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治疗相关性急性髓系白血病患者的临床结局。法国一家大学医院和癌症中心的真实经验。

Clinical outcome of therapy-related acute myeloid leukemia patients. Real-life experience in a University Hospital and a Cancer Center in France.

机构信息

Department of Hematology, Leon Berard Cancer Center, Lyon, France.

Department of Hematology, University Hospital Lyon Sud, Pierre Benite, France.

出版信息

Cancer Med. 2023 Aug;12(16):16929-16944. doi: 10.1002/cam4.6322. Epub 2023 Aug 7.

Abstract

BACKGROUND

t-AML occurs after a primary malignancy treatment and retains a poor prognosis.

AIMS

To determine the impact of primary malignancies, therapeutic strategies, and prognostic factors on clinical outcomes of t-AML.

RESULTS

A total of 112 adult patients were included in this study. Fifty-Five patients received intensive chemotherapy (IC), 33 non-IC, and 24 best supportive care. At t-AML diagnosis, 42% and 44% of patients presented an unfavorable karyotype and unfavorable 2010 ELN risk profile, respectively. Among treated patients (n = 88), 43 (49%) achieved complete remission: four out of 33 (12%) and 39 out of 55 (71%) in non-IC and IC groups, respectively. With a median follow-up of 5.5 months, the median overall survival (OS) and disease-free survival (DFS) for the whole population were 9 months and 6.3 months, respectively, and for the 88 treated patients 13.5 months and 8.2 months, respectively. Univariate analysis on OS and DFS showed a significant impact of high white blood cells (WBC) and blast counts at diagnosis, unfavorable karyotype and ELN classification. Multivariate analysis showed a negative impact of WBC count at diagnosis and a positive impact of chemotherapy on OS and DFS in the whole population. It also showed a negative impact of previous auto-HCT and high WBC count on OS and DFS and of IC on OS in treated patients which disappeared when we considered only confounding variables (age, previous cancers, marrow blasts, and 2010 ELN classification). In a pair-matched analysis comparing IC treated t-AML with de novo AML, there was no difference of OS and DFS between the two populations.

CONCLUSION

We showed, in this study that t-AML patients with unfavorable features represented almost half of the population. Best outcomes obtained in patients receiving IC must be balanced by known confounding variables and should be improved by using new innovative agents and therapeutic strategies.

摘要

背景

t-AML 发生在原发性恶性肿瘤治疗后,预后较差。

目的

确定原发性恶性肿瘤、治疗策略和预后因素对 t-AML 临床结局的影响。

结果

本研究共纳入 112 例成年患者。55 例患者接受强化化疗(IC),33 例患者接受非 IC 治疗,24 例患者接受最佳支持治疗。在 t-AML 诊断时,分别有 42%和 44%的患者存在不良核型和 2010 年 ELN 不良风险特征。在接受治疗的患者(n=88)中,43 例(49%)获得完全缓解:非 IC 组 4 例(12%)和 IC 组 39 例(71%)。中位随访 5.5 个月时,全人群的中位总生存期(OS)和无病生存期(DFS)分别为 9 个月和 6.3 个月,88 例接受治疗的患者分别为 13.5 个月和 8.2 个月。OS 和 DFS 的单因素分析显示,诊断时白细胞(WBC)和原始细胞计数高、核型不良和 ELN 分类具有显著影响。多因素分析显示,全人群中 WBC 计数和化疗对 OS 和 DFS 有负面影响,在接受治疗的患者中,IC 对 OS 和 DFS 有负面影响,而在考虑混杂变量(年龄、既往癌症、骨髓原始细胞和 2010 年 ELN 分类)后,该影响消失。在 IC 治疗的 t-AML 与初发 AML 的配对匹配分析中,两组患者的 OS 和 DFS 无差异。

结论

本研究表明,具有不良特征的 t-AML 患者几乎占人群的一半。接受 IC 治疗的患者获得的最佳结果必须与已知的混杂变量相平衡,并通过使用新的创新药物和治疗策略来改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8d0/10501294/9cc87781519b/CAM4-12-16929-g001.jpg

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