Evidence map›Paper›PMID 32748108›Full record

ArticleCancer chemotherapy and pharmacology2020

Towards better combination regimens of cytarabine and FLT3 inhibitors in acute myeloid leukemia.

Mohamed Elmeliegy, Jason Den Haese, Chetasi Talati, Meir Wetzler, William J Jusko

Open access · greenAbstract read
In one paragraph

Article in Cancer chemotherapy and pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 7 citations in OpenAlex.

  1. 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

5 authors at 3 institutions in 1 country.

Mohamed ElmeliegyPfizer, Inc., 10555 Science Center Dr., San Diego, CA, 92121, USA. Mohamed.Elmeliegy@pfizer.com.ORCID 0000-0002-9825-5890
Jason Den HaeseDepartment of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY, USA.
Chetasi TalatiDepartment of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY, USA.
Meir WetzlerDepartment of Medicine, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, NY, USA.
William J JuskoDepartment of Pharmaceutical Sciences, School of Pharmacy and Pharmaceutical Sciences, State University of New York at Buffalo, Buffalo, NY, 14214, USA.
Roswell Park Comprehensive Cancer Center · USPfizer (United States) · USUniversity at Buffalo, State University of New York · US

Funding

Two-Spirit Films in Indigenous Cancer HealthP30CA016056 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI Dean G. Tang · 1985 to 2026
$116.6M
Corticosteroid Pharmacokinetics and PharmacodynamicsR37GM024211 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JUSKO, WILLIAM J. · 2005 to 2014
$6.4M
CORTICOSTEROID PHARMACOKINETICS/DYNAMICSR01GM024211 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JUSKO, WILLIAM J. · 1985 to 2018
$4.7M
Mechanistic Pharmacokinetics and PharmacodynamicsR35GM131800 · NIGMS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI JUSKO, WILLIAM J. · 2019 to 2023
$2.9M
NCI NIH HHS P30 CA016056NIGMS NIH HHS R01 GM024211NIGMS NIH HHS R35 GM131800NIGMS NIH HHS R37 GM024211
6 · The paper itself

Abstract

backgroundAML patients with FLT3/ITD mutations have poor response to cytarabine-based chemotherapy. FLT3 inhibitors (FLT3i) may resensitize cells to cytarabine (CYT). Improving treatment outcome of this combination may benefit from a mechanistic extrapolation approach from in vitro data.

methodsThe effects of CYT and several FLT3i on cell proliferation and cell cycle kinetics were examined in AML cell lines. The effect of FLT3i (quizartinib, midostaurin, sorafenib) on cell proliferation and cell cycle kinetics was assessed in AML cell lines with differing FLT3 status; HEL (negligible expression of wild-type FLT3), EOL1 (wild-type FLT3), MV4-11 (FLT3-ITD resulting in constitutively active isoform). Semi-mechanistic cell cycle models for CYT and FLT3i were developed. Clinical CYT and quizartinib pharmacokinetic dosage regimens were modeled. Survival of AML patients was described via a hazard model. Simulations exploring different CYT/quizartinib regimens were conducted with the goal of improving treatment outcome.

resultsFLT3 status was associated with sensitivity to CYT (HEL cells most sensitive > EOL1 > MV4-11 cells). This order of sensitivity is reversed for FLT3i. Cytarabine induced apoptosis in the S-phase while all FLT3i induced apoptosis and cell cycle arrest at G1 phase. Simulations of candidate clinical regimens predict better cell kill upon adding quizartinib simultaneously with or immediately after CYT exposure. Overall survival was predicted to be significantly better with quizartinib 200 mg administered every 48 h vs every 24 h in patients with FLT3 aberrations.

conclusionSimultaneous administration of quizartinib and CYT every other day is a promising combination regimen for AML patients with FLT3 mutations.

Indexed as

Gene Expression Regulation, NeoplasticAntineoplastic Combined Chemotherapy ProtocolsApoptosisBenzothiazolesBiomarkers, TumorCell CycleCell MovementCell ProliferationCytarabinefms-Like Tyrosine Kinase 3HumansLeukemia, Myeloid, AcuteMutationPhenylurea CompoundsPrognosisSurvival RateBenzothiazolesBiomarkers, TumorCytarabineFLT3 protein, humanfms-Like Tyrosine Kinase 3Phenylurea CompoundsquizartinibAMLCell cycleCombinationCytotoxicityPharmacodynamic modeling

Identifiers

PMID32748108
PMCPMC7539618
OpenAlexW3047227866

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.