of CD4 lymphocytes is associated with tumor differentiation and lower recurrence and is an independent prognostic factor for survival in PDAC patients treated with neoadjuvant therapy.

Details

Language :
English
ISSN :
1536-4828
Volume :
46
Issue :
9
Database :
MEDLINE
Journal :
Pancreas
Publication Type :
Academic Journal
Accession number :
28902789
Full Text :
https://doi.org/10.1097/MPA.0000000000000914