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染色体断裂综合征(共济失调毛细血管扩张症或尼曼-皮克 A 型)患儿的淋巴恶性肿瘤有良好的治疗效果:回顾性调查。

Promising therapy results for lymphoid malignancies in children with chromosomal breakage syndromes (Ataxia teleangiectasia or Nijmegen-breakage syndrome): a retrospective survey.

机构信息

Department of Paediatric Oncology, Haematology and Clinical Immunology, Centre for Child and Adolescent Health, Heinrich Heine University, Düsseldorf, Germany.

出版信息

Br J Haematol. 2011 Nov;155(4):468-76. doi: 10.1111/j.1365-2141.2011.08863.x. Epub 2011 Sep 19.

DOI:10.1111/j.1365-2141.2011.08863.x
PMID:21923652
Abstract

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.

摘要

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。

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