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Current survival measures reliably reflect modern sequential treatment in CML: correlation with prognostic stratifications
T. Pavlik, E. Janousova, J. Mayer, K. Indrak, M. Jarosova, H. Klamova, D. Zackova, J. Voglova, E. Faber, M. Karas, K. Machova Polakova, Z. Racil, E. Demeckova, L. Demitrovicova, E. Tothova, J. Chudej, I. Markuljak, E. Cmunt, T. Kozak, J. Muzik, L. Dusek,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1998 to 1 year ago
Wiley Free Content
from 1996 to 1 year ago
PubMed
23760739
DOI
10.1002/ajh.23508
Knihovny.cz E-resources
- MeSH
- Survival Analysis MeSH
- Fusion Proteins, bcr-abl genetics metabolism MeSH
- Benzamides therapeutic use MeSH
- Leukemia, Myeloid, Chronic-Phase diagnosis drug therapy genetics mortality MeSH
- Adult MeSH
- Remission Induction MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger genetics metabolism MeSH
- Adolescent MeSH
- Piperazines therapeutic use MeSH
- Predictive Value of Tests MeSH
- Antineoplastic Agents therapeutic use MeSH
- Pyrimidines therapeutic use MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Treatment Outcome MeSH
- Research Design MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Using the data of 723 chronic myeloid leukemia (CML) patients in the chronic phase, we analyzed the prognostic value of the Sokal, Euro, and EUTOS scores as well as the level of BCR-ABL1 and the achievement of complete cytogenetic response (CCgR) at 3 months of imatinib therapy in relation to the so-called current survival measures: the current cumulative incidence (CCI) reflecting the probability of being alive and in CCgR after starting imatinib therapy; the current leukemia-free survival (CLFS) reflecting the probability of being alive and in CCgR after achieving the first CCgR; and the overall survival. The greatest difference between the CCI curves at 5 years after initiating imatinib therapy was observed for the BCR-ABL1 transcripts at 3 months. The 5-year CCI was 94.3% in patients with BCR-ABL1 transcripts ≤ 10% and 57.1% in patients with BCR-ABL1 transcripts > 10% (P = 0.005). Therefore, the examination of BCR-ABL1 transcripts at 3 months may help in early identification of patients who are likely to perform poorly with imatinib. On the other hand, CLFS was not significantly affected by the considered stratifications. In conclusion, our results indicate that once the CCgR is achieved, the prognosis is good irrespective of the starting prognostic risks.
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