Evidence map›Paper›PMID 36720658›Full record

Trial reportEuropean urology oncology2023

Survival by Depth of Response and Efficacy by International Metastatic Renal Cell Carcinoma Database Consortium Subgroup with Lenvatinib Plus Pembrolizumab Versus Sunitinib in Advanced Renal Cell Carcinoma: Analysis of the Phase 3 Randomized CLEAR Study.

Viktor Grünwald, Thomas Powles, Evgeny Kopyltsov, Vadim Kozlov, Teresa Alonso-Gordoa, Masatoshi Eto, Thomas Hutson, Robert Motzer, Eric Winquist, Pablo Maroto and 10 more

Open access · hybridAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in European urology oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
7.8field-weighted citation impact, top 2% of its field
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  6. Review
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  12. Review
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  14. International journal of molecular sciences · 2024
    Article
  15. Review
  16. Review
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  18. High Prognostic Value ofDiagnostics (Basel, Switzerland) · 2023
    Article
  19. Article
  20. Round up.Indian journal of urology : IJU : journal of the Urological Society of India
    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

20 authors at 18 institutions in 12 countries.

Viktor GrünwaldInterdisciplinary Genitourinary Oncology, Clinic for Urology, Clinic for Medical Oncology, University Hospital Essen, Essen, Germany. Electronic address: Viktor.Gruenwald@uk-essen.de.
Thomas PowlesThe Royal Free NHS Trust, London, England, UK.
Evgeny KopyltsovState Institution of Healthcare "Regional Clinical Oncology Dispensary", Omsk, Russia.
Vadim KozlovState Budgetary Health Care Institution "Novosibirsk Regional Clinical Oncology Dispensary", Novosibirsk, Russia.
Teresa Alonso-GordoaHospital Universitario Ramón y Cajal, Madrid, Spain.
Masatoshi EtoKyushu University, Fukuoka, Japan.
Thomas HutsonTexas Oncology, Dallas, TX, USA.
Robert MotzerMemorial Sloan Kettering Cancer Center, New York, NY, USA.
Eric WinquistUniversity of Western Ontario, London, Ontario, Canada.
Pablo MarotoHospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Bhumsuk KeamSeoul National University Hospital, Seoul, Republic of Korea.
Giuseppe ProcopioFondazione IRCCS Istituto Nazionale dei Tumori di Milano, Italy.
Shirley WongWestern Health, VIC, Australia.
Bohuslav MelicharPalacký University Medical School and Teaching Hospital, Olomouc, Czech Republic.
Frederic RollandCentre René Gauducheau Centre de Lutte Contre Le Cancer Nantes, Saint-Herblain, France.
Mototsugu OyaKeio University School of Medicine, Tokyo, Japan.
Karla Rodriguez-LopezMerck & Co., Inc, Rahway, NJ, USA.
Kenichi SaitoEisai Inc, Nutley, NJ, USA.
Jodi McKenzieEisai Inc, Nutley, NJ, USA.
Camillo PortaUniversity of Bari 'A. Moro', Bari, Italy.
Eisai (United States) · USState Healthcare Institution "Regional Clinical Oncological Dispensary" · RUEssen University Hospital · DEFondazione IRCCS Istituto Nazionale dei Tumori · ITHospital de Sant Pau · ESHospital Universitario Ramón y Cajal · ESInstitut Génétique Nantes Atlantique · FRKeio University · JPKyushu University · JPMemorial Sloan Kettering Cancer Center · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USPalacký University Olomouc · CZRoyal Free London NHS Foundation Trust · GBSeoul National University Hospital · KRTexas Oncology · USUniversity of Bari Aldo Moro · ITWestern Health · AUWestern University · CA

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundThe extent of tumor shrinkage has been deemed a predictor of survival for advanced/metastatic renal cell carcinoma (RCC), a disease with historically poor survival.

objectiveTo perform an exploratory analysis of overall survival (OS) by tumor response by 6 mo, and to assess the efficacy and survival outcomes in specific subgroups. DESIGN, SETTING, AND

participantsCLEAR was an open-label, multicenter, randomized, phase 3 trial of first-line treatment of advanced clear cell RCC.

interventionPatients were randomized 1:1:1 to lenvatinib 20 mg orally daily with pembrolizumab 200 mg intravenously once every 3 wk, lenvatinib plus everolimus (not included in this analysis), or sunitinib 50 mg orally daily for 4 wk on treatment/2 wk of no treatment. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Landmark analyses were conducted to assess the association of OS with tumor shrinkage and progressive disease status by 6 mo. Progression-free survival, duration of response, and objective response rate (ORR) were analyzed by the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk subgroup and by the presence of target kidney lesions. Efficacy was assessed by an independent review committee as per Response Evaluation Criteria in Solid Tumors version 1.1. RESULTS AND LIMITATIONS: Landmark analyses by tumor shrinkage showed that patients enrolled to lenvatinib plus pembrolizumab arm with a confirmed complete response or >75% target-lesion reduction by 6 mo had a 24-mo OS probability of ≥91.7%. A landmark analysis by disease progression showed that patients with no progression by 6 mo had lower probabilities of death in both arms. Patients with an IMDC risk classification of intermediate/poor had longer median progression-free survival (22.1 vs 5.9 mo) and a higher ORR (72.4% vs 28.8%) with lenvatinib plus pembrolizumab versus sunitinib. Similarly, results favored lenvatinib plus pembrolizumab in IMDC-favorable patients and those with/without target kidney lesions. Limitations of the study are that results were exploratory and not powered/stratified.

conclusionsLenvatinib plus pembrolizumab showed improved efficacy versus sunitinib for patients with advanced RCC; landmark analyses showed that tumor response by 6 mo correlated with longer OS. PATIENT SUMMARY: In this report of the CLEAR trial, we explored the survival of patients with advanced renal cell carcinoma by assessing how well they initially responded to treatment. We also explored how certain groups of patients responded to treatment overall. Patients were assigned to cycles of either lenvatinib 20 mg daily plus pembrolizumab 200 mg every 3 wk or sunitinib 50 mg daily for 4 wk (followed by a 2-wk break). Patients who either had a "complete response" or had their tumors shrunk by >75% within 6 mo after starting treatment with lenvatinib plus pembrolizumab had better survival than those with less tumor reduction by 6 mo. Additionally, patients who had more severe disease (as per the International Metastatic Renal Cell Carcinoma Database Consortium) at the start of study treatment survived for longer without disease progression with lenvatinib plus pembrolizumab than with sunitinib.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAntibodies, Monoclonal, HumanizedDisease ProgressionHumansPhenylurea CompoundsQuinolinesSunitinibAntibodies, Monoclonal, HumanizedlenvatinibpembrolizumabPhenylurea CompoundsQuinolinesSunitinibDepth of responseLenvatinibPembrolizumabRenal cell carcinomaSunitinib

Identifiers

PMID36720658
PMCPMC10875602
OpenAlexW4318754961

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.