Julian Ronnacker, Philippe J. Muller, Jan-Henrik Mikesch, Sven Zukunft, Barbora Weinbergerová, Jiří Šrámek, Jan Valka, Jan Novak, Pavel Zak, Tomas Szotkowski, Zdenek Koristek, Carolin Krekeler, Julia M. Unglaub, Tim Sauer, Leo Ruhnke, Sabrina Kraus, Judith Schaffrath, Lutz P. Müller, Sabrina Kaes, Dirk Niemann, Lars Fransecky, Patrick P. Hess, Martina Crysandt, Edgar Jost, Joana Millo, Johannes Gaertner, Roland Repp, Madlen Jentzsch, Lea Hoppe, Stefan Klein, Franziska Modemann, Nina Michalowski, Klaudia Fischbach, Wolfgang Blau, Marion Ruhs, Markus Ritter, Julian Lohmeyer, Björn Steffen, Sarah Hauser, Martin Kaufmann, Stefan W. Krause, Ricarda Knabe, Karsten Spiekermann, Hubert Serve, Uwe Platzbecker, Claudia D. Baldus, Carsten Müller-Tidow, Georg Lenz, Hans Christian Reinhardt, Jirí Mayer, Martin Bornhäuser, Christoph Röllig, Christoph Schliemann, Maher Hanoun
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引用次数: 0
Abstract
The addition of gemtuzumab ozogamicin (GO) to intensive chemotherapy (IC) has become a mainstay in treating patients with core binding factor acute myeloid leukemia (CBF-AML). However, evidence for the efficacy of GO in this particular subgroup is primarily based on meta-analytic data from different trials conducted more than a decade ago. In this registry-based study, we evaluated the impact of adding GO to IC in 265 CBF-AML patients from the SAL, AMLCG, and CELL cooperative study groups. Patients receiving GO had a 2-year overall survival of 90% compared with 80% in those without GO (hazard ratio [HR] 0.45, 95% confidence interval [CI] 0.21–0.95, P = 0.036) and a 2-year event-free survival of 51% versus 36% (HR 0.69, 95% CI 0.48–0.99, P = 0.046). While complete remission rates in GO vs. non-GO patients were comparable (89% vs. 90%, P = 0.81), more GO patients achieved measurable residual disease-negative remission (77% vs. 49%, P < 0.001), resulting in numerically reduced cumulative incidence of relapse (HR 0.67, 95% CI 0.43–1.02, P = 0.06). Despite delayed platelet recovery, high-grade toxicities were not increased in GO-treated patients. These findings support the integration of GO into treatment protocols for IC-eligible patients with CBF-AML.
期刊介绍:
Title: Leukemia
Journal Overview:
Publishes high-quality, peer-reviewed research
Covers all aspects of research and treatment of leukemia and allied diseases
Includes studies of normal hemopoiesis due to comparative relevance
Topics of Interest:
Oncogenes
Growth factors
Stem cells
Leukemia genomics
Cell cycle
Signal transduction
Molecular targets for therapy
And more
Content Types:
Original research articles
Reviews
Letters
Correspondence
Comments elaborating on significant advances and covering topical issues