TY - JOUR
T1 - Defining therapy goals for major molecular remission in chronic myeloid leukemia
T2 - Results of the randomized CML Study IV
AU - Saussele, Susanne
AU - Hehlmann, Rüdiger
AU - Fabarius, Alice
AU - Jeromin, Sabine
AU - Proetel, Ulrike
AU - Rinaldetti, Sebastien
AU - Kohlbrenner, Katharina
AU - Einsele, Hermann
AU - Falge, Christiane
AU - Kanz, Lothar
AU - Neubauer, Andreas
AU - Kneba, Michael
AU - Stegelmann, Frank
AU - Pfreundschuh, Michael
AU - Waller, Cornelius F.
AU - Oppliger Leibundgut, Elisabeth
AU - Heim, Dominik
AU - Krause, Stefan W.
AU - Hofmann, Wolf Karsten
AU - Hasford, Joerg
AU - Pfirrmann, Markus
AU - Müller, Martin C.
AU - Hochhaus, Andreas
AU - Lauseker, Michael
N1 - Publisher Copyright:
© 2018 The Author(s).
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Major molecular remission (MMR) is an important therapy goal in chronic myeloid leukemia (CML). So far, MMR is not a failure criterion according to ELN management recommendation leading to uncertainties when to change therapy in CML patients not reaching MMR after 12 months. At monthly landmarks, for different molecular remission status Hazard ratios (HR) were estimated for patients registered to CML study IV who were divided in a learning and a validation sample. The minimum HR for MMR was found at 2.5 years with 0.28 (compared to patients without remission). In the validation sample, a significant advantage for progression-free survival (PFS) for patients in MMR could be detected (p-value 0.007). The optimal time to predict PFS in patients with MMR could be validated in an independent sample at 2.5 years. With our model we provide a suggestion when to define lack of MMR as therapy failure and thus treatment change should be considered. The optimal response time for 1% BCR-ABL at about 12-15 months was confirmed and for deep molecular remission no specific time point was detected. Nevertheless, it was demonstrated that the earlier the MMR is achieved the higher is the chance to attain deep molecular response later.
AB - Major molecular remission (MMR) is an important therapy goal in chronic myeloid leukemia (CML). So far, MMR is not a failure criterion according to ELN management recommendation leading to uncertainties when to change therapy in CML patients not reaching MMR after 12 months. At monthly landmarks, for different molecular remission status Hazard ratios (HR) were estimated for patients registered to CML study IV who were divided in a learning and a validation sample. The minimum HR for MMR was found at 2.5 years with 0.28 (compared to patients without remission). In the validation sample, a significant advantage for progression-free survival (PFS) for patients in MMR could be detected (p-value 0.007). The optimal time to predict PFS in patients with MMR could be validated in an independent sample at 2.5 years. With our model we provide a suggestion when to define lack of MMR as therapy failure and thus treatment change should be considered. The optimal response time for 1% BCR-ABL at about 12-15 months was confirmed and for deep molecular remission no specific time point was detected. Nevertheless, it was demonstrated that the earlier the MMR is achieved the higher is the chance to attain deep molecular response later.
UR - https://www.scopus.com/pages/publications/85042542477
U2 - 10.1038/s41375-018-0055-7
DO - 10.1038/s41375-018-0055-7
M3 - Article
C2 - 29479070
AN - SCOPUS:85042542477
SN - 0887-6924
VL - 32
SP - 1222
EP - 1228
JO - Leukemia
JF - Leukemia
IS - 5
ER -