Cervantes Francisco, Hernández-Boluda Juan-Carlos, Steegmann Juan-Luis, Conde Eulogio, Alvarez-Larrán Alberto, López-Jiménez Javier, Osorio Santiago, Villalón Lucía, Camós Mireia, García-Conde Javier, Odriozola Jesús
Hematology Department, Hospital Clínic, Villarroel 170, 08036 Barcelona, Spain.
Haematologica. 2003 Oct;88(10):1117-22.
Imatinib mesylate has recently been shown to be highly effective in chronic-phase chronic myeloid leukemia (CML). The results of imatinib treatment in chronic-phase CML patients resistant or intolerant to interferon (IFN) and the factors predicting therapeutic response and progression-free survival were analyzed.
One hundred and fifty patients with chronic-phase CML resistant (n=111) or intolerant (n=39) to IFN were treated with imatinib. Prognostic factors for response and disease progression were assessed by multivariate analysis.
The median time from diagnosis was 43 months (0.5-188), median IFN therapy 21.5 months (0.5-140) and median follow-up from starting imatinib 13.6 months (range: 3-23). Complete hematologic response was achieved in 96 of 97 patients. Complete, partial and minor cytogenetic responses were present in 44%, 22%, and 8% of patients at 12 months. Grade III-IV neutropenia, thrombocytopenia, and anemia developed in 33%, 16%, and 6% of patients, respectively. Sixty-five patients discontinued treatment for a median of 4 weeks (1-36) due to toxicity. The rate of progression-free survival (lack of accelerated/blastic phase with persistent response) was 89.2% (95% CI: 84-94.4) at 12 months and 80.2% (95% CI: 72.2-88.2) at 18 months. Platelets > 450x10(9)/L and treatment discontinuation > 4 weeks were associated with a lower rate of major (complete plus partial) cytogenetic response. Patients in Sokal's high-risk group and those who did not achieve a major cytogenetic response had significantly shorter progression-free survival.
Imatinib is highly effective in chronic-phase CML patients resistant or intolerant to IFN, especially in those with normal platelet counts and in those not requiring prolonged treatment discontinuation due to neutropenia.
甲磺酸伊马替尼最近已被证明对慢性期慢性髓性白血病(CML)非常有效。分析了伊马替尼治疗对干扰素(IFN)耐药或不耐受的慢性期CML患者的结果以及预测治疗反应和无进展生存期的因素。
150例对IFN耐药(n = 111)或不耐受(n = 39)的慢性期CML患者接受伊马替尼治疗。通过多变量分析评估反应和疾病进展的预后因素。
从诊断开始的中位时间为43个月(0.5 - 188),中位IFN治疗时间为21.5个月(0.5 - 140),从开始使用伊马替尼起的中位随访时间为13.6个月(范围:3 - 23)。97例患者中有96例实现了完全血液学反应。12个月时,44%、22%和8%的患者分别出现完全、部分和微小细胞遗传学反应。分别有33%、16%和6%的患者发生III - IV级中性粒细胞减少、血小板减少和贫血。65例患者因毒性反应停药,中位停药时间为4周(1 - 36)。12个月时无进展生存期(无加速/急变期且持续有反应)的发生率为89.2%(95%CI:84 - 94.4),18个月时为80.2%(95%CI:72.2 - 88.2)。血小板计数>450×10⁹/L以及停药时间>4周与主要(完全加部分)细胞遗传学反应率较低相关。Sokal高危组患者以及未实现主要细胞遗传学反应的患者无进展生存期明显较短。
伊马替尼对IFN耐药或不耐受的慢性期CML患者非常有效,尤其是血小板计数正常且不因中性粒细胞减少而需要长时间停药的患者。