JAK2/PD-L1/PD-L2 (9p24.1) amplifications in renal cell carcinomas with sarcomatoid transformation: implications for clinical management

被引:55
作者
Gupta, Sounak [1 ]
Cheville, John C. [2 ]
Jungbluth, Achim A. [1 ]
Zhang, Yanming [1 ]
Zhang, Lei [1 ]
Chen, Ying-Bei [1 ]
Tickoo, Satish K. [1 ]
Fine, Samson W. [1 ]
Gopalan, Anuradha [1 ]
Al-Ahmadie, Hikmat A. [1 ]
Sirintrapun, Sahussapont J. [1 ]
Blum, Kyle A. [3 ,4 ,5 ]
Lohse, Christine M. [6 ]
Hakimi, A. Ari [3 ,4 ,5 ]
Thompson, R. Houston [7 ]
Leibovich, Bradley C. [7 ]
Berger, Michael F. [1 ]
Arcila, Maria E. [1 ]
Ross, Dara S. [1 ]
Ladanyi, Marc [1 ]
Antonescu, Cristina R. [1 ]
Reuter, Victor E. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
[3] Mem Sloan Kettering Canc Ctr, Dept Surg, Urol Serv, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Human Oncol, 1275 York Ave, New York, NY 10021 USA
[5] Mem Sloan Kettering Canc Ctr, Pathogenesis Program, 1275 York Ave, New York, NY 10021 USA
[6] Mayo Clin, Dept Hlth Sci Res, Rochester, MN USA
[7] Mayo Clin, Dept Urol, Rochester, MN USA
关键词
COMPREHENSIVE MOLECULAR CHARACTERIZATION; DEATH-LIGAND; GENOMIC AMPLIFICATION; HODGKIN LYMPHOMA; PD-1; BLOCKADE; NIVOLUMAB; JAK2; EXPRESSION; MUTATION; THERAPY;
D O I
10.1038/s41379-019-0269-x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Amplifications of JAK2, PD-L1, and PD-L2 at 9p24.1 lead to constitutive expression of PD-L1. This, coupled with JAK2-activation dependent upregulation of PD-L1 and adaptive/induced expression leads to higher tumor PD-L1 expression and immune evasion. Renal tumors were therefore evaluated for 9p24.1 amplifications. A combination of next generation sequencing-based copy number analysis, fluorescence in situ hybridization for JAK2/INSL6 and PD-L1/PD-L2 and immunohistochemistry for phospho-STAT3 (downstream target of JAK2), PD-L1, PD-L2, and PD-1 was performed. In this study we interrogated a "Discovery" cohort of 593 renal tumors, a "Validation" cohort of 398 high-grade renal tumors, The Cancer Genome Atlas (879 cases) and other public datasets (846 cases). 9p24.1 amplifications were significantly enriched in renal tumors with sarcomatoid transformation (5.95%, 15/252) when compared to all histologic subtypes in the combined "Discovery", "Validation" and public datasets (16/2636, 0.6%, p < 0.00001). Specifically, 9p24.1 amplifications amongst sarcomatoid tumors in public datasets, the "Discovery" and "Validation" cohorts were 7.7% (6/92), 15.1% (5/33), and 3.1% (4/127), respectively. Herein, we describe 13 cases and amplification status for these was characterized using next generation sequencing (n = 9) and/or fluorescence in situ hybridization (n = 10). Correlation with PD-L1 immunohistochemistry (n = 10) revealed constitutive expression (mean H-score: 222/300, n = 10). Analysis of outcomes based on PD-L1 expression in tumor cells performed on 282 cases ("Validation" cohort) did not reveal a significant prognostic effect and was likely reflective of advanced disease. A high incidence of constitutive PD-L1 expression in tumor cells in the "Validation" cohort (H-Score = 250/300) was noted amongst 83 rhabdoid (6%) and 127 sarcomatoid renal tumors (7.1%). This suggests additional mechanisms of constitutive expression other than amplification events. Importantly, two patients with 9p24.1-amplified sarcomatoid renal tumors showed significant response to immunotherapy. In summary, a subset of renal tumors with sarcomatoid transformation exhibits constitutive PD-L1 overexpression and these patients should be evaluated for enhanced response to immunotherapy.
引用
收藏
页码:1344 / 1358
页数:15
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