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:41
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
    Barsoum, Ivraym B.
    Smallwood, Chelsea A.
    Siemens, D. Robert
    Graham, Charles H.
    [J]. 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
    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
    [J]. CLINICAL CANCER RESEARCH, 2015, 21 (06) : 1329 - 1339
  • [4] Safety and Activity of Anti-PD-L1 Antibody in Patients with Advanced Cancer
    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.
    [J]. 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
    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.
    [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
    Di Lorenzo, Giuseppe
    Porta, Camillo
    Bellmunt, Joaquim
    Sternberg, Cora
    Kirkali, Ziya
    Staehler, Michael
    Joniau, Steven
    Montorsi, Francesco
    Buonerba, Carlo
    [J]. 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)
    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.
    [J]. EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) : 228 - 247
  • [10] Renal cell carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up
    Escudier, B.
    Eisen, T.
    Porta, C.
    Patard, J. J.
    Khoo, V.
    Algaba, F.
    Mulders, P.
    Kataja, V.
    [J]. ANNALS OF ONCOLOGY, 2012, 23 : 65 - 71