异基因干细胞移植治疗骨髓增生异常综合征后口服地西他滨加塞达脲定的维持治疗。

IF 7.9 1区 医学 Q1 HEMATOLOGY Haematologica Pub Date : 2025-08-01 Epub Date: 2025-02-27 DOI:10.3324/haematol.2024.287177
Portia Smallbone, Terri Lynn Shigle, Oren Paslovsky, Chitra Hosing, Amin Alousi, Qaiser Bashir, Yosra Aljawai, Jeremy Ramdial, Uday Popat, Richard Champlin, Elizabeth J Shpall, Betül Oran
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引用次数: 0

摘要

疾病复发仍然是接受同种异体移植(HSCT)治疗骨髓增生异常综合征(MDS)患者的主要挑战。目前正在研究使用低甲基化药物进行维持治疗,以减轻高危患者的复发。在这项回顾性研究中,我们评估了18例hsct后高危MDS患者口服地他他比西达唑定维持治疗的安全性和有效性。66.7% (n=12)在第1天和第3天接受地西他滨-cedazuridine (35/100mg)治疗,33.3% (n=6)在第1天和第3天接受治疗。患者平均完成6个治疗周期(范围;1-20),三分之一的患者完成了所有计划周期。未观察到意外的不良事件,主要毒性是骨髓抑制。4例发生1-2级上呼吸道感染,1例发生真菌性肺炎。总体而言,患者的2年无复发生存率(RFS)中位数为66.7% (95% CI, 40.4-83.4%), 2年总生存率为72.2% (95% CI, 45.6%-87.4%),复发主要发生在TP53突变病例中。前瞻性临床试验是必要的,以确认最佳耐受剂量,改善移植结果的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Maintenance therapy with oral decitabine plus cedazuridine after allogeneic stem cell transplantation for myelodysplastic syndrome.

Disease relapse remains the primary challenge for patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT) for myelodysplastic syndromes. Maintenance therapies with hypomethylating agents are under investigation for use in mitigating relapse in high-risk patients. In this retrospective study, we assessed the safety and efficacy of oral decitabine- cedazuridine maintenance in 18 high-risk myelodysplastic syndromes patients post-HSCT. A total of 66.7% (N=12) received decitabine/cedazuridine (35/100 mg) on days 1 and 3, while 33.3% (N=6) received therapy on days 1-3. Patients completed a median of six treatment cycles (range, 1-20), with one third of patients completing all planned cycles. No unexpected adverse events were observed, with the primary toxicity being myelosuppression. Grade 1-2 upper respiratory tract infections occurred in four patients, and fungal pneumonia in one patient. Overall, patients achieved a median 2-year relapse- free survival of 66.7% (95% confidence interval [CI]: 40.4-83.4) and 2-year overall survival of 72.2% (95% CI: 45.6-87.4), with relapses occurring predominantly in TP53-mutated cases. Prospective clinical trials are essential to confirm the best tolerated dose with potential to improve transplant outcomes.

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来源期刊
Haematologica
Haematologica 医学-血液学
CiteScore
14.10
自引率
2.00%
发文量
349
审稿时长
3-6 weeks
期刊介绍: Haematologica is a journal that publishes articles within the broad field of hematology. It reports on novel findings in basic, clinical, and translational research. Scope: The scope of the journal includes reporting novel research results that: Have a significant impact on understanding normal hematology or the development of hematological diseases. Are likely to bring important changes to the diagnosis or treatment of hematological diseases.
期刊最新文献
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