PD-L1 Expression and Clinical Outcomes to Cabozantinib, Everolimus, and Sunitinib in Patients with Metastatic Renal Cell Carcinoma: Analysis of the Randomized Clinical Trials METEOR and CABOSUN

被引:50
作者
Flaifel, Abdallah [1 ]
Xie, Wanling [2 ]
Braun, David A. [3 ]
Ficial, Miriam [1 ]
Bakouny, Ziad [3 ]
Nassar, Amin H. [3 ]
Jennings, Rebecca B. [1 ]
Escudier, Bernard [4 ]
George, Daniel J. [5 ]
Motzer, Robert J. [6 ]
Morris, Michael J. [6 ]
Powles, Thomas [7 ]
Wang, Evelyn [8 ]
Huang, Ying [9 ]
Freeman, Gordon J. [3 ]
Choueiri, Toni K. [3 ]
Signoretti, Sabina [1 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Harvard Med Sch, Dana Farber Canc Inst, Dept Data Sci, Boston, MA 02115 USA
[3] Harvard Med Sch, Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Gustave Roussy Canc Campus, Dept Med Oncol, Villejuif, France
[5] Duke Univ, Med Ctr, Duke Canc Inst, Dept Med Oncol, Durham, NC USA
[6] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[7] Barts Canc Inst, Dept Expt Canc Med, London, England
[8] Exelixis Inc, San Francisco, CA USA
[9] Harvard Med Sch, Dana Farber Canc Inst, Dept Oncol Pathol, Boston, MA 02115 USA
关键词
DIFFERENTIAL EXPRESSION; INTERFERON-ALPHA; CANCER; THERAPY; PAZOPANIB; HETEROGENEITY; INTERMEDIATE; ANTIBODIES; NIVOLUMAB; SURVIVAL;
D O I
10.1158/1078-0432.CCR-19-1135
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Programmeddeath-ligand1(PD-L1) status by IHC is prognostic in metastatic renal cell carcinoma (mRCC), and its role as a potential predictive biomarker is under investigation. Using tumor tissue from the METEOR (NCT01865747) and CABOSUN (NCT01835158) clinical trials, we explored whether PD-L1 expression and the extent of the immune cell infiltrate can serve as prognostic and/or predictive biomarkers for cabozantinib and other targeted agents. Experimental Design: IHC double staining for PD-L1 and CD45/CD163 (immune cell markers) was performed on tumor tissue from METEOR (n = 306) and CABOSUN (n = 110) clinical trials. Immune cell density and MET expression levels were also analyzed. Our primary aim was to correlate progression-free survival (PFS) by independent central review with PD-L1 status in patients treated with cabozantinib, everolimus (METEOR), or sunitinib (CABOSUN). Overall survival (OS) was also interrogated. Results: Tumor cell (TC) PD-L1 expression (>= 1% cutoff) was detected in 29% and 23% of tumors from patients in the METEOR and CABOSUN trials, respectively. On univariate analysis, patients with PD-L1-positive TC had poorer PFS and OS than patients with PD-L1-negative TC on both trials, independent of therapy. On multivariable analysis and when combining the two trials, the association between TC PD-L1 expression and OS was statistically significant for all patients (P = 0.034) and for patients treated with cabozantinib only (P = 0.038). Cabozantinib was associated with improved PFS (HR < 0.70) and OS (HR < 0.85) compared with everolimus and sunitinib irrespective of PD-L1 expression. Conclusions: Higher PD-L1 expression results in worse clinical outcomes in mRCC treated with targeted therapy. Furthermore, PD-L1 expression is not predictive of response to cabozantinib therapy.
引用
收藏
页码:6080 / 6088
页数:9
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