Evidence map›Paper›PMID 26141814›Full record

Trial reportJournal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy2015

Pharmacokinetics of posaconazole prophylaxis of patients with acute myeloid leukemia.

Gloria Mattiuzzi, Musa Yilmaz, Hagop Kantarjian, Gautam Borthakur, Marina Konopleva, Elias Jabbour, Yolanda Brown, Sherry Pierce, Jorge Cortes

Abstract readClinical Trial
In one paragraph

Trial report in Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 37% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Updated antimicrobial dosing recommendations for obese patients.Antimicrobial agents and chemotherapy · 2024
    Pooled it
  2. Article
  3. Article
  4. A Review of Population Pharmacokinetic Models of Posaconazole.Drug design, development and therapy · 2022
    Review
  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

9 authors at 2 institutions in 1 country.

Gloria MattiuzziDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Musa YilmazDepartment of Hematology and Oncology, Baylor College of Medicine, Houston, TX, USA.
Hagop KantarjianDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Gautam BorthakurDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Marina KonoplevaDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Elias JabbourDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Yolanda BrownDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Sherry PierceDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Jorge CortesDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA. Electronic address: jcortes@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USBaylor College of Medicine · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Antifungal prophylaxis is routinely given to patients with hematologic malignancies at high risk for invasive fungal infections (IFI), yet breakthrough IFI may still occur. Posaconazole emerged as an excellent alternative for fungal prophylaxis in high-risk patients. There is limited data about pharmacokinetics and plasma concentrations of posaconazole when given as prophylaxis in patients with hematologic malignancies. We recruited 20 adult patients for prospective, open label trial of posaconazole given as a prophylaxis in patients with newly diagnosed acute myeloid leukemia (AML) undergoing induction chemotherapy or first salvage therapy. The median age of all patients was 65 years and received prophylaxis for a median of 38 days (range: 5-42 days).Ten patients (50%) completed 42 days on posaconazole prophylaxis. Median plasma posaconazole levels showed no statistical difference across gender, body surface area, patients developing IFI, and patients acquiring grade 3 or 4 elevation of liver enzymes. However, there was an overall trend for higher trough concentrations among patients with no IFI than those with IFI. Pharmacokinetics of posaconazole varies from patient to patient, and AML patients receiving induction chemotherapy who never develop IFI tend to have higher plasma concentrations after oral administration of posaconazole.

Indexed as

AdultAgedAntifungal AgentsAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansInduction ChemotherapyLeukemia, Myeloid, AcuteMaleMiddle AgedMycosesProspective StudiesSalvage TherapyTriazolesAntifungal AgentsposaconazoleTriazolesAcute leukemiaAntifungal prophylaxisPosaconazole

Identifiers

PMID26141814
PMCPMC5459324
OpenAlexW2141336537

What OpenQuestion holds

Textmetadata
LicenceTDM
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.