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在首次复发晚期,年龄超过 55 岁的急性髓系白血病患者中,分次 gemtuzumab ozogamicin 和标准剂量阿糖胞苷治疗可延长第二次缓解期。

Fractionated gemtuzumab ozogamicin and standard dose cytarabine produced prolonged second remissions in patients over the age of 55 years with acute myeloid leukemia in late first relapse.

机构信息

Service d'Hématologie et d'Oncologie, Hôpital André Mignot, Le Chesnay, France.

出版信息

Am J Hematol. 2014 Apr;89(4):399-403. doi: 10.1002/ajh.23653. Epub 2014 Mar 7.

Abstract

Gemtuzumab ozogamicin (fGO), a humanized anti-CD33 monoclonal antibody linked to calicheamicin in combination with intensive chemotherapy gives high response rates in adult acute myeloid leukemia (AML) patients in relapse. However, reduced intensity chemotherapy in combination with fractionated GO has not been tested in aged relapsing patients. Patients from our institution with CD33+ AML aged 55 years or more in first late relapse (≥ 6 months) were proposed participation in a GO compassionate use program. Induction therapy consisted in fractionated GO (fGO; 3 mg/m², days 1, 4, 7) with standard-dose cytarabine (200 mg/m² /day, 7 days). Patients were consolidated with two courses of GO and intermediate dose cytarabine. Twenty-four patients (median age 68 years) received fGO with cytarabine. Median follow-up was 42 months. The response rate was 75%, including complete remission (CR) in 16 patients and CR with incomplete platelet recovery (CRp) in two patients. Two-year overall survival (OS) was 51% (95% CI: 28-69) and 2 years relapse-free survival (RFS) was 51% (95%CI: 25-72). Duration of second CR (CR2) was longer than first CR (CR1) in 9 out of 18 patients. Minimal residual disease (MRD) was negative in evaluable patients in CR2, particularly in NPM1 mutated cases. Toxicity was in line with that of the same fractionated single agent GO schedule. Fractionated GO with low intensity chemotherapy produced high response rates and prolonged CR2 in aged AML patients in first late relapse.

摘要

吉妥珠单抗奥佐米星(fGO)是一种人源化抗 CD33 单克隆抗体,与加利车霉素相连,与强化化疗联合用于成人复发急性髓细胞白血病(AML)患者,可获得高反应率。然而,在老年复发患者中尚未测试过低强度化疗联合分割 GO。我们机构的患者为年龄在 55 岁及以上的初发晚期复发(≥6 个月)的 CD33+AML 患者,被提议参与 GO 同情使用计划。诱导治疗包括分割 GO(fGO;3mg/m²,第 1、4、7 天)与标准剂量阿糖胞苷(200mg/m²/天,7 天)。患者接受两个疗程的 GO 和中剂量阿糖胞苷巩固治疗。24 例患者(中位年龄 68 岁)接受 fGO 和阿糖胞苷治疗。中位随访时间为 42 个月。反应率为 75%,包括 16 例完全缓解(CR)和 2 例 CR 伴不完全血小板恢复(CRp)。2 年总生存率(OS)为 51%(95%CI:28-69),2 年无复发生存率(RFS)为 51%(95%CI:25-72)。18 例中有 9 例患者的第二次 CR(CR2)持续时间长于第一次 CR(CR1)。在可评估的 CR2 患者中,MRD 阴性,特别是在 NPM1 突变病例中。毒性与相同的分割单药 GO 方案一致。在初发晚期复发的老年 AML 患者中,低强度化疗联合分割 GO 可产生高反应率并延长 CR2。

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