Hochhaus Andreas, Druker Brian, Sawyers Charles, Guilhot Francois, Schiffer Charles A, Cortes Jorge, Niederwieser Dietger W, Gambacorti-Passerini Carlo, Stone Richard M, Goldman John, Fischer Thomas, O'Brien Stephen G, Reiffers Jose J, Mone Manisha, Krahnke Tillmann, Talpaz Moshe, Kantarjian Hagop M
Medizinische Fakultaet Mannheim, University of Heidelberg, Mannheim, Germany.
Blood. 2008 Feb 1;111(3):1039-43. doi: 10.1182/blood-2007-07-103523. Epub 2007 Oct 11.
Imatinib mesylate, a targeted inhibitor of BCR-ABL tyrosine kinase, is the standard of care for chronic myeloid leukemia (CML). A phase 2 trial of imatinib in late chronic-phase (CP) CML after interferon-alpha (IFNalpha) failure enrolled 532 patients, 454 with a confirmed diagnosis of CP CML. Median time from diagnosis was 34 months; median duration of imatinib treatment was 65 months. Cumulative best rates of major cytogenetic response (MCyR) and complete cytogenetic response (CCyR) were 67% and 57%, respectively. At the 5-year landmark, 184 (41%) of the 454 patients are in CCyR. At more than 6 years, 199 (44%) of the 454 patients remain on imatinib. Most responses occurred within 12 months of starting imatinib; however, some patients achieved initial MCyR and CCyR more than 5 years after imatinib initiation. Estimated rates of freedom from progression to accelerated phase (AP) and blastic phase (BP) and overall survival at 6 years were 61% and 76%, respectively. Both freedom from progression to AP/BP and overall survival (OS) were associated with cytogenetic response level at 12 months. No increase in rates of serious adverse events was observed with continuous use of imatinib for up to 6.5 years, compared with earlier time points. Imatinib continues to be an effective and safe therapy for patients with CP CML after failure of IFN.
甲磺酸伊马替尼是一种BCR-ABL酪氨酸激酶的靶向抑制剂,是慢性髓性白血病(CML)的标准治疗药物。一项关于伊马替尼用于α干扰素(IFNα)治疗失败后的晚期慢性期(CP)CML的2期试验纳入了532例患者,其中454例确诊为CP CML。从诊断到入组的中位时间为34个月;伊马替尼治疗的中位持续时间为65个月。主要细胞遗传学反应(MCyR)和完全细胞遗传学反应(CCyR)的累积最佳率分别为67%和57%。在5年节点时,454例患者中有184例(41%)处于CCyR状态。超过6年时,454例患者中有199例(44%)仍在接受伊马替尼治疗。大多数反应在开始使用伊马替尼的12个月内出现;然而,一些患者在开始使用伊马替尼5年多后才达到初始MCyR和CCyR。估计6年时进展为加速期(AP)和急变期(BP)的无进展率以及总生存率分别为61%和76%。进展为AP/BP的无进展率和总生存率(OS)均与12个月时的细胞遗传学反应水平相关。与早期时间点相比,连续使用伊马替尼长达6.5年未观察到严重不良事件发生率增加。对于IFN治疗失败后的CP CML患者,伊马替尼仍然是一种有效且安全的治疗方法。