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维奈托克联合阿扎胞苷作为不适合接受异基因干细胞移植的急性髓系白血病患者进行同种异体干细胞移植的桥接治疗

Venetoclax Plus Azacitidine as a Bridge Treatment to Allogeneic Stem Cell Transplantation in Unfit Patients with Acute Myeloid Leukemia.

作者信息

Chen Tzu-Ting, Lin Ching-Chan, Lo Wen-Jyi, Hsieh Ching-Yun, Lein Ming-Yu, Lin Che-Hung, Lin Chen-Yuan, Bai Li-Yuan, Chiu Chang-Fang, Yeh Su-Peng

机构信息

Division of Hematology and Oncology, Department of Internal Medicine, China Medical University Hospital, Taichung 404, Taiwan.

Division of Hematology and Oncology, Department of Internal Medicine, An Nan Hospital, Tainan 700, Taiwan.

出版信息

Cancers (Basel). 2024 Mar 7;16(6):1082. doi: 10.3390/cancers16061082.

DOI:10.3390/cancers16061082
PMID:38539418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10968407/
Abstract

BACKGROUND

Allogeneic hematopoietic stem cell transplantation (HSCT) is rarely recommended for unfit patients with newly diagnosed acute myeloid leukemia (AML). Patient survival can improve with venetoclax plus azacitidine (VEN plus AZA). However, the long-term outcome of this treatment strategy is still unsatisfactory. The high response and low treatment toxicity rates of patients receiving VEN plus AZA can provide an opportunity for HSCT among unfit patients. Nevertheless, the outcomes and complications of VEN plus AZA, followed by HSCT, remain unclear.

METHODS

This single-center retrospective study aimed to compare patients with newly diagnosed AML receiving VEN plus AZA as induction therapy ( = 27) to those receiving the conventional I3A7 regimen as induction therapy ( = 34).

RESULT

The 1-year overall survival, relapse, and non-relapse mortality rates in the two groups were similar. The cytogenetic risks and the hematopoietic cell transplantation-specific comorbidity index are the most significant predictive factors of overall survival.

CONCLUSION

In older patients unfit for intensive chemotherapy, a low-intensity regimen with VEN plus AZA is a suitable bridge therapy. Furthermore, allo-HSCT is feasible and can be a curative option.

摘要

背景

对于新诊断的急性髓系白血病(AML)不适合进行强化疗的患者,很少推荐进行异基因造血干细胞移植(HSCT)。维奈克拉联合阿扎胞苷(VEN联合AZA)可提高患者生存率。然而,这种治疗策略的长期疗效仍不尽人意。接受VEN联合AZA治疗的患者缓解率高且治疗毒性低,这为不适合进行HSCT的患者提供了进行HSCT的机会。尽管如此,VEN联合AZA后序贯HSCT的疗效和并发症仍不明确。

方法

本单中心回顾性研究旨在比较新诊断的AML患者接受VEN联合AZA作为诱导治疗(n = 27)与接受传统I3A7方案作为诱导治疗(n = 34)的情况。

结果

两组的1年总生存率、复发率和非复发死亡率相似。细胞遗传学风险和造血细胞移植特异性合并症指数是总生存的最显著预测因素。

结论

对于不适合进行强化疗的老年患者,VEN联合AZA的低强度方案是合适的桥接治疗。此外,异基因HSCT是可行的,并且可以作为一种治愈性选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be8d/10968407/c04ceda79538/cancers-16-01082-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be8d/10968407/8b4d5d1e7cbe/cancers-16-01082-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be8d/10968407/c04ceda79538/cancers-16-01082-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be8d/10968407/8b4d5d1e7cbe/cancers-16-01082-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be8d/10968407/c04ceda79538/cancers-16-01082-g002.jpg

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