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Imatinib mesylate (STI571) treatment in patients with chronic-phase chronic myelogenous leukaemia previously submitted to autologous stem cell transplantation.

Authors :
Cervantes, Francisco
Hernández-Boluda, Juan-Carlos
Odriozola, Jesús
Camós, Mireia
Villalón, Lucía
Martínez-Climent, José-Angel
del Campo, Raquel
García-Conde, Javier
Montserrat, Emilio
Source :
British Journal of Haematology; Feb2003, Vol. 120 Issue 3, p500-504, 5p
Publication Year :
2003

Abstract

Summary. Imatinib mesylate (STI571) is a highly effective and well-tolerated treatment for patients with chronic-phase chronic myeloid leukaemia (CML), but information on its efficacy and tolerance in intensively pretreated patients is scarce. Thirty-three chronic-phase CML patients who were resistant or intolerant to interferon (IFN) and had been previously submitted to autologous stem cell transplantation were treated with imatinib for a median of 14 months (range: 6–19 months). Seven patients were in haematological response (HR) at the start of treatment; the remaining 26 attained a HR at a median of 3 weeks (range: 1–4 weeks). Major cytogenetic response rates at 3, 6 and 12 months were 42%, 45% and 55%, respectively, including 21%, 24% and 33% complete responses. Grade 3–4 neutropenia, thrombocytopenia and anaemia developed in 33%, 27% and 12% of patients respectively. Non-haematological toxicity included superficial oedema (21% of patients), gastrointestinal symptoms (18%), muscle cramps (15%), skin rash and liver enzyme increase (3% each). These results were not significantly different from those in 65 chronic-phase CML patients, resistant or intolerant to interferon without a previous ASCT, who were included in the same protocol. Imatinib mesylate is effective and safe in chronic-phase CML patients with a previous history of intensive treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00071048
Volume :
120
Issue :
3
Database :
Complementary Index
Journal :
British Journal of Haematology
Publication Type :
Academic Journal
Accession number :
9079188
Full Text :
https://doi.org/10.1046/j.1365-2141.2003.04077.x