[环磷酰胺单药治疗t细胞大颗粒淋巴细胞白血病疗效及停药后疗效维持分析]。

Q3 Medicine
L L Zhang, L Z Tian, H Pan, Z Gao, W W Li, R N Li, J Y Zhao, J B Huang, X Zhao, J P Li, N Nie, X Yu, L Y Li, Z X Kuang, L W Fang, J Shi
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引用次数: 0

摘要

目的:评价环磷酰胺治疗t细胞大颗粒淋巴细胞白血病(T-LGLL)的疗效及停药后无治疗缓解(TFR)的维持情况。方法:收集2019年6月至2024年3月在血液学血液病研究所再生医学门诊接受口服环磷酰胺治疗的37例T-LGLL患者的临床数据。分析患者临床特征、治疗效果及长期TFR。结果:37例患者中位年龄为60岁(37 ~ 86岁),男性22例(59.5%)。30例(81.1%)出现贫血,28例(75.7%)符合继发性纯红细胞发育不全诊断标准。中性粒细胞减少15例(40.5%),淋巴细胞增多11例(29.7%),血小板减少3例(8.1%)。16例患者(43.2%)未接受过免疫抑制治疗(初治组),21例患者(56.8%)免疫抑制治疗难治性或复发(难治性/复发组)。所有患者均符合治疗标准,接受50- 100mg /天的口服环磷酰胺治疗。在36例可评估的患者中,25例(69.4%)患者血液学缓解,中位时间为2.0个月(范围:0.7-7.0)。初治组和难治/复发组的缓解率无统计学差异(68.5% vs 66.7%, P=0.589)。在25例血液学缓解的患者中,24例停用环磷酰胺。中位随访时间为39.0个月(范围:8.0-56.0),中位TFR持续时间未达到。12个月TFR为(90.87±6.16)%,36个月TFR为(75.72±11.04)%。未治疗组和难治/复发组的TFR无显著差异(P=0.451)。结论:口服环磷酰胺治疗T-LGLL有效,停药后患者可维持长期TFR。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

[Analysis of treatment response and post-discontinuation efficacy maintenance of cyclophosphamide monotherapy in T-cell large granular lymphocytic leukemia].

[Analysis of treatment response and post-discontinuation efficacy maintenance of cyclophosphamide monotherapy in T-cell large granular lymphocytic leukemia].

Objective: To evaluate the efficacy of cyclophosphamide in patients with T-cell large granular lymphocytic leukemia (T-LGLL) and the maintenance of treatment-free remission (TFR) following drug discontinuation. Methods: Clinical data were collected from 37 patients with T-LGLL who received oral cyclophosphamide at the Regenerative Medicine Clinic of the Institute of Hematology and Blood Diseases Hospital between June 2019 and March 2024. Patient clinical characteristics, treatment efficacy, and long-term TFR were analyzed. Results: The median age of the 37 patients was 60 years (range: 37-86), and 22 (59.5%) were male. Anemia was observed in 30 patients (81.1%), and 28 (75.7%) met the diagnostic criteria for secondary pure red cell aplasia. Neutropenia occurred in 15 patients (40.5%), lymphocytosis in 11 (29.7%), and thrombocytopenia in three (8.1%). Sixteen patients (43.2%) had not received prior immunosuppressive therapy (treatment-naive group), while 21 patients (56.8%) were refractory to or had relapsed after immunosuppressive treatment (refractory/relapsed group). All patients met the treatment criteria and received oral cyclophosphamide at doses of 50-100 mg/day. Among the 36 evaluable patients, hematologic remission was achieved in 25 (69.4%), with a median time of 2.0 months (range: 0.7-7.0). There was no statistically significant difference in remission rates between the treatment-naive and refractory/relapsed groups (68.5% vs. 66.7%, P=0.589). Among the 25 patients who achieved hematologic remission, 24 discontinued cyclophosphamide. With a median follow-up of 39.0 months (range: 8.0-56.0), the median TFR duration was not reached. The estimated TFR rates were (90.87± 6.16) % at 12 months and (75.72±11.04) % at 36 months. No significant difference in TFR was observed between the treatment-naive and refractory/relapsed groups (P=0.451) . Conclusion: Oral cyclophosphamide is effective in the treatment of T-LGLL, and patients may maintain long-term TFR following drug discontinuation.

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