Evidence map›Paper›PMID 31858327›Full record

Trial reportInvestigational new drugs2020

Evaluation of the potential effect of dacomitinib, an EGFR tyrosine kinase inhibitor, on ECG parameters in patients with advanced non-small cell lung cancer.

Weiwei Tan, Nagdeep Giri, Susan Quinn, Keith Wilner, Kourosh Parivar

Registry-linked trialAbstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Investigational new drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01858389 (Phase 2 Open Label Trial Of Oral Intermittent Dacomitinib In Patients With Advanced Nsclc), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 32% 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.

NCT01858389 phase2completednot on this map

Phase 2 Open Label Trial Of Oral Intermittent Dacomitinib In Patients With Advanced Nsclc

TypeinterventionalSponsorPfizerRan2013 to 2015Enrolled41ConditionsNon-small Cell Lung CancerArmsDacomitinib
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
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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

5 authors at 1 institution in 1 country.

Weiwei TanGlobal Product Development, Pfizer Inc., 10555 Science Center Drive, San Diego, CA, 92121, USA. weiwei.tan@pfizer.com.ORCID 0000-0001-8915-1152
Nagdeep GiriGlobal Product Development, Pfizer Inc., 10555 Science Center Drive, San Diego, CA, 92121, USA.
Susan QuinnPfizer Inc., 300 Technology Square, Suite 302, Cambridge, MA, 02139, USA.
Keith WilnerGlobal Product Development, Pfizer Inc., 10555 Science Center Drive, San Diego, CA, 92121, USA.
Kourosh ParivarGlobal Product Development, Pfizer Inc., 10555 Science Center Drive, San Diego, CA, 92121, USA.
Pfizer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose The study evaluated the potential effect of dacomitinib, a small molecule epidermal growth factor receptor (EGFR) inhibitor, on the electrocardiogram (ECG) parameters in adult patients with advanced non-small cell lung cancer enrolled in a multicenter, open-label, phase 2 study. Methods Patients received dacomitinib for six doses of 45 mg every 12 h in a 7-day lead-in cycle (cycle 0), then 60 mg every 12 h for six doses in a 14-day cycle (cycle 1). Clock time-matched triplicate ECGs were performed at 0, 2, 4, 6, 8 and 10 h on day 1 (baseline) and day 4 of cycle 0, and prior to dose on days 1 and 4 of cycle 1. The QT interval was corrected for heart rate using Fridericia's correction (QTcF) and a study specific correction factor (QTcS). Results Thirty-two patients in the study comprised the QTc-evaluable population. Dacomitinib had no effect on the heart rate. The upper limits of the 95% confidence interval (CI) for the mean change from baseline in QTcF and QTcS were < 10 ms at all time points. A lack of relationship between plasma concentrations of dacomitinib or total active moiety on QTcF and QTcS was evidenced. All upper 90% CIs of the PR intervals were < 200 ms, although a small mean increase from baseline (2.7-6.6 ms) was observed. Conclusions There was a lack of a clinically relevant effect of dacomitinib on ECG parameters at dacomitinib concentrations comparable to those obtained at its highest therapeutic dosing regimen of 45 mg once daily. ClinicalTrials.gov identifier: NCT01858389.

Indexed as

AdultAgedAged, 80 and overCarcinoma, Non-Small-Cell LungDose-Response Relationship, DrugElectrocardiographyErbB ReceptorsFemaleHeart RateHumansLong QT SyndromeLung NeoplasmsMaleMiddle AgedProtein Kinase InhibitorsQuinazolinonesdacomitinibEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsQuinazolinonesConcentration-QTc modellingDacomitinibECGQT interval

Identifiers

PMID31858327
OpenAlexW2996019668

What OpenQuestion holds

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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.