Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia.
Pediatric Hematology Oncology, Washington University School of Medicine, St. Louis, Missouri.
Clin Cancer Res. 2017 Jun 1;23(11):e14-e22. doi: 10.1158/1078-0432.CCR-17-0428.
Leukemia, the most common childhood cancer, has long been recognized to occasionally run in families. The first clues about the genetic mechanisms underlying familial leukemia emerged in 1990 when Li-Fraumeni syndrome was linked to mutations. Since this discovery, many other genes associated with hereditary predisposition to leukemia have been identified. Although several of these disorders also predispose individuals to solid tumors, certain conditions exist in which individuals are specifically at increased risk to develop myelodysplastic syndrome (MDS) and/or acute leukemia. The increasing identification of affected individuals and families has raised questions around the efficacy, timing, and optimal methods of surveillance. As part of the AACR Childhood Cancer Predisposition Workshop, an expert panel met to review the spectrum of leukemia-predisposing conditions, with the aim to develop consensus recommendations for surveillance for pediatric patients. The panel recognized that for several conditions, routine monitoring with complete blood counts and bone marrow evaluations is essential to identify disease evolution and enable early intervention with allogeneic hematopoietic stem cell transplantation. However, for others, less intensive surveillance may be considered. Because few reports describing the efficacy of surveillance exist, the recommendations derived by this panel are based on opinion, and local experience and will need to be revised over time. The development of registries and clinical trials is urgently needed to enhance understanding of the natural history of the leukemia-predisposing conditions, such that these surveillance recommendations can be optimized to further enhance long-term outcomes.
白血病是最常见的儿童癌症,长期以来一直被认为偶尔会在家族中出现。1990 年,当 Li-Fraumeni 综合征与 突变相关联时,有关家族性白血病遗传机制的第一个线索出现了。自这一发现以来,已经确定了许多与遗传性白血病易感性相关的其他基因。尽管其中一些疾病也使个体易患实体肿瘤,但某些情况下,个体患骨髓增生异常综合征(MDS)和/或急性白血病的风险会增加。越来越多的受影响个体和家庭的出现引发了关于疗效、时间和最佳监测方法的问题。作为 AACR 儿童癌症易感性研讨会的一部分,一个专家小组开会审查了白血病易感性疾病的范围,旨在为儿科患者的监测制定共识建议。专家组认识到,对于几种情况,通过全血细胞计数和骨髓评估进行常规监测对于确定疾病的演变和能够进行同种异体造血干细胞移植的早期干预至关重要。然而,对于其他情况,可以考虑较少的密集监测。由于很少有描述监测效果的报告,因此该小组提出的建议是基于意见、当地经验,并且需要随着时间的推移进行修订。迫切需要制定登记册和临床试验,以增强对白血病易感性疾病自然史的理解,以便能够优化这些监测建议,进一步提高长期结果。