Epigenetic Therapy With Hydralazine and Magnesium Valproate Reverses Imatinib Resistance in Patients With Chronic Myeloid Leukemia

被引:24
作者
Cervera, Eduardo [2 ]
Candelaria, Myrna [2 ,3 ]
Lopez-Navarro, Omar [2 ]
Labardini, Juan [2 ]
Gonzalez-Fierro, Aurora [4 ]
Taja-Chayeb, Lucia [4 ]
Cortes, Jorge [5 ]
Gordillo-Bastidas, Daniela [2 ]
Duenas-Gonzalez, Alfonso [1 ]
机构
[1] UNAM Inst Nacl Cancerol, Inst Invest Biomed, Unidad Invest Biomed Canc, Mexico City, DF, Mexico
[2] Inst Nacl Cancerol, Dept Hematol, Mexico City, DF, Mexico
[3] Inst Nacl Cancerol, Div Clin Res, Mexico City, DF, Mexico
[4] Inst Nacl Cancerol, Basic Res Div, Mexico City, DF, Mexico
[5] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
关键词
Chronic myeloid leukemia; Epigenetic therapy; Imatinib resistance; CHRONIC MYELOGENOUS LEUKEMIA; TYROSINE KINASE INHIBITOR; LOW-DOSE DECITABINE; PHASE-II; BCR-ABL; INTERFERON-ALPHA; BLASTIC PHASE; SOLID TUMORS; FOLLOW-UP; MESYLATE;
D O I
10.1016/j.clml.2012.01.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The epigenetic drugs hydralazine and valproate were administered in a compassionate manner to 8 patients with chronic myeloid leukemia (CML) refractory to imatinib. Two patients had a complete hematologic response (25%), 1 major cytogenetic response, 1 complete cytogenetic response (25% any cytogenetic response), and 3 (37.5%) stable disease. No grade 3 or 4 toxicity was observed. These results show the ability of epigenetic therapy to revert imatinib resistance. Background: Epigenetic alterations participate in the development of acquired resistance to imatinib, hence, the DNA methylation, and histone deacetylase inhibitors hydralazine and valproate, respectively, has the potential to overcome it. Patient and Methods: A series of 8 patients with chronic myeloid leukemia (CML) refractory to imatinib mesylate with no access to second-generation tyrosine kinase inhibitors were treated with hydralazine and valproate in a compassionate manner. Clinical efficacy and safety of these drugs added to imatinib mesylate were evaluated. Results: Two patients were in the blast phase, 5 were in the accelerated phase, and 1 was in the chronic phase. All the patients continued with the same dose of imatinib that they had been receiving at the time of development of resistance, with a median dose of 600 mg daily (range, 400-800 mg). The median time from diagnosis of CML to the start of hydralazine and valproate was 53.6 months (range, 19-84 months). Two (25%) patients had a complete hematologic response, one (12.5%) had an major cytogenetic response, and one (12.5%) had a complete cytogenetic response. Three (37.5%) patients had stable disease, and only one (12.5%) patient failed to respond. At a median follow-up time of 18 months (range, 3-18 months), the median survival had not been reached, and the projected overall survival was 63%. All the patients had mild neurologic toxicity, including distal tremor and somnolence. No grade 3 or 4 toxicity was observed. Conclusions: Our results suggest that the epigenetic drugs hydralazine and valproate revert the resistance to imatinib in patients with CML. Clinical Lymphoma, Myeloma & Leukemia, Vol. 12, No. 3, 207-12 (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:207 / 212
页数:6
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