# Efficacy of selinexor combined with subcutaneous decitabine in myeloid malignancies refractory to or relapsed after venetoclax therapy

**Authors:** 瑞华 米, 琳 王, 宁 胡, 超 李, 琳 陈, 轶轩 马, 旭东 魏

PMC · DOI: 10.3760/cma.j.cn121090-20240920-00358 · Chinese Journal of Hematology · 2025-05-01

## TL;DR

This study explores the effectiveness and safety of combining selinexor and subcutaneous decitabine in treating myeloid malignancies that have failed venetoclax therapy.

## Contribution

The study introduces a novel treatment combination for patients refractory or relapsed after venetoclax therapy.

## Key findings

- The treatment showed partial responses in some AML and MDS patients.
- Most patients experienced manageable side effects like bone marrow suppression and mild gastrointestinal reactions.
- The median duration of response was 2 months for the six effective cases.

## Abstract

维奈克拉（Ven）目前在临床应用的范围越来越广，不管是急性髓系白血病（AML）还是高危骨髓增生异常综合征（MDS），既往Ven治疗后失败的患者，再诱导方案的选择尚无统一标准。本文对10例既往Ven治疗失败的AML和伴原始细胞增多1/2型MDS患者，采用塞利尼索（Selinxor）联合皮下注射地西他滨进行治疗，对其疗效和安全性进行回顾性总结，并结合文献复习。7例AML患者中，完全缓解（CR）1例，CR伴不完全血液学恢复2例，部分缓解1例，未缓解2例，疾病进展1例；3例MDS患者中，骨髓完全缓解2例，疾病稳定1例。6例有效患者的中位缓解持续时间为2（0.5～6）个月。10例患者均出现不同程度的骨髓抑制，5例患者出现轻微胃肠道反应，但均在可控的范围内，整体耐受性良好，没有患者因治疗不良反应而死亡。表明塞利尼索联合皮下注射地西他滨为Ven治疗失败的患者提供了一种新的治疗手段，且耐受性良好。

## Linked entities

- **Chemicals:** selinexor (PubChem CID 71481097), decitabine (PubChem CID 451668), venetoclax (PubChem CID 49846579)
- **Diseases:** acute myeloid leukemia (MONDO:0015667), myelodysplastic syndrome (MONDO:0018881), AML (MONDO:0018874), MDS (MONDO:0018881)

## Full-text entities

- **Diseases:** AML (MESH:D054218), MDS (MESH:D009190), gastrointestinal reactions (MESH:D005767), deaths (MESH:D003643), myeloid malignancies (MESH:D009369)
- **Chemicals:** selinexor (MESH:C585161), Ven (MESH:C579720), DAC (MESH:D000077209)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12268302/full.md

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Source: https://tomesphere.com/paper/PMC12268302