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