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未经治疗的急性非淋巴细胞白血病体外骨髓培养生长模式的预后意义

Prognostic significance of in vitro marrow culture growth pattern in untreated acute nonlymphocytic leukemia.

作者信息

Shih L Y, Dunn P, Liaw S J

出版信息

Acta Haematol. 1986;76(1):20-4. doi: 10.1159/000206012.

DOI:10.1159/000206012
PMID:3098023
Abstract

The growth pattern of marrow cells in agar culture was studied in 90 adult patients with acute nonlymphocytic leukemia (ANLL) at diagnosis. We classified the abnormal growth patterns into 4 groups, A: no growth, B: decreased growth, C: excessive microcluster formation and D: excessive cluster growth with more than 20 colonies. There was a good correlation between growth pattern and FAB subtype. A predominance of group A growth was observed in M1, while group B growth was found in 50% of patients with M2 and M5. No relationships between the growth patterns and other clinical parameters were detected. Sixty-six patients were evaluable for treatment outcome. The growth pattern significantly correlated with complete remission rate. The remission rates were 52, 87, 80, and 25% for patients with group A, B, C and D growth, respectively. Analyses of remission duration and survival curves showed significant differences among the different growth patterns. Patients with D growth experienced a shorter remission duration and a lower survival rate than other groups. These results indicate that the in vitro culture growth pattern in untreated ANLL is of prognostic significance in predicting the response to therapy.

摘要

对90例初诊的成年急性非淋巴细胞白血病(ANLL)患者的骨髓细胞在琼脂培养中的生长模式进行了研究。我们将异常生长模式分为4组,A组:无生长;B组:生长减少;C组:过度微集落形成;D组:有超过20个集落的过度集落生长。生长模式与FAB亚型之间存在良好的相关性。在M1中观察到A组生长占优势,而在50%的M2和M5患者中发现B组生长。未检测到生长模式与其他临床参数之间的关系。66例患者可评估治疗结果。生长模式与完全缓解率显著相关。A、B、C和D组生长的患者缓解率分别为52%、87%、80%和25%。缓解持续时间和生存曲线分析显示不同生长模式之间存在显著差异。D组生长的患者缓解持续时间较短,生存率低于其他组。这些结果表明,未经治疗的ANLL体外培养生长模式在预测治疗反应方面具有预后意义。

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引用本文的文献

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In vitro culture studies of blood and marrow cells in chronic myeloid leukemia at different phases of the disease.慢性髓性白血病不同疾病阶段血液和骨髓细胞的体外培养研究。
Blut. 1988 Sep;57(3):125-30. doi: 10.1007/BF00320152.