Evidence map›Paper›PMID 33090357›Full record

ArticleClinical drug investigation2020

Concomitant Administration of Direct Oral Anticoagulants in Chronic Phase Chronic Myeloid Leukemia Patients Treated with Tyrosine Kinase Inhibitors.

Alessandra Serrao, Emilia Scalzulli, Luciano Fiori, Alessio Di Prima, Massimo Breccia, Antonio Chistolini

Abstract read
PubMed Publisher
In one paragraph

Article in Clinical drug investigation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 36% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

6 authors at 1 institution in 1 country.

Alessandra SerraoDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy.
Emilia ScalzulliDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy.
Luciano FioriDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy.
Alessio Di PrimaDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy.
Massimo BrecciaDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy.
Antonio ChistoliniDepartment of Translational and Precision Medicine, Hematology, Sapienza University of Rome, 00161, Rome, Italy. antonio.chistolini@uniroma1.it.ORCID http://orcid.org/0000-0002-2593-1376
Sapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveIn the last decades, the chronic myeloid leukemia (CML) therapeutic landscape has changed dramatically with the introduction of tyrosine kinase inhibitors (TKIs), with 10-year survival rates improving to up to 80%. Long-lasting TKI treatment, in particular with second-generation TKIs, has enabled clinicians to manage the onset of several side effects and other co-morbidities, such as atrial fibrillation or venous thromboembolism (VTE).

methodsWe retrospectively evaluated nine CML patients treated with TKIs between 2017 and 2020 who experienced atrial fibrillation or VTE and received concomitant administration of TKIs and direct oral anticoagulants (DOACs) outside clinical trials, to evaluate the efficacy and safety of this combination.

resultsMedian age was 66 years at CML diagnosis (range 52-73 years) and 69 years at the time of starting DOACs. A female predominance was observed. The median follow-up of concomitant DOAC and TKI administration was 8.5 months; edoxaban was administered in six patients and apixaban in two patients, and one patient received rivaroxaban. Regarding CML treatment, four patients received imatinib, two patients bosutinib, and three nilotinib. In eight patients DOACs were started for atrial fibrillation and in one patient for VTE. In none of the patients treated with the combination were additional symptomatic thrombotic adverse events or major bleedings reported.

conclusionIn this small case series, the use of DOACs in CML patients seemed feasible. Additional data on long-term outcomes including a larger cohort of CML patients treated with DOACs are, however, needed.

Indexed as

Administration, OralAdultAgedAniline CompoundsAnticoagulantsCohort StudiesFemaleHemorrhageHumansImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedNitrilesProtein Kinase InhibitorsPyrimidinesAniline CompoundsAnticoagulantsbosutinibImatinib MesylatenilotinibNitrilesProtein Kinase InhibitorsPyrimidinesQuinolines

Identifiers

PMID33090357
OpenAlexW3094278404

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.