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[甲磺酸伊马替尼治疗费城染色体阳性慢性髓性白血病患者后异常费城染色体阴性细胞的克隆进化]

[Clonal evolution of abnormal Philadelphia chromosome-negative cells after imatinib mesylate therapy in patients with Philadelphia chromosome-positive chronic myelogenous leukemia].

作者信息

Jiang Qian, Chen Shan-shan, Jiang Bin, Jiang Hao, Lu Ying, Qiu Jing-ying, Lu Dao-pei

机构信息

Institute of Hematology of People's Hospital, Peking University, Beijing 100044, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2005 Jan;26(1):23-6.

Abstract

OBJECTIVE

To investigate clonal evolution of abnormal Philadelphia chromosome-negative cells (Ph- CE) after imatinib mesylate therapy in patients with Philadelphia chromosome-positive chronic myelogenous leukemia (Ph+ CML).

METHODS

Bone marrow cells G-banding karyotype was evaluated every 3 months in 100 patients with Ph+ CML after achieving hematologic responses on the course of imatinib therapy. There were 54 patients in chronic phase (CP), 37 in accelerated phase (AP) and 9 in blast phase (BP).

RESULTS

After a median follow-up of 32 months (ranged 25-34 months), 11 patients, including 5 cases in CP, 5 in AP and 1 in BP, developed transient, interrupted or continuous Ph- CE after 3 - 29 months on imatinib therapy. Ph- CE emerged at the beginning of Ph+ cells decreasing or after Ph+ cells disappearing. The proportion of Ph- CE, was negatively correlated with the proportion of Ph+ cells (P < 0.05). Ph- CE commonly included +8 (45.5%) and +Y (27.3%). Five patients had additional cytogenetic abnormalities besides Ph+ in Ph- CE. Seven of the patients with Ph- CE achieved a major cytogenetic response while 9 of them achieved a complete hematologic response. One patient with Ph- CE in AP progressed to BP 20 months after the initiation of the therapy while the rests remained in hematologic or cytogenetic responses.

CONCLUSION

Ph- CE occurred in about 11% of the patients with Ph+ CML who achieved major or minor cytogenetic responses on imatinib therapy. After a median follow-up of more than 2 years, most of the patients with Ph- CE were in a stable status with no disease progression.

摘要

目的

探讨甲磺酸伊马替尼治疗费城染色体阳性慢性髓性白血病(Ph+CML)患者后异常费城染色体阴性细胞(Ph-CE)的克隆演变。

方法

对100例接受伊马替尼治疗并获得血液学缓解的Ph+CML患者,每3个月评估一次骨髓细胞G显带核型。其中慢性期(CP)54例,加速期(AP)37例,急变期(BP)9例。

结果

中位随访32个月(范围25 - 34个月),11例患者在伊马替尼治疗3 - 29个月后出现短暂、间断或持续的Ph-CE,其中CP期5例,AP期5例,BP期1例。Ph-CE在Ph+细胞开始减少时或Ph+细胞消失后出现。Ph-CE的比例与Ph+细胞的比例呈负相关(P<0.05)。Ph-CE常见的有+8(45.5%)和+Y(27.3%)。5例患者的Ph-CE除Ph+外还有其他细胞遗传学异常。7例有Ph-CE的患者获得了主要细胞遗传学缓解,9例获得了完全血液学缓解。1例AP期有Ph-CE的患者在治疗开始20个月后进展为BP期,其余患者维持血液学或细胞遗传学缓解状态。

结论

在接受伊马替尼治疗获得主要或次要细胞遗传学缓解的Ph+CML患者中,约11%出现Ph-CE。中位随访超过2年后,大多数有Ph-CE的患者病情稳定,无疾病进展。

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