Evidence map›Paper›PMID 29845477›Full record

Trial reportInternational journal of clinical oncology2018

Plasma concentrations of dasatinib have a clinical impact on the frequency of dasatinib dose reduction and interruption in chronic myeloid leukemia: an analysis of the DARIA 01 study.

Shuichi Mizuta, Masashi Sawa, Hisashi Tsurumi, Kana Matsumoto, Kotaro Miyao, Takeshi Hara, Takeshi Takahashi, Reona Sakemura, Hiroshi Kojima, Akio Kohno and 4 more

Abstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in International journal of clinical oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Therapeutic drug monitoring of oral targeted antineoplastic drugs.European journal of clinical pharmacology · 2021
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Is There a Role for Dose Modification of TKI Therapy in CML?Current hematologic malignancy reports · 2019
    Review
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

14 authors.

Shuichi MizutaDepartment of Hematology, Fujita Health University School of Medicine, Toyoake, Japan. mizuta@spacelan.ne.jp.ORCID http://orcid.org/0000-0001-6690-5409
Masashi SawaDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Hisashi TsurumiDepartment of Hematology, Graduate School of Medicine, Gifu University, Gifu, Japan.
Kana MatsumotoDepartment of Clinical Pharmaceutics, Doshisha Women's College of Liberal Arts, Kyoto, Japan.
Kotaro MiyaoDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Takeshi HaraDepartment of Hematology, Graduate School of Medicine, Gifu University, Gifu, Japan.
Takeshi TakahashiDepartment of Hematology, Gifu Municipal Hospital, Gifu, Japan.
Reona SakemuraDepartment of Hematology and Oncology, Anjo Kosei Hospital, Anjo, Japan.
Hiroshi KojimaDepartment of Hematology, Daido Hospital, Nagoya, Japan.
Akio KohnoDepartment of Hematology and Oncology, JA Aichi Konan Kosei Hospital, Konan, Japan.
Mari S ObaDepartment of Medical Statistics, Faculty of Medicine, Toho University, Tokyo, Japan.
Satoshi MoritaDepartment of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Junichi SakamotoTokai Central Hospital, Kagamigahara, Japan.
Nobuhiko EmiDepartment of Hematology, Fujita Health University School of Medicine, Toyoake, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDasatinib has shown promising anti-leukemic activity against chronic myeloid leukemia (CML). However, patients receiving dasatinib frequently require dose reductions and treatment interruptions (treatment alteration).

methodsWe prospectively analyzed the frequency and significance of treatment alteration during dasatinib therapy in patients with CML. In all patients, trough plasma concentrations of dasatinib (C

results28% of patients had their doses reduced at a median of 42 days, and 25% of patients had temporarily interrupted at a median of 54 days after treatment initiation. The overall dasatinib treatment alteration-free rate at 1 year was 66%. Age was significantly correlated with C

conclusionCurrent data demonstrate that patients treated with dasatinib who displayed a high C

Indexed as

AdultAgedAged, 80 and overDasatinibDose-Response Relationship, DrugFemaleHumansJapanLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedProspective StudiesProtein Kinase InhibitorsSurvival RateTreatment FailureYoung AdultDasatinibProtein Kinase InhibitorsChronic myeloid leukemiaDasatinibIndividualized dasatinib therapyPlasma concentrationTreatment adherence

Identifiers

PMID29845477
PMCPMC6154123

What OpenQuestion holds

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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.