Jansen J H, de Ridder M C, Geertsma W M, Erpelinck C A, van Lom K, Smit E M, Slater R, vd Reijden B A, de Greef G E, Sonneveld P, Löwenberg B
Institute of Hematology, the Department of Clinical Genetics, Erasmus University Rotterdam, Rotterdam, The Netherlands.
Blood. 1999 Jul 1;94(1):39-45.
The combined use of retinoic acid and chemotherapy has led to an important improvement of cure rates in acute promyelocytic leukemia. Retinoic acid forces terminal maturation of the malignant cells and this application represents the first generally accepted differentiation-based therapy in leukemia. Unfortunately, similar approaches have failed in other types of hematological malignancies suggesting that the applicability is limited to this specific subgroup of patients. This has been endorsed by the notorious lack of response in acute promyelocytic leukemia bearing the variant t(11;17) translocation. Based on the reported synergistic effects of retinoic acid and the hematopoietic growth factor granulocyte colony-stimulating factor (G-CSF), we studied maturation of t(11;17) positive leukemia cells using several combinations of retinoic acid and growth factors. In cultures with retinoic acid or G-CSF the leukemic cells did not differentiate into mature granulocytes, but striking granulocytic differentiation occurred with the combination of both agents. At relapse, the patient was treated with retinoic acid and G-CSF before reinduction chemotherapy. With retinoic acid and G-CSF treatment alone, complete granulocytic maturation of the leukemic cells occurred in vivo, followed by a complete cytogenetical and hematological remission. Bone marrow and blood became negative in fluorescense in situ hybridization analysis and semi-quantitative polymerase chain reaction showed a profound reduction of promyelocytic leukemia zinc finger-retinoic acid receptor-alpha fusion transcripts. This shows that t(11;17) positive leukemia cells are not intrinsically resistant to retinoic acid, provided that the proper costimulus is administered. These observations may encourage the investigation of combinations of all-trans retinoic acid and hematopoietic growth factors in other types of leukemia.
维甲酸与化疗联合使用已使急性早幼粒细胞白血病的治愈率有了显著提高。维甲酸促使恶性细胞终末成熟,这种应用代表了白血病中首个被普遍接受的基于分化的疗法。不幸的是,类似方法在其他类型的血液系统恶性肿瘤中失败了,这表明其适用性仅限于这一特定亚组患者。急性早幼粒细胞白血病伴有变异型t(11;17)易位时明显缺乏反应就证实了这一点。基于报道的维甲酸与造血生长因子粒细胞集落刺激因子(G-CSF)的协同作用,我们使用维甲酸和生长因子的几种组合研究了t(11;17)阳性白血病细胞的成熟情况。在含有维甲酸或G-CSF的培养物中,白血病细胞未分化为成熟粒细胞,但两种药物联合使用时出现了显著的粒细胞分化。复发时,患者在再次诱导化疗前接受了维甲酸和G-CSF治疗。单独使用维甲酸和G-CSF治疗时,白血病细胞在体内发生了完全的粒细胞成熟,随后实现了完全的细胞遗传学和血液学缓解。荧光原位杂交分析显示骨髓和血液呈阴性,半定量聚合酶链反应显示早幼粒细胞白血病锌指-维甲酸受体-α融合转录本显著减少。这表明,只要给予适当的共刺激,t(11;17)阳性白血病细胞并非固有地对维甲酸耐药。这些观察结果可能会促使人们研究全反式维甲酸与造血生长因子在其他类型白血病中的联合应用。