TY - JOUR
T1 - Safety and efficacy of the combination of pegylated interferon-α2b and dasatinib in newly diagnosed chronic-phase chronic myeloid leukemia patients
AU - Hjorth-Hansen, H.
AU - Stentoft, J.
AU - Richter, J.
AU - Koskenvesa, P.
AU - Höglund, M.
AU - Dreimane, A.
AU - Porkka, K.
AU - Gedde-Dahl, T.
AU - Gjertsen, B. T.
AU - Gruber, F. X.
AU - Stenke, L.
AU - Eriksson, K. M.
AU - Markevärn, B.
AU - Lübking, A.
AU - Vestergaard, H.
AU - Udby, L.
AU - Bjerrum, O. W.
AU - Persson, I.
AU - Mustjoki, S.
AU - Olsson-Strömberg, U.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Dasatinib (DAS) and interferon-α have antileukemic and immunostimulatory effects and induce deep responses in chronic myeloid leukemia (CML). We assigned 40 newly diagnosed chronic-phase CML patients to receive DAS 100 mg o.d. followed by addition of pegylated interferon-α2b (PegIFN) after 3 months (M3). The starting dose of PegIFN was 15 μg/week and it increased to 25 μg/week at M6 until M15. The combination was well tolerated with manageable toxicity. Of the patients, 84% remained on PegIFN at M12 and 91% (DAS) and 73% (PegIFN) of assigned dose was given. Only one patient had a pleural effusion during first year, and three more during the second year. After introduction of PegIFN we observed a steep increase in response rates. Major molecular response was achieved in 10%, 57%, 84% and 89% of patients at M3, M6, M12 and M18, respectively. At M12, MR 4 was achieved by 46% and MR 4.5 by 27% of patients. No patients progressed to advanced phase. In conclusion, the combination treatment appeared safe with very promising efficacy. A randomized comparison of DAS±PegIFN is warranted.
AB - Dasatinib (DAS) and interferon-α have antileukemic and immunostimulatory effects and induce deep responses in chronic myeloid leukemia (CML). We assigned 40 newly diagnosed chronic-phase CML patients to receive DAS 100 mg o.d. followed by addition of pegylated interferon-α2b (PegIFN) after 3 months (M3). The starting dose of PegIFN was 15 μg/week and it increased to 25 μg/week at M6 until M15. The combination was well tolerated with manageable toxicity. Of the patients, 84% remained on PegIFN at M12 and 91% (DAS) and 73% (PegIFN) of assigned dose was given. Only one patient had a pleural effusion during first year, and three more during the second year. After introduction of PegIFN we observed a steep increase in response rates. Major molecular response was achieved in 10%, 57%, 84% and 89% of patients at M3, M6, M12 and M18, respectively. At M12, MR 4 was achieved by 46% and MR 4.5 by 27% of patients. No patients progressed to advanced phase. In conclusion, the combination treatment appeared safe with very promising efficacy. A randomized comparison of DAS±PegIFN is warranted.
UR - http://www.scopus.com/inward/record.url?scp=84973163267&partnerID=8YFLogxK
U2 - 10.1038/leu.2016.121
DO - 10.1038/leu.2016.121
M3 - Article
C2 - 27133821
AN - SCOPUS:84973163267
VL - 30
SP - 1853
EP - 1860
JO - Leukemia
JF - Leukemia
SN - 1476-5551
IS - 9
ER -