Evidence map›Paper›PMID 35291210›Full record

ArticleHemaSphere2022

Monitoring of Leukemia Clones in B-cell Acute Lymphoblastic Leukemia at Diagnosis and During Treatment by Single-cell DNA Amplicon Sequencing.

Sarah Meyers, Llucia Alberti-Servera, Olga Gielen, Margot Erard, Toon Swings, Jolien De Bie, Lucienne Michaux, Barbara Dewaele, Nancy Boeckx, Anne Uyttebroeck and 5 more

Open access · goldAbstract read
In one paragraph

Article in HemaSphere, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 20 citations in OpenAlex.

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  10. XBP1 promotes NRASJournal of cellular and molecular medicine · 2023
    Article
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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

15 authors at 3 institutions in 1 country.

Sarah MeyersDepartment of Human Genetics, KU Leuven, Belgium.
Llucia Alberti-ServeraDepartment of Human Genetics, KU Leuven, Belgium.
Olga GielenDepartment of Human Genetics, KU Leuven, Belgium.
Margot ErardDepartment of Human Genetics, KU Leuven, Belgium.
Toon SwingsVIB Technology Watch, Technology Innovation Lab, VIB, Gent, Belgium.
Jolien De BieDepartment of Human Genetics, KU Leuven, Belgium.
Lucienne MichauxDepartment of Human Genetics, KU Leuven, Belgium.
Barbara DewaeleDepartment of Human Genetics, KU Leuven, Belgium.
Nancy BoeckxDepartment of Laboratory Medicine, UZ Leuven, Belgium.
Anne UyttebroeckLeuvens Kanker Instituut (LKI), KU Leuven-UZ Leuven, Belgium.
Kim De KeersmaeckerLeuvens Kanker Instituut (LKI), KU Leuven-UZ Leuven, Belgium.
Johan MaertensLeuvens Kanker Instituut (LKI), KU Leuven-UZ Leuven, Belgium.
Heidi SegersLeuvens Kanker Instituut (LKI), KU Leuven-UZ Leuven, Belgium.
Jan CoolsDepartment of Human Genetics, KU Leuven, Belgium.
Sofie DemeyerDepartment of Human Genetics, KU Leuven, Belgium.
KU Leuven · BEUniversitair Ziekenhuis Leuven · BEVIB-KU Leuven Center for Cancer Biology · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL) is characterized by the presence of chromosomal changes, including numerical changes, translocations, and deletions, which are often associated with additional single-nucleotide mutations. In this study, we used single cell-targeted DNA sequencing to evaluate the clonal heterogeneity of B-ALL at diagnosis and during chemotherapy treatment. We designed a custom DNA amplicon library targeting mutational hotspot regions (in 110 genes) present in ALL, and we measured the presence of mutations and small insertions/deletions (indels) in bone marrow or blood samples from 12 B-ALL patients, with a median of 7973 cells per sample. Nine of the 12 cases showed at least 1 subclonal mutation, of which cases with

Identifiers

PMID35291210
PMCPMC8916209
OpenAlexW4220842813

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.