Evidence map›Paper›PMID 30992690›Full record

ArticleCancer cell international2019

The assessment of minimal residual disease versus that of somatic mutations for predicting the outcome of acute myeloid leukemia patients.

Serena Salehzadeh, Francesca Guerrini, Umberto Pizzano, Susanna Grassi, Elena Ciabatti, Lorenzo Iovino, Gabriele Buda, Francesco Caracciolo, Edoardo Benedetti, Enrico Orciuolo and 12 more

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 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

22 authors at 2 institutions in 1 country.

Serena Salehzadeh1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.ORCID 0000-0002-2701-2947
Francesca Guerrini1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Umberto Pizzano1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Susanna Grassi1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Elena Ciabatti1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Lorenzo Iovino1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Gabriele Buda1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Francesco Caracciolo1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Edoardo Benedetti1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Enrico Orciuolo1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Matteo Pelosini1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Giovanni Consani1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Giovanni Carulli1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Maria Rita MetelliMolecular Laboratory of Hematology, AOUP, Pisa, Italy.
Francesca Martini1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Francesco Mazziotta1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Elisa Mazzantini1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Pietro Rossi1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Rita Tavarozzi1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Federica Ricci1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Mario Petrini *1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
Sara Galimberti *1Department of Clinical and Experimental Medicine, Section of Hematology, University of Pisa, Pisa, Italy.
University of Pisa · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn addition to morphological and cytogenetic features, acute myeloid leukemias are characterized by mutations that can be used for target-therapy; also the minimal/measurable residual disease (MRD) could be an important prognostic factor. The purpose of this retrospective study was to investigate if somatic mutations could represent an additional prognostic value in respect of MRD alone.

methodAt baseline, 98 patients were tested for

resultsOverall, 60.2% of our patients resulted mutated: 24.5% carried mutations of

conclusionsWe demonstrated that additional somatic mutations are able to impair outcome of the already MRD-negative subjects. About MRD, we suggest a prognostic role also for the

Indexed as

Additional mutationsAMLAML outcomeASXL1FLT3IDHNPM1RUNX1TP53WT1

Identifiers

PMID30992690
PMCPMC6449954
OpenAlexW2942834671

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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.