Evidence map›Paper›PMID 32152879›Full record

ArticleInternational journal of hematology2020

Pharmacokinetics of dasatinib in a hemodialysis patient with chronic myeloid leukemia and chronic kidney disease.

Jinichi Mori, Kumi Oshima, Tetsuya Tanimoto, Hikari Ishizuka, Shinya Kimura, Masatomo Miura, Naoto Takahashi

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In one paragraph

Article in International journal of hematology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. How to manage CML patients with comorbidities.Hematology. American Society of Hematology. Education Program · 2020
    Review
  6. Article
  7. 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

7 authors.

Jinichi MoriDepartment of Hematology, Jyoban Hospital, Tokiwa Foundation, 57 Kaminodai Kamiyunagayamachi Jyoban, Iwaki, Fukushima, 972-8322, Japan. jinichi-mori@tokiwa.or.jp.
Kumi OshimaDepartment of Hematology, Jyoban Hospital, Tokiwa Foundation, 57 Kaminodai Kamiyunagayamachi Jyoban, Iwaki, Fukushima, 972-8322, Japan.
Tetsuya TanimotoDepartment of Hematology, Jyoban Hospital, Tokiwa Foundation, 57 Kaminodai Kamiyunagayamachi Jyoban, Iwaki, Fukushima, 972-8322, Japan.
Hikari IshizukaDepartment of Internal Medicine, Fukushima Rosai Hospital, Iwaki, Fukushima, Japan.
Shinya KimuraDivision of Hematology, Respiratory Medicine and Oncology, Department of Internal Medicine, Faculty of Medicine, Saga University, Saga, Japan.
Masatomo MiuraDepartment of Pharmacy, Akita University Hospital, Akita, Japan.
Naoto TakahashiDepartment of Hematology, Nephrology, and Rheumatology, Akita University Graduate School of Medicine, Akita, Japan.

Funding

Grant-in-Aid for Scientific Research 17K08408
6 · The paper itself

Abstract

Until now, no studies have addressed the use of dasatinib in hemodialysis patients. Herein, we report the case of a 73-year-old hemodialysis patient with chronic myeloid leukemia (CML) who was treated with dasatinib. For 5 years prior, the patient had received nilotinib for the treatment of CML. Regular hemodialysis was initiated due to progression of hypertensive nephrosclerosis, whereupon nilotinib was discontinued and the patient began receiving 100 mg dose of dasatinib once daily. On dialysis days, dasatinib was administered immediately after completion of dialysis. Four months after starting dasatinib, we performed a pharmacokinetic study. The plasma concentrations of dasatinib before, immediately, and 2 h after the completion of hemodialysis were 7.4, 6.1, and 59.5 ng/mL, respectively. Ultrasound cardiography revealed a gradual decline in ejection fraction during dasatinib therapy. Because the patient's dasatinib trough concentration was higher (6.1 ng/mL) than the target level (1.5 ng/mL), we suspected the development of dasatinib-related heart dysfunction; thus, dasatinib was discontinued 6 months after its initiation. We concluded that hemodialysis patients are potentially vulnerable to the cardiotoxic effects of dasatinib; monitoring of cardiac function and plasma drug concentration may thus be useful in assessing their condition.

Indexed as

CardiotoxinsRenal DialysisAgedBiomarkers, PharmacologicalDasatinibHeart FailureHumansHypertensionLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleRenal Insufficiency, ChronicStroke VolumeTime FactorsWithholding TreatmentBiomarkers, PharmacologicalCardiotoxinsDasatinibCardiotoxicityCMLDasatinibHemodialysisPharmacokinetics

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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.