Evidence map›Paper›PMID 24357015›Full record

Trial reportInternational journal of hematology2014

Efficacy and safety of dasatinib versus imatinib in Japanese patients with newly diagnosed chronic-phase chronic myeloid leukemia (CML-CP): Subset analysis of the DASISION trial with 2-year follow-up.

Shin Fujisawa, Hirohisa Nakamae, Michinori Ogura, Ken-ichi Ishizawa, Masafumi Taniwaki, Atae Utsunomiya, Kosei Matsue, Yasushi Takamatsu, Kensuke Usuki, Mitsune Tanimoto and 3 more

Registry-linked trialAbstract readClinical Trial, Phase IIIComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02690922 (The Combination of Lower Dosage of Chemotherapy With Tyrosine Kinase Inhibitor to Treat Newly Diagnosed ph+ Acute Lymphoblastic Leukemia Patients), which is not on this map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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.

NCT02690922 phase4unknown statusnot on this mapstarted 2016, after this paper: background citation

The Combination of Lower Dosage of Chemotherapy With Tyrosine Kinase Inhibitor to Treat Newly Diagnosed ph+ Acute Lymphoblastic Leukemia Patients

TypeinterventionalSponsorTongji HospitalRan2016 to 2017Enrolled40Conditionsph+ Acute Lymphoblastic LeukemiaArmsDasatinib, prednisone, dexamethasone, methotrexate
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 28 citations in OpenAlex.

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  18. Personalized medicine in hematology - A landmark from bench to bed.Computational and structural biotechnology journal · 2014
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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

13 authors at 13 institutions in 1 country.

Shin FujisawaDepartment of Hematology, Yokohama City University Medical Center, 4-57 Urafune-cho, Minami-ku, Yokohama, Kanagawa, Japan, shin-fji@urahp.yokohama-cu.ac.jp.
Hirohisa Nakamae
Michinori Ogura
Ken-ichi Ishizawa
Masafumi Taniwaki
Atae Utsunomiya
Kosei Matsue
Yasushi Takamatsu
Kensuke Usuki
Mitsune Tanimoto
Yoji Ishida
Hideki Akiyama
Shintaro Onishi
Fukuoka University · JPImamura Hospital · JPIwate Medical University · JPJapanese Red Cross Nagoya Daini Hospital · JPKameda Medical Center · JPNTT Medical Center · JPOkayama University Hospital · JPOsaka City University Hospital · JPOtsuka (Japan) · JPTohoku University · JPTokyo Metropolitan Komagome Hospital · JPUniversity Hospital Kyoto Prefectural University of Medicine · JPYokohama City University Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dasatinib is a highly potent BCR-ABL kinase inhibitor with established efficacy and safety in imatinib-resistant or -intolerant patients with chronic myeloid leukemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukemia. In the global phase III DASISION trial in patients with newly diagnosed chronic phase CML (CML-CP), dasatinib was found to have an acceptable safety profile and demonstrated significantly faster and higher rates of complete cytogenetic response (CCyR) and major molecular response (MMR) compared with imatinib. Here, we report the results of a subset analysis of Japanese patients enrolled in the DASISION trial, showing safety and efficacy profiles generally consistent with patients enrolled worldwide, including higher response rates (CCyR, MMR) with dasatinib compared with imatinib and similar high rates of progression-free and overall survival with both therapies. However, the small sample size of the present study limits the strength of these conclusions, and further exploration is needed to confirm any differences observed in Japanese patients compared with the total treated population. These findings support the use of dasatinib 100 mg QD as a first-line treatment in Japanese patients with newly diagnosed CML-CP.

Indexed as

AdultAgedAntineoplastic AgentsBenzamidesDasatinibDrug Resistance, NeoplasmFemaleFollow-Up StudiesFusion Proteins, bcr-ablHumansImatinib MesylateJapanLeukemia, Myeloid, Chronic-PhaseMaleMiddle AgedMutationAntineoplastic AgentsBenzamidesDasatinibFusion Proteins, bcr-ablImatinib MesylatePiperazinesProtein Kinase InhibitorsPyrimidinesThiazoles

Identifiers

PMID24357015
OpenAlexW2007586468

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.