Prognostic value of MRD-dynamics in childhood acute lymphoblastic leukemia treated according to the MB-2002/2008 protocols

Abstract Detection of minimal residual disease (MRD) during the treatment of acute lymphoblastic leukemia (ALL) by RQ-PCR analysis of clonal Ig/TCR rearrangements is used for risk group stratification in European treatment protocols. In Belarus patients with childhood ALL are treated according to AL...

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Veröffentlicht in:Leukemia research 2011-10, Vol.35 (10), p.1312-1320
Hauptverfasser: Meleshko, Alexander N, Savva, Natalia N, Fedasenka, Uladzimir U, Romancova, Alexandra S, Krasko, Olga V, Eckert, Cornelia, von Stackelberg, Arend, Aleinikova, Olga V
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Sprache:eng
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Zusammenfassung:Abstract Detection of minimal residual disease (MRD) during the treatment of acute lymphoblastic leukemia (ALL) by RQ-PCR analysis of clonal Ig/TCR rearrangements is used for risk group stratification in European treatment protocols. In Belarus patients with childhood ALL are treated according to ALL-MB protocols, which do not use MRD-based risk stratification. To evaluate the prognostic significance of MRD for ALL-MB-2002/2008 protocols, MRD was quantified by RQ-PCR in 68 ALL patients at four time points: on day 15, on day 36, before and after maintenance therapy (MT). MRD positivity, as well as quantitative level of MRD were analyzed and compared between patients who stayed in remission and relapsed. Relapse-free survival revealed to be significantly associated with MRD levels at different time points. Unfavorable prognosis was shown for MRD ≥ 10−3 on day 36 ( p < 0.001), and any positive MRD before ( p < 0.001) and after ( p = 0.001) MT. Multivariate Cox regression analysis proved MRD as independent significant prognosis factor at day 36 ( p = 0.005) and before MT ( p = 0.001). We conclude, that MRD quantified by RQ-PCR in children with ALL treated with ALL-MB protocols is feasible and independently associated with outcome. MRD may be a suitable parameter for treatment stratification in MB protocols in future.
ISSN:0145-2126
1873-5835
DOI:10.1016/j.leukres.2011.04.013