Roy Lydia, Guilhot Joëlle, Krahnke Tillmann, Guerci-Bresler Agnès, Druker Brian J, Larson Richard A, O'Brien Steve, So Charlene, Massimini Giorgio, Guilhot François
Department of Oncology-Hematology and Cell Therapy, EA 3805, CHU La Milétrie, 2 Rue de la Milétrie, 86021 POITIERS CEDEX, France.
Blood. 2006 Sep 1;108(5):1478-84. doi: 10.1182/blood-2006-02-001495. Epub 2006 Apr 20.
In the multinational IRIS study comparing imatinib with interferon plus cytarabine (IFN/Ara-C) in patients with newly diagnosed chronic-phase chronic myelogenous leukemia (CP CML), imatinib demonstrated significantly higher rates of complete cytogenetic responses (CCyRs) and improved progression-free survival (PFS). However, because of a high early crossover rate to imatinib, survival benefit was not assessable. Here, we report the result of a study comparing long-term outcome of patients included in 2 prospective randomized trials: 551 patients assigned to imatinib in the IRIS trial from 2000 to 2001 and 325 patients who received the combination IFN/Ara-C in the CML91 trial between 1991 and 1996 before imatinib was available. With a follow-up of 42 months for both groups of patients, estimated CCyR, survival free of transformation, and overall survival were significantly higher with imatinib compared with IFN/Ara-C (P < .001, P = .004, and P < .001, respectively). Improved overall survival was also confirmed within different Sokal prognostic risk groups. Of interest, among all patients who achieved major cytogenetic response or CCyR at 12 months, the survival rate was similar irrespective of their treatment. In conclusion, within the limitation of this historical comparison, there is a survival advantage from first-line therapy with imatinib over IFN/Ara-C.
在一项多国IRIS研究中,对新诊断的慢性期慢性髓性白血病(CP CML)患者比较了伊马替尼与干扰素加阿糖胞苷(IFN/Ara-C)的疗效,结果显示伊马替尼的完全细胞遗传学缓解(CCyR)率显著更高,无进展生存期(PFS)也有所改善。然而,由于早期交叉使用伊马替尼的比例较高,生存获益无法评估。在此,我们报告一项研究结果,该研究比较了两项前瞻性随机试验中患者的长期预后:2000年至2001年IRIS试验中分配接受伊马替尼治疗的551例患者,以及1991年至1996年在伊马替尼上市之前CML91试验中接受IFN/Ara-C联合治疗的325例患者。两组患者均随访42个月,结果显示伊马替尼组的估计CCyR、无转化生存期和总生存期均显著高于IFN/Ara-C组(P分别<0.001、P = 0.004和P < 0.001)。在不同的索卡尔预后风险组中也证实了伊马替尼组总生存期的改善。有趣的是,在所有12个月时达到主要细胞遗传学缓解或CCyR的患者中,无论接受何种治疗,生存率相似。总之,在这项历史对照研究的局限性内,一线使用伊马替尼治疗相对于IFN/Ara-C具有生存优势。