Prognostic rote of tumoral PDL1 expression and peritumoral FoxP3+lymphocytes in vulvar melanomas

被引:20
作者
Chlopik, Agata [1 ,2 ]
Selim, M. Angelica [3 ]
Peng, Yan [4 ]
Wu, Cheng-Lin [5 ]
Tell-Marti, Gemma [6 ,7 ]
Paral, Kristen M. [3 ]
Shalin, Sara C. [8 ]
Kraft, Stefan [9 ]
Hsu, Chao-Kai [10 ]
Shea, Christopher R. [11 ]
Puig, Susana [6 ,7 ]
Fernandez-Figueras, Maria-Teresa [12 ]
Biernat, Wojciech [13 ]
Rys, Janusz [14 ]
Marszalek, Andrzej [1 ,2 ]
Hoang, Mai P. [15 ,16 ]
机构
[1] Poznan Univ Med Sci, Dept Pathol, PL-60206 Poznan, Poland
[2] Greater Poland Canc Ctr, PL-60206 Poznan, Poland
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Univ Texas Southwestern Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
[5] Natl Cheng Kung Univ, Coll Med, Natl Cheng Kung Univ Hosp, Dept Pathol, Tainan 70403, Taiwan
[6] Hosp Clin Barcelona, IDIBAPS, Melanoma Unit, Dept Dermatol, Barcelona 08193, Spain
[7] ISCIII, Ctr Biomed Res Rare Dis CIBERER, Barcelona 08193, Spain
[8] Univ Arkansas, Dept Pathol, Little Rock, AR 72204 USA
[9] Ctr Dermatopathol, Dept Pathol, D-79016 Freiburg, Germany
[10] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Dermatol, Tainan 70403, Taiwan
[11] Univ Chicago, Dermatol Sect, Dept Med, Chicago, IL 60637 USA
[12] Univ Autonoma Barcelona, Hosp Univ Germans Trias & Pujol, Dept Pathol, E-08193 Barcelona, Spain
[13] Med Univ Gdansk, Dept Pathol, PL-80309 Gdansk, Poland
[14] M Sklodowska Curie Mem Inst, Ctr Oncol, Dept Pathol, PL-31115 Krakow, Poland
[15] Massachusetts Gen Hosp, Dept Pathol, 55 Fruit St,Warren 820, Boston, MA 02114 USA
[16] Harvard Med Sch, Boston, MA 02114 USA
关键词
Vulvar melanoma; Survival; PDL1; CD8; FoxP3; Immunohistochemistry; REGULATORY T-CELLS; INFILTRATING IMMUNE CELLS; MALIGNANT-MELANOMA; METASTATIC MELANOMA; MUCOSAL MELANOMA; CANCER; LYMPHOCYTES; RESISTANCE; BLOCKADE; SURVIVAL;
D O I
10.1016/j.humpath.2017.12.022
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The prognostic role of PDL1 expression, CD8+ and FoxP3+ lymphocytes in vulvar melanomas has not been studied. We correlated PDL1 expression and CD8+ and FoxP3+ immune infiltrates with dinicopathologic variables and patient outcomes in a series of 75 vulvar melanomas. Tumoral PDL1 expression (>5%) was seen in 23% of cases. By Fisher exact test, PDL1 expression and peritumoral FoxP3+ lymphocytes significantly correlated with less disease-specific death. By linear regression analysis, correlations between tumoral PDL1 expression with the density of tumoral CD8+ and peritumoral CD8+ lymphocytes, tumoral FoxP3+ with tumoral CD8+ lymphocytes, and peritumoral FoxP3+ with peritumoral CD8+ lymphocytes were observed. By univariate analyses, tumor thickness >4 mm predicted poorer progression-free survival, melanoma-specific survival, and overall survival. PDL1 expression >5% and peritumoral CD8+, peritumoral FoxP3+, and tumoral FoxP3+ lymphocytes correlated with better overall survival. By multivariate analyses, high peritumoral FoxP3+ lymphocytes independently predicted better melanoma-specific survival (P = .023), and tumor thickness independently predicted poorer progression-free survival (P = .05) and overall survival (P = .039). In conclusion, our study shows that, independent from tumor thickness, an increased density of peritumoral FoxP3+ lymphocytes may positively impact survival in a subset of vulvar melanomas. Tumoral PDL1 expression correlated with tumoral as well as peritumoral CD8+ and FoxP3+ lymphocytes, supportive of an adaptive immune response. Although the frequency of PDLI expression is low in vulvar melanoma, its expression may identify a subset of vulvar melanoma that might respond to immunotherapy. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:176 / 183
页数:8
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