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ETV6::RUNX1 急性淋巴细胞白血病:治愈需要多少治疗?

ETV6::RUNX1 Acute Lymphoblastic Leukemia: how much therapy is needed for cure?

机构信息

Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.

Mathematical Institute, Leiden University, Leiden, The Netherlands.

出版信息

Leukemia. 2024 Jul;38(7):1477-1487. doi: 10.1038/s41375-024-02287-7. Epub 2024 Jun 6.

Abstract

Recent trials show 5-year survival rates >95% for ETV6::RUNX1 Acute Lymphoblastic Leukemia (ALL). Since treatment has many side effects, an overview of cumulative drug doses and intensities between eight international trials is presented to characterize therapy needed for cure. A meta-analysis was performed as a comprehensive summary of survival outcomes at 5 and 10 years. For drug dose comparison in non-high risk trial arms, risk group distribution was applied to split the trials into two groups: trial group A with ~70% (range: 63.5-75%) of patients in low risk (LR) (CCLSG ALL2004, CoALL 07-03, NOPHO ALL2008, UKALL2003) and trial group B with ~45% (range: 38.7-52.7%) in LR (AIEOP-BFM ALL 2000, ALL-IC BFM ALL 2002, DCOG ALL10, JACLS ALL-02). Meta-analysis did not show evidence of heterogeneity between studies in trial group A LR and medium risk (MR) despite differences in treatment intensity. Statistical heterogeneity was present in trial group B LR and MR. Trials using higher cumulative dose and intensity of asparaginase and pulses of glucocorticoids and vincristine showed better 5-year event-free survival but similar overall survival. Based on similar outcomes between trials despite differences in therapy intensity, future trials should investigate, to what extent de-escalation is feasible for ETV6::RUNX1 ALL.

摘要

最近的试验显示,ETV6::RUNX1 急性淋巴细胞白血病(ALL)的 5 年生存率>95%。由于治疗有许多副作用,因此对八项国际试验之间的累积药物剂量和强度进行了概述,以确定治愈所需的治疗方法。进行了荟萃分析,作为 5 年和 10 年生存结果的综合总结。对于非高风险试验臂中的药物剂量比较,应用风险组分布将试验分为两组:试验组 A 中约 70%(范围:63.5-75%)的患者为低危(LR)(CCLSG ALL2004、CoALL 07-03、NOPHO ALL2008、UKALL2003),试验组 B 中约 45%(范围:38.7-52.7%)的患者为 LR(AIEOP-BFM ALL 2000、ALL-IC BFM ALL 2002、DCOG ALL10、JACLS ALL-02)。尽管治疗强度存在差异,但在试验组 A LR 和中危(MR)中,荟萃分析并未显示研究之间存在异质性的证据。在试验组 B LR 和 MR 中存在统计学异质性。使用更高累积剂量和强度的 asparaginase 以及糖皮质激素和长春新碱脉冲的试验显示出更好的 5 年无事件生存率,但总体生存率相似。基于尽管治疗强度存在差异,但试验之间仍具有相似的结果,未来的试验应研究在多大程度上可以对 ETV6::RUNX1 ALL 进行降级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/518e/11216990/70e8c5863ab1/41375_2024_2287_Fig1_HTML.jpg

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