Hematology, University "Sapienza", Via Benevento 6, 00161 Rome; Italy.
Haematologica. 2010 May;95(5):837-40. doi: 10.3324/haematol.2009.009035. Epub 2010 Jan 27.
The clinical outcome of 21 adults with ALL1(MLL)/AF4 positive acute lymphoblastic leukemia enrolled in the GIMEMA LAL 2000 trial and of 25 patients entered into the previous 0496 study is reported. LAL 2000 included more intensive consolidation and transplants. Complete remission rates were 90% and 88% in the LAL 2000 and 0496 trials, respectively. Fifteen patients were transplanted (5 autologous, 10 allogeneic). At 36 months, overall and disease free survivals were 32.9%, 31.8%, 28% and 27.3%, in LAL 2000 and 0496 trials, respectively. Relapses remained the main reason of failure occurring in 10 and 16 of the 19 and 22 responding patients. In the LAL 2000 study, 4 relapses were observed before transplant. Thus, ALL1(MLL)/AF4 abnormality characterized a subset of patients with adverse prognosis in which the overall strategy adopted in the LAL 2000 study, rather than transplants per se, failed to improve the patient clinical outcome.
报道了 21 例 ALL1(MLL)/AF4 阳性急性淋巴细胞白血病成人患者在 GIMEMA LAL 2000 试验中的临床结果,以及 25 例入组前 0496 研究患者的临床结果。LAL 2000 试验包括更强化的巩固和移植。在 LAL 2000 和 0496 试验中,完全缓解率分别为 90%和 88%。15 例患者接受了移植(5 例自体,10 例异基因)。在 36 个月时,LAL 2000 和 0496 试验的总生存率和无病生存率分别为 32.9%、31.8%、28%和 27.3%。复发仍然是失败的主要原因,19 例和 22 例有反应的患者中分别有 10 例和 16 例发生复发。在 LAL 2000 研究中,有 4 例复发发生在移植前。因此,ALL1(MLL)/AF4 异常是具有不良预后的患者亚群的特征,在该亚群中,LAL 2000 研究中采用的总体策略,而不是移植本身,未能改善患者的临床结果。