Fianchi L, Pagano L, Leoni F, Storti S, Voso M T, Valentini C G, Rutella S, Scardocci A, Caira M, Gianfaldoni G, Leone G
Istituto di Ematologia, Università Cattolica del Sacro Cuore, Roma, Italy.
Ann Oncol. 2008 Jan;19(1):128-34. doi: 10.1093/annonc/mdm451. Epub 2007 Sep 28.
Gemtuzumab ozogamicin (GO) is effective as single agent in the treatment of acute myeloid leukemia (AML). We evaluated efficacy and safety of a chemotherapy including growth factors, cytarabine, and GO (G-AraMy) in the treatment of poor-prognosis AML in elderly patients.
In three Italian hematology departments from September 2003 to September 2006, 53 elderly patients [median age 69 years (range 65-77)] with untreated or primary refractory/relapsed AML were enrolled on the combination G-AraMy administered according to two consecutive schedules (G-AraMy1 and G-AraMy2), with intensified consolidation in the second. Twenty-three of 53 patients had a secondary acute myeloid leukemia (sAML).
The overall response rate was 57%. The most common adverse event was myelosuppression. Seven patients died in induction (13%). No differences for response rate and toxicity profile were observed between untreated and primary resistant/relapsed patients, de novo AML and sAML, and in the two treatment trials. Median disease-free survival and overall survival were 8 months (range 2-23+) and 9 months (range 2-24+).
G-AraMy therapy may be considered an useful treatment approach for poor-risk elderly AML patients, with a complete remission rate comparable to literature data with reduced side-effects, also in a poor-prognosis population.
吉妥单抗奥唑米星(GO)作为单一药物治疗急性髓系白血病(AML)有效。我们评估了一种包含生长因子、阿糖胞苷和GO(G - AraMy)的化疗方案治疗老年预后不良AML患者的疗效和安全性。
2003年9月至2006年9月期间,在意大利三个血液科,53例未治疗或原发性难治/复发AML的老年患者[中位年龄69岁(范围65 - 77岁)]入组接受根据两个连续方案(G - AraMy1和G - AraMy2)给予的G - AraMy联合治疗,第二个方案有强化巩固治疗。53例患者中有23例患有继发性急性髓系白血病(sAML)。
总缓解率为57%。最常见的不良事件是骨髓抑制。7例患者在诱导期死亡(13%)。未治疗患者与原发性耐药/复发患者、初发AML与sAML之间以及两个治疗试验之间在缓解率和毒性特征方面未观察到差异。中位无病生存期和总生存期分别为8个月(范围2 - 23 +)和9个月(范围2 - 24 +)。
G - AraMy疗法可被认为是老年高危AML患者的一种有效治疗方法,完全缓解率与文献数据相当,副作用减少,在预后不良人群中也是如此。