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[诱导化疗后行异基因造血干细胞移植治疗核型正常的FLT3-ITD(+)急性髓系白血病的临床研究]

[Clinical study of induction chemotherapy followed by allogeneic hematopoietic stem cell transplantation in the treatment of FLT3-ITD(+) acute myeloid leukemia with normal karyotype].

作者信息

Li F, Liu Y P, Zhu H, Hong M, Qian S X, Zhu Y, Shen W Y, Chen L J, He G S, Wu H X, Lu H, Li J Y, Miao K R

机构信息

Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2023 Mar 14;44(3):230-235. doi: 10.3760/cma.j.issn.0253-2727.2023.03.009.

DOI:10.3760/cma.j.issn.0253-2727.2023.03.009
PMID:37356985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10119728/
Abstract

To assess the efficacy of induction chemotherapy followed by allogeneic hematopoietic stem cell transplantation (allo-HSCT) in the treatment of FLT3-ITD(+) acute myeloid leukemia (AML) with normal karyotype. The clinical data of FLT3-ITD(+) AML patients with normal karyotype in the First Affiliated Hospital of Nanjing Medical University from Jan 2018 to March 2021 were retrospectively analyzed. The study included 49 patients with FLT3-ITD(+)AML, 31 males, and 18 females, with a median age of 46 (16-59) years old. All patients received induction chemotherapy, and 24 patients received sequential allo-HSCT (transplantation group) . The median follow-up time was 465 days, the one-year overall survival (OS) from diagnosis was (70.0 ± 7.4) %, and one-year disease-free survival (DFS) was (70.3±7.4) %. The one-year OS was significantly different between the transplantation group and the non-transplantation group [ (85.2 ± 7.9) % (52.6 ± 12.3) %, =0.049]. but one-year DFS [ (84.7 ± 8.1) % (55.2 ± 11.9) %, =0.061] was not. No significance was found in one-year OS between patients with low-frequency and high-frequency FLT3-ITD(+) (>0.05) . There were 12 patients with high-frequency FLT3-ITD(+) in the transplantation and the non-transplantation groups, respectively. The one-year OS [ (68.8 ± 15.7) % in the transplantation group (26.2 ± 15.3) % in the non-transplantation group, =0.027] and one-year DFS [ (45.5 ± 21.3) % in the transplantation group (27.8±15.8) % in the non-transplantation group, =0.032] were significantly different between the two groups. Induction chemotherapy followed by allo-HSCT can enhance the prognosis of FLT3-ITD(+) patients, particularly those with FLT3-ITD high-frequency mutation.

摘要

评估诱导化疗后行异基因造血干细胞移植(allo-HSCT)治疗核型正常的FLT3-ITD(+)急性髓系白血病(AML)的疗效。回顾性分析2018年1月至2021年3月南京医科大学第一附属医院核型正常的FLT3-ITD(+) AML患者的临床资料。该研究纳入49例FLT3-ITD(+)AML患者,其中男性31例,女性18例,中位年龄46(16 - 59)岁。所有患者均接受诱导化疗,24例患者接受序贯allo-HSCT(移植组)。中位随访时间为465天,诊断后1年总生存(OS)率为(70.0±7.4)%,1年无病生存(DFS)率为(70.3±7.4)%。移植组与非移植组1年OS率有显著差异[(85.2±7.9)% 对(52.6±12.3)%,P = 0.049],但1年DFS率[(84.7±8.1)% 对(55.2±11.9)%,P = 0.061]无显著差异。低频和高频FLT3-ITD(+)患者(>0.05)的1年OS率无显著差异。移植组和非移植组分别有12例高频FLT3-ITD(+)患者。两组间1年OS率[移植组为(68.8±15.7)%,非移植组为(26.2±15.3)%,P = 0.027]和1年DFS率[移植组为(45.5±21.3)%,非移植组为(27.8±15.8)%,P = 0.032]有显著差异。诱导化疗后行allo-HSCT可改善FLT3-ITD(+)患者的预后,尤其是FLT3-ITD高频突变患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/b27d94ca5e8b/cjh-44-03-230-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/6802eddc4fc3/cjh-44-03-230-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/52fda8fc6a7e/cjh-44-03-230-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/b27d94ca5e8b/cjh-44-03-230-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/6802eddc4fc3/cjh-44-03-230-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/52fda8fc6a7e/cjh-44-03-230-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33bc/10119728/b27d94ca5e8b/cjh-44-03-230-g003.jpg

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