Evidence map›Paper›PMID 35235189›Full record

ArticleInternational journal of hematology2022

Safety profile of bosutinib in Japanese versus non-Japanese patients with chronic myeloid leukemia: a pooled analysis.

Naoto Takahashi, Jorge E Cortes, Emiko Sakaida, Kenichi Ishizawa, Takaaki Ono, Noriko Doki, Itaru Matsumura, Valentín García-Gutiérrez, Gianantonio Rosti, Chiho Ono and 4 more

7 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in International journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 7 registered trials, which are not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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.

NCT00261846 phase2completednot on this map

A Phase 1/2 Study Of Bosutinib (Ski-606) In Philadelphia Chromosome Positive Leukemias

TypeinterventionalSponsorPfizerRan2006 to 2015Enrolled571ConditionsChronic Myeloid LeukemiaArmsBosutinib
NCT00574873 phase3completednot on this map

A phase 3 randomized, open-label study of bosutinib versus imatinib in subjects with newly diagnosed chronic phase philadelphia chromosome positive chronic myelogenous leukemia

TypeinterventionalSponsorPfizerRan2008 to 2015Enrolled502ConditionsChronic Myeloid LeukemiaArmsBosutinib, imatinib
NCT00811070 phase2completednot on this map

A Phase 1/2 Study Of SKI-606 Administered As A Single Agent In Japanese Subjects With Philadelphia Chromosome Positive Leukemias

TypeinterventionalSponsorPfizerRan2007 to 2015Enrolled63ConditionsChronic Myelogenous LeukemiaArmsSKI-606 (Bosutinib)
NCT01903733 nacompletednot on this map

An open-label bosutinib treatment extension study for subjects with chronic myeloid leukemia (cml) who have previously participated in bosutinib studies b1871006 or b1871008

TypeinterventionalSponsorPfizerRan2013 to 2020Enrolled281ConditionsChronic Myeloid LeukemiaArmsbosutinib
NCT02130557 phase3completednot on this map

A multicenter phase 3 randomized, open-label study of bosutinib versus imatinib in adult patients with newly diagnosed chronic phase chronic myelogenous leukemia

TypeinterventionalSponsorPfizerRan2014 to 2020Enrolled536ConditionsLeukemia, Myelogenous, Chronic, Breakpoint Cluster Region-Abelson Proto-oncogene (BCR-ABL) PositiveArmsBosutinib, Imatinib
NCT02228382 phase4terminatednot on this map

A phase 4 safety and efficacy study of bosutinib (bosulif (registered)) in patients with philadelphia chromosome positive chronic myeloid leukemia previously treated with one or more tyrosine kinase inhibitors

TypeinterventionalSponsorPfizerRan2014 to 2020Enrolled163ConditionsPreviously Treated PH + CMLArmsBosutinib
NCT03128411 phase2completednot on this map

A phase 2, open-label, single-arm study to evaluate efficacy and safety of bosutinib monotherapy in japanese adult patients with newly diagnosed chronic phase chronic myelogenous leukemia

TypeinterventionalSponsorPfizerRan2017 to 2021Enrolled64ConditionsLeukemia, Chronic MyelogenousArmsBosutinib
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. 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

14 authors at 11 institutions in 5 countries.

Naoto TakahashiDepartment of Hematology, Nephrology and Rheumatology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita City, Akita, 010-8543, Japan. naotot@doc.med.akita-u.ac.jp.ORCID http://orcid.org/0000-0002-6758-3787
Jorge E CortesGeorgia Cancer Center, Augusta, GA, USA.
Emiko SakaidaChiba University Hospital, Chiba, Japan.
Kenichi IshizawaYamagata University Hospital, Yamagata, Japan.
Takaaki OnoHamamatsu University Hospital, Shizuoka, Japan.
Noriko DokiTokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan.
Itaru MatsumuraKindai University Hospital, Osaka, Japan.
Valentín García-GutiérrezHospital Universitario Ramón Y Cajal, Ramón Y Cajal Health Research Institute, Madrid, Spain.
Gianantonio RostiIRCCS Istituto Romagnolo Per Lo Studio Dei Tumori (IRST) "Dino Amadori", Meldola (FC), Italy.
Chiho OnoPfizer Japan Inc, Tokyo, Japan.
Masayuki OhkuraPfizer R&D Japan GK, Tokyo, Japan.
Yusuke TanetsuguPfizer R&D Japan GK, Tokyo, Japan.
Andrea ViqueiraPfizer SLU, Madrid, Spain.
Tim H BrümmendorfUniversitätsklinikum RWTH Aachen, Aachen, Germany.
Pfizer (Japan) · JPAkita University · JPChiba University Hospital · JPHamamatsu University Hospital · JPIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITKindai University Hospital · JPNational Cancer Center of Georgia · GESaint Louis University · ESTokyo Metropolitan Komagome Hospital · JPUniversitätsklinikum Aachen · DEYamagata University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bosutinib has been investigated in multiple clinical trials globally, including Japan, for treatment of chronic myeloid leukemia (CML). A pooled analysis of seven Pfizer-sponsored clinical trials evaluated the safety of bosutinib in Japanese (n = 138) vs non-Japanese (n = 1210) patients with CML. First-line bosutinib was administered in 54.3% vs 41.4% of patients, and second-line or later bosutinib in the remainder. Median treatment duration was 1.4 vs 2.3 years, and median relative dose intensity 78.1% vs 90.0%. Any-grade treatment-emergent adverse events (TEAEs) occurred in 100.0% vs 98.9% (grade ≥ 3: 81.9% vs 75.2%). In both groups, the most common TEAEs relevant to bosutinib were gastrointestinal (92.8% vs 84.7%), liver function (72.5% vs 34.8%), rash (63.8% vs 37.4%), and myelosuppression (55.1% vs 50.7%). TEAEs led to dose reduction in 65.2% vs 50.6%, dose interruption in 78.3% vs 68.8%, and permanent treatment discontinuation in 30.4% vs 25.4% of patients. The safety profile of bosutinib in Japanese patients was generally consistent with that in non-Japanese patients, despite a higher incidence of gastrointestinal, liver function, and rash events. TEAEs were largely manageable with dose modifications and supportive care in both groups. These data may help optimize TEAE management and outcomes in Japanese patients receiving bosutinib for CML. Trial registration ClinicalTrials.gov: NCT02130557, NCT03128411, NCT00574873, NCT00261846, NCT01903733, NCT00811070, NCT02228382.

Indexed as

Antineoplastic AgentsExanthemaLeukemia, Myelogenous, Chronic, BCR-ABL PositiveAniline CompoundsHumansJapanNitrilesProtein Kinase InhibitorsQuinolinesAniline CompoundsAntineoplastic AgentsbosutinibNitrilesProtein Kinase InhibitorsQuinolinesBosutinibChronic myeloid leukemiaJapanSafetyTyrosine kinase inhibitor

Identifiers

PMID35235189
OpenAlexW4214806085

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 1 more above

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.