Prognostic Value of Programmed Death Ligand 1 and Programmed Death 1 Expression in Thymic Carcinoma. 2016

Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
Department of Surgery, Kurume University School of Medicine, Kurume, Japan.

OBJECTIVE The immune checkpoint of the programmed death 1/programmed death ligand 1 (PD-1/PD-L1) pathway is believed to play an important role in evasion of host antitumor immune surveillance in various malignancies; however, little is known about its role in thymic carcinoma. This study investigated PD-1/PD-L1 expression and its association with clinicopathologic features, the expression of immune-related proteins in tumor-infiltrating lymphocytes (TIL), and patient prognosis. METHODS PD-L1 and PD-1 expression was evaluated by IHC in 25 thymic carcinoma tissue specimens. Copy number alterations of the PD-L1 gene in 11 cases were assessed in formalin-fixed, paraffin-embedded material using qRT-PCR. RESULTS Compared with normal subjects, 3 thymic carcinoma patients showed an increase in PD-L1 copy number, whereas 8 did not. PD-L1 was significantly overexpressed in cases with copy number gain as compared with normal cases. High PD-L1 expression was associated with higher disease-free and overall survival rates as compared to cases with low expression. Prognostic analysis revealed low PD-L1 expression and high number of PD-1(+) TILs as significant predictors of poor survival, together with Masaoka-Koga stage IVa/IVb disease and incomplete resection. In the quantitative analysis of TILs, PD-L1 expression correlated proportionally with the number of infiltrating CTLs. CONCLUSIONS Here, for the first time, we report that PD-L1 and PD-1 expression might be useful prognostic predictors in thymic carcinoma. Further studies are expected to substantiate the prognostic value of PD-L1 and PD-1 expression, and the potential efficacy of targeting the PD-1/PD-L1 pathway in thymic carcinoma via immunotherapy. Clin Cancer Res; 22(18); 4727-34. ©2016 AACR.

UI MeSH Term Description Entries
D007150 Immunohistochemistry Histochemical localization of immunoreactive substances using labeled antibodies as reagents. Immunocytochemistry,Immunogold Techniques,Immunogold-Silver Techniques,Immunohistocytochemistry,Immunolabeling Techniques,Immunogold Technics,Immunogold-Silver Technics,Immunolabeling Technics,Immunogold Silver Technics,Immunogold Silver Techniques,Immunogold Technic,Immunogold Technique,Immunogold-Silver Technic,Immunogold-Silver Technique,Immunolabeling Technic,Immunolabeling Technique,Technic, Immunogold,Technic, Immunogold-Silver,Technic, Immunolabeling,Technics, Immunogold,Technics, Immunogold-Silver,Technics, Immunolabeling,Technique, Immunogold,Technique, Immunogold-Silver,Technique, Immunolabeling,Techniques, Immunogold,Techniques, Immunogold-Silver,Techniques, Immunolabeling
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D009367 Neoplasm Staging Methods which attempt to express in replicable terms the extent of the neoplasm in the patient. Cancer Staging,Staging, Neoplasm,Tumor Staging,TNM Classification,TNM Staging,TNM Staging System,Classification, TNM,Classifications, TNM,Staging System, TNM,Staging Systems, TNM,Staging, Cancer,Staging, TNM,Staging, Tumor,System, TNM Staging,Systems, TNM Staging,TNM Classifications,TNM Staging Systems
D002277 Carcinoma A malignant neoplasm made up of epithelial cells tending to infiltrate the surrounding tissues and give rise to metastases. It is a histological type of neoplasm and not a synonym for "cancer." Carcinoma, Anaplastic,Carcinoma, Spindle-Cell,Carcinoma, Undifferentiated,Carcinomatosis,Epithelial Neoplasms, Malignant,Epithelioma,Epithelial Tumors, Malignant,Malignant Epithelial Neoplasms,Neoplasms, Malignant Epithelial,Anaplastic Carcinoma,Anaplastic Carcinomas,Carcinoma, Spindle Cell,Carcinomas,Carcinomatoses,Epithelial Neoplasm, Malignant,Epithelial Tumor, Malignant,Epitheliomas,Malignant Epithelial Neoplasm,Malignant Epithelial Tumor,Malignant Epithelial Tumors,Neoplasm, Malignant Epithelial,Spindle-Cell Carcinoma,Spindle-Cell Carcinomas,Tumor, Malignant Epithelial,Undifferentiated Carcinoma,Undifferentiated Carcinomas
D005260 Female Females
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000369 Aged, 80 and over Persons 80 years of age and older. Oldest Old

Related Publications

Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
November 2023, BJU international,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
November 2017, Journal of gynecologic oncology,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
September 2019, Chronic diseases and translational medicine,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
May 2016, Oncotarget,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
January 2020, Applied immunohistochemistry & molecular morphology : AIMM,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
January 2019, Frontiers in oncology,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
July 2021, Histopathology,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
October 2016, World journal of gastroenterology,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
November 2021, International journal of clinical oncology,
Shintaro Yokoyama, and Hiroaki Miyoshi, and Kazutaka Nakashima, and Joji Shimono, and Toshihiro Hashiguchi, and Masahiro Mitsuoka, and Shinzo Takamori, and Yoshito Akagi, and Koichi Ohshima
May 2017, Cancer science,
Copied contents to your clipboard!