Evidence map›Paper›PMID 28153029›Full record

ReviewJournal of hematology & oncology2017

New treatment options for metastatic renal cell carcinoma with prior anti-angiogenesis therapy.

Kevin Zarrabi, Chunhui Fang, Shenhong Wu

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03813394 (A Randomised Phase II Study of Pembrolizumab With or Without Bevacizumab in Platinum-resistant Recurrent/Metastatic Nasopharyngeal Carcinoma), which is not on this map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
8.8field-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.

NCT03813394 phase1 / phase2active not recruitingnot on this mapstarted 2019, after this paper: background citation

A Randomised Phase II Study of Pembrolizumab With or Without Bevacizumab in Platinum-resistant Recurrent/Metastatic Nasopharyngeal Carcinoma

TypeinterventionalSponsorNational University Hospital, SingaporeRan2019 to 2025Enrolled48ConditionsLocally Recurrent Cancer, Metastatic Nasopharyngeal CancerArmspembrolizumab, bevacizumab
3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 105 citations in OpenAlex.

  1. Pooled it
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  4. Tumor Microvessel Density as a Prognostic Marker in High-Risk Renal Cell Carcinoma Patients Treated on ECOG-ACRIN E2805.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
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  18. NMolecular cancer · 2022
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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

3 authors at 2 institutions in 1 country.

Kevin ZarrabiDepartment of Medicine, Stony Brook University Hospital, 9447 Suny, Stony Brook, NY, 11794-9447, USA.
Chunhui FangDepartment of Medicine, Stony Brook University Hospital, 9447 Suny, Stony Brook, NY, 11794-9447, USA.
Shenhong WuDepartment of Medicine, Stony Brook University Hospital, 9447 Suny, Stony Brook, NY, 11794-9447, USA. Shenhong.Wu@Stonybrookmedicine.edu.
Stony Brook University Hospital · USNorthport VA Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is a critical process in the progression of advanced renal cell carcinoma. Agents targeting angiogenesis have played a primary role in the treatment of metastatic renal cell carcinoma. However, resistance to anti-angiogenesis therapy almost always occurs, and major progress has been made in understanding its underlying molecular mechanism. Axitinib and everolimus have been used extensively in patients whom have had disease progression after prior anti-angiogenesis therapy. Recently, several new agents have been shown to improve overall survival in comparison with everolimus. This review provides an in-depth summary of drugs employable in the clinical setting, the rationale to their use, and the studies conducted leading to their approval for use and provides perspective on the paradigm shift in the treatment of renal cell carcinoma. Highlighted are the newly approved agents cabozantinib, nivolumab, and lenvatinib for advanced renal cell carcinoma patients treated with prior anti-angiogenesis therapy.

Indexed as

Therapies, InvestigationalAngiogenesis InhibitorsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalCarcinoma, Renal CellClinical Trials as TopicDrug Resistance, NeoplasmForecastingHumansKidney NeoplasmsMolecular Targeted TherapyNeoplasm ProteinsProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsProtein-Tyrosine KinasesRandomized Controlled Trials as TopicAngiogenesis InhibitorsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalMTOR protein, humanNeoplasm ProteinsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorProtein Kinase InhibitorsProtein-Tyrosine KinasesTOR Serine-Threonine KinasesAnti-angiogenesisCabozantinibLenvatinibNivolumabRenal cell carcinoma

Identifiers

PMID28153029
PMCPMC5288948
OpenAlexW2584812602

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.