[Treatment of residual disease in chronic myeloid leukemia with STI-571 (Glivec)].

Acta medica Austriaca. Supplement Pub Date : 2002-01-01
K Geissler, Hermine Agis, Verena Sagaster
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Abstract

Cytoreductive therapy can ameliorate symptoms in chronic myeloid leukemia (CML) but only treatment beyond hematologic remission aiming to affect the leukemic clone can improve prognosis. Up to now bone marrow transplantation is the only established therapy with the potential to completely eliminate the BCR-ABL positive cell population. Interferon-alpha (IFN-alpha) as well as cytosine arabinoside (ARA-C), particularly in combination, have been shown to be effective in achieving cytogenetic remission in some patients. With Glivec (STI-571) there is now a drug available which can induce major cytogenetic response in more than half of the patients who have failed IFN-alpha treatment and thus possibly delay or prevent blast crisis. Recent reports, however, have shown that primitive, quiescent, Philadelphia-positive stem cells are insensitive to STI-571 in vitro. Such cells could be the basis of relapse after termination of Glivec-therapy.

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[STI-571 (Glivec)治疗慢性髓系白血病残留病变]。
细胞减少治疗可以改善慢性髓性白血病(CML)的症状,但只有在血液学缓解之外的治疗才能改善预后。到目前为止,骨髓移植是唯一确定的有可能完全消除BCR-ABL阳性细胞群的治疗方法。干扰素- α (ifn - α)和阿拉伯糖胞嘧啶(ARA-C),特别是联合使用,已被证明对某些患者的细胞遗传学缓解是有效的。Glivec (STI-571)现在是一种可用的药物,可以在超过一半的ifn - α治疗失败的患者中诱导主要的细胞遗传学反应,从而可能延迟或预防原细胞危象。然而,最近的报道表明,原始的、静止的、philadelphia阳性的干细胞在体外对STI-571不敏感。这些细胞可能是格列韦治疗终止后复发的基础。
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