J 2010

Dasatinib in imatinib-resistant or -intolerant CML patients: data from the clinical practice of 6 hematological centers in the Czech Republic

KLAMOVA, H.; E. FABER; Daniela ŽÁČKOVÁ; M. MARKOVA; J. VOGLOVA et al.

Základní údaje

Originální název

Dasatinib in imatinib-resistant or -intolerant CML patients: data from the clinical practice of 6 hematological centers in the Czech Republic

Autoři

KLAMOVA, H.; E. FABER; Daniela ŽÁČKOVÁ; M. MARKOVA; J. VOGLOVA; E. CMUNT; L. NOVAKOVA; K. MACHOVA-POLAKOVA; J. MORAVCOVA; Dana DVOŘÁKOVÁ; K. MICHALOVA; J. BREZINOVA; Alexandra OLTOVÁ; Marie JAROŠOVÁ; Petr CETKOVSKÝ; K. INDRAK a Jiří MAYER

Vydání

Neoplasma, Slovakia, Slovak Academic Press, Ltd, 2010, 0028-2685

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30200 3.2 Clinical medicine

Stát vydavatele

Slovensko

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 1.449

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14110/10:00051558

Organizační jednotka

Lékařská fakulta

Klíčová slova anglicky

chronic myeloid leukemia; dasatinib; cytogenetic response; mutation

Příznaky

Mezinárodní význam
Změněno: 20. 4. 2012 15:03, Mgr. Michal Petr

Anotace

V originále

Dasatinib is effective second line treatment for patients with chronic myeloid leukemia (CML) resistant or intolerant to imatinib. We report here the first experiences with dasatinib therapy in 71 CML patients resistant or intolerant to imatinib from the real clinical practice of 6 hematological centers in the Czech Republic. Dose 100 mg daily and 70 mg twice daily was administered to patients with chronic phase (CP) and advanced phases (AP) CML. In chronic phase (n=46), complete hematological reponse (CHR) was achieved in 97%, major cytogenetic reponse (MCgR) in 77% and complete cytogenetic response (CCgR) in 67%. Major molecular reponse (MMR) was achieved in 19/31 patients in median of 10 months. In advanced phase (n=25), CHR was attained in 77%, MCgR in 39%, CCgR in 33% and MMR in 2/18 patients. Eleven different baseline mutations were followed up in 15 patients. Dasatinib eliminated mutations in most of the patients, but 3 patients acquired a new one. Novel mutations were detected under dasatinib therapy in 2 patients. Dasatinib was well tolerated, cytopenias were common and was managed by dose modification. The estimated progression free survival (PFS) at 12 months was 97+/-3% in CP and 62+/-21% in AP. The median time to treatment failure was 605 days in AP while it was not reached in CP patients. Our clinical experiences, described here, confirmed that dasatinib is associated with high response rates especially in imatinib resistant or intolerant CML patients in chronic phase.