Attarbaschi Andishe, Dworzak Michael, Steiner Manuel, Urban Christian, Fink Franz-Martin, Reiter Alfred, Gadner Helmut, Mann Georg
St. Anna Children's Hospital, Vienna, Austria.
Pediatr Blood Cancer. 2005 Jan;44(1):70-6. doi: 10.1002/pbc.20121.
Children and adolescents with Non-Hodgkin lymphoma (NHL) and mature B-cell leukemia (B-ALL) have an excellent prognosis with contemporary chemotherapy stratified according to the histologic subtype and clinical stage of disease. However, a small subset of patients does not respond to front-line therapy or suffers from an early relapse.
A retrospective analysis was performed to assess the incidence, treatment, and outcome of all children with relapsed or progressed NHL and B-ALL diagnosed in Austria between 1986 and 2003 (n = 22/234).
Nine of 140 (6.5%) patients with B-cell NHL/B-ALL (relapse, n = 6; progress, n = 3) failed initial treatment. Four of them underwent a hematopoietic stem cell transplantation (HSCT) as second-line therapy, two patients received intensive chemotherapy alone and in three patients treatment was palliative. Eight of the nine patients died of their disease. Four of 65 (6%) patients with lymphoblastic lymphoma (LBL) (relapse, n = 2; progress, n = 2) had a treatment failure. High-dose chemotherapy followed by HSCT was performed in two of the four patients; another two patients received chemotherapy alone. Three of the four patients died of resistant disease. Nine of 29 (31%) patients with anaplastic large cell lymphoma (ALCL) (relapse, n = 7; progress, n = 2) failed first-line therapy. Six underwent a HSCT (autologous, n = 3; allogeneic, n = 3) and are currently in second complete remission. Treatment of the other three patients consisted of chemotherapy alone-they all died of tumor progression.
Conclusively, patients with early relapsed and progressive B-cell neoplasia or LBL have a very poor prognosis with current treatment approaches, while those with ALCL have a respectable chance to achieve a sustained complete second remission with high-dose chemotherapy and HSCT.
非霍奇金淋巴瘤(NHL)和成熟B细胞白血病(B-ALL)的儿童及青少年患者,采用根据疾病组织学亚型和临床分期分层的当代化疗方案,预后良好。然而,一小部分患者对一线治疗无反应或早期复发。
进行一项回顾性分析,以评估1986年至2003年间在奥地利诊断的所有复发或进展性NHL和B-ALL儿童患者的发病率、治疗情况及预后(n = 22/234)。
140例B细胞NHL/B-ALL患者中有9例(6.5%)(复发6例,进展3例)初始治疗失败。其中4例接受造血干细胞移植(HSCT)作为二线治疗,2例仅接受强化化疗,3例采用姑息治疗。9例患者中有8例死于疾病。65例淋巴细胞淋巴瘤(LBL)患者中有4例(6%)(复发2例,进展2例)治疗失败。4例患者中的2例接受了高剂量化疗后进行HSCT;另外2例仅接受化疗。4例患者中有3例死于耐药性疾病。29例间变性大细胞淋巴瘤(ALCL)患者中有9例(31%)(复发7例,进展2例)一线治疗失败。6例接受了HSCT(自体移植3例,异体移植3例),目前处于第二次完全缓解期。其他3例患者仅接受化疗,均死于肿瘤进展。
总之,早期复发和进展性B细胞肿瘤或LBL患者采用当前治疗方法预后很差,而ALCL患者通过高剂量化疗和HSCT有相当大的机会实现持续的第二次完全缓解。