Plasma KIM-1 Is Associated with Recurrence Risk after Nephrectomy for Localized Renal Cell Carcinoma: A Trial of the ECOG-ACRIN Research Group (E2805)

被引:16
作者
Xu, Wenxin [1 ]
Puligandla, Maneka [1 ]
Halbert, Brian [2 ]
Haas, Naomi B. [3 ]
Flaherty, Keith T. [4 ]
Uzzo, Robert G. [5 ]
Dutcher, Janice P. [6 ]
DiPaola, Robert S. [7 ]
Sabbisetti, Venkata [8 ]
Bhatt, Rupal S. [2 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[3] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[4] Massachusetts Gen Hosp, Boston, MA 02114 USA
[5] Fox Chase Canc Ctr, 7701 Burholme Ave, Philadelphia, PA 19111 USA
[6] Canc Res Fdn, Chappaqua, NY USA
[7] Univ Kentucky, Lexington, KY USA
[8] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
关键词
KIDNEY INJURY MOLECULE-1; PHASE-III TRIAL; ADJUVANT SUNITINIB; DOUBLE-BLIND; SORAFENIB; MARKER; BIOMARKER; CYTOKINE; PLACEBO;
D O I
10.1158/1078-0432.CCR-21-0025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: No circulating biomarkers are currently available to identify patients at highest risk of recurrence after nephrectomy for renal cell carcinoma (RCC). Kidney injury molecule-1 (KIM-1) is overexpressed in RCC and its ectodomain circulates in plasma. We investigated whether plasma KIM-1 is a prognostic biomarker in patients with localized RCC after nephrectomy. Experimental Design: The ECOG-ACRIN E2805 (ASSURE) trial evaluated adjuvant sunitinib, sorafenib, or placebo in resected high-risk RCC. KIM-1 levels were measured from banked plasma at trial enrollment 4-12 weeks after nephrectomy. Lognormal accelerated failure time models were used to test for association between KIM-1 and disease-free survival (DFS) as well as overall survival (OS). Results: Plasma from 418 patients was analyzed. Higher postnephrectomy KIM-1 was associated with worse DFS across all study arms after adjustment for Fuhrman grade, T stage, N stage, and tumor histology [survival time ratio 056 for 75th vs. 25th percentile of KIM-1; 95% confidence interval (CI), 0.42-0.73; P < 0.001]. The association between KIM-1 and DFS was stronger among patients with pathologic nodal involvement (P-interaction = 0.0086). The addition of post-nephrectomy KIM-1 improved the concordance of clinical prognostic models (Stage, Size, Grade, and Necrosis (SSIGN) concordance 057 vs. 0.43, P = 0.05; UCLA International Staging System (UISS) concordance 0.60 vs. 0.40, P = 0.0005]. Higher post-nephrectomy KIM-1 was also associated with worse OS after multivariable adjustment (survival time ratio 0.71 for 75th vs. 25th percentile of MM-1; 95% CI, 0.56-0.91; P < 0.001). Conclusions: Post-nephrectomy plasma KIM-1 is associated with DFS and OS in RCC, and may be a biomarker for microscopic residual disease.
引用
收藏
页码:3397 / 3403
页数:7
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