학술논문
The High-Dose Aldesleukin “Select” Trial: A Trial to Prospectively Validate Predictive Models of Response to Treatment in Patients with Metastatic Renal Cell Carcinoma
Document Type
article
Author
McDermott, David F; Cheng, Su-Chun; Signoretti, Sabina; Margolin, Kim A; Clark, Joseph I; Sosman, Jeffrey A; Dutcher, Janice P; Logan, Theodore F; Curti, Brendan D; Ernstoff, Marc S; Appleman, Leonard; Wong, Michael KK; Khushalani, Nikhil I; Oleksowicz, Leslie; Vaishampayan, Ulka N; Mier, James W; Panka, David J; Bhatt, Rupal S; Bailey, Alexandra S; Leibovich, Bradley C; Kwon, Eugene D; Kabbinavar, Fairooz F; Belldegrun, Arie S; Figlin, Robert A; Pantuck, Allan J; Regan, Meredith M; Atkins, Michael B
Source
Clinical Cancer Research. 21(3)
Subject
Language
Abstract
PurposeHigh-dose aldesleukin (HD IL2) received FDA approval for the treatment of metastatic renal cell carcinoma (MRCC) in 1992, producing a 14% objective response rate (ORR) and durable remissions. Retrospective studies suggested that clinical and pathologic features could predict for benefit. The Cytokine Working Group conducted this prospective trial to validate proposed predictive markers of response to HD IL2.Experimental designStandard HD IL2 was administered to prospectively evaluate whether the ORR of patients with mRCC with "good" predictive pathologic features based on an "integrated selection" model [ISM (e.g., clear-cell histology subclassification and carbonic anhydrase-9 (CA-9) IHC staining] was significantly higher than the ORR of a historical, unselected population. Archived tumor was collected for pathologic analysis including tumor programmed death-ligand 1 (PD-L1) expression.ResultsOne hundred and twenty eligible patients were enrolled between June 11 and September 7; 70% were Memorial Sloan Kettering Cancer Center (New York, NY) intermediate risk, 96% had clear cell RCC, and 99% had prior nephrectomy. The independently assessed ORR was 25% (30/120, 95% CI, 17.5%-33.7%, P = 0.0014; 3 complete responses, 27 partial responses) and was higher than a historical ORR. Thirteen patients (11%) remained progression free at 3 years and the median overall survival was 42.8 months. ORR was not statistically different by ISM classification ("good-risk" 23% vs. "poor-risk" 30%; P = 0.39). ORR was positively associated with tumor PD-L1 expression (P = 0.01) by IHC.ConclusionsIn this prospective, biomarker validation study, HD IL2 produced durable remissions and prolonged survival in both "good" and "poor-risk" patients. The proposed ISM was unable to improve the selection criteria. Novel markers (e.g., tumor PD L1 expression) appeared useful, but require independent validation.