Tumor B7-H3 expression in diagnostic biopsy specimens and survival in patients with metastatic prostate cancer

被引:19
作者
Amori, Gulanbar [1 ,2 ]
Sugawara, Emiko [1 ,2 ]
Shigematsu, Yasuyuki [1 ,2 ]
Akiya, Masashi [1 ,2 ]
Kunieda, Junko [1 ,3 ]
Yuasa, Takeshi [4 ]
Yamamoto, Shinya [4 ]
Yonese, Junji [4 ]
Takeuchi, Kengo [1 ,2 ,5 ]
Inamura, Kentaro [1 ,2 ]
机构
[1] Japanese Fdn Canc Res, Inst Canc, Div Pathol, Tokyo, Japan
[2] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Pathol, Tokyo, Japan
[3] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Comprehens Pathol, Tokyo, Japan
[4] Japanese Fdn Canc Res, Canc Inst Hosp, Dept Urol, Tokyo, Japan
[5] Japanese Fdn Canc Res, Canc Inst Hosp, Pathol Project Mol Targets, Tokyo, Japan
关键词
T-CELLS; CD276; EXPRESSION; TARGETING B7-H3; ACTIVATION; PATHWAYS; CAPACITY; ABLATION; RECEPTOR;
D O I
10.1038/s41391-021-00331-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Prostate cancer spans a broad spectrum from indolent to deadly disease. In the management of prostate cancer, diagnostic biopsy specimens are important sources of data that inform the selection of treatment. B7-H3 (CD276), an immune checkpoint molecule, has emerged as a promising immunotherapy target. B7-H3 expression is related to adverse clinical outcomes in various types of cancer; however, little is known concerning the association between tumor B7-H3 expression in diagnostic biopsy specimens and clinical outcome in patients with metastatic prostate cancer. Methods We evaluated tumor B7-H3 expression levels in diagnostic biopsy specimens from 135 patients with metastatic prostate cancer and 113 patients with localized prostate cancer. Results High B7-H3 expression was more frequently observed in patients with metastatic cancer than in those with localized cancer (31 vs. 12%; p = 0.0003). In patients with localized cancer, the B7-H3 expression status was not associated with biochemical recurrence-free survival. However, among patients with metastatic cancer, high B7-H3 expression was independently associated with high disease-specific mortality (multivariable hazard ratio [HR] = 2.72; p = 0.047) and overall mortality rates (multivariable HR = 2.04; p = 0.025). Conclusions Tumor B7-H3 expression in diagnostic biopsy specimens may be a useful biomarker for identifying highly aggressive metastatic prostate cancer. Given the potential utility of anti-B7-H3 immunotherapy, this information may aid in stratifying prostate cancer based on its responsiveness to B7-H3-targeted treatment.
引用
收藏
页码:767 / 774
页数:8
相关论文
共 42 条
[1]   Tumor exosomes expressing Fas ligand mediate CD8+ T-cell apoptosis [J].
Abusamra, AJ ;
Zhong, ZH ;
Zheng, XF ;
Li, M ;
Ichim, TE ;
Chin, JL ;
Min, WP .
BLOOD CELLS MOLECULES AND DISEASES, 2005, 35 (02) :169-173
[2]   Correlation of B7-H3 with androgen receptor, immune pathways and poor outcome in prostate cancer: an expression-based analysis [J].
Benzon, B. ;
Zhao, S. G. ;
Haffner, M. C. ;
Takhar, M. ;
Erho, N. ;
Yousefi, K. ;
Hurley, P. ;
Bishop, J. L. ;
Tosoian, J. ;
Ghabili, K. ;
Alshalalfa, M. ;
Glavaris, S. ;
Simons, B. W. ;
Tran, P. ;
Davicioni, E. ;
Karnes, R. J. ;
Boudadi, K. ;
Antonarakis, E. S. ;
Schaeffer, E. M. ;
Drake, C. G. ;
Feng, F. ;
Ross, A. E. .
PROSTATE CANCER AND PROSTATIC DISEASES, 2017, 20 (01) :28-35
[3]   Past, Current, and Future of Immunotherapies for Prostate Cancer [J].
Boettcher, Adeline N. ;
Usman, Ahmed ;
Morgans, Alicia ;
VanderWeele, David J. ;
Sosman, Jeffrey ;
Wu, Jennifer D. .
FRONTIERS IN ONCOLOGY, 2019, 9
[4]  
Castellanos JR, 2017, AM J CLIN EXP IMMUNO, V6, P66
[5]   B7 family checkpoint regulators in immune regulation and disease [J].
Ceeraz, Sabrina ;
Nowak, Elizabeth C. ;
Noelle, Randolph J. .
TRENDS IN IMMUNOLOGY, 2013, 34 (11) :556-563
[6]   B7-H3:: A costimulatory molecule for T cell activation and IFN-γ production [J].
Chapoval, AI ;
Ni, J ;
Lau, JS ;
Wilcox, RA ;
Flies, DB ;
Liu, D ;
Dong, HD ;
Sica, GL ;
Zhu, GF ;
Tamada, K ;
Chen, LP .
NATURE IMMUNOLOGY, 2001, 2 (03) :269-274
[7]   Immunotherapy in Prostate Cancer: Teaching an Old Dog New Tricks [J].
Comiskey, Michael C. ;
Dallos, Matthew C. ;
Drake, Charles G. .
CURRENT ONCOLOGY REPORTS, 2018, 20 (09)
[8]   Antitumor Responses in the Absence of Toxicity in Solid Tumors by Targeting B7-H3 via Chimeric Antigen Receptor T Cells [J].
Du, Hongwei ;
Hirabayashi, Koichi ;
Ahn, Sarah ;
Kren, Nancy Porterfield ;
Montgomery, Stephanie Ann ;
Wang, Xinhui ;
Tiruthani, Karthik ;
Mirlekar, Bhalchandra ;
Michaud, Daniel ;
Greene, Kevin ;
Herrera, Silvia Gabriela ;
Xu, Yang ;
Sun, Chuang ;
Chen, Yuhui ;
Ma, Xingcong ;
Ferrone, Cristina Rosa ;
Pylayeva-Gupta, Yuliya ;
Yeh, Jen Jen ;
Liu, Rihe ;
Savoldo, Barbara ;
Ferrone, Soldano ;
Dotti, Gianpietro .
CANCER CELL, 2019, 35 (02) :221-+
[9]   B7-H3 Immune Checkpoint Protein in Human Cancer [J].
Flem-Karlsen, Karine ;
Fodstad, Oystein ;
Nunes-Xavier, Caroline E. .
CURRENT MEDICINAL CHEMISTRY, 2020, 27 (24) :4062-4086
[10]   B7-H3 in Cancer - Beyond Immune Regulation [J].
Flem-Karlsen, Karine ;
Fodstad, Oystein ;
Tan, Ming ;
Nunes-Xavier, Caroline E. .
TRENDS IN CANCER, 2018, 4 (06) :401-404