定性和实时定量逆转录酶聚合酶链反应分子随访在TEL/ amm1阳性儿童急性淋巴细胞白血病中的预后意义

Gisella Volpe , Nicoletta Bertorello , Elena Barisone , Stefano Ulisciani , Enrico Gottardi , Daniela Cilloni , Marco Vignetti , Carlo Lanza , Franca Fagioli , Enrico Madon , Giuseppe Saglio
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引用次数: 0

摘要

采用定性和定量聚合酶链反应(PCR)对28例统一治疗的TEL/ aml1阳性急性淋巴细胞白血病患儿进行微量残留病(MRD)检测和定量。患者和方法在2年的治疗和随访期间,分析了600多份骨髓或外周血样本。结果所有患者在治疗第42天达到血液学完全缓解,并计划进行BM评估。此时,28例患者中有22例在定性和定量PCR分析中BM已呈阴性,28例患者中有6例显示可量化的MRD,持续时间在1 - 10个月之间,只有1例患者持续PCR阳性,最终复发并因疾病进展而死亡。中位随访104个月后,28例患者中有18例(64%)持续完全缓解且持续PCR阴性。28例患者中10例复发,4例因病情进展死亡,6例经挽救性治疗后第二次血液和分子完全缓解。8年无事件生存率为64%,总生存率为86%。值得注意的是,所有复发之前,在血液学复发前1.5至8个月之间,PCR阳性恢复。此外,诱导治疗后第42天,在10例复发患者中有5例观察到PCR阳性,在18例仍处于持续完全缓解的患者中只有1例观察到PCR阳性。结论:这支持了诱导后第42天可检测到的MRD持续存在与随后复发风险增加相关的观点。
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Prognostic Significance of Molecular Follow-up by Qualitative and Real-Time Quantitative Reverse-Transcriptase Polymerase Chain Reaction in TEL/AML1–Positive Childhood Acute Lymphoblastic Leukemia

Background

Minimal residual disease (MRD) detection and quantification in children with TEL/AML1–positive acute lymphoblastic leukemia was performed by qualitative and quantitative polymerase chain reaction (PCR) in 28 patients, uniformly treated.

Patients and Methods

More than 600 bone marrow (BM) or peripheral blood samples were analyzed during 2 years of therapy and subsequent follow-up.

Results

All the patients reached complete hematologic remission at day 42 of treatment, when a BM evaluation was scheduled. At this time, 22 of 28 patients were already negative in the BM at qualitative and quantitative PCR analysis, 6 of 28 showed a quantifiable MRD that lasted between 1 and 10 months, and only 1 patient remained persistently PCR positive and finally relapsed and died of progressive disease. After a median follow-up of 104 months, 18 of 28 patients (64%) are in continuous complete remission and persistently PCR negative. Ten of 28 patients relapsed: 4 died of progressive disease, and 6 are in second complete hematologic and molecular remission after salvage therapy. The event-free survival at 8 years is 64%, and the overall survival is 86%. Notably, all relapses were preceded by a return to PCR positivity between 1.5 and 8 months before hematologic relapse. Moreover, PCR positivity in the BM taken at day 42 after induction therapy was observed in 5 of the 10 patients who subsequently relapsed and only in 1 of the 18 patients who are still in continuous complete remission.

Conclusion

This supports the notion that persistence of detectable MRD at day 42 after induction is associated with an increased risk of subsequent relapse.

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