Evidence map›Paper›PMID 32291161›Full record

ArticleClinical genitourinary cancer2020

The Efficacy of Lenvatinib Plus Everolimus in Patients with Metastatic Renal Cell Carcinoma Exhibiting Primary Resistance to Front-Line Targeted Therapy or Immunotherapy.

Lana Hamieh, Rachel L Beck, Valerie H Le, James J Hsieh

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Clinical genitourinary cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
2.8field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 25 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Lana HamiehDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO; Department of Medicine, Saint Louis University School of Medicine, St Louis, MO.
Rachel L BeckDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
Valerie H LeDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO.
James J HsiehDivision of Oncology, Department of Medicine, Washington University School of Medicine, St Louis, MO. Electronic address: Jhsieh@wustl.edu.
Washington University in St. Louis · USSaint Louis University · US

Funding

Genetic Loss-of-Function Studies of SETD2 in Kidney TumorigenesisR01CA223231 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI CHENG, EMILY H · 2018 to 2022
$2.7M
NCI NIH HHS R01 CA223231
6 · The paper itself

Abstract

backgroundPatients with primary refractory metastatic renal cell carcinoma (mRCC) have a dismal prognosis and poor response to subsequent treatments. While there are several approved second-line therapies, it remains critical to choose the most effective treatment regimen. PATIENTS AND

methodsWe identified 7 patients with clear cell mRCC who had primary resistance to vascular endothelial growth factor (VEGF)-targeted tyrosine kinase inhibitors (TKIs) or immune checkpoint inhibitor (ICI) combination therapy. The patients were treated with lenvatinib (a multitargeted TKI) plus everolimus (a mammalian target of rapamycin inhibitor). Among these 7 patients, 2 had prior TKI therapy, 3 had prior ICI therapy, and 2 had prior TKI and ICI therapy. We collected the patients' clinical characteristics, molecular profiles, treatment durations, and toxicity outcomes.

resultsThe median time to progression on prior therapies was 1.5 months. Lenvatinib plus everolimus was used either as a second-line (n = 4) or third-line (n = 3) therapy. As best responses, 3 patients had partial responses and 3 achieved stable disease. Patients were followed for ≥17 months; progression-free survival ranged from 3 to 15 months, and overall survival ranged from 4 to 17 months.

conclusionThese 7 cases provide real-world data for the use of lenvatinib plus everolimus in patients with mRCC with primary resistance to first-line VEGF-targeted TKIs or ICI combination therapy.

Indexed as

AdultAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Renal CellDrug Resistance, NeoplasmEverolimusFemaleFollow-Up StudiesHumansImmunotherapyKidney NeoplasmsMaleMiddle AgedPhenylurea CompoundsPrognosisProtein Kinase InhibitorsQuinolinesEverolimuslenvatinibPhenylurea CompoundsProtein Kinase InhibitorsQuinolinesSirolimusImmune checkpoint inhibitorKidney cancermTOR inhibitorPrimary refractorySecond-line therapy tyrosine kinase inhibitor

Identifiers

PMID32291161
PMCPMC7415534
OpenAlexW3011419056

What OpenQuestion holds

Textmetadata
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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.