Bone Marrow Transplant Unit, Cancer Center, Massachusetts General Hospital, Boston, USA.
Am J Hematol. 2011 Jul;86(7):625-7. doi: 10.1002/ajh.22041.
We retrospectively analyzed clinical outcomes of patients aged 18–59 with cytogenetically normal AML (CN-AML) and mutations in the FLT3 receptor according to type of postremission therapy. Specifically, we compared the outcomes of patients who underwent autologous SCT versus consolidation chemotherapy. There were 37 patients with an ITD mutation (7 also had a TKD mutation) and 19 patients with an isolated TKD mutation at diagnosis. In all, patients with an isolated TKD (n=16) had an improved DFS and OS (p=.031 and .014, respectively) compared to ITD patients (n=21). For individuals with an isolated TKD mutation, survival outcomes were similar irrespective of the type of postremission therapy (n=7 for SCT and 9 for chemotherapy) (p=0.97 and 0.082, respectively). However, ITD positive patients who underwent an SCT in CR1 (n=10) had an improved DFS but similar OS compared to those who received consolidation chemotherapy (n=11) (p=.05 and .27). These results suggest that high dose chemotherapy with autologous SCT may be a reasonable therapeutic choice over consolidation chemotherapy for young CN-AML patients with a FLT3ITD mutation.
我们回顾性分析了根据缓解后治疗类型,年龄在 18-59 岁、细胞遗传学正常的急性髓系白血病(CN-AML)且存在 FLT3 受体突变患者的临床结局。具体而言,我们比较了接受自体 SCT 与巩固化疗的患者的结局。在诊断时,有 37 例患者存在 ITD 突变(7 例还存在 TKD 突变),19 例患者存在单纯的 TKD 突变。所有,与 ITD 患者(n=21)相比,单纯 TKD 患者(n=16)具有更好的DFS 和 OS(p=.031 和.014)。对于存在单纯 TKD 突变的个体,无论缓解后治疗类型如何(n=7 例接受 SCT,n=9 例接受化疗),生存结局均相似(p=0.97 和 0.082)。然而,在 CR1 期接受 SCT 的 ITD 阳性患者(n=10)与接受巩固化疗的患者(n=11)相比,DFS 改善,但 OS 相似(p=.05 和.27)。这些结果表明,对于存在 FLT3-ITD 突变的年轻 CN-AML 患者,高剂量化疗联合自体 SCT 可能是比巩固化疗更合理的治疗选择。