Larson Richard A, Sievers Eric L, Stadtmauer Edward A, Löwenberg Bob, Estey Elihu H, Dombret Hervé, Theobald Matthias, Voliotis Dimitris, Bennett John M, Richie Maria, Leopold Lance H, Berger Mark S, Sherman Matthew L, Loken Michael R, van Dongen Jacques J M, Bernstein Irwin D, Appelbaum Frederick R
Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Cancer. 2005 Oct 1;104(7):1442-52. doi: 10.1002/cncr.21326.
In this study, the authors analyzed the efficacy and safety of gemtuzumab ozogamicin (GO) (Mylotarg), an antibody-targeted chemotherapy for CD33-positive acute myeloid leukemia (AML).
Patients with CD33-positive AML in first recurrence were entered in 3 open-label, single-arm, Phase II studies. Patients received monotherapy with GO 9 mg/m(2) as a 2-hour intravenous infusion in 2 doses separated by 2 weeks. Patients were evaluated for remission, survival, and treatment-emergent adverse events.
Two hundred seventy-seven patients (median age, 61 yrs) were treated with GO, and 71 patients (26%) achieved remission, which was defined as < or = 5% blasts in the bone marrow without leukemic blasts in the peripheral blood, neutrophil recovery to > or = 1500/microL, hemoglobin > or = 9 g/dL, and independence from red blood cell and platelet transfusions. Complete remission (CR) with platelet recovery (> or = 100,000/microL) or without full platelet recovery (< 100,000/microL) (CRp) was observed in 35 patients (13%) and 36 patients (13%), respectively. The median recurrence-free survival was 6.4 months for patients who achieved CR and 4.5 months for patients who achieved CRp. Although expected incidences of Grade 3 or 4 neutropenia (98%) and thrombocytopenia (99%) were observed, the incidence of Grade 3 or 4 sepsis (17%) and pneumonia (8%) was relatively low. Grade 3 or 4 hyperbilirubinemia and hepatic aspartate aminotransferase and alanine aminotransferase elevations were reported in 29%, 18%, and 9% of patients, respectively; 0.9% of patients who did not undergo prior or subsequent hematopoietic stem cell transplantation developed hepatic venoocclusive disease after GO treatment.
When it was administered to patients with CD33-positive AML in first recurrence, single-agent GO induced a 26% remission rate with a generally acceptable safety profile.
在本研究中,作者分析了吉妥单抗奥唑米星(GO)(商品名:麦罗塔)治疗CD33阳性急性髓性白血病(AML)的疗效和安全性,这是一种抗体靶向化疗药物。
首次复发的CD33阳性AML患者进入3项开放标签、单臂、II期研究。患者接受GO单药治疗,剂量为9 mg/m²,静脉输注2小时,分2剂给药,间隔2周。对患者的缓解情况、生存率和治疗中出现的不良事件进行评估。
277例患者(中位年龄61岁)接受了GO治疗,71例患者(26%)达到缓解,缓解定义为骨髓中原始细胞≤5%,外周血无白血病原始细胞,中性粒细胞恢复至≥1500/μL,血红蛋白≥9 g/dL,且无需输注红细胞和血小板。分别有35例患者(13%)和36例患者(13%)观察到血小板恢复(≥100,000/μL)或未完全恢复(<100,000/μL)的完全缓解(CR)。达到CR的患者中位无复发生存期为6.4个月,达到CRp的患者为4.5个月。虽然观察到3/4级中性粒细胞减少(98%)和血小板减少(99%)的预期发生率,但3/4级败血症(17%)和肺炎(8%)的发生率相对较低。分别有29%、18%和9%的患者报告出现3/4级高胆红素血症以及肝天冬氨酸氨基转移酶和丙氨酸氨基转移酶升高;未接受过造血干细胞移植的患者中,0.9%在GO治疗后发生肝静脉闭塞病。
对于首次复发的CD33阳性AML患者,单药GO诱导缓解率为26%,安全性总体可接受。