Evidence map›Paper›PMID 31522242›Full record

ArticleCancer chemotherapy and pharmacology2019

Phase I trial of belinostat in combination with 13-cis-retinoic acid in advanced solid tumor malignancies: a California Cancer Consortium NCI/CTEP sponsored trial.

Thehang Luu, Paul Frankel, Jan H Beumer, Dean Lim, Mihaela Cristea, Leonard J Appleman, Heinz J Lenz, David R Gandara, Brian F Kiesel, Richard L Piekarz and 1 more

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

Article in Cancer chemotherapy and pharmacology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-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

8 citing papers in PubMed, 15 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

11 authors at 6 institutions in 1 country.

Thehang LuuDepartment of Medical Oncology, City of Hope, Duarte, USA.
Paul FrankelDepartment of Biostatistics, City of Hope, Duarte, USA.
Jan H BeumerUPMC Hillman Cancer Center, Pittsburgh, USA.
Dean LimDepartment of Medical Oncology, City of Hope, Duarte, USA.
Mihaela CristeaDepartment of Medical Oncology, City of Hope, Duarte, USA.
Leonard J ApplemanUPMC Hillman Cancer Center, Pittsburgh, USA.
Heinz J LenzUniversity of Southern California/Norris Comprehensive Cancer Center, Los Angeles, CA, 90033, USA.
David R GandaraUniversity of California Davis Cancer Center, Sacramento, CA, 95817, USA.
Brian F KieselUPMC Hillman Cancer Center, Pittsburgh, USA.
Richard L PiekarzCancer Therapy Evaluation Program, National Cancer Institute, 9609 Medical Center Dr., MSC 9739, Bethesda, MD, 20892, USA.
Edward M NewmanBeckman Research Institute City of Hope, Duarte, CA, 91010, USA. enewman@coh.org.ORCID 0000-0001-6988-5909
City Of Hope National Medical Center · USUPMC Hillman Cancer Center · USCity of Hope · USNational Cancer Institute · USUniversity of California, Davis · USUniversity of Southern California · US

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD · 1988 to 2026
$158.0M
Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI XIWEI WU · 1985 to 2026
$86.3M
Phase I Molecular and Clinical Pharmacodynamic Trials ETCTNUM1CA186717 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI A. Dimitrios Colevas, Alexey V. Danilov · 2014 to 2026
$19.8M
NCI ET-CTN with Phase i Emphasis at UPCIUM1CA186690 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI JOHN C. BYRD, Farshid Dayyani · 2014 to 2026
$9.1M
PHASE I MOLECULAR AND CLINICAL PHARMACODYNAMIC TRIALSU01CA062505 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI NEWMAN, EDWARD M · 1994 to 2013
$8.1M
National Cancer Institute (US) P30CA033572National Cancer Institute (US) P30CA047904National Cancer Institute (US) U01CA062505National Cancer Institute (US) UM1CA186690National Cancer Institute (US) UM1CA186717NCI NIH HHS P30 CA033572NCI NIH HHS P30 CA047904NCI NIH HHS U01 CA062505NCI NIH HHS UM1 CA186690NCI NIH HHS UM1 CA186717
6 · The paper itself

Abstract

purposeThe reported maximum tolerated dose (MTD) of single-agent belinostat is 1000 mg/m

methodsBelinostat was administered days 1-5 and 13-cRA days 1-14, every 21 days. Dose-limiting toxicity (DLT) was defined as cycle 1 hematologic toxicity grade ≥ 3 not resolving to grade ≤ 1 within 1 week or non-hematologic toxicity grade ≥ 3 (except controlled nausea and vomiting and transient liver function abnormalities) attributable to belinostat.

resultsAmong 51 patients, two DLTs were observed: grade 3 hypersensitivity with dizziness and hypoxia at 1700 mg/m

conclusionsThe combination of belinostat 2000 mg/m

Indexed as

Maximum Tolerated DoseAdministration, OralAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsDose-Response Relationship, DrugDrug Administration ScheduleFemaleHumansHydroxamic AcidsInfusions, IntravenousIsotretinoinMaleMiddle AgedNeoplasmsbelinostatHydroxamic AcidsIsotretinoinSulfonamidesHistone deacetylase (HDAC) inhibitorsPharmacokineticsPhase I clinical trialRetinoids

Identifiers

PMID31522242
PMCPMC6821594
OpenAlexW2973034045

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.