Evidence map›Paper›PMID 33612681›Full record

ArticleInternal medicine (Tokyo, Japan)2021

Efficacy and Cardiovascular Adverse Events of Long-term Treatment with Tyrosine Kinase Inhibitors for Chronic Myeloid Leukemia: A Report from the Nagasaki CML Study Group.

Masahiko Chiwata, Hidehiro Itonaga, Shinya Sato, Miki Hashimoto, Machiko Fujioka, Sachie Kasai, Hikaru Sakamoto, Eo Toriyama, Jun Nakashima, Rena Kamijo and 24 more

Abstract read
In one paragraph

Article in Internal medicine (Tokyo, Japan), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

34 authors.

Masahiko ChiwataDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Hidehiro ItonagaDepartment of Hematology, Nagasaki University Hospital, Japan.
Shinya SatoDepartment of Hematology, Nagasaki University Hospital, Japan.
Miki HashimotoDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Machiko FujiokaDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Sachie KasaiDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Hikaru SakamotoDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Eo ToriyamaDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Jun NakashimaDepartment of Hematology, Nagasaki University Hospital, Japan.
Rena KamijoDepartment of Hematology, Nagasaki University Hospital, Japan.
Hideaki KitanosonoDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Yuji KobayashiDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Makiko HoraiDepartment of Hematology, Nagasaki University Hospital, Japan.
Masataka TaguchiDepartment of Hematology, Nagasaki University Hospital, Japan.
Masatoshi MatsuoDepartment of Hematology, Nagasaki University Hospital, Japan.
Junya MakiyamaDepartment of Hematology, Sasebo City General Hospital, Japan.
Yumi TakasakiDepartment of Hematology, Saint Francis Hospital, Japan.
Emi MatsuoDepartment of Hematology, National Hospital Organization Nagasaki Medical Center, Japan.
Kensuke HorioDepartment of Hematology, Nagasaki Prefecture Shimabara Hospital, Japan.
Koji AndoDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Atomic Bomb Disease Institute, Nagasaki University, Japan.
Yasushi SawayamaDepartment of Hematology, Nagasaki University Hospital, Japan.
Jun TaguchiDepartment of Hematology, Nagasaki University Hospital, Japan.
Yasuhisa KawaguchiDepartment of Internal Medicine, National Hospital Organization Nagasaki Hospital, Japan.
Hideki TsushimaDepartment of Hematology, Nagasaki Harbor Medical Center, Japan.
Daisuke ImanishiDepartment of Internal Medicine, Nagasaki Prefecture Gotochuoh Hospital, Japan.
Yoshitaka ImaizumiDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Shinichiro YoshidaDepartment of Hematology, National Hospital Organization Nagasaki Medical Center, Japan.
Tatsuro JoDepartment of Hematology, Japanese Red Cross Nagasaki Genbaku Hospital, Japan.
Hiroaki NonakaDepartment of Laboratory Medicine, Nagasaki Rosai Hospital, Japan.
Yukiyoshi MoriuchiDepartment of Hematology, Sasebo City General Hospital, Japan.
Kazuhiro NagaiTransfusion and Cell Therapy Unit, Nagasaki University Hospital, Japan.
Ken-Ichi YokotaBiostatistics Section, Division of Scientific Data Registry, Atomic Bomb Disease Institute, Nagasaki University, Japan.
Tomoko HataDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.
Yasushi MiyazakiDepartment of Hematology, Atomic Bomb Disease and Hibakusha Medicine Unit, Nagasaki University Graduate School of Biomedical Sciences, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective The standard treatment for chronic myeloid leukemia (CML) is the continuous use of tyrosine kinase inhibitors (TKIs), which results in a favorable prognosis for the majority of patients. Recent studies have identified cardiovascular diseases (CVDs) as late adverse events (AEs) related to TKIs. In this study, we evaluated the long-term efficacy and AEs of TKIs, focusing on CVDs. Methods We performed a retrospective survey of CML patients (diagnosed from 2001 to 2016) treated with TKIs in Nagasaki Prefecture. Clinical data were obtained from their medical records. We analyzed the survival, estimated cumulative incidence of CVDs, and risk factors for CVD among CML patients treated with TKIs. Results The overall survival rate of 264 CML patients treated with TKIs (median age 58 years old) was 89.6% [95% confidence interval (CI), 84.9-92.9%], and 80.5% (95% CI, 73.4-85.9%) at 5 and 10 years after the CML diagnosis, respectively. CVD events occurred in 26 patients (9.8%, median age 67.5 years old) with a median 65.5 months of TKI treatment. The cumulative incidences at 2 and 5 years was 2.4% (95% CI, 1.0-4.8%) and 5.2% (95% CI, 2.8-8.6%), respectively. Hypertension and a high SCORE chart risk at the diagnosis of CML were associated with CVD events during TKI treatment. Conclusion TKI treatment contributed to the long-term survival of CML patients in Nagasaki Prefecture in a "real-world" setting, but the incidence of CVDs seemed to be increased in these patients. A proper approach to managing risk factors for CVD is warranted to reduce CVD events during TKI treatment.

Indexed as

Cardiovascular DiseasesLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAgedHumansMiddle AgedProtein Kinase InhibitorsRetrospective StudiesRisk FactorsProtein Kinase Inhibitorsadverse eventcardiovascular diseasechronic myeloid leukemiatyrosine kinase inhibitor

Identifiers

PMID33612681
PMCPMC8355380

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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.