Evidence map›Paper›PMID 28449393›Full record

ArticlePediatric blood & cancer2017

A phase 1 study of the c-Met inhibitor, tivantinib (ARQ197) in children with relapsed or refractory solid tumors: A Children's Oncology Group study phase 1 and pilot consortium trial (ADVL1111).

James I Geller, John P Perentesis, Xiaowei Liu, Charles G Minard, Rachel A Kudgus, Joel M Reid, Elizabeth Fox, Susan M Blaney, Brenda J Weigel

Open access · greenAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Pediatric blood & cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 16 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

9 authors at 7 institutions in 1 country.

James I GellerCincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH.
John P PerentesisCincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH.
Xiaowei LiuChildren's Oncology Group, Monrovia, CA.
Charles G MinardDan L. Duncan Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, TX.
Rachel A KudgusMayo Clinic, Rochester, MN.
Joel M ReidMayo Clinic, Rochester, MN.
Elizabeth FoxChildren's Hospital of Philadelphia, Philadelphia, PA.
Susan M BlaneyDan L. Duncan Institute for Clinical and Translational Research, Baylor College of Medicine, Houston, TX.
Brenda J WeigelMasonic Children's Hospital, University of Minnesota Medical Center, Minneapolis, MN.
Baylor College of Medicine · USMayo Clinic in Arizona · USChildren's Hospital of Philadelphia · USChildren's Oncology Group · USCincinnati Children's Hospital Medical Center · USUniversity of Cincinnati · USUniversity of Minnesota Children's Hospital · US

Funding

Pediatric Phase 1/Pilot ConsortiumUM1CA097452 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI WEIGEL, BRENDA J. · 2009 to 2018
$17.7M
NCI NIH HHS UM1 CA097452
6 · The paper itself

Abstract

backgroundThe c-Met receptor tyrosine kinase is dysregulated in many pediatric cancers. Tivantinib is an oral small molecule that inhibits the c-Met receptor tyrosine kinase. A phase 1 and pharmacokinetic (PK) trial evaluating tivantinib was conducted in children with relapsed/refractory solid tumors.

methodsOral tivantinib capsules were administered twice daily with food, continuously in 28-day cycles. Dose levels 170, 200, and 240 mg/m

resultsThirty-six patients were enrolled: 20 in Part A, 6 in a PK expansion cohort, and 10 in Part B. Fifteen patients had primary central nervous system tumors and 21 had solid tumors. In Part A, there were no dose-limiting toxicities. One grade 4 intracranial hemorrhage occurred in a patient with a progressive brain tumor in the expanded PK cohort (240 mg/m

conclusionsThe RP2D of tivantinib given with food in children with refractory solid tumors is 240 mg/m

Indexed as

Salvage TherapyAdolescentAdultChildChild, PreschoolDrug Resistance, NeoplasmFemaleHumansInfantMaleMaximum Tolerated DoseNeoplasm Recurrence, LocalNeoplasmsNeoplasm StagingPilot ProjectsPrognosisARQ 197MET protein, humanProto-Oncogene Proteins c-metPyrrolidinonesQuinolines

Identifiers

PMID28449393
PMCPMC5657151
OpenAlexW2608296346

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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.