Evidence map›Paper›PMID 33590711›Full record

ArticleCancer medicine2021

Change of right ventricular systolic pressure can indicate dasatinib-induced pulmonary arterial hypertension in chronic myeloid leukemia.

Sung-Eun Lee, Jee Hyun Kong, Soo-Hyun Kim, Eun-Jung Jang, Nack-Gyun Chung, Bin Cho, Suk Joong Oh, Hae-Eok Jung, Ho-Joong Youn, Woo-Baek Chung and 1 more

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Article in Cancer medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

3 citing papers in PubMed, 5 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

11 authors at 3 institutions in 1 country.

Sung-Eun LeeDepartment of Hematology, Catholic Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.ORCID 0000-0002-9810-2050
Jee Hyun KongDivision of Hematology, Department of Internal Medicine, Wonju Christian Hospital, Yonsei University College of Medicine, Wonju, South Korea.
Soo-Hyun KimLeukemia Research Institute, The Catholic University of Korea, Seoul, South Korea.
Eun-Jung JangLeukemia Research Institute, The Catholic University of Korea, Seoul, South Korea.
Nack-Gyun ChungDepartment of Pediatrics, Catholic Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Bin ChoDepartment of Pediatrics, Catholic Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Suk Joong OhDepartment of Hematology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Hae-Eok JungDivision of Cardiology, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Ho-Joong YounDivision of Cardiology, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Woo-Baek ChungDivision of Cardiology, College of Medicine, The Catholic University of Korea, Seoul, South Korea.ORCID 0000-0002-6933-2957
Dong-Wook KimDepartment of Hematology, Catholic Hematology Hospital, College of Medicine, The Catholic University of Korea, Seoul, South Korea.
Catholic University of Korea · KRKangbuk Samsung Hospital · KRYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated the feasibility of the clinical application of non-invasive transthoracic echocardiography for diagnosis of pulmonary arterial hypertension induced by dasatinib (D-PAH) in chronic myeloid leukemia (CML).

methodsA total of 451 CML patients who were examined by 2D-echocardiography at least once at baseline and/or during dasatinib therapy as frontline (n = 196) and subsequent line (n = 255) therapies were included in this study. D-PAH was defined as right ventricular systolic pressure (RVSP) >40 mm Hg with relevant symptoms and the absence of other specific etiologies.

resultsA total of 847 echocardiographies were performed including at baseline (n = 255) and during dasatinib treatment (n = 592). During the median of 36.2 (0.1-181.8) months of dasatinib therapy, the level of RVSP gradually increased (Spearman's r = 0.2819, p < 0.001) and the mean RVSP was significantly increased after taking dasatinib therapy compared with baseline. During dasatinib therapy, 56 (12.4%) patients had RVSP >40 mm Hg without (asymptomatic, n = 27, 48.2%) or with symptoms (D-PAH, n = 29, 51.8%). All asymptomatic patients maintained dasatinib therapy without further symptoms and the D-PAH patients ultimately switched to other tyrosine kinase inhibitors. After dasatinib discontinuation, 13 (45%) and 15 (52%) patients showed RVSP normalization and gradual decrease, respectively.

conclusionsOur large cohort study demonstrated that the gradual increment of RVSP might be induced by dasatinib and non-invasive echocardiography can be fast way for early diagnosis as well as for monitoring of D-PAH.

Indexed as

AdultAgedAntineoplastic AgentsBlood PressureDasatinibDrug SubstitutionEchocardiographyFeasibility StudiesFemaleHumansLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedProtein Kinase InhibitorsPulmonary Arterial HypertensionSystoleAntineoplastic AgentsDasatinibProtein Kinase Inhibitorschronic myeloid leukemiadasatinibechocardiographypulmonary arterial hypertensionright ventricular systolic pressure

Identifiers

PMID33590711
PMCPMC7940235
OpenAlexW3131466586

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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.