In a study of patients with high-risk renal cell carcinoma, those who took the drug everolimus daily for up to one year after surgery lived longer without their disease returning (recurrence-free survival, or RFS) than those who did not take everolimus, although the results narrowly missed the clinical trial’s prespecified level for statistical significance. Improvement was seen primarily in patients with very high-risk disease, while patients with intermediate high-risk disease saw no improvement in RFS.
The results are from the phase III S0931 trial, also known as the EVEREST study, conducted by SWOG Cancer Research Network, a cancer clinical trials group funded by the National Cancer Institute (NCI). They will be presented at the 2022 annual meeting of the American Society of Clinical Oncology (ASCO) in Chicago on June 3.
The study was led by Christopher W. Ryan, MD, a SWOG investigator who is professor of medicine at Oregon Health & Science University.
“This is the only adjuvant study in renal carcinoma of the class of therapies called mTOR inhibitors,” Ryan said. “While there were fewer recurrences in patients who took everolimus, the results fell just shy of statistical significance. Patients at the highest risk of recurrence – those with locally advanced tumors or lymph node involvement – appeared to garner the most benefit from treatment.”
The EVEREST trial enrolled patients who had been diagnosed with intermediate high-risk or very high-risk renal cell carcinoma and who had had their cancer surgically removed by a partial or radical nephrectomy. The study randomized 1,545 of these patients to a year of either everolimus (a 10 mg pill daily) or a placebo, starting within 12 weeks of their surgery.
Overall across all patients, RFS was improved on the everolimus arm: a hazard ratio (HR) of 0.85, with a 95 percent confidence interval (CI) of 0.72-1.00 with a one-sided P value of 0.025. These results, however, narrowly missed the pre-specified significance level of 0.022.
Median RFS has not yet been reached for patients on either arm, but the estimates for five-year RFS are 67 percent for patients on the everolimus arm and 63 percent for those on the placebo arm.
EVEREST patients with very high-risk disease (55 percent of those enrolled) who took everolimus saw a 21 percent improvement in RFS (HR: 0.79; 95 percent CI 0.65-0.97), whereas RFS was essentially unchanged for those in the intermediate high-risk group (HR: 0.99; 95 percent CI 0.73-1.35).
Adverse events (side effects) such as oral mucositis (an inflammation of the lining of the mouth) led many patients to discontinue treatment. On the everolimus arm, 37 percent of patients stopped treatment because of adverse events they were experiencing. In fact, only 45 percent of patients on the everolimus arm completed all 54 weeks of study treatment, versus 69 percent on the placebo arm.
“High discontinuation rates of oral adjuvant therapies are common in cancer,” Dr. Ryan said. “Despite the large number of patients who stopped everolimus early, we still observed favorable results for everolimus, which brings into question the duration of adjuvant therapy that is actually needed.”
Study S0931 is supported by the National Cancer Institute (NCI), part of the National Institutes of Health (NIH), led by SWOG, and conducted by the NIH-funded National Clinical Trials Network (NCTN). The Alliance for Clinical Trials in Oncology, the ECOG-ACRIN Cancer Research Group, and NRG Oncology also enrolled patients to the trial.
S0931 was funded by the NIH/NCI through grants CA180888, CA180819, CA180820, and CA180821; in part by Novartis Pharmaceuticals Corporation; and in part by a grant from The Hope Foundation through the SWOG Trial Support (STrS) program.
In addition to Dr. Ryan, the S0931 study team included Catherine M. Tangen, DrPH, of SWOG Statistics and Data Management Center and Fred Hutch Cancer Center; Elisabeth I. Heath, MD, of Wayne State University/Karmanos Cancer Institute; Mark N. Stein, MD, of Rutgers Cancer Institute of New Jersey; Maxwell V. Meng, MD, of University of California at San Francisco; Ajjai S. Alva, MD, of University of Michigan; Sumanta K. Pal, MD, of City of Hope Comprehensive Cancer Center; Igor Puzanov, MD, MSCI, of Vanderbilt University/Ingram Cancer Center (during trial) and Roswell Park Comprehensive Cancer Center (currently); Joseph I. Clark, MD, of Loyola University Medical Center; Toni K. Choueiri, MD, of Dana-Farber Cancer Institute/Harvard Cancer Center; Neeraj Agarwal, MD, of Huntsman Cancer Institute at the University of Utah; Robert G. Uzzo, MD, MBA, of Fox Chase Cancer Center; Naomi B. Haas, MD, University of Pennsylvania; Timothy W. Synold, PharmD, City of Hope Comprehensive Cancer Center; Melissa Plets, MS, of SWOG Statistics and Data Management Center and Fred Hutch Cancer Center; Ulka N. Vaishampayan, MD, of University of Michigan; Brian M. Shuch, MD, of University of California at Los Angeles; Nicholas J. Vogelzang, MD, of Comprehensive Cancer Centers of Nevada; Ian M. Thompson, MD, of Children’s Hospital of San Antonio; and Primo N. Lara, MD, of University of California at Davis.
Reference: Ryan CW et al, “EVEREST: Everolimus for renal cancer ensuing surgical therapy—A phase III study (SWOG S0931, NCT01120249),” J Clin Oncol 40, 2022 (suppl 16; abstr LBA4500)
SWOG Cancer Research Network is part of the National Cancer Institute's National Clinical Trials Network and the NCI Community Oncology Research Program and is part of the oldest and largest publicly funded cancer research network in the nation. SWOG has nearly 12,000 members in 47 states and nine foreign countries who design and conduct clinical trials to improve the lives of people with cancer. SWOG trials have led to the approval of 14 cancer drugs, changed more than 100 standards of cancer care, and saved more than 3 million years of human life. Learn more at swog.org, and follow us on Twitter at @SWOG.
Method of Research
Randomized controlled/clinical trial
Subject of Research