Discontinuation of imatinib in patients with chronic myeloid leukaemia who have maintained complete molecular remission for at least 2 years: the prospective, multicentre Stop Imatinib (STIM) trial

被引:1184
作者
Mahon, Francois-Xavier [1 ,2 ,3 ]
Rea, Delphine [4 ,5 ]
Guilhot, Joelle [6 ]
Guilhot, Francois [6 ]
Huguet, Francoise [7 ]
Nicolini, Franck [8 ]
Legros, Laurence [9 ]
Charbonnier, Aude [10 ]
Guerci, Agnes [11 ]
Varet, Bruno [12 ]
Etienne, Gabriel [13 ]
Reiffers, Josy [13 ]
Rousselot, Philippe [14 ]
机构
[1] Univ Bordeaux 2, Hematol Lab, Ctr Hosp Univ Bordeaux, Lab Hematopoiese Normale & Pathol,INSERM E217, F-33076 Bordeaux, France
[2] Univ Bordeaux 2, Serv Malad Sang, Ctr Hosp Univ Bordeaux, F-33076 Bordeaux, France
[3] INSERM U876, Bordeaux, France
[4] Hop St Louis, Serv Malad Sang, Paris, France
[5] EA3518, Paris, France
[6] Ctr Hosp Univ Poitiers, INSERM, CIC 802, Poitiers, France
[7] Hop Purpan, Serv Hematol, Toulouse, France
[8] Hop Edouard Herriot, Dept Hematol, Lyon 03, France
[9] Ctr Hosp Univ Nice, Serv Hematol Clin, Hop Archet, UMR CNRS UNSA Ctr Antoine Lacassagne 6543, Nice, France
[10] Inst Paoli Calmette, Marseille, France
[11] Ctr Hosp Univ Brabois, Vandoeuvre Les Nancy, France
[12] Hop Necker Enfants Malad, Serv Malad Sang, Paris, France
[13] Inst Bergonie, Dept Hematol, Bordeaux, France
[14] Univ Versailles St Quentin En Yvelines, Hop Mignot, CIC INSERM U940, Versailles, France
关键词
STEM-CELL TRANSPLANTATION; FOLLOW-UP; INTERFERON; MESYLATE; RESPONSES; CYTARABINE; THERAPY;
D O I
10.1016/S1470-2045(10)70233-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Imatinib treatment significantly improves survival in patients with chronic myeloid leukaemia (CML), but little is known about whether treatment can safely be discontinued in the long term. We aimed to assess whether imatinib can be discontinued without occurrence of molecular relapse in patients in complete molecular remission (CMR) while on imatinib. Methods In our prospective, multicentre, non-randomised Stop Imatinib (STIM) study, imatinib treatment (of >2 years duration) was discontinued in patients with CML who were aged 18 years and older and in CMR (>5-log reduction in BCR-ABL and ABL levels and undetectable transcripts on quantitative RT-PCR). Patients who had undergone immunomodulatory treatment (apart from interferon alpha), treatment for other malignancies, or allogeneic haemopoietic stem-cell transplantation were not included. Patients were enrolled at 19 participating institutions in France. In this interim analysis, rate of relapse was assessed by use of RT-PCR for patients with at least 12 months of follow-up. Imatinib was reintroduced in patients who had molecular relapse. This study is registered with ClinicalTrials.gov, number NCT00478985. Findings 100 patients were enrolled between July 9, 2007, and Dec 17, 2009. Median follow-up was 17 months (range 1-30), and 69 patients had at least 12 months follow-up (median 24 months, range 13-30). 42 (61%) of these 69 patients relapsed (40 before 6 months, one patient at month 7, and one at month 19). At 12 months, the probability of persistent CMR for these 69 patients was 41% (95% CI 29-52). All patients who relapsed responded to reintroduction of imatinib: 16 of the 42 patients who relapsed showed decreases in their BCR-ABL levels, and 26 achieved CMR that was sustained after imatinib rechallenge. Interpretation Imatinib can be safely discontinued in patients with a CMR of at least 2 years duration. Imatinib discontinuation in this setting yields promising results for molecular relapse-free survival, raising the possibility that, at least in some patients, CML might be cured with tyrosine kinase inhibitors.
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收藏
页码:1029 / 1035
页数:7
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