The Association Between PD-L1 Expression and the Clinical Outcomes to Vascular Endothelial Growth Factor-Targeted Therapy in Patients With Metastatic Clear Cell Renal Cell Carcinoma

被引:42
作者
Shin, Su-Jin [1 ]
Jeon, Yoon Kyung [3 ]
Cho, Yong Mee [1 ]
Lee, Jae-Lyun [2 ]
Chung, Doo Hyun [3 ,4 ]
Park, Ji Young [5 ]
Go, Heounjeong [1 ]
机构
[1] Univ Ulsan, Coll Med, Dept Pathol, Asan Med Ctr, Seoul 138736, South Korea
[2] Univ Ulsan, Coll Med, Dept Oncol, Asan Med Ctr, Seoul 138736, South Korea
[3] Seoul Natl Univ Hosp, Dept Pathol, Seoul 110744, South Korea
[4] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul, South Korea
[5] Kyungpook Natl Univ, Sch Med, Med Ctr, Dept Pathol, Daegu, South Korea
关键词
Metastatic clear cell renal cell carcinoma; Programmed death ligand-2; Programmed death ligand-1; Vascular endothelial growth factor pathway-tyrosine kinase inhibitor; Responsiveness; Prognosis; SUNITINIB; PAZOPANIB; HYPOXIA;
D O I
10.1634/theoncologist.2015-0151
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Vascular endothelial growth factor pathway (VEGF)tyrosine kinase inhibitors (TKIs) are used as the first-line treatment for patients with metastatic clear cell renal cell carcinoma (mCCRCC). Recently, programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) blockade emerged as promising therapy for renal cell carcinoma. However, the expression pattern and prognostic implication of programmed death-ligands (PD-Ls) in mCCRCC patients receiving VEGF-TKI remain unclear. Patients and Methods. PD-L1 and PD-L2 expression in tumor cells and the quantities of PD-1+ tumor-infiltrating lymphocytes were immunohistochemically evaluated in 91 mCCRCC patients treated with VEGF-TKI, and their associations with VEGF-TKI responsiveness and clinical outcome were analyzed. Results. PD-L1 immunopositivity was observed in 17.6% and significantly associated with a high International Society of Urological Pathology grade (p = .031) and sarcomatoid features (p = .014). PD-L2 immunopositivity was observed in 39.6% and was not associated with any of the assessed clinicopathological variables. PD-L1-positive cases showed poor VEGF-TKI responsiveness (p = .012) compared with PD-L1-negative cases. In univariate survival analysis, PD-L1 immunopositivity was significantly associated with shorter overall survival (OS) (p = .037) and progression-free survival (PFS) (p = .043). Multivariate survival analysis revealed that PD-L1 expression was independently associated with poor OS (p = .038) and PFS (p = .013) in addition totumor necrosis (p = .006; p = .029, respectively) and Memorial Sloan Kettering Cancer Center score (p = .018; p = .032, respectively). PD-L2 expression was neither associated with VEGF-TKI responsiveness nor patients' outcome. Conclusion. PD-L1 expression was significantly related to lack of VEGF-TKI responsiveness and independently associated with shorter survival in mCCRCC patients after VEGF-TKI treatment. PD-L1 may have a predictive and prognostic value for determining the value of VEGF-TKI treatment in patients with mCCRCC.
引用
收藏
页码:1253 / 1260
页数:8
相关论文
共 28 条
[1]  
AMIN A, 2014, J CLIN ONCOL, V32, pA5010
[2]   A Mechanism of Hypoxia-Mediated Escape from Adaptive Immunity in Cancer Cells [J].
Barsoum, Ivraym B. ;
Smallwood, Chelsea A. ;
Siemens, D. Robert ;
Graham, Charles H. .
CANCER RESEARCH, 2014, 74 (03) :665-674
[3]   Molecular Subtypes of Clear Cell Renal Cell Carcinoma Are Associated with Sunitinib Response in the Metastatic Setting [J].
Beuselinck, Benoit ;
Job, Sylvie ;
Becht, Etienne ;
Karadimou, Alexandra ;
Verkarre, Virginie ;
Couchy, Gabrielle ;
Giraldo, Nicolas ;
Rioux-Leclercq, Nathalie ;
Molinie, Vincent ;
Sibony, Mathilde ;
Elaidi, Reza ;
Teghom, Corinne ;
Patard, Jean-Jacques ;
Mejean, Arnaud ;
Fridman, Wolf Herman ;
Sautes-Fridman, Catherine ;
de Reynies, Aurelien ;
Oudard, Stephane ;
Zucman-Rossi, Jessica .
CLINICAL CANCER RESEARCH, 2015, 21 (06) :1329-1339
[4]   Safety and Activity of Anti-PD-L1 Antibody in Patients with Advanced Cancer [J].
Brahmer, Julie R. ;
Tykodi, Scott S. ;
Chow, Laura Q. M. ;
Hwu, Wen-Jen ;
Topalian, Suzanne L. ;
Hwu, Patrick ;
Drake, Charles G. ;
Camacho, Luis H. ;
Kauh, John ;
Odunsi, Kunle ;
Pitot, Henry C. ;
Hamid, Omid ;
Bhatia, Shailender ;
Martins, Renato ;
Eaton, Keith ;
Chen, Shuming ;
Salay, Theresa M. ;
Alaparthy, Suresh ;
Grosso, Joseph F. ;
Korman, Alan J. ;
Parker, Susan M. ;
Agrawal, Shruti ;
Goldberg, Stacie M. ;
Pardoll, Drew M. ;
Gupta, Ashok ;
Wigginton, Jon M. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (26) :2455-2465
[5]   Correlation of PD-L1 Tumor Expression and Treatment Outcomes in Patients with Renal Cell Carcinoma Receiving Sunitinib or Pazopanib: Results from COMPARZ, a Randomized Controlled Trial [J].
Choueiri, Toni K. ;
Figueroa, David J. ;
Fay, Andre P. ;
Signoretti, Sabina ;
Liu, Yuan ;
Gagnon, Robert ;
Deen, Keith ;
Carpenter, Christopher ;
Benson, Peter ;
Ho, Thai H. ;
Pandite, Lini ;
de Souza, Paul ;
Powles, Thomas ;
Motzer, Robert J. .
CLINICAL CANCER RESEARCH, 2015, 21 (05) :1071-1077
[6]  
Delahunt B, 2013, AM J SURG PATHOL, V37, P1490, DOI 10.1097/PAS.0b013e318299f0fb
[7]   Toxicities of Targeted Therapy and Their Management in Kidney Cancer [J].
Di Lorenzo, Giuseppe ;
Porta, Camillo ;
Bellmunt, Joaquim ;
Sternberg, Cora ;
Kirkali, Ziya ;
Staehler, Michael ;
Joniau, Steven ;
Montorsi, Francesco ;
Buonerba, Carlo .
EUROPEAN UROLOGY, 2011, 59 (04) :526-540
[8]  
Eble J., 2004, WHO CLASSIFICATION T
[9]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[10]   Renal cell carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up [J].
Escudier, B. ;
Eisen, T. ;
Porta, C. ;
Patard, J. J. ;
Khoo, V. ;
Algaba, F. ;
Mulders, P. ;
Kataja, V. .
ANNALS OF ONCOLOGY, 2012, 23 :65-71