Evidence map›Paper›PMID 37778952›Full record

Trial reportEuropean urology2024

Pembrolizumab with or Without Lenvatinib as First-line Therapy for Patients with Advanced Urothelial Carcinoma (LEAP-011): A Phase 3, Randomized, Double-Blind Trial.

Nobuaki Matsubara, Ronald de Wit, Arjun Vasant Balar, Arlene O Siefker-Radtke, Jakub Zolnierek, Tibor Csoszi, Sang Joon Shin, Se Hoon Park, Vagif Atduev, Mahmut Gumus and 11 more

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
PubMed Publisher
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. It is linked to trial NCT03898180 (A Phase 3, Randomized, Double-blind Study to Compare the Efficacy and Safety of Pembrolizumab), which is not on this map. Cited by 20 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 4 pooled it
7.0field-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.

NCT03898180 phase3completednot on this map

A Phase 3, Randomized, Double-blind Study to Compare the Efficacy and Safety of Pembrolizumab (MK-3475) in Combination With Lenvatinib (E7080/MK-7902) Versus Pembrolizumab and Placebo as First Line Treatment for Locally Advanced or Metastatic Urothelial Carcinoma in Cisplatin-ineligible Participants Whose Tumors Express PD-L1, and in Participants Ineligible for Any Platinum-containing Chemotherapy Regardless of PD-L1 Expression (LEAP-011)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2019 to 2024Enrolled505ConditionsUrothelial CarcinomaArmsPembrolizumab, Lenvatinib, Placebo for lenvatinib
3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 4 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Pooled it
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  17. Landscape of targeted therapies for advanced urothelial carcinoma.Exploration of targeted anti-tumor therapy · 2024
    Review
  18. Review
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  20. Combination therapy for advanced urothelial cancer: LEAP-011 trial.Indian journal of urology : IJU : journal of the Urological Society of India
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 15 institutions in 10 countries.

Nobuaki MatsubaraNational Cancer Center Hospital East, Chiba, Japan.
Ronald de WitErasmus MC Cancer Institute, Rotterdam, The Netherlands.
Arjun Vasant BalarPerlmutter Cancer Center, NYU Langone Health, New York, NY, USA.
Arlene O Siefker-RadtkeThe University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Jakub ZolnierekLUX MED Onkologia Hospital, Warsaw, Poland.
Tibor CsosziJász-Nagykun-Szolnok County Hospital, Szolnok, Hungary.
Sang Joon ShinYosnei University College of Medicine, Seoul, South Korea.
Se Hoon ParkSamsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Vagif AtduevVolga District Medical Center, Federal Medical-Biological Agency, Nizhny Novgorod, Russia.
Mahmut GumusIstanbul Medeniyet University, Istanbul, Turkey.
Yu-Li SuKaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Saziye Burcak KaracaTülay Aktaş Onkoloji Hastanesi, İzmir Bornova, Turkey.
Hernán Javier CutuliInstitute for Diagnosis and Metabolic Research (IDIM), Buenos Aires, Argentina.
Mehmet A N SendurAnkara Yildirim Beyazıt University Faculty of Medicine and Ankara City Hospital, Ankara, Turkey.
Liji ShenMerck & Co., Inc., Rahway, NJ, USA.
Karen O'HaraEisai LTD, Hatfield, UK.
Chinyere E OkparaEisai LTD, Hatfield, UK.
Sonia FrancoMerck & Co., Inc., Rahway, NJ, USA.
Blanca Homet MorenoMerck & Co., Inc., Rahway, NJ, USA.
Petros GrivasUniversity of Washington, Fred Hutchinson Cancer Center, Seattle, WA, USA. Electronic address: pgrivas@uw.edu.
Yohann LoriotGustave Roussy, Cancer Campus, Villejuif, France; Université Paris-Saclay, Villejuif, France. Electronic address: Yohann.loriot@gustaveroussy.fr.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USEisai (United Kingdom) · GBAnkara Yıldırım Beyazıt University · TRChang Gung University · TWErasmus MC Cancer Institute · NLFederal Medical-Biological Agency · RUInstituto de Diagnóstico e Investigaciones Metabólicas · ARIstanbul Medeniyet University · TRNational Cancer Center Hospital East · JPNYU Langone Health · USSamsung Medical Center · KRThe University of Texas MD Anderson Cancer Center · USUniversité Paris-Saclay · FRUniversity of Washington · USYonsei University Health System · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPembrolizumab plus lenvatinib has shown antitumor activity and acceptable safety in patients with platinum-refractory urothelial carcinoma (UC).

objectiveTo evaluate pembrolizumab plus either lenvatinib or placebo as first-line therapy for advanced UC in the phase 3 LEAP-011 study. DESIGN, SETTING, AND

participantsPatients with advanced UC who were ineligible for cisplatin-based therapy or any platinum-based chemotherapy were enrolled.

interventionPatients were randomly assigned (1:1) to pembrolizumab 200 mg intravenously every 3 wk plus either lenvatinib 20 mg or placebo orally once daily. OUTCOME MEASUREMENTS AND STATISTICAL ANALYSIS: Dual primary endpoints were progression-free survival (PFS) and overall survival (OS). An external data monitoring committee (DMC) regularly reviewed safety and efficacy data every 3 mo. RESULTS AND LIMITATIONS: Between June 25, 2019 and July 21, 2021, 487 patients were allocated to receive lenvatinib plus pembrolizumab (n = 245) or placebo plus pembrolizumab (n = 242). The median time from randomization to the data cutoff date (July 26, 2021) was 12.8 mo (interquartile range, 6.9-19.3). The median PFS was 4.5 mo in the combination arm and 4.0 mo in the pembrolizumab arm (hazard ratio [HR] 0.90 [95% confidence interval {CI} 0.72-1.14]). The median OS was 11.8 mo for the combination arm and 12.9 mo for the pembrolizumab arm (HR 1.14 [95% CI 0.87-1.48]). Grade 3-5 adverse events attributed to trial treatment occurred in 123 of 241 patients (51%) treated with lenvatinib plus pembrolizumab and in 66 of 242 patients (27%) treated with placebo plus pembrolizumab. This trial was terminated earlier than initially planned based on recommendation from the DMC.

conclusionsThe benefit-to-risk ratio for first-line lenvatinib plus pembrolizumab was not considered favorable versus pembrolizumab plus placebo as first-line therapy in patients with advanced UC. PATIENT SUMMARY: Lenvatinib plus pembrolizumab was not more effective than pembrolizumab plus placebo in patients with advanced urothelial carcinoma.

Indexed as

Carcinoma, Transitional CellPhenylurea CompoundsQuinolinesUrinary Bladder NeoplasmsAntibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsHumansAntibodies, Monoclonal, HumanizedlenvatinibpembrolizumabPhenylurea CompoundsQuinolinesBladder cancerCheckpoint inhibitorCisplatin IneligibleImmunotherapyLenvatinibPembrolizumabPlatinum ineligibleUrothelial carcinoma

Identifiers

PMID37778952
OpenAlexW4387190801

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.