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首页> 外文期刊>Haematologica >A prospective study of alpha-interferon and autologous bone marrow transplantation in chronic myeloid leukemia. The Italian Co-operative Study Group on Chronic Myeloid Leukemia | Haematologica
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A prospective study of alpha-interferon and autologous bone marrow transplantation in chronic myeloid leukemia. The Italian Co-operative Study Group on Chronic Myeloid Leukemia | Haematologica

机译:慢性髓细胞性白血病中α-干扰素和自体骨髓移植的前瞻性研究。意大利慢性粒细胞白血病合作研究小组|血液学

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摘要

BACKGROUND AND OBJECTIVE: Alpha-interferon (alphaIFN) can induce cytogenetic remissions in chronic myeloid leukemia (CML). Hemopoietic progenitors can be collected from the marrow in remission and utilized for autologous repopulation after high dose chemotherapy. This study was designed with the purpose of evaluating the feasibility of a combined treatment policy of alphaIFN followed by autologous bone marrow transplantation (autoBMT). DESIGN AND METHODS: A prospective study of alphaIFN and autoBMT was begun in 1989. Two hundred and seventy-two consecutive previously untreated non-blastic Ph positive chronic myeloid leukemia (CML) patients, who were less than 56 years old, were enrolled over a 3-year period (1989-1991) and were assigned to receive human recombinant alphaIFN 2a (Roferon-A) at a dose of 9 MIU daily for at least one year. If they achieved a cytogenetic response consisting in a percentage of Ph neg metaphases of more than 25%, they were eligible for marrow harvesting and subsequent autografting after high dose busulfan (16 mg/kg) and melphalan (60 mg/m(2)). RESULTS: Seventy-six patients (28%) were eligible for a marrow harvest but the marrow was harvested in only 37 cases (14%), and only twenty-three patients (8%) were actually autografted. One patient died of infection nine days after autoBMT. The other patients recovered and did not suffer any late adverse events. Five patients progressed to blastic phase, six are alive in complete hematologic remission and eleven are alive in complete hematologic and cytogenetic remission. AlphaIFN treatment was reinstituted after autoBMT in 18 of 22 cases, but four patients who are in continuous complete cytogenetic remission were not given alphaIFN anymore. The progression-free survival of the autografted patients is 65% 8 years after registration. INTERPRETATION AND CONCLUSIONS: This study shows that bone marrow hemopoietic progenitors (Ph neg and Ph pos) can be collected from patients who respond to alphaIFN and can be used to rescue hemopoietic activity after high dose chemotherapy. Though some complete and durable cytogenetic remissions were obtained, the treatment could be applied only to a small group of good risk patients, highlighting that selection is very important and results cannot be extrapolated to the average patient.
机译:背景与目的:干扰素(αIFN)可以诱导慢性粒细胞白血病(CML)的细胞遗传学缓解。可以从骨髓中回收造血祖细胞,以减轻其剂量,并在高剂量化疗后用于自体繁殖。本研究旨在评估αIFN联合自体骨髓移植(autoBMT)联合治疗策略的可行性。设计与方法:于1989年开始对αIFN和autoBMT进行前瞻性研究。研究纳入了连续接受治疗的连续56例年龄小于56岁的非原发性Ph阳性慢性粒细胞白血病(CML)患者。期限为3年(1989年至1991年),并被指定每天接受9 MIU剂量的人重组αIFN2a(Roferon-A)至少一年。如果他们达到了包括超过25%的Ph neg中期百分比在内的细胞遗传学反应,则有资格进行大剂量白消安(16 mg / kg)和美法仑(60 mg / m(2))后的骨髓收获和随后的自体移植。结果:76例患者(28%)有资格进行骨髓移植,但只有37例(14%)获得了骨髓,而实际上只有23例患者(8%)被移植了。 autoBMT后9天,一名患者死于感染。其他患者康复并且没有遭受任何后期不良事件。五名患者发展为成骨期,六名患者血液学完全缓解还活着,十一名患者血液学和细胞遗传学完全缓解。 22例中有18例在autoBMT后重新开始使用αIFN治疗,但有4例持续完全细胞遗传学缓解的患者不再给予αIFN治疗。自体移植患者的无进展生存期是注册后8年的65%。解释和结论:这项研究表明,可以从对αIFN有反应的患者中收集骨髓造血祖细胞(Ph neg和Ph pos),并可以在大剂量化疗后用于挽救造血活动。尽管获得了一些完全和持久的细胞遗传学缓解,但是该治疗仅可用于一小群高风险患者,这突出表明选择非常重要,并且结果无法外推到普通患者。

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