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Checkpoint inhibitors in patients with metastatic renal cell carcinoma: Results from the International Metastatic Renal Cell Carcinoma Database Consortium
Author(s) -
Yip Steven M.,
Wells Connor,
Moreira Raphael,
Wong Alex,
Srinivas Sandy,
Beuselinck Benoit,
Porta Camillo,
Sim HaoWen,
Ernst D. Scott,
Rini Brian I.,
Yuasa Takeshi,
Basappa Naveen S.,
Kanesvaran Ravindran,
Wood Lori A.,
Canil Christina,
Kapoor Anil,
Fu Simon Y.F.,
Choueiri Toni K.,
Heng Daniel Y.C.
Publication year - 2018
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.31595
Subject(s) - medicine , nivolumab , renal cell carcinoma , ipilimumab , oncology , clear cell renal cell carcinoma , retrospective cohort study , carcinoma , cancer , gastroenterology , immunotherapy
BACKGROUND To the authors' knowledge, outcomes and prognostic tools have yet to be clearly defined in patients with metastatic renal cell carcinoma (mRCC) who are treated with immuno‐oncology (IO) checkpoint inhibitors (programmed death‐ligand 1 [PD‐L1] inhibitors). In the current study, the authors aimed to establish IO efficacy benchmarks in patients with mRCC and update patient outcomes in each International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) prognostic class. METHODS A retrospective analysis was performed using the IMDC database with data from 38 centers. It included patients with mRCC who were treated with ≥1 line of IO. Overall response rates (ORRs), duration of treatment (DOT), and overall survival (OS) were calculated. Patients were stratified using IMDC prognostic factors. RESULTS A total of 687 patients (90% with clear cell and 10% with non‐clear cell) were included. The ORR was 27% in evaluable patients (461 patients). In patients treated with first‐line nivolumab and ipilimumab (49 patients), the combination of PD‐L1 inhibitor and vascular endothelial growth factor inhibitor (72 patients), and PD‐L1 inhibitor (51 patients), the ORR was 31%, 39%, and 40%, respectively, and the median DOT was 8.3 months, 14.7 months, and 8.3 months, respectively. The ORR for second‐line, third‐line, and fourth‐line nivolumab was 22%, 24%, and 26%, respectively. The median DOT was 5.7 months, 6.2 months, and 8.3 months, respectively, in the second‐line, third‐line, and fourth‐line settings. When segregated into IMDC favorable‐risk, intermediate‐risk, and poor‐risk groups, the median OS rates for the first‐line, second‐line, third‐line, and fourth‐line treatment settings were not reached (NR), NR, and NR, respectively ( P = .163); NR, 26.7 months, and 7.4 months, respectively ( P < 0. 0001); 36.1 months, 28.2 months, and 11.1 months, respectively ( P = .016); and NR, NR, and 6.7 months, respectively ( P = .047). CONCLUSIONS The ORR was not found to deteriorate from the first‐line to the fourth‐line of IO therapy. In the second line through fourth line, the IMDC criteria appropriately stratified patients into favorable‐risk, intermediate‐risk, and poor‐risk groups for OS.