Evidence map›Paper›PMID 34689693›Full record

ArticleLeukemia & lymphoma2022

The pharmacokinetics of therapeutic arsenic trioxide in acute promyelocytic leukemia patients.

Cristina M Ghiuzeli, Miroslav Stýblo, Jesse Saunders, Anthony Calabro, Daniel Budman, Steven Allen, Craig Devoe, Radhika Dhingra

Open access · greenAbstract read
In one paragraph

Article in Leukemia & lymphoma, 2022. 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 40% 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, 7 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Review
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

8 authors at 3 institutions in 1 country.

Cristina M GhiuzeliNorthwell Health Cancer Institute, Zucker School of Medicine at Hofstra/Northwell, New York, NY, USA.
Miroslav StýbloDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Jesse SaundersDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Anthony CalabroDepartment of Medicine, Icahn School of Medicine at Mount Sinai Hospital, New York, NY, USA.
Daniel BudmanNorthwell Health Cancer Institute, Zucker School of Medicine at Hofstra/Northwell, New York, NY, USA.
Steven AllenNorthwell Health Cancer Institute, Zucker School of Medicine at Hofstra/Northwell, New York, NY, USA.
Craig DevoeNorthwell Health Cancer Institute, Zucker School of Medicine at Hofstra/Northwell, New York, NY, USA.
Radhika DhingraInstitute for Environmental Health Solutions, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.ORCID 0000-0003-0202-1860
Northwell Health · USUniversity of North Carolina at Chapel Hill · USMount Sinai Hospital · US

Funding

UNC-CH CENTER FOR ENVIRONMENTAL HEALTH &SUSCEPTIBILITYP30ES010126 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Stephanie Engel · 2001 to 2026
$36.3M
UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
The UNC Chapel Hill Superfund Research Program (UNC-SRP)P42ES031007 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Rebecca Fry · 2020 to 2026
$22.2M
Genetic underpinning of diabetes associated with arsenic exposureR01ES029925 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FRY, REBECCA, PARDO-MANUEL DE VILLENA, FERNANDO · 2019 to 2023
$3.3M
Humanized mouse models for arsenic toxicologyR01ES032643 · NIEHS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOLLER, BEVERLY H, STYBLO, MIROSLAV · 2021 to 2025
$2.1M
Optimized Hydride Generation Systems for Arsenic Specia*R03TW007057 · FIC · UNIV OF NORTH CAROLINA CHAPEL HILL · PI STYBLO, MIROSLAV · 2004 to 2006
$120k
FIC NIH HHS R03 TW007057NIDDK NIH HHS P30 DK056350NIEHS NIH HHS P30 ES010126NIEHS NIH HHS P42 ES031007NIEHS NIH HHS R01 ES029925NIEHS NIH HHS R01 ES032643
6 · The paper itself

Abstract

Arsenic trioxide (ATO) treats Acute Promyelocytic Leukemia (APL). ATO is converted from inorganic arsenic (iAs) to methylated (MAs) and dimethylated (DMAs) metabolites, which are excreted in the urine. Methylation of iAs is important in detoxification, as iAs exposure is deleterious to health. We examined ATO metabolism in 25 APL patients, measuring iAs, MAs, and DMAs. Plasma total iAs increased after ATO administration, followed by a rapid decline, reaching trough levels by 4-6 h. We identified two patterns of iAs metabolism between 6 and 24 h after infusion: in Group 1, iAs increased and were slowly converted to MAs and DMAs, whereas in Group 2, iAs was rapidly metabolized. These patterns were associated with smoking and different treatments: ATO with all-trans retinoic acid (ATRA) alone vs. ATO preceded by ATRA and chemotherapy. Our data suggest that smoking and prior chemotherapy exposure may be associated with ATO metabolism stimulation, thus lowering the effective blood ATO dose.

Indexed as

ArsenicalsLeukemia, Promyelocytic, AcuteAntineoplastic Combined Chemotherapy ProtocolsArsenic TrioxideHumansOxidesTretinoinArsenicalsArsenic TrioxideOxidesTretinoinacute promyelocytic leukemiaArsenic trioxidemetabolismpharmacokinetics

Identifiers

PMID34689693
PMCPMC8891048
OpenAlexW3208871305

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.