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Verfasst von:Hehlmann, Rüdiger [VerfasserIn]   i
 Lauseker, Michael [VerfasserIn]   i
 Jung-Munkwitz, Susanne [VerfasserIn]   i
 Leitner, Armin [VerfasserIn]   i
 Müller, Martin Christian [VerfasserIn]   i
 Pletsch, Nadine [VerfasserIn]   i
 Proetel, Ulrike [VerfasserIn]   i
 Haferlach, Claudia [VerfasserIn]   i
 Schlegelberger, Brigitte [VerfasserIn]   i
 Balleisen, Leopold [VerfasserIn]   i
 Hänel, Mathias [VerfasserIn]   i
 Pfirrmann, Markus [VerfasserIn]   i
 Krause, Stefan W. [VerfasserIn]   i
 Nerl, Christoph [VerfasserIn]   i
 Pralle, Hans [VerfasserIn]   i
 Gratwohl, Alois [VerfasserIn]   i
 Hossfeld, Dieter K. [VerfasserIn]   i
 Hasford, Joerg [VerfasserIn]   i
 Hochhaus, Andreas [VerfasserIn]   i
 Saußele, Susanne [VerfasserIn]   i
Titel:Tolerability-adapted imatinib 800 mg/d versus 400 mg/d versus 400 mg/d plus interferon-α in newly diagnosed chronic myeloid leukemia
Verf.angabe:Rüdiger Hehlmann, Michael Lauseker, Susanne Jung-Munkwitz, Armin Leitner, Martin C. Müller, Nadine Pletsch, Ulrike Proetel, Claudia Haferlach, Brigitte Schlegelberger, Leopold Balleisen, Mathias Hänel, Markus Pfirrmann, Stefan W. Krause, Christoph Nerl, Hans Pralle, Alois Gratwohl, Dieter K. Hossfeld, Joerg Hasford, Andreas Hochhaus, and Susanne Saussele
E-Jahr:2011
Jahr:March 21, 2011
Umfang:9 S.
Fussnoten:Gesehen am 03.05.2022
Titel Quelle:Enthalten in: Journal of clinical oncology
Ort Quelle:Alexandria, Va. : American Society of Clinical Oncology, 1983
Jahr Quelle:2011
Band/Heft Quelle:29(2011), 12, Seite 1634-1642
ISSN Quelle:1527-7755
Abstract:PURPOSE: Treatment of chronic-phase (CP) chronic myeloid leukemia (CML) with imatinib 400 mg/d can be unsatisfactory. Optimization of treatment is warranted. - PATIENTS AND METHODS: In all, 1,014 newly diagnosed CP-CML patients were randomly assigned to imatinib 800 mg/d (n = 338), imatinib 400 mg/d (n = 325), or imatinib 400 mg/d plus interferon alfa (IFN-α; n = 351). Dose adaptation to avoid higher-grade toxicity was recommended. First primary end point was major molecular remission (MMR) at 12 months. - RESULTS: A higher rate of MMR at 12 months occurred with tolerability-adapted imatinib 800 mg/d than with imatinib 400 mg/d (59% [95% CI, 53% to 65%] v 44% [95% CI, 37% to 50%]; P < .001) or imatinib 400 mg/d plus IFN-α (59% v 46% [95% CI, 40% to 52%]; P = .002). Median dose in the 800-mg/d arm was 628 mg/d with a maximum dose of 737 mg/d during months 4 to 6 and a maintenance dose of 600 mg/d. All three treatment approaches were well tolerated with similar grade 3 and 4 adverse events. Independent of treatment approach, MMR at 12 months showed better progression-free survival (99% v 94%; P = .0023) and overall survival (99% v 93%; P = .0011) at 3 years when compared with > 1% on the international scale or no MMR but showed no difference in 0.1% to < 1% on the international scale, which closely correlates with complete cytogenetic remission. - CONCLUSION: Treatment of early-phase CML with imatinib can be optimized. Early high-dose therapy followed by rapid adaptation to good tolerability increases the rate of MMR at 12 months. Achievement of MMR by month 12 is directly associated with improved survival.
DOI:doi:10.1200/JCO.2010.32.0598
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

DOI: https://doi.org/10.1200/JCO.2010.32.0598
Datenträger:Online-Ressource
Sprache:eng
Bibliogr. Hinweis:Erscheint auch als : Druck-Ausgabe: Hehlmann, Rüdiger, 1941 - : Tolerability-adapted imatinib 800 mg/d versus 400 mg/d versus 400 mg/d plus interferon-α in newly diagnosed chronic myeloid leukemia. - 2011
Sach-SW:Adolescent
 Adult
 Aged
 Aged, 80 and over
 Antineoplastic Combined Chemotherapy Protocols
 Benzamides
 Chi-Square Distribution
 Disease-Free Survival
 Dose-Response Relationship, Drug
 Female
 Germany
 Humans
 Imatinib Mesylate
 Interferon-alpha
 Kaplan-Meier Estimate
 Leukemia, Myelogenous, Chronic, BCR-ABL Positive
 Male
 Middle Aged
 Piperazines
 Protein Kinase Inhibitors
 Pyrimidines
 Remission Induction
 Risk Assessment
 Risk Factors
 Survival Rate
 Time Factors
 Treatment Outcome
 Young Adult
K10plus-PPN:180073123X
Verknüpfungen:→ Zeitschrift

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