Treatment of chronic granulocytic leukemia in the accelerated phase by transfusion of autologous buffy-coat cells--a case report.

A Takeshita, N Hirabayashi, M Ichihara, Y Miwa
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Abstract

We treated a patient with chronic granulocytic leukemia (CGL), in the accelerated phase by intensive chemotherapy followed by the infusion of cryopreserved peripheral blood buffy-coat cells. The cells had been stored for 32 months. The chemotherapy consisted of daunorubicin 40 mg X 2 days, vincristine 2 mg X 1 day, cytosine arabinoside (Ara-C) 200 mg X 6 days and prednisolone 30 mg X 7 days in the first week, then Ara-C 3 g/m2 X 3 days and cyclophosphamide 60 mg/kg X 2 days in the second week, but reversion to the chronic phase was not achieved. Therefore, total body irradiation (TBI) was added to repeated intensive chemotherapy followed by infusion of the remaining cells. Marrow recovery was good. The patient is currently alive and has been in the chronic phase for 22 months. This preliminary result indicates that this therapy may be tried soon after transformation in CGL and that TBI is an important part of therapy in BMT in the accelerated or blastic phase of CGL.

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自体黄皮细胞输注治疗加速期慢性粒细胞白血病1例。
我们治疗了一位慢性粒细胞白血病(CGL)患者,在加速期,通过强化化疗和输注冷冻保存的外周血白皮细胞。细胞保存32个月。化疗方案为:第一周给予柔红霉素40 mg × 2天、长春新碱2 mg × 1天、阿糖胞苷(Ara-C) 200 mg × 6天、强的松龙30 mg × 7天,第2周给予Ara-C 3 g/m2 × 3天、环磷酰胺60 mg/kg × 2天,但未见缓缓期逆转。因此,全身照射(TBI)在重复强化化疗后再输注剩余细胞。骨髓恢复良好。患者目前还活着,处于慢性期已22个月。这一初步结果表明,这种治疗方法可以在CGL转化后不久进行试验,并且在CGL加速或成形期,TBI是BMT治疗的重要组成部分。
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