Evidence map›Paper›PMID 33619261›Full record

ReviewBlood cancer journal2021

Acute myeloid leukemia: current progress and future directions.

Hagop Kantarjian, Tapan Kadia, Courtney DiNardo, Naval Daver, Gautam Borthakur, Elias Jabbour, Guillermo Garcia-Manero, Marina Konopleva, Farhad Ravandi

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Blood cancer journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07432100 (Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia), which is not on this map. Cited by 457 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
457citing papers in PubMed, 3 pooled it
78.4field-weighted citation impact, top 1% 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.

NCT07432100 phase1not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Clinical Study on the Safety, Efficacy and Pharmacokinetics of Universal CLL1 Chimeric Antigen Receptor T-Cell in Relapsed/Refractory Acute Myeloid Leukemia

TypeinterventionalSponsorMingfeng ZhaoRan2026 to 2028Enrolled20ConditionsAcute Myeloid Leukemia, Chimeric Antigen Receptor T-cell, Universal CLL1 CAR-TArmsuniversal CLL1 CAR-T cells
3 · Its place in the literature

Who cites it

457 citing papers in PubMed, 3 syntheses or guidelines pooled it, 732 citations in OpenAlex.

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397 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

Hagop KantarjianDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA. hkantarjian@mdanderson.org.ORCID 0000-0002-1908-3307
Tapan KadiaDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-9892-9832
Courtney DiNardoDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-9003-0390
Naval DaverDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-7103-373X
Gautam BorthakurDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0001-7679-6453
Elias JabbourDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
Guillermo Garcia-ManeroDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-3631-2482
Marina KonoplevaDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-9347-2212
Farhad RavandiDepartment of Leukemia, MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
University of Texas M.D. Anderson Cancer SPORE-LeukemiaP50CA100632 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SHPALL, ELIZABETH J · 2003 to 2023
$43.7M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA100632
6 · The paper itself

Abstract

Progress in the understanding of the biology and therapy of acute myeloid leukemia (AML) is occurring rapidly. Since 2017, nine agents have been approved for various indications in AML. These included several targeted therapies like venetoclax, FLT3 inhibitors, IDH inhibitors, and others. The management of AML is complicated, highlighting the need for expertise in order to deliver optimal therapy and achieve optimal outcomes. The multiple subentities in AML require very different therapies. In this review, we summarize the important pathophysiologies driving AML, review current therapies in standard practice, and address present and future research directions.

Indexed as

AnimalsAntineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsChromosome AberrationsDisease ManagementHumansLeukemia, Myeloid, AcuteMolecular Targeted TherapyMutationPrognosisProtein Kinase InhibitorsAntineoplastic AgentsProtein Kinase Inhibitors

Identifiers

PMID33619261
PMCPMC7900255
OpenAlexW3130903278

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.