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青年人高危急性淋巴细胞白血病的治疗(CCG-1961):儿童肿瘤协作组的长期随访研究报告。

Treatment of higher risk acute lymphoblastic leukemia in young people (CCG-1961), long-term follow-up: a report from the Children's Oncology Group.

机构信息

Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Children's National Health System, George Washington University School of Medicine and Health Sciences, Washington, DC, USA.

出版信息

Leukemia. 2019 Sep;33(9):2144-2154. doi: 10.1038/s41375-019-0422-z. Epub 2019 Feb 28.

Abstract

Children's Cancer Group CCG-1882 improved outcome for 1-21-year old with high risk acute lymphoblastic leukemia and Induction Day 8 marrow blasts ≥25% (slow early responders, SER) with longer and stronger post induction intensification (PII). This CCG-1961 explored alternative PII strategies. We report 10-year follow-up for patients with rapid early response (RER) and for the first time details our experience for SER patients. A total of 2057 patients were enrolled, and 1299 RER patients were randomized to 1 of 4 PII regimens: standard vs. augmented intensity and standard vs. increased length. At the end of interim maintenance, 447 SER patients were randomized to idarubicin/cyclophosphamide or weekly doxorubicin in the delayed intensification phases. The 10-year EFS for RER were 79.4 ± 2.4% and 70.9 ± 2.6% (hazard ratio = 0.65, 95% CI 0.52-0.82, p < 0.001) for augmented and standard strength PII; the 10-year OS rates were 87.2 ± 2.0% and 81.0 ± 2.2% (hazard ratio = 0.64, 95% CI 0.48-0.86, p = 0.003). Outcomes remain similar for standard and longer PII, and for SER patients assigned to idarubicin/cyclophosphamide and weekly doxorubicin. The EFS and OS advantage of augmented PII is sustained at 10 years for RER patients. Longer PII for RER patients and sequential idarubicin/cyclophosphamide for SER patients offered no advantage. CCG-1961 is the platform for subsequent COG studies.

摘要

儿童癌症组 CCG-1882 通过延长和强化诱导后强化治疗(PII),改善了高危急性淋巴细胞白血病且诱导第 8 天骨髓 blast≥25%(慢早期反应者,SER)的 1-21 岁患者的预后。CCG-1961 探索了替代 PII 策略。我们报告了快速早期反应(RER)患者的 10 年随访结果,并且首次详细介绍了 SER 患者的治疗经验。共有 2057 名患者入组,1299 名 RER 患者随机分为 4 种 PII 方案中的 1 种:标准强度 vs. 增强强度,以及标准长度 vs. 增加长度。在中期维持治疗结束时,447 名 SER 患者随机分配到延迟强化阶段的阿糖胞苷/环磷酰胺或每周多柔比星。RER 的 10 年 EFS 分别为 79.4±2.4%和 70.9±2.6%(危险比=0.65,95%CI 0.52-0.82,p<0.001),增强和标准强度 PII 组;10 年 OS 率分别为 87.2±2.0%和 81.0±2.2%(危险比=0.64,95%CI 0.48-0.86,p=0.003)。对于标准强度和更长强度的 PII,以及接受阿糖胞苷/环磷酰胺和每周多柔比星治疗的 SER 患者,结果仍然相似。对于 RER 患者,增强 PII 的 EFS 和 OS 优势持续 10 年。对于 RER 患者延长 PII 和 SER 患者序贯阿糖胞苷/环磷酰胺并没有带来优势。CCG-1961 是 COG 后续研究的平台。

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