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基于高三尖杉酯碱方案治疗儿童急性髓系白血病的疗效与安全性:一项中国的回顾性研究

The efficacy and safety of a homoharringtonine-based protocol for children with acute myeloid leukemia: A retrospective study in China.

作者信息

Tang Yanjing, Luo Chengjuan, Shen Shuhong, Xue Huiliang, Pan Ci, Hu Wenting, Chen Xiaoxiao, Cai Jiaoyang, Chen Jing, Tang Jingyan

机构信息

Department of Hematology/Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Key Lab of Pediatric Hematology & Oncology of China Ministry of Health, Shanghai, China.

出版信息

Pediatr Hematol Oncol. 2021 Mar;38(2):97-107. doi: 10.1080/08880018.2020.1820649. Epub 2020 Oct 5.

Abstract

The standard chemotherapy for acute myeloid leukemia (AML) is usually composed of anthracyclines and cytarabine. We previously reported that homoharringtonine (HHT) was incorporated into regimens for pediatric AML with acceptable efficacy and tolerable toxicity. We treated newly diagnosed AML patients aged 0-18 years on the AML-SCMC-2009 protocol. A total of 102 de novo newly diagnosed AML patients aged 0-18 years were enrolled. All patients were treated with ten courses of chemotherapy including double induction, high dose cytarabine consolidation, and maintenance. The cumulative dose of HHT was 165 mg/m and the daunorubicin dose was 120 mg/m. Complete remission (CR), overall survival (OS) rate, event free survival (EFS) rate, adverse effect response and prognosis factors were retrospectively evaluated to investigate the long-term outcome and safety of this protocol. Eighty-two patients (80.4%) achieved complete remission with the first induction. The 5-year overall survival and event-free survival rates were 65.0% (, 4.9%) and 53.3% (, 5.2%), respectively. A first induction failure, age older than 2 years, and BCR-ABL translocation were associated with a significantly worse outcome ( < 0.05). No significant drug-related cardiac toxicity was observed. AML-SCMC-2009 protocol which use HHT as backbone drug is efficacious and tolerated. HHT could partially replace anthracycline to be an effective option for childhood AML.

摘要

急性髓系白血病(AML)的标准化疗通常由蒽环类药物和阿糖胞苷组成。我们之前报道过高三尖杉酯碱(HHT)被纳入小儿AML治疗方案中,疗效尚可且毒性可耐受。我们按照AML-SCMC-2009方案治疗0至18岁新诊断的AML患者。总共纳入了102例0至18岁初发新诊断的AML患者。所有患者均接受了十个疗程的化疗,包括双重诱导、大剂量阿糖胞苷巩固和维持治疗。HHT的累积剂量为165mg/m,柔红霉素剂量为120mg/m。对完全缓解(CR)、总生存率(OS)、无事件生存率(EFS)、不良反应反应及预后因素进行回顾性评估,以研究该方案的长期疗效和安全性。82例患者(80.4%)首次诱导即达到完全缓解。5年总生存率和无事件生存率分别为65.0%(,4.9%)和53.3%(,5.2%)。首次诱导失败、年龄大于2岁以及BCR-ABL易位与显著更差的预后相关(<0.05)。未观察到明显的药物相关心脏毒性。以HHT作为骨干药物的AML-SCMC-2009方案有效且耐受性良好。HHT可部分替代蒽环类药物,成为儿童AML的有效选择。

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