Pastorczak Agata, Szczepanski Tomasz, Mlynarski Wojciech
Department of Pediatrics, Hematology, Oncology and Diabetology, Medical University of Lodz, Poland.
Department of Pediatric Hematology and Oncology, Medical University of Silesia, Zabrze, Poland.
Eur J Med Genet. 2016 Mar;59(3):126-32. doi: 10.1016/j.ejmg.2016.01.007. Epub 2016 Jan 27.
Nijmegen breakage syndrome (NBS, MIM #251260) is an autosomal recessive chromosomal instability disorder. Majority of patients affected are of Slavic origin and share the same founder mutation of 657del5 within the NBN gene encoding protein involved in DNA double-strand breaks repair. Clinically, this is characterized by a microcephaly, immunodeficiency and a high incidence of pediatric malignancies, mostly lymphomas and leukemias. Anticancer treatment among patients with NBS is challenging because of a high risk of life threatening therapy-related toxicity including severe infections, bone marrow failure, cardio- and nephrotoxicity and occurrence of secondary cancer. Based on systemic review of available literature and the Polish acute lymphoblastic leukemia database we concluded that among patients with NBS, these who suffered from clinically proven severe immunodeficiency are at risk of the complications associated with oncological treatment. Thus, in this group it reasonable to reduce chemotherapy up to 50% especially concerning anthracyclines methotrexate, alkylating agents and epipodophyllotoxines, bleomycin and radiotherapy should be omitted. Moreover, infection prophylaxis using intravenous immunoglobulin supplementation together with antifungal and antibacterial agent is recommended. To replace radiotherapy or some toxic anticancer agents targeted therapy using monoclonal antibodies and kinase inhibitors or bone marrow transplantation with reduced-intensity conditioning should be considered in some cases, however, this statement needs further studies.
奈梅亨断裂综合征(NBS,MIM #251260)是一种常染色体隐性染色体不稳定疾病。大多数受影响的患者来自斯拉夫族裔,并且在参与DNA双链断裂修复的蛋白质编码基因NBN内共享相同的657del5奠基者突变。临床上,其特征为小头畸形、免疫缺陷以及儿童恶性肿瘤(主要是淋巴瘤和白血病)的高发病率。由于存在危及生命的治疗相关毒性的高风险,包括严重感染、骨髓衰竭、心脏和肾脏毒性以及继发性癌症的发生,奈梅亨断裂综合征患者的抗癌治疗具有挑战性。基于对现有文献和波兰急性淋巴细胞白血病数据库的系统评价,我们得出结论,在奈梅亨断裂综合征患者中,那些临床证实患有严重免疫缺陷的患者有发生与肿瘤治疗相关并发症的风险。因此,在这组患者中,将化疗剂量减少多达50%是合理的,尤其是关于蒽环类药物、甲氨蝶呤、烷化剂和表鬼臼毒素,应省略博来霉素和放疗。此外,建议使用静脉注射免疫球蛋白补充剂以及抗真菌和抗菌剂进行感染预防。为了替代放疗或一些有毒的抗癌药物,在某些情况下应考虑使用单克隆抗体和激酶抑制剂进行靶向治疗或采用降低强度预处理的骨髓移植,然而,这一说法需要进一步研究。