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治疗相关型与初发型急性早幼粒细胞白血病患者异基因造血细胞移植的比较分析:一项回顾性研究

Comparative analysis of allogeneic hematopoietic cell transplantation in patients with therapy-related and de novo acute promyelocytic leukemia A retrospective study.

作者信息

Yamasaki Satoshi, Yanada Masamitsu, Araie Hiroaki, Fukuda Takahiro, Kanda Yoshinobu, Tashiro Haruko, Uchida Naoyuki, Ozeki Kazutaka, Ota Shuichi, Onishi Yasushi, Doki Noriko, Oyake Tatsuo, Takada Satoru, Sakurai Masatoshi, Kondo Yukio, Nakamae Hirohisa, Kawakita Toshiro, Onizuka Makoto, Atsuta Yoshiko, Konuma Takaaki

机构信息

Department of Hematology, St. Mary's Hospital, 422 Tsubukuhonmachi, Kurume, Fukuoka, 830-8543, Japan.

Department of Hematology and Oncology, Nagoya City University East Medical Center, Nagoya, Japan.

出版信息

Sci Rep. 2025 Mar 31;15(1):10967. doi: 10.1038/s41598-025-95471-3.

Abstract

Although allogeneic hematopoietic cell transplantation (HCT) is an alternative treatment for relapsed or refractory (R/R) acute promyelocytic leukemia (APL), little is known regarding the utility of allogeneic HCT for R/R therapy-related APL (t-APL). We retrospectively analyzed data for 144 patients with APL (t-APL, n = 20 and de novo APL, n = 124) who received a first allogeneic HCT between 2008 and 2020. We found no significant differences in survival between the t-APL and de novo APL groups. The 3-year overall survival (OS) rates were 53.8% in the t-APL group and 52.4% in the de novo APL group. However, as previously reported, patients without complete remission (CR) at HCT had significantly worse OS than those with CR (P = 0.004). The 3-year OS rates were 61.1% in patients with CR and 36.5% in those without CR. These findings suggest that allogeneic HCT may be considered a viable treatment option for patients with t-APL and de novo APL, with an emphasis on achieving CR before transplantation to optimize outcomes. However, clinicians should be aware of the potential for worse outcomes in male patients and those with lower performance status, highlighting the need for personalized treatment approaches and careful patient selection.

摘要

尽管异基因造血细胞移植(HCT)是复发或难治性(R/R)急性早幼粒细胞白血病(APL)的一种替代治疗方法,但关于异基因HCT用于治疗R/R治疗相关APL(t-APL)的效用知之甚少。我们回顾性分析了2008年至2020年间接受首次异基因HCT的144例APL患者(t-APL,n = 20例;初发APL,n = 124例)的数据。我们发现t-APL组和初发APL组之间的生存率无显著差异。t-APL组的3年总生存率(OS)为53.8%,初发APL组为52.4%。然而,如先前报道,HCT时未达到完全缓解(CR)的患者的OS明显差于达到CR的患者(P = 0.004)。达到CR的患者3年OS率为61.1%,未达到CR的患者为36.5%。这些发现表明,异基因HCT可被视为t-APL和初发APL患者的一种可行治疗选择,重点是在移植前实现CR以优化结局。然而,临床医生应意识到男性患者和体能状态较低患者结局较差的可能性,这突出了个性化治疗方法和仔细选择患者的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4537/11958742/688c98c1ff6e/41598_2025_95471_Fig1_HTML.jpg

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