Evidence map›Paper›PMID 33851349›Full record

Trial reportInternational journal of hematology2021

Efficacy and safety of bosutinib versus imatinib for newly diagnosed chronic myeloid leukemia in the Asian subpopulation of the phase 3 BFORE trial.

Charles Chuah, Liang Piu Koh, Tontanai Numbenjapon, Dae Young Zang, Kiat Hoe Ong, Young Rok Do, Masayuki Ohkura, Chiho Ono, Andrea Viqueira, Jorge E Cortes and 1 more

Registry-linked trialAbstract readClinical Trial, Phase IIIMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in International journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02130557 (A MULTICENTER PHASE 3 RANDOMIZED, OPEN-LABEL STUDY OF BOSUTINIB VERSUS IMATINIB IN ADULT PATIENTS WITH NEWLY DIAGNOSED CHRONIC PHASE CHRONIC MYELOGENOUS LEUKEMIA), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

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
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

11 authors at 10 institutions in 7 countries.

Charles ChuahSingapore General Hospital, Duke-NUS Medical School, 20 College Road, Singapore, 169856, Singapore. charles.chuah.t.h@singhealth.com.sg.ORCID http://orcid.org/0000-0002-0834-9333
Liang Piu KohNational University Cancer Institute, Singapore, Singapore.
Tontanai NumbenjaponPhramongkutklao Hospital, Phramongkutklao College of Medicine, Bangkok, Thailand.
Dae Young ZangHallym University Sacred Heart Hospital, Anyang, Republic of Korea.
Kiat Hoe OngTan Tock Seng Hospital, Singapore, Singapore.
Young Rok DoDongsan Medical Center, Keimyung University, Daegu, Republic of Korea.
Masayuki OhkuraPfizer R&D Japan GK, Tokyo, Japan.
Chiho OnoPfizer Japan Inc, Tokyo, Japan.
Andrea ViqueiraPfizer SLU, Madrid, Spain.
Jorge E CortesGeorgia Cancer Center at Augusta University, Augusta, GA, USA.
Tim H BrümmendorfUniversitätsklinikum RWTH Aachen, Aachen, Germany.
Pfizer (Japan) · JPAugusta University Health · USHallym University Sacred Heart Hospital · KRKeimyung University Dongsan Medical Center · KRNational University Cancer Institute, Singapore · SGPhramongkutklao Hospital · THSaint Louis University · ESSingHealth · SGTan Tock Seng Hospital · SGUniversitätsklinikum Aachen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bosutinib is approved in the United States, Europe, Japan, and other countries for treatment of newly diagnosed chronic phase (CP) chronic myeloid leukemia (CML), and CML resistant/intolerant to prior therapy. In the phase 3 BFORE trial (Clinicaltrials.gov, NCT02130557), patients were randomized 1:1 to first-line bosutinib or imatinib 400 mg once daily. We examined efficacy, safety, and patient-reported outcomes of bosutinib vs imatinib and pharmacokinetics of bosutinib in the Asian (n = 33 vs 34) and non-Asian (n = 235 vs 234) subpopulations of BFORE followed for at least 24 months. At the data cutoff date, 72.7 vs 66.7% of Asian and 70.6 vs 66.4% of non-Asian patients remained on treatment. The major molecular response rate at 24 months favored bosutinib vs imatinib among Asian (63.6 vs 38.2%) and non-Asian (60.9 vs 52.6%) patients, as did the complete cytogenetic response rate by 24 months (86.7 vs 76.7%, 81.5 vs 76.3%). Treatment-emergent adverse events in both subpopulations were consistent with the primary BFORE results. Trough bosutinib concentration levels tended to be higher in Asian patients. Health-related quality of life was maintained after 12 months of bosutinib in both subpopulations. These results support bosutinib as a first-line treatment option in Asian patients with CP CML.

Indexed as

AdultAgedAged, 80 and overAniline CompoundsAntineoplastic AgentsAsiaFemaleHumansImatinib MesylateLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleMiddle AgedNitrilesProtein Kinase InhibitorsQuinolinesTreatment OutcomeAniline CompoundsAntineoplastic AgentsbosutinibImatinib MesylateNitrilesProtein Kinase InhibitorsQuinolinesAsianBosutinibChronic myeloid leukemiaFirst-lineImatinib

Identifiers

PMID33851349
OpenAlexW3156088103

What OpenQuestion holds

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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.