Hassan Inaam Bashir, Kristensen Jorgen, Al Qawasmeh Khalid, Alam Arif
Department of Internal Medicine, Faculty of Medicine and Health Sciences, United Arab Emirates University, P.O. Box 17666, Al Ain, United Arab Emirates.
Department of Hematology, Oncology Tawam Hospital, Al Ain, United Arab Emirates.
Int J Hematol. 2018 Oct;108(4):390-401. doi: 10.1007/s12185-018-2478-3. Epub 2018 Jun 27.
We studied the outcome of 47 adult patients with relapsed acute leukaemia (AML = 25 and ALL = 22) treated with FLAG-mitoxantrone regimen. Median time to relapse was 10.7 months (range 1.9-27.7). Complete remission (CR2) was 60.1% which was significantly more frequent in ALL compared to AML (P = 0.049). WBC count < 100 × 10/L at initial diagnosis and time to relapse > 1 year were significantly predictor for CR2 in AML (P = 0.005 for both). Induction death was significantly higher in ALL compared to AML (P = 0.039). Median follow-up was 4.0 months (0.9-119.8) for AML and 2.1 months (range 0.6-118.1) for ALL. Nine patients underwent allogeneic stem-cell transplantation (allo-SCT). Estimated overall survival (OS) at 12 and 18 months was 60.5 and 34.6%, respectively, for AML, and 39.9 and 29.9%, respectively, for ALL. For AML patients failure to achieve CR, WBC count at initial diagnosis > 5 × 10/L and poor cytogenetic risk group was significant predictors of poor OS (P = 0.010, P = 0.025, and P = 0.015, respectively). For ALL patients failure to achieve of CR, WBC count at relapse < 5 × 10/L (CR patients) and lack of any type of consolidation therapy were significant predictor of poor OS (P < 0.001, P = 0.008, P = 0.008, respectively).
我们研究了47例复发急性白血病成年患者(急性髓系白血病[AML]=25例,急性淋巴细胞白血病[ALL]=22例)接受FLAG-米托蒽醌方案治疗的结果。复发的中位时间为10.7个月(范围1.9 - 27.7个月)。完全缓解(CR2)率为60.1%,ALL患者的CR2率显著高于AML患者(P = 0.049)。初诊时白细胞计数<100×10⁹/L以及复发时间>1年是AML患者CR2的显著预测因素(两者P均=0.005)。ALL患者的诱导死亡显著高于AML患者(P = 0.039)。AML患者的中位随访时间为4.0个月(0.9 - 119.8个月),ALL患者为2.1个月(范围0.6 - 118.1个月)。9例患者接受了异基因干细胞移植(allo - SCT)。AML患者12个月和18个月的估计总生存率(OS)分别为60.5%和34.6%,ALL患者分别为39.9%和29.9%。对于未达到CR的AML患者,初诊时白细胞计数>5×10⁹/L以及细胞遗传学风险分组不良是OS不良的显著预测因素(分别为P = 0.010、P = 0.025和P = 0.015)。对于未达到CR的ALL患者,复发时白细胞计数<5×10⁹/L(达到CR的患者)以及未进行任何类型的巩固治疗是OS不良的显著预测因素(分别为P< = <0.001、P = 0.008、P = 0.008)。