Ohanian Maro, Kantarjian Hagop M, Quintas-Cardama Alfonso, Jabbour Elias, Abruzzo Lynne, Verstovsek Srdan, Borthakur Gautam, Ravandi Farhad, Garcia-Manero Guillermo, Champlin Richard, Pierce Sherry, Alattar Mona Lisa, Trinh Long Xuan, Luthra Raja, Ferrajoli Alessandra, Kadia Tapan, O'Brien Susan, Cortes Jorge E
Department of Leukemia, M.D. Anderson Cancer Center, Houston, TX.
Department of Leukemia, M.D. Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2014 Apr;14(2):155-162.e1. doi: 10.1016/j.clml.2013.08.008. Epub 2013 Dec 9.
Accelerated phase CML most frequently represents a progression state in CML. However, some patients present with AP features at the time of diagnosis. There is limited information on the outcome of these patients who received TKIs as initial therapy.
We analyzed the outcome of 51 consecutive patients with CML who presented with features of AP at the time of diagnosis, including blasts ≥ 15% (n = 6), basophils ≥ 20% (n = 22), platelets < 100 × 10(9)/L (n = 3), cytogenetic clonal evolution (n = 17), or more than 1 feature (n = 3). Patients received initial therapy with imatinib (n = 30), dasatinib (n = 5), or nilotinib (n = 16).
The rate of complete cytogenetic response for patients treated with imatinib was 80%, and with dasatinib or nilotinib was 90%. Major molecular response (MMR) (Breakpoint Cluster Region (BCR)-Abelson (ABL)/ABL ≤ 0.1%, International Scale [IS]) was achieved in 69% of patients including complete molecular response (BCR-ABL/ABL ≤ 0.0032% IS) in 49%. MMR rates for patients treated with imatinib were 63%, and with 2GTKIs, 76%. Overall survival at 36 months was 87% with imatinib and 95% with 2GTKIs.
TKIs should be considered standard initial therapy for patients with AP at the time of diagnosis.
加速期慢性髓性白血病(CML)通常是CML的一种进展状态。然而,一些患者在诊断时就表现出加速期特征。关于这些接受酪氨酸激酶抑制剂(TKIs)作为初始治疗的患者的预后信息有限。
我们分析了51例连续诊断时具有加速期特征的CML患者的预后,这些特征包括原始细胞≥15%(n = 6)、嗜碱性粒细胞≥20%(n = 22)、血小板<100×10⁹/L(n = 3)、细胞遗传学克隆演变(n = 17)或不止一项特征(n = 3)。患者接受伊马替尼(n = 30)、达沙替尼(n = 5)或尼洛替尼(n = 16)作为初始治疗。
接受伊马替尼治疗的患者完全细胞遗传学反应率为80%,接受达沙替尼或尼洛替尼治疗的患者为90%。69%的患者达到主要分子反应(MMR)(断裂点簇集区(BCR)-阿贝尔森(ABL)/ABL≤0.1%,国际标准[IS]),其中49%达到完全分子反应(BCR-ABL/ABL≤0.0032% IS)。接受伊马替尼治疗的患者MMR率为63%,接受两种TKIs治疗的患者为76%。伊马替尼治疗组36个月总生存率为87%,两种TKIs治疗组为95%。
对于诊断时处于加速期的患者,应将TKIs视为标准的初始治疗。