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首页> 外文期刊>Leukemia >Minimal residual disease (MRD) analysis in the non-MRD-based ALL IC-BFM 2002 protocol for childhood ALL: is it possible to avoid MRD testing?
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Minimal residual disease (MRD) analysis in the non-MRD-based ALL IC-BFM 2002 protocol for childhood ALL: is it possible to avoid MRD testing?

机译:基于非MRD的ALL IC-BFM 2002方案中对儿童ALL的最小残留疾病(MRD)分析:是否可以避免MRD测试?

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摘要

The ALL IC-BFM 2002 protocol was created as an alternative to the MRD-based AIEOP-BFM ALL 2000 study, to integrate early response criteria into risk-group stratification in countries not performing routine PCR-based MRD testing. ALL IC stratification comprises the response to prednisone, bone marrow (BM) morphology at days 15 and 33, age, WBC and BCR/ABL or MLL/AF4 presence. Here, we compared this stratification to the MRD-based criteria using MRD evaluation in 163 patients from four ALL IC member countries at days 8, 15 and 33 and week 12. MRD negativity at day 33 was associated with an age of 1–5 years, WBC-1, non-T immunophenotype, good prednisone response and non-M3 morphology at day 15. There were no significant associations with gender or hyperdiploidy in the study group, or with TEL/AML1 fusion within BCP-ALL. Patients with M1/2 BM at day 8 tended to be MRD negative at week 12. Patients stratified into the standard-risk group had a better response than intermediate-risk group patients. However, 34% of them were MRD positive at day 33 and/or week 12. Our findings revealed that morphology-based ALL IC risk-group stratification allows the identification of most MRD high-risk patients, but fails to discriminate the MRD low-risk group assigned to therapy reduction.
机译:ALL IC-BFM 2002协议是对基于MRD的AIEOP-BFM ALL 2000研究的替代方案,旨在将早期响应标准纳入未进行基于PCR的常规MRD测试的国家的风险人群分层中。所有IC分层包括对泼尼松,第15天和第33天,年龄,WBC和BCR / ABL或MLL / AF4存在的骨髓(BM)形态的反应。在这里,我们将第4天,第15天,第33天和第12周来自四个ALL IC成员国的163名患者的MRD评估结果与基于MRD的标准进行了比较,第33天的MRD阴性与1-5岁相关,第15天的WBC-1,非T免疫表型,良好的泼尼松反应和非M3形态。在研究组中,性别或超二倍体与BCP-ALL内的TEL / AML1融合无明显关联。在第8天出现M1 / 2 BM的患者在第12周时往往呈MRD阴性。分层为标准风险组的患者比中风险组患者的反应更好。但是,其中有34%的患者在第33天和/或第12周时MRD阳性。我们的研究结果表明,基于形态学的ALL IC风险组分层可以识别大多数MRD高危患者,但不能区分MRD低-减少治疗的风险组。

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