Randomized comparison of interferon α and hydroxyurea with hydroxyurea monotherapy in chronic myeloid leukemia (CML-study II): prolongation of survival by the combination of interferon α and hydroxyurea

The optimum treatment conditions of interferon (IFN) α therapy in chronic myeloid leukemia (CML) are still controversial. To evaluate the role of hydroxyurea (HU) for the outcome of IFN therapy, we conducted a randomized trial to compare the combination of IFN and HU vs HU monotherapy (CML-study II)...

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Hauptverfasser: Hehlmann, Rüdiger (VerfasserIn) , Berger, Ute (VerfasserIn) , Pfirrmann, M. (VerfasserIn) , Hochhaus, Andreas (VerfasserIn) , Metzgeroth, Georgia (VerfasserIn) , Maywald, O. (VerfasserIn) , Hasford, J. (VerfasserIn) , Reiter, Andreas (VerfasserIn) , Hossfeld, D. K. (VerfasserIn) , Kolb, H.-J. (VerfasserIn) , Löffler, H. (VerfasserIn) , Pralle, H. (VerfasserIn) , Queißer, Wolfgang (VerfasserIn) , Griesshammer, M. (VerfasserIn) , Nerl, C. (VerfasserIn) , Kuse, R. (VerfasserIn) , Tobler, A. (VerfasserIn) , Eimermacher, H. (VerfasserIn) , Tichelli, A. (VerfasserIn) , Aul, C. (VerfasserIn) , Wilhelm, M. (VerfasserIn) , Fischer, J. T. (VerfasserIn) , Perker, M. (VerfasserIn) , Scheid, C. (VerfasserIn) , Schenk, M. (VerfasserIn) , Weiß, J. (VerfasserIn) , Meier, C. R. (VerfasserIn) , Kremers, S. (VerfasserIn) , Labedzki, L. (VerfasserIn) , Schmeiser, T. (VerfasserIn) , Lohrmann, H.-P. (VerfasserIn) , Heimpel, H. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 29 July 2003
In: Leukemia
Year: 2003, Jahrgang: 17, Heft: 8, Pages: 1529-1537
ISSN:1476-5551
DOI:10.1038/sj.leu.2403006
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1038/sj.leu.2403006
Verlag, lizenzpflichtig, Volltext: https://www.nature.com/articles/2403006
Volltext
Verfasserangaben:R. Hehlmann, U. Berger, M. Pfirrmann, A. Hochhaus, G. Metzgeroth, O. Maywald, J. Hasford, A. Reiter, D.K. Hossfeld, H.-J. Kolb, H. Löffler, H. Pralle, W. Queißer, M. Griesshammer, C. Nerl, R. Kuse, A. Tobler, H. Eimermacher, A. Tichelli, C. Aul, M. Wilhelm, J.T. Fischer, M. Perker, C. Scheid, M. Schenk, J. Weiß, C.R. Meier, S. Kremers, L. Labedzki, T. Schmeiser, H.-P. Lohrmann, H. Heimpel and the German CML-Study Group

MARC

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245 1 0 |a Randomized comparison of interferon α and hydroxyurea with hydroxyurea monotherapy in chronic myeloid leukemia (CML-study II)  |b prolongation of survival by the combination of interferon α and hydroxyurea  |c R. Hehlmann, U. Berger, M. Pfirrmann, A. Hochhaus, G. Metzgeroth, O. Maywald, J. Hasford, A. Reiter, D.K. Hossfeld, H.-J. Kolb, H. Löffler, H. Pralle, W. Queißer, M. Griesshammer, C. Nerl, R. Kuse, A. Tobler, H. Eimermacher, A. Tichelli, C. Aul, M. Wilhelm, J.T. Fischer, M. Perker, C. Scheid, M. Schenk, J. Weiß, C.R. Meier, S. Kremers, L. Labedzki, T. Schmeiser, H.-P. Lohrmann, H. Heimpel and the German CML-Study Group 
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520 |a The optimum treatment conditions of interferon (IFN) α therapy in chronic myeloid leukemia (CML) are still controversial. To evaluate the role of hydroxyurea (HU) for the outcome of IFN therapy, we conducted a randomized trial to compare the combination of IFN and HU vs HU monotherapy (CML-study II). From February 1991 to December 1994, 376 patients with newly diagnosed CML in chronic phase were randomized. In all, 340 patients were Ph/BCR-ABL positive and evaluable. Randomization was unbalanced 1:2 in favor of the combination therapy, since study conditions were identical to the previous CML-study I and it had been planned in advance to add the HU patients of study I (n=194) to the HU control group. Therefore, a total of 534 patients were evaluable (226 patients with IFN/HU and 308 patients with HU). Analyses were according to intention-to-treat. Median observation time of nontransplanted living patients was 7.6 years (7.9 years for IFN/HU and 7.3 years for HU). The risk profile (new CML score) was available for 532 patients: 200 patients (38%) were low, 239 patients (45%) intermediate, and 93 patients (17%) high risk. Complete hematologic response rates were higher in IFN/HU-treated patients (59 vs 32%). Of 169 evaluable IFN/HU-treated patients (75%), 104 patients (62%) achieved a cytogenetic response that was complete in 12% (n=21), major in 14% (n=24), and at least minimal in 35% (n=59). Of the 534 patients, 105 (20%) underwent allogeneic stem cell transplantation in first chronic phase. In the low-risk group, 65 of 200 patients were transplanted (33%), 30 (13%) in the intermediate-risk group, and nine (10%) in the high-risk group. Duration of chronic phase was 55 months for IFN/HU and 41 months for HU (P<0.0001). Median survival was 64 months for IFN/HU and 53 months for HU-treated patients (P=0.0063). We conclude that IFN in combination with HU achieves a significant long-term survival advantage over HU monotherapy. In view of the data of CML-study I, these results suggest that IFN/HU is also superior to IFN alone. HU should be combined with IFN in IFN-based therapies and for comparisons with new therapies. 
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