Medina Jorge, Kantarjian Hagop, Talpaz Moshe, O'Brien Susan, Garcia-Manero Guillermo, Giles Francis, Rios Mary Beth, Hayes Kimberly, Cortes Jorge
Department of Leukemia, The University of Texas, M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2003 Nov 1;98(9):1905-11. doi: 10.1002/cncr.11729.
Anecdotal cases of chromosomal abnormalities in Philadelphia chromosome (Ph)-negative metaphases have been reported in patients with chronic myelogenous leukemia (CML) in the chronic phase during treatment with interferon and, more recently, with imatinib. This phenomenon is different from true clonal evolution in that the additional cytogenetic abnormality occurs in Ph-negative cells.
The authors analyzed their experience with 342 patients with CML in chronic phase treated with imatinib to investigate the frequency and significance of this event.
After a median follow-up of 30 months (range, 16-35 months), 21 patients (6%; 95% confidence interval, 0.04, 0.09) developed 25 chromosomal abnormalities in Ph-negative cells. Thirteen (54%) of these abnormalities were seen in 2 or more metaphases. The median time from the start of treatment with imatinib to the appearance of the abnormalities was 6 months (range, 3-22 months). The most common cytogenetic abnormality detected was trisomy 8 (33%). Twenty of 21 patients (95%) achieved a major (Ph < 35%) cytogenetic response (complete cytogenetic response in 13-62%). After a median follow-up of 22 months (range, 4-33 months), all 21 patients were alive, 20 of them in chronic phase and in complete hematologic response. None of the patients showed features of myelodysplasia.
Cytogenetic abnormalities occur in Ph-negative cells in a fraction of patients with CML in chronic phase treated with imatinib. With a short follow-up, no clear clinical consequences can be identified.
有报道称,慢性粒细胞白血病(CML)慢性期患者在接受干扰素治疗期间,以及最近在接受伊马替尼治疗期间,费城染色体(Ph)阴性中期出现染色体异常的个别病例。这种现象与真正的克隆进化不同,因为额外的细胞遗传学异常发生在Ph阴性细胞中。
作者分析了342例接受伊马替尼治疗的慢性期CML患者的情况,以研究这一事件的发生率和意义。
中位随访30个月(范围16 - 35个月)后,21例患者(6%;95%置信区间,0.04, 0.09)在Ph阴性细胞中出现了25种染色体异常。其中13种(54%)异常在2个或更多中期可见。从开始伊马替尼治疗到出现异常的中位时间为6个月(范围3 - 22个月)。检测到的最常见细胞遗传学异常是8号染色体三体(33%)。21例患者中有20例(95%)获得了主要(Ph < 35%)细胞遗传学反应(13 - 62%为完全细胞遗传学反应)。中位随访22个月(范围4 - 33个月)后,所有21例患者均存活;其中20例处于慢性期且完全血液学缓解。所有患者均未表现出骨髓增生异常的特征。
接受伊马替尼治疗的慢性期CML患者中,一部分患者的Ph阴性细胞会出现细胞遗传学异常。由于随访时间短,尚未发现明确的临床后果。