Leukemia Department, The University of Texas M.D. Anderson Cancer Center, Houston, TX, USA.
Clin Lymphoma Myeloma Leuk. 2013 Aug;13(4):477-84. doi: 10.1016/j.clml.2013.02.025. Epub 2013 Jun 14.
The outcome of patients with CML who discontinue 2G-TKI initial therapy is unknown. We analyzed the characteristics of patients in whom treatment with first-line 2G-TKIs had failed.
A total of 218 patients with CML were treated with dasatinib (n = 101) or nilotinib (n = 117; 12 in AP). After a median follow-up of 23 months, 40 patients (18%) discontinued therapy: 25 initially treated with nilotinib (21% of all treated with nilotinib; 6 treated in AP) and 15 (15%) initially treated with dasatinib. Median age of the patients was 47 (range, 19-79) years, and they had received therapy for a median of 8 (range, 0-62) months.
Reasons for treatment discontinuation include: toxicity, 16 patients; resistance in CP, 5 patients; transformation to blast phase, 4 patients (2 treated in AP); and other reasons, 15 patients. Subsequent treatment was imatinib in 11 patients, nilotinib in 7, dasatinib in 4, ponatinib in 2, chemotherapy plus dasatinib in 3, stem cell transplant in 2, bafetinib in 1, and unknown or none in 8 patients. A complete cytogenetic response was achieved in 19 patients, including 17 with major molecular response. Fourteen of the patients who achieved a complete molecular response or major molecular response with subsequent TKIs were in CP at the time of 2G-TKI discontinuation.
We conclude that treatment failure after first-line therapy with 2G-TKIs is mostly associated with toxicity or patient preference, and these patients respond well to alternative TKIs.
停止使用 2G-TKI 初始治疗的 CML 患者的结局尚不清楚。我们分析了一线 2G-TKI 治疗失败患者的特征。
共有 218 例 CML 患者接受达沙替尼(n=101)或尼罗替尼(n=117;AP 中 12 例)治疗。中位随访 23 个月后,40 例(18%)停止治疗:25 例最初接受尼罗替尼治疗(所有接受尼罗替尼治疗患者的 21%;AP 中 6 例),15 例(15%)最初接受达沙替尼治疗。患者中位年龄为 47 岁(范围,19-79 岁),中位治疗时间为 8 个月(范围,0-62 个月)。
停止治疗的原因包括:毒性,16 例;CP 耐药,5 例;转化为急变期,4 例(AP 中 2 例);其他原因,15 例。随后的治疗包括伊马替尼 11 例、尼罗替尼 7 例、达沙替尼 4 例、波那替尼 2 例、化疗加达沙替尼 3 例、干细胞移植 2 例、巴非替尼 1 例,8 例患者未知或无后续治疗。19 例患者获得完全细胞遗传学缓解,其中 17 例获得主要分子学缓解。在停止使用 2G-TKI 时处于 CP 的 14 例获得完全分子学缓解或主要分子学缓解的患者随后使用 TKI 治疗效果良好。
我们的结论是,一线 2G-TKI 治疗失败主要与毒性或患者偏好相关,这些患者对替代 TKI 反应良好。