Patient-reported outcomes in the phase 3 BFORE trial of bosutinib versus imatinib for newly diagnosed chronic phase chronic myeloid leukemia.


Journal

Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 19 01 2019
accepted: 12 03 2019
pubmed: 17 4 2019
medline: 14 6 2019
entrez: 17 4 2019
Statut: ppublish

Résumé

In the phase 3 BFORE trial (NCT02130557), treatment with bosutinib resulted in a significantly higher major molecular response rate at 12 months versus imatinib in the modified intent-to-treat (mITT) population of patients with newly diagnosed chronic phase chronic myeloid leukemia (CP CML). Assessment of patient-reported outcomes (PROs) was an exploratory objective. Patients with newly diagnosed CP CML were randomized 1:1 to receive once-daily bosutinib 400 mg or imatinib 400 mg as first-line therapy. Patients completed the Functional Assessment of Cancer Therapy-Leukemia (FACT-Leu) and EuroQoL-5 Dimensions (EQ-5D) questionnaires at baseline, every 3 months for the first 24 months of treatment, every 6 months thereafter, and at treatment completion. We report PRO results at month 12 in the mITT population (bosutinib: n = 246; imatinib: n = 241). Mean FACT-Leu combined and subscale scores were similar at baseline in the bosutinib and imatinib arms; at month 12, all scores demonstrated improvement or maintenance of health-related quality of life (HRQoL) in both treatment arms. Repeated-measures mixed-effects models showed no significant difference between bosutinib and imatinib for any FACT-Leu score. Functional health status, as measured by EQ-5D, also demonstrated improvement or maintenance with bosutinib and imatinib at month 12. Similar improvements in PROs compared with baseline were seen after 12 months of treatment with first-line bosutinib or imatinib in the BFORE trial. Newly diagnosed patients with CP CML receiving bosutinib or imatinib can preserve or improve HRQoL during treatment, although clinical efficacy was superior with bosutinib.

Sections du résumé

BACKGROUND BACKGROUND
In the phase 3 BFORE trial (NCT02130557), treatment with bosutinib resulted in a significantly higher major molecular response rate at 12 months versus imatinib in the modified intent-to-treat (mITT) population of patients with newly diagnosed chronic phase chronic myeloid leukemia (CP CML). Assessment of patient-reported outcomes (PROs) was an exploratory objective.
METHODS METHODS
Patients with newly diagnosed CP CML were randomized 1:1 to receive once-daily bosutinib 400 mg or imatinib 400 mg as first-line therapy. Patients completed the Functional Assessment of Cancer Therapy-Leukemia (FACT-Leu) and EuroQoL-5 Dimensions (EQ-5D) questionnaires at baseline, every 3 months for the first 24 months of treatment, every 6 months thereafter, and at treatment completion. We report PRO results at month 12 in the mITT population (bosutinib: n = 246; imatinib: n = 241).
RESULTS RESULTS
Mean FACT-Leu combined and subscale scores were similar at baseline in the bosutinib and imatinib arms; at month 12, all scores demonstrated improvement or maintenance of health-related quality of life (HRQoL) in both treatment arms. Repeated-measures mixed-effects models showed no significant difference between bosutinib and imatinib for any FACT-Leu score. Functional health status, as measured by EQ-5D, also demonstrated improvement or maintenance with bosutinib and imatinib at month 12.
CONCLUSIONS CONCLUSIONS
Similar improvements in PROs compared with baseline were seen after 12 months of treatment with first-line bosutinib or imatinib in the BFORE trial. Newly diagnosed patients with CP CML receiving bosutinib or imatinib can preserve or improve HRQoL during treatment, although clinical efficacy was superior with bosutinib.

Identifiants

pubmed: 30989330
doi: 10.1007/s00432-019-02894-3
pii: 10.1007/s00432-019-02894-3
doi:

Substances chimiques

Aniline Compounds 0
Nitriles 0
Quinolines 0
bosutinib 5018V4AEZ0
Imatinib Mesylate 8A1O1M485B

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1589-1599

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Auteurs

Jorge E Cortes (JE)

University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 428, Houston, TX, 77030, USA. jcortes@mdanderson.org.

Carlo Gambacorti-Passerini (C)

University of Milano-Bicocca, Monza, Italy.

Michael W Deininger (MW)

University of Utah, Salt Lake City, UT, USA.

Michael J Mauro (MJ)

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Charles Chuah (C)

Singapore General Hospital, Duke-NUS Graduate Medical School, Singapore, Singapore.

Dong-Wook Kim (DW)

Seoul St. Mary's Hematology Hospital, Leukemia Research Institute, The Catholic University of Korea, Seoul, Republic of Korea.

Dragana Milojkovic (D)

Hammersmith Hospital, Imperial College London, London, UK.

Philipp le Coutre (P)

Charité-Universitätsmedizin Berlin, Berlin, Germany.

Valentin Garcia-Gutierrez (V)

Hospital Universitario Ramón y Cajal, IRYCIS, Madrid, Spain.

Rocco Crescenzo (R)

Pfizer Inc, Collegeville, PA, USA.

Carla Mamolo (C)

Pfizer Inc, Groton, CT, USA.

Arlene Reisman (A)

Pfizer Inc, New York, NY, USA.

Andreas Hochhaus (A)

Klinik für Innere Medizin II, Universitätsklinikum Jena, Jena, Germany.

Tim H Brümmendorf (TH)

Department of Hematology and Oncology, Universitätsklinikum RWTH Aachen, Aachen, Germany.

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Classifications MeSH