Evidence map›Paper›PMID 32026180›Full record

ReviewHeart failure reviews2020

Early diagnosis, clinical management, and follow-up of cardiovascular events with ponatinib.

Grazia Casavecchia, Maurizio Galderisi, Giuseppina Novo, Matteo Gravina, Ciro Santoro, Eustachio Agricola, Silvana Capalbo, Stefano Zicchino, Matteo Cameli, Luisa De Gennaro and 6 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Heart failure reviews, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  14. Lifelong TKI therapy: how to manage cardiovascular and other risks.Hematology. American Society of Hematology. Education Program · 2021
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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

16 authors at 9 institutions in 1 country.

Grazia CasavecchiaOspedali Riuniti University Hospital, Foggia, Italy.
Maurizio GalderisiDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Giuseppina NovoBiomedic Department of Internal Medicine and Specialities (DIBIMIS), University of Palermo, Palermo, Italy.
Matteo GravinaOspedali Riuniti University Hospital, Foggia, Italy.
Ciro SantoroDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Eustachio AgricolaEchocardiography Laboratory, San Raffaele University Hospital IRRCS Milan, Milan, Italy.
Silvana CapalboOspedali Riuniti University Hospital, Foggia, Italy.
Stefano ZicchinoDepartment of Medical & Surgical Sciences, University of Foggia, Foggia, Italy.
Matteo CameliDepartment of Cardiovascular Diseases, University of Siena, Siena, Italy.
Luisa De GennaroSan Paolo Hospital, Bari, Italy.
Francesca Maria RighiniDepartment of Cardiovascular Diseases, University of Siena, Siena, Italy.
Ines MonteGeneral surgery and Medical-Surgery Specialities, University of Catania, Catania, Italy.
Carlo Gabriele TocchettiDepartment of Translational Medical Sciences, Federico II University, Naples, Italy.
Natale Daniele BrunettiDepartment of Medical & Surgical Sciences, University of Foggia, Foggia, Italy. natale.brunetti@unifg.it.ORCID 0000-0001-9610-7408
Cristian CadedduDepartment of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
Giuseppe MercuroDepartment of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
Federico II University Hospital · ITOspedali Riuniti di Foggia · ITUniversity of Cagliari · ITUniversity of Foggia · ITUniversity of Siena · ITOspedale San Paolo · ITSan Raffaele University of Rome · ITUniversity of Catania · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by neoplastic transformation of pluripotent cells due to a typical cytogenetic and molecular mutation known as Philadelphia (Ph) chromosome. In 2001, the introduction of the tyrosine kinasis inhibitor (TKI) imatinib as a therapeutic strategy for CML with PH chromosome mutation represented an important step towards treatment of these patients, and nowadays, this drug represents the gold therapeutic standard in this clinical setting. A second generation of TKIs (dasatinib, nilotinib, and bosutinib) showed an effective action in all patients with mutations resistant to imatinib. Ponatinib is a third-generation TKI and is the only inhibitor with activity against T3151 mutation. The impact of ponatinib on cardiovascular events was first evaluated in the PACE trial. We therefore report and discuss most relevant evidence currently available on cardiovascular events associated with the use of ponatinib. Though many exams can be used for diagnosis and follow-up of this kind of cardiotoxicity, echocardiography seems to have a pivotal role thanks to its feasibility, availability, and low cost.

Indexed as

Disease ManagementEarly DiagnosisCardiovascular DiseasesFollow-Up StudiesHumansImidazolesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein Kinase InhibitorsPyridazinesRisk FactorsImidazolesponatinibProtein Kinase InhibitorsPyridazinesCardio-oncologyChronic myeloid leukemiaPonatinibReviewTyrosine kinase inhibitors

Identifiers

PMID32026180
OpenAlexW3004564242

What OpenQuestion holds

Textmetadata
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.