Department of Hematology/Oncology, Hospital de Pediatría Prof. Dr. Juan P. Garrahan, Buenos Aires, Argentina.
Leuk Lymphoma. 2011 Jul;52(7):1215-21. doi: 10.3109/10428194.2011.565436. Epub 2011 May 3.
Historically, t(1;19)(q23;p13.3) has been related to pre-B acute lymphoblastic leukemia (ALL) and associated with a poor prognosis. Current treatments have overcome this dismal outcome, but advantages in survival for the unbalanced group have been reported. We compared the outcome of balanced and unbalanced der(19)t(1;19) cases and also patients with t(1;19)/TCF3-PBX1 versus patients without this translocation, to assess its prognostic value. From January 1990 to December 2010, t(1;19)(q23;p13)/TCF3-PBX1 was detected in 48 cases. Patients were treated with Berlin-Frankfurt-Münster (BFM)-based protocols and classified into balanced (n = 17) and unbalanced (n = 23) groups. The probability of event-free survival (pEFS) (standard error) of patients with t(1;19)/TCF3-PBX1 was 85% (6%), for the unbalanced group 78% (10%), and 88% (8%) for the balanced. The pEFS of patients with t(1;19)/TCF3-PBX1 was significantly superior to that of patients without t(1;19)/TCF3-PBX1 (p-value <0.0001). Patients with t(1;19)/TCF3-PBX1 presented a good outcome with no differences between balanced and unbalanced subgroups. Thus, risk-adjustment therapy would not be necessary for cases with t(1;19)/TCF3-PBX1.
从历史上看,t(1;19)(q23;p13.3) 与前 B 急性淋巴细胞白血病 (ALL) 相关,并与预后不良相关。目前的治疗方法已经克服了这种糟糕的结果,但据报道,不平衡组的生存优势有所提高。我们比较了平衡和不平衡 der(19)t(1;19) 病例的结果,以及 t(1;19)/TCF3-PBX1 与没有这种易位的患者的结果,以评估其预后价值。从 1990 年 1 月至 2010 年 12 月,检测到 48 例 t(1;19)(q23;p13)/TCF3-PBX1。患者接受柏林-法兰克福-慕尼黑 (BFM)- 为基础的方案治疗,并分为平衡 (n = 17) 和不平衡 (n = 23) 组。t(1;19)/TCF3-PBX1 患者的无事件生存 (pEFS) (标准误差) 为 85% (6%),不平衡组为 78% (10%),平衡组为 88% (8%)。t(1;19)/TCF3-PBX1 患者的 pEFS 明显优于无 t(1;19)/TCF3-PBX1 患者 (p 值<0.0001)。t(1;19)/TCF3-PBX1 患者预后良好,平衡和不平衡亚组之间无差异。因此,对于 t(1;19)/TCF3-PBX1 病例,不需要进行风险调整治疗。