Evidence map›Paper›PMID 42123630›Full record

ArticleInternational journal of molecular sciences2026

Analysis of Clinical Impact of CD33 rs12459419 Single-Nucleotide Polymorphism in AML Treated with Intensive Chemotherapy Without Gemtuzumab Ozogamicin.

Sophie Helfenstein, Inna Shaforostova, Katja Seipel, Marie-Noelle Kronig, Myriam Legros, Ulrike Bacher, Thomas Pabst

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Sophie HelfensteinDepartment of Medical Oncology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
Inna ShaforostovaDepartment of Medical Oncology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
Katja SeipelDepartment of Medical Oncology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
Marie-Noelle KronigDepartment of Medical Oncology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
Myriam LegrosDepartment of Hematology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.
Ulrike BacherDepartment of Hematology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.ORCID 0000-0001-8771-947X
Thomas PabstDepartment of Medical Oncology, Inselspital, Bern University Hospital, 3010 Bern, Switzerland.ORCID 0000-0002-6055-5257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CD33 rs12459419 (C>T; Ala14Val) single-nucleotide polymorphism (SNP) has been reported to modulate treatment response and survival in pediatric patients with acute myeloid leukemia (AML) receiving gemtuzumab ozogamicin (GO), an anti-CD33 antibody linked to the cytotoxic compound calicheamicin. However, it remains unclear whether this SNP also affects CD33 expression on leukemic blasts. Moreover, its prognostic significance in adult AML patients treated with standard chemotherapy without GO has not been investigated. In this study, we retrospectively genotyped 184 adult AML patients who received standard induction chemotherapy for the CD33

Indexed as

Leukemia, Myeloid, AcutePolymorphism, Single NucleotideSialic Acid Binding Ig-like Lectin 3AdolescentAdultAgedAged, 80 and overAminoglycosidesFemaleGemtuzumabGenotypeHumansMaleMiddle AgedPrognosisRetrospective StudiesAminoglycosidesCD33 protein, humanGemtuzumabSialic Acid Binding Ig-like Lectin 3acute myeloid leukemia (AML)CD33rs12459419single nucleotide polymorphism (SNP)

Identifiers

PMID42123630
PMCPMC13163365

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Registered trials

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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.