Incidence and prognostic value of central nervous system involvement in infants with B‐cell precursor acute lymphoblastic leukemia treated according to the MLL‐Baby protocol

医学 微小残留病 入射(几何) 脑脊液 中枢神经系统 负效应 内科学 化疗 肿瘤科 白血病 心理学 社会心理学 光学 物理
作者
А. М. Попов,Grigory Tsaur,Zh. V. Permikin,Veronika Fominikh,Tatiana Verzhbitskaya,Tatiana Riger,Anna Demina,Egor Shorikov,Anatoly Kustanovich,Liudmila Movchan,Olga Streneva,Olga Khlebnikova,О. В. Макарова,О. R. Arakaev,Alexander Solodovnikov,Э Г Бойченко,К. Л. Кондратчик,Natalia Ponomareva,Elena Lapotentova,Olga Aleinikova
出处
期刊:Pediatric Blood & Cancer [Wiley]
卷期号:69 (9) 被引量:4
标识
DOI:10.1002/pbc.29860
摘要

The aim of the study was to evaluate the incidence and prognostic impact of central nervous system (CNS) involvement in infants with B-cell precursor acute lymphoblastic leukemia (BCP-ALL), as well as its relation with minimal residual disease (MRD) data.A total of 139 consecutive infants with BCP-ALL from the MLL-Baby trial were studied. Cerebrospinal fluid (CSF) samples were investigated by microscopy of cytospin slides. MRD was evaluated according to the protocol schedule by flow cytometry and PCR for fusion gene transcripts (FGT).Involvement of the CNS at any level was found in 50 infants (36.0%). The incidence of CNS involvement was higher in patients with KMT2A gene rearrangements (44.0% for KMT2A-r vs. 15.4% for KMT2A-g, p = .003). The outcome of CNS-positive infants was significantly worse than that of CNS-negative infants, although this prognostic impact was limited to the KMT2A-r group (event-free survival 0.21 for CNS-positive vs. 0.48 for CNS-negative infants, p = .044). CNS-positive infants could not be treated successfully by conventional chemotherapy alone, irrespective of the rapidity of MRD response. In contrast, the combination of initial CNS negativity and FGT-MRD negativity identified a group comprising up to one-third of infants with KMT2A-r ALL who can be treated with chemotherapy and achieve very good outcomes (disease-free survival above 95%), and remaining patients should be allocated to receive other types of treatment.We can conclude that this combination of initial CNS involvement and MRD data can significantly improve risk-group allocation in future clinical trials enrolling infants with ALL.
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