Survival Outcomes for Clonal Evolution in Chronic Myeloid Leukemia Patients on Second Generation Tyrosine Kinase Inhibitor Therapy

被引:46
作者
Verma, Dushyant [1 ]
Kantarjian, Hagop [1 ]
Shan, Jianqin [1 ]
O'Brien, Susan [1 ]
Estrov, Zeev [1 ]
Garcia-Manero, Guillermo [1 ]
Koller, Charles [1 ]
Borthakur, Gautam [1 ]
Cortes, Jorge [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
clonal expression; clonal evolution; chronic myeloid leukemia; dasatinib; nilotinib; CHRONIC MYELOGENOUS LEUKEMIA; ADDITIONAL CYTOGENETIC ABNORMALITIES; IMATINIB MESYLATE; ACCELERATED PHASE; PROGNOSTIC-SIGNIFICANCE; INTERFERON-ALPHA; RESPONSES; RESISTANCE; DIAGNOSIS; DISEASE;
D O I
10.1002/cncr.25015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Clonal evolution is frequently detected in patients developing resistance to imatinib. The outcome of patients with clonal evolution treated with second generation tyrosine kinase inhibitors is not known. METHODS: The authors analyzed the outcome of 177 CML patients after second tyrosine kinase inhibitor therapy. RESULTS: Ninety-five patients were in chronic phase, 30 had clonal evolution, 28 were in accelerated phase (AP), and 24 were in AP plus clonal evolution. Major cytogenetic response rates were 58%, 54%, 28%, and 13%; 2-year overall survival (OS) rates were 86%, 73%, 68%, and 33%; and 2-year event-free survival (EFS) rates were 69%, 67%, 31%, and 8%, respectively. The hematologic and cytogenetic response rates, OS, and EFS were no different between patients in chronic phase with clonal evolution and patients with chronic phase and no clonal evolution. However, clonal evolution had a significant adverse impact when associated with other features of AP. On multivariate analysis, clonal evolution had no independently significant effect on achieving major cytogenetic response on the second generation tyrosine kinase inhibitors. The factors predicting increasing major cytogenetic response to second generation tyrosine kinase inhibitors were prior achievement of major cytogenetic response with imatinib, higher hemoglobin levels, no splenomegaly, lower percentage of Philadelphia chromosome-positive metaphases, and no prior chemotherapy. CONCLUSIONS: Clonal evolution constitutes a heterogeneous entity with variable outcome with second generation tyrosine kinase inhibitors, with trisomy 8, chromosome 17, and complex abnormalities having the worst outcome, regardless of the number of metaphases involved. The molecular events behind these abnormalities and potential therapeutic approaches directed at them need to be defined. Cancer 2010;116:2673-81. (C) 2010 American Cancer Society.
引用
收藏
页码:2673 / 2681
页数:9
相关论文
共 26 条
[1]  
ANASTASI J, 1995, LEUKEMIA, V9, P628
[2]   MARROW TRANSPLANTATION FOR PATIENTS IN ACCELERATED PHASE OF CHRONIC MYELOID-LEUKEMIA [J].
CLIFT, RA ;
BUCKNER, CD ;
THOMAS, ED ;
BRYANT, E ;
ANASETTI, C ;
BENSINGER, WI ;
BOWDEN, R ;
DEEG, HJ ;
DONEY, KC ;
FISHER, LD ;
HANSEN, JA ;
MARTIN, P ;
MCDONALD, GB ;
SANDERS, JE ;
SCHOCH, G ;
SINGER, J ;
STORB, R ;
SULLIVAN, KM ;
WITHERSPOON, RP ;
APPELBAUM, FR .
BLOOD, 1994, 84 (12) :4368-4373
[3]   Suppression of cytogenetic clonal evolution with interferon alfa therapy in patients with Philadelphia chromosome-positive chronic myelogenous leukemia [J].
Cortes, J ;
Talpaz, M ;
O'Brien, S ;
Rios, MB ;
Majlis, A ;
Keating, M ;
Freireich, EJ ;
Kantarjian, H .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (10) :3279-3285
[4]   Molecular responses in patients with chronic myelogenous leukemia in chronic phase treated with imatinib mesylate [J].
Cortes, J ;
Talpaz, M ;
O'Brien, S ;
Jones, D ;
Luthra, R ;
Shan, J ;
Giles, F ;
Faderl, S ;
Verstovsek, S ;
Garcia-Manero, G ;
Rios, MB ;
Kantarjian, H .
CLINICAL CANCER RESEARCH, 2005, 11 (09) :3425-3432
[5]   Clonal evolution in chronic myelogenous leukemia [J].
Cortes, J ;
O'Dwyer, ME .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2004, 18 (03) :671-+
[6]   Prognostic significance of cytogenetic clonal evolution in patients with chronic myelogenous leukemia on imatinib mesylate therapy [J].
Cortes, JE ;
Talpaz, M ;
Giles, F ;
O'Brien, S ;
Rios, MB ;
Shan, J ;
Garcia-Manero, G ;
Faclerl, S ;
Thomas, DA ;
Wierda, W ;
Ferrajoli, A ;
Jeha, S ;
Kantarjian, HM .
BLOOD, 2003, 101 (10) :3794-3800
[7]   Dynamics of cytogenetic aberrations in Philadelphia chromosome positive and negative hematopoiesis during dasatinib therapy of chronic myeloid leukemia patients after imatinib failure [J].
Fabarius, Alice ;
Haferlach, Claudia ;
Mueller, Martin C. ;
Erben, Philipp ;
Lahaye, Tanja ;
Giehl, Michelle ;
Frank, Oliver ;
Seifarth, Wolfgang ;
Hehlmann, Ruediger ;
Hochhaus, Andreas .
HAEMATOLOGICA, 2007, 92 (06) :834-837
[8]   Dasatinib induces significant hematologic and cytogenetic responses in patients with imatinib-resistant or -intolerant chronic myeloid leukemia in accelerated phase [J].
Guilhot, Francois ;
Apperley, Jane ;
Kim, Dong-Wook ;
Bullorsky, Eduardo O. ;
Baccarani, Michele ;
Roboz, Gail J. ;
Amadori, Sergio ;
de Souza, Carmino A. ;
Lipton, Jeffrey H. ;
Hochhaus, Andreas ;
Heim, Dominik ;
Larson, Richard A. ;
Branford, Susan ;
Muller, Martin C. ;
Agarwal, Prasheen ;
Gollerkeri, Ashwin ;
Talpaz, Moshe .
BLOOD, 2007, 109 (10) :4143-4150
[9]   Molecular and chromosomal mechanisms of resistance to imatinib (ST1571) therapy [J].
Hochhaus, A ;
Kreil, S ;
Corbin, AS ;
La Rosée, P ;
Müller, MC ;
Lahaye, T ;
Hanfstein, B ;
Schoch, C ;
Cross, N ;
Berger, U ;
Gschaidmeier, H ;
Druker, BJ ;
Hehlmann, R .
LEUKEMIA, 2002, 16 (11) :2190-2196
[10]   Frequency and clinical significance of BCR-ABL mutations in patients with chronic myeloid leukemia treated with imatinib mesylate [J].
Jabbour, E. ;
Kantarjian, H. ;
Jones, D. ;
Talpaz, M. ;
Bekele, N. ;
O'Brien, S. ;
Zhou, X. ;
Luthra, R. ;
Garcia-Manero, G. ;
Giles, F. ;
Rios, M. B. ;
Verstovsek, S. ;
Cortes, J. .
LEUKEMIA, 2006, 20 (10) :1767-1773