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对α干扰素细胞遗传学反应不佳的慢性髓性白血病(CML)患者进行费城阴性祖细胞自体移植。

Autologous transplantation with Philadelphia-negative progenitor cells for patients with chronic myeloid leukaemia (CML) failing to attain a cytogenetic response to alpha interferon.

作者信息

McBride N C, Cavenagh J D, Newland A C, Lillington D M, Murrell C, Kelsey S M

机构信息

Department of Haematology, St Bartholomew's and Royal London Hospital School of Medicine and Dentistry, UK.

出版信息

Bone Marrow Transplant. 2000 Dec;26(11):1165-72. doi: 10.1038/sj.bmt.1702671.

Abstract

Between October 1993 and March 1999, 29 patients with CML who were ineligible for allogeneic BMT underwent PBSC harvest using idarubicin, cytarabine and G-CSF. In 9/29 (31%) patients all collected stem cells were Ph-negative, and 15/29 patients' (52%) collections were substantially (>95%) Ph-negative. The proportion of patients from whom Ph-negative stem cells were obtained was similar between patients who had, or had not, received prior alphaIFN. Fifteen patients in chronic phase (median age 45) proceeded to PBSCT following busulphan 16 mg/m2 and cyclophosphamide 120 mg/m2. Nine of the 13 patients who had failed to respond to prior alphaIFN proceeded to stem cell transplantation as soon as was feasible and six of the newly diagnosed patients were transplanted after failing to achieve a cytogenetic response after a minimum of 12 months on alphaIFN following progenitor cell harvest. The median number of days to neutrophils >0.5 and platelet >50 was 18 (range 13-69) and 28 (range 13-234), respectively. There was no procedure-related mortality. At median follow-up of 2.3 years post autograft 10 of 15 patients remain alive and in chronic phase. Overall survival for all 27 patients at 5 years after initial diagnosis is 70% and median survival from diagnosis 7.3 years. Survival for alphaIFN non-responders who were transplanted is 74% at 5 years from diagnosis and 75% at 3 years from transplant. Cytogenetic analysis performed 3 months post transplant demonstrated one patient with a complete cytogenetic response, seven with a partial response and three with no response. Six patients remain partially Ph-negative, with one major CR. Survival for all patients in the protocol is favourable compared with conventional therapy and is particularly encouraging following PBSCT for alphaIFN non-responsive patients. Patients not responding to alphaIFN can be induced into Ph-negativity with PBSCT but this may not always be sustainable. There seems to be no obvious disadvantage in harvesting stem cells after prior exposure to alphaIFN, providing an adequate alphaIFN-free rest period is used.

摘要

1993年10月至1999年3月期间,29例不符合异基因骨髓移植条件的慢性粒细胞白血病患者使用伊达比星、阿糖胞苷和粒细胞集落刺激因子进行了外周血干细胞采集。29例患者中有9例(31%)采集的所有干细胞均为Ph阴性,15例患者(52%)采集的干细胞大部分(>95%)为Ph阴性。接受或未接受过α干扰素治疗的患者中,获得Ph阴性干细胞的患者比例相似。15例慢性期患者(中位年龄45岁)在接受16 mg/m²白消安和120 mg/m²环磷酰胺治疗后进行了外周血干细胞移植。13例既往对α干扰素治疗无反应的患者中有9例尽快进行了干细胞移植,6例新诊断患者在祖细胞采集后接受α干扰素治疗至少12个月仍未获得细胞遗传学反应后进行了移植。中性粒细胞>0.5和血小板>50的中位天数分别为18天(范围13 - 69天)和28天(范围13 - 234天)。无手术相关死亡。自体移植后中位随访2.3年,15例患者中有10例仍存活且处于慢性期。所有27例患者初始诊断后5年的总生存率为70%,诊断后的中位生存期为7.3年。移植的α干扰素无反应者诊断后5年生存率为74%,移植后3年生存率为75%。移植后3个月进行的细胞遗传学分析显示,1例患者完全缓解,7例部分缓解,3例无反应。6例患者仍部分为Ph阴性,其中1例为主要完全缓解(CR)。与传统治疗相比,该方案中所有患者的生存率良好,对于α干扰素无反应患者进行外周血干细胞移植后尤其令人鼓舞。对α干扰素无反应的患者可通过外周血干细胞移植诱导为Ph阴性,但这可能并不总是可持续的。在先接触α干扰素后采集干细胞似乎没有明显弊端,前提是使用足够的无α干扰素休息期。

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