Angiogenic and Immune-Related Biomarkers and Outcomes Following Axitinib/Pembrolizumab Treatment in Patients with Advanced Renal Cell Carcinoma

被引:14
|
作者
Martini, Jean-Fran Comma Cois [1 ]
Plimack, Elizabeth R. [2 ]
Choueiri, Toni K. [3 ]
McDermott, David F. [4 ]
Puzanov, Igor [5 ,6 ]
Fishman, Mayer N. [7 ]
Cho, Daniel C. [8 ]
Vaishampayan, Ulka [9 ]
Rosbrook, Bradley [1 ]
Fernandez, Kathrine C. [10 ]
Tarazi, Jamal C. [1 ]
George, Saby [6 ]
Atkins, Michael B. [11 ]
机构
[1] Pfizer Global Prod Dev Oncol, San Diego, CA USA
[2] Fox Chase Canc Ctr, 333 Cottman Ave, Philadelphia, PA 19111 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[5] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[6] Roswell Pk Comprehens Canc Ctr, Buffalo, NY USA
[7] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[8] NYU Langone Med Ctr, Perlmutter Canc Ctr, New York, NY USA
[9] Wayne State Univ, Karmanos Canc Inst, Detroit, MI USA
[10] Pfizer Global Prod Dev Oncol, Cambridge, MA USA
[11] Georgetown Lombardi Comprehens Canc Ctr, Washington, DC USA
关键词
BLIND PHASE-III; INTERFERON-ALPHA; OPEN-LABEL; SURVIVAL; SUNITINIB; PAZOPANIB; AXITINIB; THERAPY;
D O I
10.1158/1078-0432.CCR-20-1408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Combined axitinib/pembrolizumab is approved for advanced renal cell carcinoma (aRCC). This exploratory analysis examined associations between angiogenic and immune-related biomarkers and outcomes following axitinib/pembrolizumab treatment. Patients and Methods: Prospectively defined retrospective correlative exploratory analyses tested biospecimens from 52 treatment-naive patients receiving axitinib and pembrolizumab (starting doses 5 mg twice daily and 2 mg/kg respectively, every 3 weeks). Tumor tissue, serum, and whole blood samples were collected at baseline, at cycle 2 day 1 (C2D1), and end of treatment (EOT) for blood-based samples. Clinical outcomes were objective response rate (ORR) and progression-free survival (PFS). Results: Higher baseline tumor levels of CD8 showed a trend toward longer PFS (HR 0.4; P = 0.091). Higher baseline serum levels of CXCL10 (P = 0.0197) and CEACAM1 (P = 0.085) showed a trend toward better ORR and longer PFS, respectively. Patients for whom IL6 was not detected at baseline had longer PFS versus patients for whom it was detected (HR 0.4; P = 0.028). At C2D1 and/or EOT, mainly immune-related biomarkers showed any association with better outcomes. The genes CA9 (P = 0.084), HIF1A (P = 0.064), and IFNG (P = 0.073) showed trending associations with ORR, and AKT3 (P = 0.0145), DDX58 (P = 0.0726), GZMA (P = 0.0666), LCN2 (NGAL; P = 0.0267), and PTPN11 (P = 0.0287) with PFS. Conclusions: With combined axitinib/pembrolizumab treatment in patients with aRCC, mostly immune-related biomarkers are associated with better treatment outcomes. This exploratory analysis has identified some candidate biomarkers to consider in future prospective testing.
引用
收藏
页码:5598 / 5608
页数:11
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