Department of Paediatric Oncology, Haematology and Clinical Immunology, Centre for Child and Adolescent Health, Heinrich Heine University, Düsseldorf, Germany.
Br J Haematol. 2011 Nov;155(4):468-76. doi: 10.1111/j.1365-2141.2011.08863.x. Epub 2011 Sep 19.
Children with chromosomal instability syndromes have an increased risk of developing lymphoma and leukaemia. The treatment of these malignancies is hampered by therapy-associated toxicity and infectious complications. This retrospective analysis evaluated the therapy outcome of 38 children with Ataxia teleangiectasia or Nijmegen-breakage syndrome with acute lymphoblastic leukaemia (ALL, n = 9), Non-Hodgkin lymphoma (NHL, n = 28) and Hodgkin lymphoma (HL, n = 1). All patients with NHL or ALL were treated in accordance to Berlin-Frankfurt-Münster (BFM)- or Co-operative study group for childhood ALL (CoALL)-oriented chemotherapy schedules. 22 patients received significantly reduced-intensity chemotherapy. After a median follow-up of 3·7 years the 10-year overall survival was 58%. Dosage-reduction of chemotherapeutic drugs seemed to have no disadvantages and reduced toxic side effects. On the other hand, reduced-intensity chemotherapy did not prevent second malignancies, which occurred in ten patients with a 10-year incidence of 25%. After individual treatment approaches three of these patients with second malignancies were in complete clinical remission for more than 5 years. We conclude that BFM- or CoALL-oriented chemotherapy is effective and can be administered in children with AT or NBS. Moreover, we show that even second lymphoid malignancies can successfully be treated in these patients.
患有染色体不稳定性综合征的儿童发生淋巴瘤和白血病的风险增加。这些恶性肿瘤的治疗受到与治疗相关的毒性和感染性并发症的阻碍。这项回顾性分析评估了 38 例共济失调毛细血管扩张症或尼曼-皮克氏病合并急性淋巴细胞白血病(ALL,n=9)、非霍奇金淋巴瘤(NHL,n=28)和霍奇金淋巴瘤(HL,n=1)的患儿的治疗结果。所有 NHL 或 ALL 患儿均按照柏林-法兰克福-明斯特(BFM)或儿童急性淋巴细胞白血病合作组(CoALL)导向的化疗方案进行治疗。22 例患者接受了强度降低的化疗。中位随访 3.7 年后,10 年总生存率为 58%。化疗药物的剂量减少似乎没有带来劣势,反而减少了毒副作用。另一方面,强度降低的化疗并不能预防第二恶性肿瘤,10 例患儿在 10 年内的发病率为 25%。在个体化治疗方法后,这 3 例患有第二恶性肿瘤的患儿中有 3 例完全缓解超过 5 年。我们得出结论,BFM 或 CoALL 导向的化疗是有效的,可以在 AT 或 NBS 患儿中进行。此外,我们表明,即使是二次淋巴恶性肿瘤也可以成功地治疗这些患者。