Evidence map›Paper›PMID 20577839›Full record

Trial reportInternational journal of hematology2010

Imatinib for newly diagnosed chronic-phase chronic myeloid leukemia: results of a prospective study in Japan.

Tadashi Nagai, Jin Takeuchi, Nobuaki Dobashi, Yuzuru Kanakura, Shuichi Taniguchi, Koji Ezaki, Chiaki Nakaseko, Akira Hiraoka, Masaya Okada, Yasushi Miyazaki and 10 more

Abstract readClinical TrialMulticenter Study
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. 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

20 authors at 19 institutions in 1 country.

Tadashi NagaiDivision of Hematology, Jichi Medical University Hospital, Shimotsuke, Japan. t-nagai@jichi.ac.jp
Jin Takeuchi
Nobuaki Dobashi
Yuzuru Kanakura
Shuichi Taniguchi
Koji Ezaki
Chiaki Nakaseko
Akira Hiraoka
Masaya Okada
Yasushi Miyazaki
Toshiko Motoji
Masaaki Higashihara
Norifumi Tsukamoto
Hitoshi Kiyoi
Shinji Nakao
Katsuji Shinagawa
Ryuzo Ohno
Tomoki Naoe
Kazunori Ohnishi
Noriko Usui
Nagoya University Hospital · JPAichi Cancer Center · JPChiba University · JPFujita Health University Hospital · JPGunma University Hospital · JPHamamatsu University School of Medicine · JPHyogo Medical University · JPJichi Medical University · JPJikei University School of Medicine · JPKanazawa University · JPKitasato University Hospital · JPNagasaki University Hospital · JPNihon University Itabashi Hospital · JPOkayama University Hospital · JPOsaka Medical Center for Cancer and Cardiovascular Diseases · JPOsaka University Hospital · JPThe Jikei University Hospital · JPTokyo Women's Medical University · JPToranomon Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although imatinib has become the current standard treatment for chronic myeloid leukemia (CML), there is limited information regarding its efficacy and safety among Japanese patients. We therefore conducted a prospective multi-center open-label study of imatinib for Japanese patients with newly diagnosed chronic-phase CML (CP-CML). A total of 107 patients were enrolled and treated with imatinib at an initial daily dose of 400 mg. Eighty-three patients completed 3 years of study treatment. The cumulative rates of major cytogenetic response and complete cytogenetic response (CCyR) were 90.9 and 90.2% at 3 years, respectively. The safety profile was not very different from that reported in the IRIS study, although grade > or =3 neutropenia occurred relatively frequently (31.8 vs. 14.3%). Only seven patients discontinued the study due to adverse events, as did four patients due to insufficient efficacy. The 3-year probabilities of overall survival and progression-free survival were 93.2 and 91.4%, respectively. Higher average daily doses (i.e., > or =350 mg) were significantly associated not only with higher rates of achieving CCyR, but also with longer duration of CCyR. These findings confirm the clinical utility of imatinib in Japanese patients with newly diagnosed CP-CML, and suggest detrimental effect of low average daily dose on treatment results.

Indexed as

AdolescentAdultAgedBenzamidesChildDrug-Related Side Effects and Adverse ReactionsFemaleHumansImatinib MesylateJapanLeukemia, Myeloid, Chronic-PhaseMaleMiddle AgedPiperazinesProspective StudiesPyrimidinesBenzamidesImatinib MesylatePiperazinesPyrimidines

Identifiers

PMID20577839
OpenAlexW2000354804

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.