Evidence map›Paper›PMID 29784193›Full record

SynthesisEuropean urology2018

Adjuvant Vascular Endothelial Growth Factor-targeted Therapy in Renal Cell Carcinoma: A Systematic Review and Pooled Analysis.

Maxine Sun, Lorenzo Marconi, Tim Eisen, Bernard Escudier, Rachel H Giles, Naomi B Haas, Lauren C Harshman, David I Quinn, James Larkin, Sumanta K Pal and 6 more

Open access · greenAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in European urology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

29 citing papers in PubMed, 89 citations in OpenAlex.

  1. Trial
  2. Adjuvant Sorafenib for Renal Cell Carcinoma at Intermediate or High Risk of Relapse: Results From the SORCE Randomized Phase III Intergroup Trial.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2020
    Trial
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 14 institutions in 6 countries.

Maxine SunLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Lorenzo MarconiDepartment of Urology, Coimbra University Hospital, Coimbra, Portugal.
Tim EisenDepartment of Oncology, Addenbrooke's Hospital, Cambridge Biomedical Research Centre, UK.
Bernard EscudierDepartment of Cancer Medicine, Institut Gustave Roussy, Villejuif, France.
Rachel H GilesPatient Advocate, International Kidney Cancer Coalition, Duivendrecht, The Netherlands; Department Nephrology and Hypertension, Regenerative Medicine Center Utrecht, University Medical Center Utrecht, University of Utrecht, The Netherlands.
Naomi B HaasAbramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
Lauren C HarshmanLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
David I QuinnSection of Genitourinary Medical Oncology, University of Southern California Norris Comprehensive Cancer Center, Los Angeles, CA, USA.
James LarkinRoyal Marsden NHS Trust Foundation Trust, London, UK.
Sumanta K PalDepartment of Medical Oncology & Therapeutics Research, City of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Thomas PowlesThe Royal Free NHS Trust and Barts Cancer Institute, Queen Mary University of London, London, UK.
Christopher W RyanKnight Cancer Institute, Oregon Health & Science University, Portland, OR, USA.
Cora N SternbergDepartment of Medical Oncology, San Camillo Forlanini Hospital, Rome, Italy.
Robert UzzoDepartment of Surgery, Fox Chase Cancer Center - Temple University Health System, Philadelphia, PA, USA.
Toni K ChoueiriLank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Boston, MA, USA. Electronic address: Toni_Choueiri@dfci.harvard.edu.
Axel BexDepartment of Urology, The Netherlands Cancer Institute, Antoni van Leeuwenhoek Hospital, Amsterdam, The Netherlands. Electronic address: a.bex@nki.nl.
Dana-Farber Cancer Institute · USAddenbrooke's Hospital · GBCarlo Forlanini Hospital · ITCity of Hope · USFox Chase Cancer Center · USInstitut Gustave Roussy · FROregon Health & Science University · USRoyal Marsden NHS Foundation Trust · GBThe Netherlands Cancer Institute · NLThe Royal Free Hospital · GBUniversity Medical Center Utrecht · NLUniversity of Coimbra · PTUniversity of Pennsylvania · USUniversity of Southern California · US

Funding

USC/NORRIS COMPREHENSIVE CANCER CENTER (CORE) SUPPORTP30CA014089 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Fumito Ito · 1985 to 2026
$181.4M
Cancer Research UK 6858NCI NIH HHS P30 CA014089
6 · The paper itself

Abstract

contextContradictory data exist with regard to adjuvant vascular endothelial growth factor receptor (VEGFR)-targeted therapy in surgically managed patients for localized renal cell carcinoma (RCC).

objectiveTo systematically evaluate the current evidence regarding the therapeutic benefit (disease-free survival [DFS] and overall survival [OS]) and grade 3-4 adverse events (AEs) for adjuvant VEGFR-targeted therapy for resected localized RCC. EVIDENCE ACQUISITION: A critical review of PubMed/Medline, Embase, and the Cochrane Library in January 2018 according to the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) statement was performed. We identified reports and reviewed them according to the Consolidated Standards of Reporting Trials and Standards for the Reporting of Diagnostic Accuracy Studies criteria. Of eight full-text articles that were eligible for inclusion, five studies (two of five were updated analyses) were retained in the final synthesis. Study characteristics were abstracted and the number needed to treat (NNT) per trial was estimated. EVIDENCE SYNTHESIS: The three randomized controlled phase III trials included the following comparisons: sunitinib versus placebo or sorafenib versus placebo (Adjuvant Sorafenib or Sunitinib for Unfavorable Renal Carcinoma [ASSURE] study, n=1943), sunitinib versus placebo (S-TRAC, n=615), and pazopanib versus placebo (Pazopanib As Adjuvant Therapy in Localized/Locally Advanced RCC After Nephrectomy study, n=1135). The NNT ranged from 10 (S-TRAC) to 137 (ASSURE study). The pooled analysis showed that VEGFR-targeted therapy was not statistically significantly associated with improved DFS (hazard ratio [HR

conclusionsThis pooled analysis of reported randomized trials did not reveal a statistically significant effect between adjuvant VEGFR-targeted therapy and improved DFS or OS in patients with intermediate/high-risk local or regional fully resected RCC. Improvement in DFS may be more likely with the use of full-dose regimens, pending further results. However, adjuvant treatment was associated with high-grade AEs. PATIENT SUMMARY: Vascular endothelial growth factor receptor-targeted therapy after nephrectomy for localized kidney cancer is not associated with consistent improvements in delaying cancer recurrence or prolonging life and comes at the expense of potentially significant side effects.

Indexed as

Neovascularization, PathologicAngiogenesis InhibitorsCarcinoma, Renal CellChemotherapy, AdjuvantClinical Trials, Phase III as TopicDisease-Free SurvivalDisease ProgressionHumansKidney NeoplasmsNeoplasm Recurrence, LocalNephrectomyProgression-Free SurvivalRandomized Controlled Trials as TopicReceptors, Vascular Endothelial Growth FactorRisk FactorsSignal TransductionAngiogenesis InhibitorsReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor AVEGFA protein, humanAdjuvant therapyMeta-analysisMetastatic renal cell carcinomaSystemic therapyTargeted therapy

Identifiers

PMID29784193
PMCPMC7515772
OpenAlexW2804762794

What OpenQuestion holds

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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.