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吉妥珠单抗奥佐米星作为一线治疗药物用于 70 岁及以上急性髓系白血病患者。

Gemtuzumab ozogamicin as first-line treatment in patients aged 70 years or older with acute myeloid leukemia.

机构信息

Division of Hematology-Oncology, University of Pittsburgh School of Medicine, University of Pittsburgh Cancer Institute, Pittsburgh, PA 15232, USA.

出版信息

Cancer. 2010 Jun 15;116(12):3001-5. doi: 10.1002/cncr.25078.

Abstract

BACKGROUND

Elderly patients with acute myeloid leukemia (AML) are generally unable to withstand the rigors of intensive induction chemotherapy and its attendant complications. Gemtuzumab ozogamicin (GO) is an immunoconjugate that had demonstrated activity in recurrent AML.

METHODS

The objective of the current study was to determine the prognostic factors for achievement of complete remission (CR) in newly diagnosed elderly AML patients treated with GO as initial induction therapy. A retrospective study was performed of efficacy and toxicity associated with GO therapy, and factors potentially predictive of response were assessed in 49 previously untreated AML patients.

RESULTS

CR was achieved in 14% of all treated patients. Among the patients with an intermediate-risk karyotype, the CR rate was 30%, compared with none with an unfavorable karyotype. The median duration of overall survival was 3.7 months (95% confidence interval [95% CI], 1.4-6.9 months), and the median recurrence-free survival in patients who achieved CR was 11.8 months (95% CI, 5.0-ind months).

CONCLUSIONS

These data suggest that GO should be considered as a first-line treatment option in older patients with AML with intermediate-risk cytogenetics who cannot tolerate high-dose induction chemotherapy.

摘要

背景

老年急性髓系白血病(AML)患者通常无法承受强化诱导化疗及其相关并发症的严峻考验。吉妥珠单抗奥佐米星(GO)是一种免疫偶联物,在复发性 AML 中具有活性。

方法

本研究的目的是确定新诊断的老年 AML 患者接受 GO 作为初始诱导治疗时达到完全缓解(CR)的预后因素。对 49 例未经治疗的 AML 患者进行了 GO 治疗相关疗效和毒性的回顾性研究,并评估了潜在的反应预测因素。

结果

所有治疗患者的 CR 率为 14%。在具有中危核型的患者中,CR 率为 30%,而核型不良的患者无一例达到 CR。总生存的中位数为 3.7 个月(95%置信区间 [95%CI],1.4-6.9 个月),达到 CR 的患者无复发生存的中位数为 11.8 个月(95%CI,5.0-13.6 个月)。

结论

这些数据表明,GO 应被视为不能耐受大剂量诱导化疗的中危细胞遗传学老年 AML 患者的一线治疗选择。

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