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Outcome of allogeneic hematopoietic stem cell transplantation for T-cell lymphoblastic leukemia/lymphoma: a single-center study
Leukemia Research ( IF 2.1 ) Pub Date : 2021-05-18 , DOI: 10.1016/j.leukres.2021.106627
Shunichiro Yasuda 1 , Yuho Najima 2 , Tatsuya Konishi 2 , Yuta Yamada 2 , Akihito Nagata 2 , Toshiaki Takezaki 2 , Satoshi Kaito 2 , Shuhei Kurosawa 2 , Masahiro Sakaguchi 2 , Kaito Harada 2 , Naoki Shingai 2 , Kosuke Yoshioka 2 , Kyoko Inamoto 2 , Junichi Mukae 2 , Takashi Toya 2 , Aiko Igarashi 2 , Hiroaki Shimizu 2 , Takeshi Kobayashi 2 , Kazuhiko Kakihana 2 , Hisashi Sakamaki 2 , Norihiko Kawamata 3 , Kazuteru Ohashi 2 , Noriko Doki 2
Affiliation  

Although the indications for allogeneic hematopoietic stem cell transplantation (allo-HSCT) as a treatment for T-cell acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) and Philadelphia chromosome (Ph)-negative B-cell acute lymphoblastic leukemia (B-ALL) are similar, few studies have compared its outcomes for T-ALL/LBL and Ph-negative B-ALL. The clinical data of 28 patients with T-ALL, 16 with T-LBL, and 99 with Ph-negative B-ALL who underwent the first allo-HSCT from 2000–2019 were retrospectively analyzed. Complete remission (CR) rates at allo-HSCT were 79%, 63%, and 75% for T-ALL, T-LBL, and B-ALL, respectively; the 3-year overall survival (OS) rates were 55.7%, 56.2%, and 58.6%, respectively (p = 0.92). Univariate analysis revealed that disease subtypes were not significantly associated with OS (B-ALL vs. T-ALL: hazard ratio [HR]=0.89, p = 0.70; T-LBL vs. T-ALL: HR=0.87, p = 0.75), and CR at allo-HSCT was the only prognostic factor for OS (HR=0.25, p < 0.001). Multivariate analysis demonstrated that CR at allo-HSCT was the only predictor of OS (HR=0.24, p < 0.001). In all three disease subtypes, patients in CR at allo-HSCT tended to have a lower cumulative incidence of relapse than did those in non-CR (T-ALL: 13.6% vs. 50.0%, p = 0.10; T-LBL: 20.0% vs. 50.0%, p = 0.21; B-ALL: 10.0% vs. 56.0%, p < 0.01). Thus, the outcomes of allo-HSCT for T-ALL/LBL were comparable to those of Ph-negative B-ALL. Irrespective of the disease subtypes, achieving CR before allo-HSCT was associated with a favorable OS. Further advances in chemotherapy before allo-HSCT and defining the optimal timing of allo-HSCT would improve the prognosis of patients with T-ALL/LBL.



中文翻译:

异基因造血干细胞移植治疗 T 细胞淋巴细胞白血病/淋巴瘤的结果:一项单中心研究

尽管异基因造血干细胞移植 (allo-HSCT) 作为治疗 T 细胞急性淋巴细胞白血病/淋巴瘤 (T-ALL/LBL) 和费城染色体 (Ph) 阴性 B 细胞急性淋巴细胞白血病 (B- ALL) 相似,但很少有研究比较其对 T-ALL/LBL 和 Ph 阴性 B-ALL 的结果。回顾性分析了 28 例 T-ALL 患者、16 例 T-LBL 患者和 99 例 Ph 阴性 B-ALL 患者的临床资料,这些患者在 2000-2019 年期间接受了第一次 allo-HSCT。allo-HSCT 中 T-ALL、T-LBL 和 B-ALL 的完全缓解 (CR) 率分别为 79%、63% 和 75%;3 年总生存 (OS) 率分别为 55.7%、56.2% 和 58.6%(p = 0.92)。单变量分析显示疾病亚型与 OS 无显着相关性(B-ALL 与 T-ALL:风险比 [HR]=0.89,p  = 0.70;T-LBL 与 T-ALL:HR=0.87,p  = 0.75 ),allo-HSCT 的 CR 是 OS 的唯一预后因素(HR=0.25,p  < 0.001)。多变量分析表明,allo-HSCT 的 CR 是 OS 的唯一预测因子​​(HR=0.24,p  < 0.001)。在所有三种疾病亚型中,allo-HSCT 的 CR 患者的累积复发率往往低于非 CR 的患者(T-ALL:13.6% vs. 50.0%,p  = 0.10;T-LBL:20.0 % 与 50.0%,p  = 0.21;B-ALL:10.0% 与 56.0%,p < 0.01)。因此,allo-HSCT 对 T-ALL/LBL 的结果与 Ph 阴性 B-ALL 的结果相当。无论疾病亚型如何,在 allo-HSCT 之前实现 CR 与有利的 OS 相关。allo-HSCT 前化疗的进一步进展和确定 allo-HSCT 的最佳时机将改善 T-ALL/LBL 患者的预后。

更新日期:2021-05-19
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