Evidence map›Paper›PMID 38811313›Full record

Trial reportEuropean urology2024

Adjuvant Everolimus in Patients with Completely Resected, Very High-risk Renal Cell Carcinoma of Clear Cell Histology: Results from the Phase 3 Placebo-controlled SWOG S0931 (EVEREST) Trial.

Primo N Lara, Catherine Tangen, Elisabeth I Heath, Shuchi Gulati, Mark N Stein, Maxwell Meng, Ajjai Shivaram Alva, Sumanta K Pal, Igor Puzanov, Joseph I Clark and 11 more

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in European urology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Clinical advances and practice updates in genitourinary cancers: a 2024 review from the multidisciplinary Spanish 'Cambados annual meeting'.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  2. Advances in Adjuvant Therapy for Renal Cell Carcinoma: Perspectives on Risk Stratification and Treatment Outcomes.International journal of urology : official journal of the Japanese Urological Association · 2025
    Review
  3. Review
  4. 2024 CUA-KCRNC Expert Report: Management of non-clear cell renal cell carcinoma.Canadian Urological Association journal = Journal de l'Association des urologues du Canada · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Primo N LaraUniversity of California Davis Comprehensive Cancer Center, Sacramento, CA, USA. Electronic address: pnlara@ucdavis.edu.
Catherine TangenSWOG Statistical Center, Seattle, WA, USA.
Elisabeth I HeathKarmanos Cancer Institute, Wayne State University, Detroit, MI, USA.
Shuchi GulatiUniversity of California Davis Comprehensive Cancer Center, Sacramento, CA, USA.
Mark N SteinColumbia University, New York, NY, USA.
Maxwell MengUC San Francisco Diller Comprehensive Cancer Center, San Francisco, CA, USA.
Ajjai Shivaram AlvaUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Sumanta K PalCity of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Igor PuzanovRoswell Park Comprehensive Cancer Center, Buffalo, NY, USA.
Joseph I ClarkLoyola University Medical Center, Chicago, IL, USA.
Toni K ChoueiriDana Farber Cancer Institute, Boston, MA, USA.
Neeraj AgarwalHuntsman Cancer Institute, Salt Lake City, UT, USA.
Robert UzzoFox Chase Comprehensive Cancer Center, Philadelphia, PA, USA.
Naomi B HaasAbramson Comprehensive Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
Timothy W SynoldCity of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Melissa PletsSWOG Statistical Center, Seattle, WA, USA.
Ulka N VaishampayanUniversity of Michigan Rogel Cancer Center, Ann Arbor, MI, USA.
Brian M ShuchUCLA Jonsson Comprehensive Cancer Center, Los Angeles, CA, USA.
Seth LernerBaylor College of Medicine, Houston, TX, USA.
Ian M ThompsonChristus Santa Rosa Health System San Antonio, TX Health, San Antonio, TX, USA.
Christopher W RyanOregon Health and Science University, Portland OR, USA.

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$167.6M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
SWOG Statistics & Data Management Center complex - extension supplement for GY06U10CA180819 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Michael L. LeBlanc · 2014 to 2026
$115.2M
Staff InvestigatorsP30CA093373 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI Laura Marcu · 2002 to 2026
$84.9M
UM LAPs -UG1 GrantUG1CA233160 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANNE F SCHOTT · 2019 to 2026
$5.4M
Huntsman Cancer Institute/ University of Utah Network Lead Academic Participating Site ApplicationUG1CA233178 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Matthew Poppe, Heloisa Prado Soares · 2019 to 2026
$4.9M
UCDCCC NCTN UG1 PROGRAMUG1CA233340 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GANDARA, DAVID R, VALICENTI, RICHARD · 2019 to 2025
$3.7M
NCI National Clinical Trials Network – Network Lead Academic Participating SiteUG1CA233163 · NCI · WAYNE STATE UNIVERSITY · PI FLAHERTY, LAWRENCE E, SHIELDS, ANTHONY FRANK · 2019 to 2025
$3.5M
Network Lead Academic Participating Site Grant from the Roswell Park Cancer InstituteUG1CA233191 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI LELE, SHASHIKANT, LEVINE, ELLIS G · 2019 to 2025
$3.1M
Combination of Transcriptomic and Metallomic Biomarkers for Risk Assessment in Locoregional Clear Cell Renal Cell CarcinomaK08CA273542 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Shuchi Gulati · 2022 to 2026
$1.3M
NCI NIH HHS K08 CA273542NCI NIH HHS P30 CA093373NCI NIH HHS U10 CA180819NCI NIH HHS U10 CA180820NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA233160NCI NIH HHS UG1 CA233163NCI NIH HHS UG1 CA233178NCI NIH HHS UG1 CA233191NCI NIH HHS UG1 CA233340
6 · The paper itself

Abstract

BACKGROUND AND

objectiveEVEREST is a phase 3 trial in patients with renal cell cancer (RCC) at intermediate-high or very high risk of recurrence after nephrectomy who were randomized to receive adjuvant everolimus or placebo. Longer recurrence-free survival (RFS) was observed with everolimus (hazard ratio [HR] 0.85, 95% confidence interval [CI] 0.72-1.00; p = 0.051), but the nominal significance level (p = 0.044) was not reached. To contextualize these results with positive phase 3 trials of adjuvant sunitinib and pembrolizumab, we conducted a secondary analysis in a similar population of EVEREST patients with very high-risk disease and clear cell histology.

methodsPostnephrectomy patients with any clear cell component and very high-risk disease, defined as pT3a (grade 3-4), pT3b-c (any grade), T4 (any grade), or node-positive status (N+), were identified. A Cox regression model stratified by performance status was used to compare RFS and overall survival (OS) between the treatment arms. KEY FINDINGS AND LIMITATIONS: Of 1499 patients, 717 had clear cell histology and very high-risk disease; 699 met the eligibility criteria, of whom 348 were randomized to everolimus arm, and 351 to the placebo arm. Patient characteristics were similar between the arms. Only 163/348 (47%) patients in the everolimus arm completed all treatment as planned, versus 225/351 (64%) in the placebo arm. Adjuvant everolimus resulted in a statistically significant improvement in RFS (HR 0.80; 95%CI 0.65-0.99, p = 0.041). Evidence of a survival benefit was not seen (HR 0.85; 95%CI 0.64-1.14, p = 0.3) CONCLUSIONS AND CLINICAL IMPLICATIONS: In patients with clear cell RCC at very high-risk for recurrence, adjuvant everolimus resulted in significantly improved RFS compared to placebo but resulted in a high discontinuation rate due to adverse events. Although the treatment HR for OS was consistent with RFS findings, it did not reach statistical significance. With a focus on risk stratification tools and/or biomarkers to minimize toxicity risk in those not likely to benefit, this information can help inform the design of future adjuvant trials in high-risk RCC.

Indexed as

Carcinoma, Renal CellEverolimusKidney NeoplasmsNephrectomyAgedAntineoplastic AgentsChemotherapy, AdjuvantFemaleHumansMaleMiddle AgedNeoplasm StagingRisk AssessmentAntineoplastic AgentsEverolimusAdjuvantEverolimusHigh riskKidney cancer

Identifiers

PMID38811313
PMCPMC12036081

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.