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儿童复发急性淋巴细胞白血病的治疗:日本儿童癌症研究组的观察性研究。

Treatment of relapsed acute lymphoblastic leukemia in children: an observational study of the Japan Children's Cancer Group.

机构信息

Division of Hematology/Oncology, Kanagawa Children's Medical Center, 2-138-4 Mutsukawa Minami-Ku, Yokohama, Kanagawa, Japan.

Clinical Research Center, NHO Nagoya Medical Center, Aichi, Japan.

出版信息

Int J Hematol. 2024 Nov;120(5):631-638. doi: 10.1007/s12185-024-03838-5. Epub 2024 Aug 27.

DOI:10.1007/s12185-024-03838-5
PMID:39190256
Abstract

The Japan Children's Cancer Group Relapsed Acute Lymphoblastic Leukemia (ALL) Committee conducted a prospective observational study (ALL-R14) to explore promising reinduction therapy regimens for relapsed ALL to investigate in future trials. In Japan, clofarabine- and bortezomib-based regimens were of interest since they were newly introduced for ALL in the study period (2015-2018). Seventy-five pediatric patients were enrolled in total. The 2-year event-free/overall survival rates in patients with first (n = 59) or second (n = 11) relapse were 40.1% (95% confidence interval [CI]: 25.5-52.3%)/66.3% (95% CI 52.3-77.0%) and 34.1% (95% CI 9.1-61.6%)/62.3% (95% CI 27.7-84.0%), respectively. Clofarabine- or bortezomib-based regimens were used only in patients with high-risk disease. The first reinduction therapy used in the 41 patients with early or multiple relapsed B-cell precursor ALL was clofarabine in 7 patients and bortezomib in 9 patients. The odds ratio for reinduction failure risk with a clofarabine- or bortezomib-based regimen compared with other regimens was 9.0 (95% CI 0.9-86.4, P = 0.057) or 1.9 (95% CI 0.4-8.7, P = 0.42), respectively. Thus, clofarabine- or bortezomib-based regimens had no obvious advantage as reinduction therapy for relapsed ALL in children.

摘要

日本儿童癌症研究组(JCRCG)复发急性淋巴细胞白血病(ALL)委员会进行了一项前瞻性观察性研究(ALL-R14),旨在探索复发 ALL 有前途的再诱导治疗方案,以便在未来的试验中进行研究。在日本,由于在研究期间(2015-2018 年)氯法拉滨和硼替佐米方案被新引入 ALL,因此这些方案受到关注。总共有 75 名儿科患者入组。首次(n=59)或第二次(n=11)复发患者的 2 年无事件/总生存率分别为 40.1%(95%置信区间 [CI]:25.5-52.3%)/66.3%(95% CI 52.3-77.0%)和 34.1%(95% CI 9.1-61.6%)/62.3%(95% CI 27.7-84.0%)。氯法拉滨或硼替佐米方案仅用于高危疾病患者。41 例早期或多次复发 B 细胞前体 ALL 患者的首次再诱导治疗中,7 例患者使用氯法拉滨,9 例患者使用硼替佐米。与其他方案相比,基于氯法拉滨或硼替佐米方案的再诱导失败风险的优势比为 9.0(95% CI 0.9-86.4,P=0.057)或 1.9(95% CI 0.4-8.7,P=0.42)。因此,氯法拉滨或硼替佐米方案作为儿童复发 ALL 的再诱导治疗并没有明显优势。

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本文引用的文献

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Temporal changes in incidence of relapse and outcome after relapse of childhood acute lymphoblastic leukemia over three decades; a Nordic population-based cohort study.三十年间儿童急性淋巴细胞白血病复发率及复发后结局的时间变化;一项基于北欧人群的队列研究。
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Disease Burden Affects Outcomes in Pediatric and Young Adult B-Cell Lymphoblastic Leukemia After Commercial Tisagenlecleucel: A Pediatric Real-World Chimeric Antigen Receptor Consortium Report.
商业用 tisagenlecleucel 治疗儿童和青年 B 细胞淋巴母细胞白血病后的疾病负担对结果的影响:儿科嵌合抗原受体联盟报告。
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