Suppr超能文献

早期强化强度降低不会增加标准风险急性淋巴细胞白血病患儿复发的风险 - GD-2008-ALL 方案的多中心临床研究。

Reduced intensity of early intensification does not increase the risk of relapse in children with standard risk acute lymphoblastic leukemia - a multi-centric clinical study of GD-2008-ALL protocol.

机构信息

Department of Pediatrics, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, 510120, China.

出版信息

BMC Cancer. 2021 Jan 13;21(1):59. doi: 10.1186/s12885-020-07752-x.

Abstract

BACKGROUND

The prognosis of childhood acute lymphoblastic leukemia (ALL) is optimistic with a 5-year event-free survival (EFS) rate of 70-85%. However, the major causes of mortality are chemotherapy toxicity, infection and relapse. The Guangdong (GD)-2008-ALL collaborative protocol was carried out to study the effect of reduced intensity on treatment related mortality (TRM) based on Berlin-Frankfurt-Münster (BFM) 2002 backbone treatment. The study was designed to elucidate whether the reduced intensity is effective and safe for children with ALL.

METHODS

The clinical data were obtained from February 28, 2008 to June 30, 2016. A total of 1765 childhood ALL cases from 9 medical centers were collected and data were retrospectively analyzed. Patients were stratified into 3 groups according to bone marrow morphology, prednisone response, age, genotype, and karyotype information: standard risk (SR), intermediate risk (IR) and high risk (HR). For SR group, daunorubicin was decreased in induction IA while duration was reduced in Induction Ib (2 weeks in place of 4 weeks). Doses for CAM were same in all risk groups - SR patients received one CAM, others got two CAMs.

RESULTS

The 5-year and 8-year overall survival (OS), event-free survival (EFS) and cumulative incidence of relapse (CIR) were 83.5±0.9% and 83.1±1.0%, 71.9±1.1% and 70.9±1.2%, and 19.5±1.0% and 20.5±1.1%, respectively. The 2-year treatment-related mortality (TRM) was 5.2±0.5%. The 5-year and 8-year OS were 90.7±1.4% and 89.6±1.6% in the SR group, while the 5-year and 8-year EFS were 81.5±1.8% and 80.0±2.0%. In the SR group, 74 (15.2%) patients measured minimal residual disease (MRD) on Day 15 and Day 33 of induction therapy. Among them, 7 patients (9.46%) were MRD positive (≥ 0.01%) on Day 33. The incidence of relapse in the MRD Day 33 positive group (n=7) was 28.6%, while in the MRD Day 33 negative group (n=67) was 7.5% (p=0.129).

CONCLUSIONS

The results of GD-2008-ALL protocol are outstanding for reducing TRM in childhood ALL in China with excellent long term EFS. This protocol provided the evidence for further reducing intensity of induction therapy in the SR group according to the risk stratification. MRD levels on Day 15 and Day 33 are appropriate indexes for stratification.

摘要

背景

儿童急性淋巴细胞白血病(ALL)的预后乐观,5 年无事件生存率(EFS)为 70-85%。然而,导致死亡率的主要原因是化疗毒性、感染和复发。广东(GD)-2008-ALL 协作方案基于柏林-法兰克福-慕尼黑(BFM)2002 骨干治疗,旨在研究减少强度对治疗相关死亡率(TRM)的影响。该研究旨在阐明减少强度对 ALL 儿童是否有效和安全。

方法

临床数据来自 2008 年 2 月 28 日至 2016 年 6 月 30 日。共收集了来自 9 家医疗中心的 1765 例儿童 ALL 病例,并进行了回顾性分析。根据骨髓形态学、泼尼松反应、年龄、基因型和核型信息,患者分为 3 组:标准风险(SR)、中危(IR)和高危(HR)。对于 SR 组,诱导 IA 中的柔红霉素减少,诱导 Ib 中的持续时间缩短(2 周代替 4 周)。所有风险组的 CAM 剂量相同-SR 患者接受 1 次 CAM,其他患者接受 2 次 CAM。

结果

5 年和 8 年总生存率(OS)、无事件生存率(EFS)和累积复发率(CIR)分别为 83.5±0.9%和 83.1±1.0%、71.9±1.1%和 70.9±1.2%和 19.5±1.0%和 20.5±1.1%。2 年治疗相关死亡率(TRM)为 5.2±0.5%。SR 组的 5 年和 8 年 OS 分别为 90.7±1.4%和 89.6±1.6%,5 年和 8 年 EFS 分别为 81.5±1.8%和 80.0±2.0%。在 SR 组中,74 名(15.2%)患者在诱导治疗第 15 天和第 33 天测量微小残留病(MRD)。其中,7 名(9.46%)患者在第 33 天的 MRD 呈阳性(≥0.01%)。第 33 天 MRD 阳性组(n=7)的复发率为 28.6%,而第 33 天 MRD 阴性组(n=67)的复发率为 7.5%(p=0.129)。

结论

GD-2008-ALL 方案在中国降低儿童 ALL 的 TRM 方面取得了显著的成果,具有良好的长期 EFS。该方案为根据风险分层进一步降低 SR 组诱导治疗强度提供了证据。第 15 天和第 33 天的 MRD 水平是分层的适当指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93e0/7805214/9426fc516a36/12885_2020_7752_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验