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急性髓性白血病的治疗

Therapy of acute myelogenous leukemia.

作者信息

Gale R P, Foon K A

出版信息

Semin Hematol. 1987 Jan;24(1):40-54.

PMID:3547672
Abstract

Over the past 10 years, there have been substantial advances in the treatment of AML. Intensive induction chemotherapy using 7-day courses of cytarabine and daunorubicin or amsacrine produce remission in 60% to 85% of patients. Median remission duration is 9 to 16 months. In some series, 20% to 40% of patients are in continuous remission for 2 years or more; many of these patients remain in remission for 5 years or longer and some may be cured. Bone marrow transplantation has evolved as a useful therapeutic modality capable of achieving long-term survival in some circumstances in which chemotherapy is relatively ineffective. Its precise role in the initial therapy of AML remains to be defined, but it is likely to be beneficial in selected patients. These data indicate substantial recent progress in the treatment of this disease, which was almost uniformly fatal 30 years ago. The fact that most patients relapse within 1 to 2 years reflects a lack of progress in developing effective postremission therapy. Maintenance chemotherapy, immunotherapy, and CNS prophylaxis have little role in AML. It is unclear whether consolidation or intensification extend remissions or increase the proportion of long-term survivors; controlled randomized trials should answer this question within the next few years. Future progress in the treatment of AML awaits the development of more sensitive methods for detecting residual leukemia, more effective use of current therapeutic modalities and the introduction of new effective drugs. Most data suggest that early intensive treatment is of key importance for achieving cures. However, we cannot presently distinguish between patients cured by initial treatment and those who required further chemotherapy.

摘要

在过去10年中,急性髓系白血病(AML)的治疗取得了重大进展。使用7天疗程的阿糖胞苷和柔红霉素或安吖啶进行强化诱导化疗,可使60%至85%的患者获得缓解。中位缓解持续时间为9至16个月。在一些系列研究中,20%至40%的患者持续缓解2年或更长时间;其中许多患者缓解5年或更长时间,有些可能被治愈。骨髓移植已发展成为一种有用的治疗方式,在某些化疗相对无效的情况下能够实现长期生存。其在AML初始治疗中的精确作用仍有待确定,但可能对选定的患者有益。这些数据表明,这种30年前几乎无一例外会致命的疾病,近期在治疗方面取得了重大进展。大多数患者在1至2年内复发这一事实反映出在开发有效的缓解后治疗方面缺乏进展。维持化疗、免疫治疗和中枢神经系统预防在AML中作用不大。尚不清楚巩固或强化治疗是否能延长缓解期或增加长期存活者的比例;未来几年的对照随机试验应能回答这个问题。AML治疗的未来进展有待于开发更敏感的检测残留白血病的方法、更有效地利用当前的治疗方式以及引入新的有效药物。大多数数据表明,早期强化治疗对于实现治愈至关重要。然而,目前我们无法区分通过初始治疗治愈的患者和那些需要进一步化疗的患者。

相似文献

1
Therapy of acute myelogenous leukemia.急性髓性白血病的治疗
Semin Hematol. 1987 Jan;24(1):40-54.
2
Acute myeloid leukaemia: recent advances in therapy.急性髓系白血病:治疗的最新进展
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3
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Postremission chemotherapy for adults with acute myelogenous leukemia: improved survival with high-dose cytarabine and daunorubicin consolidation treatment.成人急性髓系白血病缓解后化疗:大剂量阿糖胞苷和柔红霉素巩固治疗可提高生存率。
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Autologous or allogeneic bone marrow transplantation compared with intensive chemotherapy in acute myelogenous leukemia. European Organization for Research and Treatment of Cancer (EORTC) and the Gruppo Italiano Malattie Ematologiche Maligne dell'Adulto (GIMEMA) Leukemia Cooperative Groups.自体或异基因骨髓移植与急性髓性白血病强化化疗的比较。欧洲癌症研究与治疗组织(EORTC)和意大利成人恶性血液病研究组(GIMEMA)白血病协作组。
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10
Bone marrow transplantation for acute leukemia: recent advances and comparison with alternative therapies.急性白血病的骨髓移植:最新进展及与其他疗法的比较
Semin Hematol. 1987 Jan;24(1):55-67.

引用本文的文献

1
Possible benefit of consolidation therapy with high-dose cytarabine on overall survival of adults with non-promyelocytic acute myeloid leukemia.大剂量阿糖胞苷巩固治疗对非早幼粒细胞急性髓系白血病成年患者总生存期的潜在益处。
Braz J Med Biol Res. 2015 Feb;48(2):178-85. doi: 10.1590/1414-431X20144059. Epub 2014 Dec 12.
2
Immunotherapy prospects for acute myeloid leukaemia.免疫疗法治疗急性髓系白血病的前景。
Clin Exp Immunol. 2010 Aug;161(2):223-32. doi: 10.1111/j.1365-2249.2010.04197.x. Epub 2010 May 31.
3
[Therapy of infections in patients with acute leukemia].
[急性白血病患者感染的治疗]
Med Klin (Munich). 1997 Jul 15;92(7):406-9. doi: 10.1007/BF03042571.
4
Cytosine arabinoside increases the binding of 125I-labelled epidermal growth factor and 125I-transferrin and enhances the in vitro targeting of human tumour cells with anti-(growth factor receptor) mAb.阿糖胞苷增加了¹²⁵I标记的表皮生长因子和¹²⁵I转铁蛋白的结合,并增强了抗(生长因子受体)单克隆抗体对人肿瘤细胞的体外靶向作用。
Cancer Immunol Immunother. 1993 Aug;37(3):150-6. doi: 10.1007/BF01525428.
5
Chemotherapy for relapsed and resistant acute nonlymphoblastic leukemia. Effect of ATA, an amsacrine-containing regime.复发和耐药性急性非淋巴细胞白血病的化疗。含安吖啶方案(ATA)的疗效。
Cancer Chemother Pharmacol. 1988;21(1):68-70. doi: 10.1007/BF00262743.
6
Treatment of promyelocytic leukemia during pregnancy. A case report and review of the literature.
Blut. 1988 Jul;57(1):51-4. doi: 10.1007/BF00320635.
7
Effective reinduction therapy for childhood acute nonlymphoid leukemia using simultaneous continuous infusions of teniposide and amsacrine.使用替尼泊苷和安吖啶同步持续输注对儿童急性非淋巴细胞白血病进行有效的再诱导治疗。
Cancer Chemother Pharmacol. 1989;24(2):123-7. doi: 10.1007/BF00263133.
8
Acute non-lymphoblastic leukemias in childhood.
Indian J Pediatr. 1989 Nov-Dec;56(6):683-92. doi: 10.1007/BF02724450.
9
Amsacrine, cytarabine and etoposide in the treatment of bad prognosis acute myeloid leukemia.安吖啶、阿糖胞苷和依托泊苷治疗预后不良的急性髓系白血病
Med Oncol Tumor Pharmacother. 1989;6(3):199-205. doi: 10.1007/BF02985191.
10
High-dose cytosine arabinoside plus etoposide as initial treatment for acute myeloid leukaemia: a single centre study.高剂量阿糖胞苷联合依托泊苷作为急性髓系白血病的初始治疗:一项单中心研究。
Br J Cancer. 1990 Nov;62(5):830-3. doi: 10.1038/bjc.1990.387.