Evidence map›Paper›PMID 36742324›Full record

ReviewFrontiers in immunology2023

A potential area of use for immune checkpoint inhibitors: Targeting bone marrow microenvironment in acute myeloid leukemia.

Başak Aru, Cemil Pehlivanoğlu, Zeynep Dal, Nida Nur Dereli-Çalışkan, Ege Gürlü, Gülderen Yanıkkaya-Demirel

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 3% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Başak AruImmunology Department, Faculty of Medicine, Yeditepe University, Istanbul, Türkiye.
Cemil PehlivanoğluImmunology Department, Faculty of Medicine, Yeditepe University, Istanbul, Türkiye.
Zeynep DalSchool of Medicine, Yeditepe University, Istanbul, Türkiye.
Nida Nur Dereli-ÇalışkanImmunology Department, Faculty of Medicine, Yeditepe University, Istanbul, Türkiye.
Ege GürlüSchool of Medicine, Yeditepe University, Istanbul, Türkiye.
Gülderen Yanıkkaya-DemirelImmunology Department, Faculty of Medicine, Yeditepe University, Istanbul, Türkiye.
Yeditepe University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) arises from the cells of myeloid lineage and is the most frequent leukemia type in adulthood accounting for about 80% of all cases. The most common treatment strategy for the treatment of AML includes chemotherapy, in rare cases radiotherapy and stem cell and bone marrow transplantation are considered. Immune checkpoint proteins involve in the negative regulation of immune cells, leading to an escape from immune surveillance, in turn, causing failure of tumor cell elimination. Immune checkpoint inhibitors (ICIs) target the negative regulation of the immune cells and support the immune system in terms of anti-tumor immunity. Bone marrow microenvironment (BMM) bears various blood cell lineages and the interactions between these lineages and the noncellular components of BMM are considered important for AML development and progression. Administration of ICIs for the AML treatment may be a promising option by regulating BMM. In this review, we summarize the current treatment options in AML treatment and discuss the possible application of ICIs in AML treatment from the perspective of the regulation of BMM.

Indexed as

Bone MarrowLeukemia, Myeloid, AcuteBone Marrow TransplantationHumansImmune Checkpoint InhibitorsNeoplastic Stem CellsTumor MicroenvironmentImmune Checkpoint Inhibitorsacute myeloid leukemiabone marrow microenvironmentimmune checkpoint inhibitors (ICI)immune checkpoint proteins (ICP)tumor microenvironment

Identifiers

PMID36742324
PMCPMC9895857
OpenAlexW4317627186

What OpenQuestion holds

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LicenceCC BY
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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.