Evidence map›Paper›PMID 33194157›Full record

ReviewMediterranean journal of hematology and infectious diseases2020

NPM1 Mutated, BCR-ABL1 Positive Myeloid Neoplasms: Review of the Literature.

Gianfranco Catalano, Pasquale Niscola, Cristina Banella, Daniela Diverio, Malgorzata Monika Trawinska, Stefano Fratoni, Rita Iazzoni, Paolo De Fabritiis, Elisabetta Abruzzese, Nelida Ines Noguera

Open access · goldAbstract readReview
In one paragraph

Review in Mediterranean journal of hematology and infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 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

10 authors at 2 institutions in 1 country.

Gianfranco CatalanoDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.
Pasquale NiscolaHematology Unit, Sant' Eugenio Hospital, Tor Vergata University of Rome, Rome, Italy.
Cristina BanellaDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.
Daniela DiverioHematology, Department of Precision and Translational Medicine, Policlinico Umberto I, "Sapienza" University of Rome, Rome, Italy.
Malgorzata Monika TrawinskaDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.
Stefano FratoniDepartment of Pathology (UOSD Anatomia Patologica) A.S.L. Roma2, Sant' Eugenio Hospital, Rome, Italy.
Rita IazzoniDepartment of Clinical Pathology (U.O.C. Laboratorio) A.S.L. Roma2, Sant' Eugenio Hospital, Rome, Italy.
Paolo De FabritiisDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.
Elisabetta AbruzzeseHematology Unit, Sant' Eugenio Hospital, Tor Vergata University of Rome, Rome, Italy.
Nelida Ines NogueraDepartment of Biomedicine and Prevention, Tor Vergata University of Rome, 00133 Rome, Italy.
University of Rome Tor Vergata · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breakpoint cluster region - Abelson (BCR-ABL1) chimeric protein and mutated Nucleophosmin (NPM1) are often present in hematological cancers, but they rarely coexist in the same disease. Both anomalies are considered founder mutations that inhibit differentiation and apoptosis, but BCR-ABL1 could act as a secondary mutation conferring a proliferative advantage to a pre-neoplastic clone. The 2016 World Health Organization (WHO) classification lists the provisional acute myeloid leukemia (AML) with BCR-ABL1, which must be diagnosed differentially from the rare blast phase (BP) onset of chronic myeloid leukemia (CML), mainly because of the different therapeutic approach in the use of tyrosine kinase inhibitors (TKI). Here we review the BCR/ABL1 plus NPMc+ published cases since 1975 and describe a case from our institution in order to discuss the clinical and molecular features of this rare combination, and report the latest acquisition about an occurrence that could pertain either to the rare AML BCR-ABL1 positive or the even rarer CML-BP with mutated NPM1 at the onset. Differential diagnosis is based on careful analysis of genotypic and phenotypic features and anamnestic, clinical evolution, and background data. Therapeutic decisions must consider the broader clinical aspects, the comparatively mild effects of TKI therapy versus the great benefit that might bring to most of the patients, as may be incidentally demonstrated by our case history.

Indexed as

AML with BCR-ABL1CML-BPNPM1TKI therapy

Identifiers

PMID33194157
PMCPMC7643801
OpenAlexW3095047504

What OpenQuestion holds

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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.