Evidence map›Paper›PMID 24755475›Full record

ArticleBMC research notes2014

Probable fatal drug interaction between intravenous fenretinide, ceftriaxone, and acetaminophen: a case report from a New Approaches to Neuroblastoma (NANT) Phase I study.

Min H Kang, Judith G Villablanca, Julia L Glade Bender, Katherine K Matthay, Susan Groshen, Richard Sposto, Scarlett Czarnecki, Matthew M Ames, C Patrick Reynolds, Araz Marachelian and 1 more

Open access · goldAbstract readCase ReportsClinical Trial, Phase I
In one paragraph

Article in BMC research notes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. The Cancer Drug Fraction of Metabolism Database.CPT: pharmacometrics & systems pharmacology · 2019
    Article
  4. Article
  5. Article
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 7 institutions in 1 country.

Min H KangCancer Center and Departments of Cell Biology and Biochemistry, Pharmacology and Neuroscience, Pediatrics, and Internal Medicine, School of Medicine, Texas Tech University Health Sciences Center, 3601 4th Street, STOP 9445 79430 Lubbock, TX, USA. min.kang@ttuhsc.edu.
Judith G Villablanca
Julia L Glade Bender
Katherine K Matthay
Susan Groshen
Richard Sposto
Scarlett Czarnecki
Matthew M Ames
C Patrick Reynolds
Araz Marachelian
Barry J Maurer
University of Southern California · USTexas Tech University Health Sciences Center · USChildren's Hospital of Los Angeles · USColumbia University · USMayo Clinic in Florida · USTexas Tech University · USUniversity of California, San Francisco · US

Funding

Vascular endothelial cell integrins in angiogenesisP01CA081403 · NCI · CHILDREN'S HOSPITAL OF LOS ANGELES · PI SEEGER, ROBERT CHARLES · 2000 to 2014
$28.5M
Novel Ceramide-based Chemotherapy for Acute LeukemiaR01CA100895 · NCI · TEXAS TECH UNIVERSITY HEALTH SCIS CENTER · PI MAURER, BARRY J · 2004 to 2007
$980k
NCI NIH HHS P01 CA81403NCI NIH HHS R01 CA100895
6 · The paper itself

Abstract

backgroundPatients with relapsed/refractory stage 4 high-risk neuroblastoma were enrolled on a phase I study (NANT2004-03) of intravenous fenretinide emulsion. Pharmacokinetic samples were collected during and after the infusion, and the levels were measured using an HPLC system. A likely case of a fatal drug interaction between fenretinide, ceftriaxone, and acetaminophen is described, including the pharmacokinetics of fenretinide, laboratory data, and post-mortem autopsy in a pediatric neuroblastoma patient treated on this study. CASE PRESENTATION: On Day 4 of a scheduled 5-day-infusion of intravenous fenretinide, the patient developed a fever, acetaminophen was started, ceftriaxone initiated for possible bacteremia, and fenretinide level doubled from 56 to 110 μM. Over the next three days, although blood cultures remained negative, the patient's condition deteriorated rapidly. Acute liver failure was diagnosed on Day 7, and the patient expired on Day 20 of fulminant hepatic failure with associated renal, cardiac, and hemorrhagic/coagulation toxicities. Autopsy showed extensive hemorrhagic necrosis of the liver, marked bile duct proliferation, and abundant hemosiderin, consistent with cholestasis and drug toxicity.

conclusionsAfter extensive review of patient data, the clinical course, and the literature, we conclude that observed hepatic toxicity was likely due to a drug interaction between fenretinide and concomitant ceftriaxone and acetaminophen. None of the other 16 patients treated on this study experienced significant hepatic toxicity. Although the prevalence of cholestasis with ceftriaxone usage is relatively high, the potential drug interaction with these concomitant medications has not been previously reported. Concomitant use of fenretinide, ceftriaxone, and acetaminophen should be avoided.

Indexed as

AcetaminophenCeftriaxoneChildDose-Response Relationship, DrugDrug InteractionsFatal OutcomeFenretinideHumansInjections, IntravenousMaleNeuroblastomaRadiographyAcetaminophenCeftriaxoneFenretinide

Identifiers

PMID24755475
PMCPMC4006848
OpenAlexW2160353682

What OpenQuestion holds

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Registered trials

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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.