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成人急性淋巴细胞白血病:近期进展与未来方向

Acute lymphoblastic leukemia in adults: recent progress, future directions.

作者信息

Hoelzer D, Gale R P

出版信息

Semin Hematol. 1987 Jan;24(1):27-39.

PMID:3547671
Abstract

The data reviewed indicate substantial recent progress in the treatment of ALL in adults. Most patients, greater than 70% to 80%, will achieve a remission following induction chemotherapy with vincristine, prednisone, and an anthracycline. Additional drugs do not convincingly increase the remission rate; their effect on remission duration is unknown. Although continuation therapy has not been critically evaluated in randomized trials, the longest remissions have been reported in individuals receiving consolidation/intensification, particularly in the immediate postremission period. Presently, a disease-free survival is 35% to 45% at greater than 5 years when this type of consolidation/intensification therapy is used. The precise value of conventional maintenance chemotherapy in adult ALL is unknown. CNS prophylaxis is necessary; the standard of treatment remains cranial radiation and intrathecal methotrexate. Alternative approaches are currently being studied such as systemic treatment with high doses of methotrexate or cytarabine. Recently, prognostic factors have been better defined. In recent studies with intensive treatment, time to response, age, WBC, immunologic subtype and cytogenetic data can be used to divide patients into a low-risk group with a projected disease-free survival of 60% or more and a high-risk group with a disease-free survival of 20% to 25%. The definition of risk groups in adult ALL may be useful in determining future further optimal therapeutic approaches.

摘要

回顾的数据表明,近期成人急性淋巴细胞白血病(ALL)的治疗取得了重大进展。大多数患者,即70%至80%以上,在接受长春新碱、泼尼松和蒽环类药物诱导化疗后可实现缓解。其他药物并不能令人信服地提高缓解率;它们对缓解持续时间的影响尚不清楚。尽管延续治疗尚未在随机试验中得到严格评估,但据报道,接受巩固/强化治疗的患者缓解期最长,尤其是在缓解后的即刻阶段。目前,采用这种巩固/强化治疗时,5年以上的无病生存率为35%至45%。成人ALL中传统维持化疗的确切价值尚不清楚。中枢神经系统预防是必要的;治疗标准仍然是颅脑放疗和鞘内注射甲氨蝶呤。目前正在研究替代方法,如高剂量甲氨蝶呤或阿糖胞苷的全身治疗。最近,预后因素得到了更好的界定。在近期的强化治疗研究中,缓解时间、年龄、白细胞计数、免疫亚型和细胞遗传学数据可用于将患者分为无病生存率预计为60%或更高的低风险组和无病生存率为20%至25%的高风险组。成人ALL风险组的定义可能有助于确定未来进一步的最佳治疗方法。

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