Increased Intratumoral FOXP3-positive Regulatory Immune Cells during Interleukin-2 Treatment in Metastatic Renal Cell Carcinoma

被引:79
作者
Jensen, Hanne Krogh [1 ,2 ]
Donskov, Frede [1 ,2 ]
Nordsmark, Marianne [1 ,2 ]
Marcussen, Niels [3 ]
von der Maase, Hans [4 ]
机构
[1] Aarhus Univ Hosp, Dept Oncol, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ Hosp, Dept Expt Clin Oncol, DK-8000 Aarhus C, Denmark
[3] Odense Univ Hosp, Dept Clin Pathol, DK-5000 Odense, Denmark
[4] Copenhagen Univ Hosp, Rigshosp, Dept Oncol, Copenhagen O, Denmark
关键词
HIGH-DOSE INTERLEUKIN-2; T-CELLS; PERIPHERAL-BLOOD; INCREASED POPULATIONS; CANCER; FOXP3; IMMUNOTHERAPY; MELANOMA; SURVIVAL; DEPLETION;
D O I
10.1158/1078-0432.CCR-08-1296
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The administration of interleukin-2 (IL-2) may increase the frequency of peripherally circulating FOXP3-positive regulatory immune cells, thus potentially compromising this treatment option for patients with metastatic renal cell carcinoma, The impact of IL-2-based therapy on the accumulation of FOXP3-positive immune cells in the tumor microenvironment in metastatic renal cell carcinoma is unknown. Experimental Design: Baseline (n = 58) and on-treatment (n = 42) tumor core biopsies were prospectively obtained from patients with clear cell metastatic renal cell carcinoma before and during IL-2-based immunotherapy. Immunohistochemical expression of FOXP3 was estimated by stereological counting technique and correlated with other immune cell subsets and overall survival. Results: A significant increase in absolute intratumoral FOXP3-positive immune cells was observed comparing baseline (median 23 cells/mm(2); range, 0-183) and on-treatment biopsies (median, 89 cells/mm(2); range, 11-388; P < 0.001). The relative increase in individual patients was median 4.7-fold, range 0.3 to 230. FOXP3-positive cells were positively correlated with CD3-positive, CD4-positive, and CD8-positive tumor-infiltrating immune cells at baseline and during treatment (P < 0.05 in all comparisons). All patients achieving high numbers (>180 cells/mm(2)) of on-treatment FOXP3-positive intratumoral immune cells were dead within 22 months (n = 11), whereas patients with low numbers (>80 cells/mm(2)) of on-treatment FOXP3-positive cells (n = 31) had a 5-year survival rate of 19% (hazard ratio, 2.2; confidence interval, 1.03-4.5; P = 0.043). All long-term survivors were characterized by low-baseline FOXP3-positive cells and a modest absolute rise in FOXP3-positive cells. Conclusion: Intratumoral FOXP3-positive regulatory immune cells significantly increased during IL-2-based immunotherapy, and high numbers of on-treatment FOXP3-positive cells were correlated with poor prognosis in patients with metastatic renal cell carcinoma.
引用
收藏
页码:1052 / 1058
页数:7
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