Suppr超能文献

80岁以上初发的无红系和/或巨核系发育异常的急性髓系白血病患者在接受经典的3+7化疗后可实现完全缓解并获得更长生存期。

[Patients older than 80 years with de novo acute myeloid leukemias without erythroblastic and/or megakaryocytic dysplasia achieve complete remission and longer survival after classical chemotherapy 3 + 7].

作者信息

Lemez P, Gáliková J, Michalová K, Dvoráková D, MacWhannell A, Zemanová Z, Stejskal J

机构信息

Hematologicko-transfuzní oddĕlení Nemocnice Jihlava.

出版信息

Vnitr Lek. 2010 Jan;56(1):37-43.

Abstract

Chemotherapy in most patients with AML over 80 years of age is not recommended because their median survival is about 1 month. The aim of our study was to identify patients in this age group who might achieve complete remission with standard dose chemotherapy. We report 9 consecutive patients with de novo AML diagnosed and treated in 1992-2008. All bone marrow samples were hypercellular, classified as FAB types M2 in 2 cases, M4 in 6, and M5 in one case. Three patients opted for supportive or palliative therapy and survived 1-4 months. Six patients received standard dose chemotherapy. Two patients with a normal karyotype had resistant AML and survived 1.0 and 2.7 months; one patient with a complex karyotype died of septic shock on the 10th day of therapy. All these three patients exhibited erythroblastic and/or megakaryocytic dysplasia (EMD) at presentation (two in more than 26% erythroblasts, all three in a half or more of megakaryocytes). Three remaining patients with AML M4, a normal karyotype but without EMD, achieved complete remission in spite of co-morbidities and a poor performance status. Two of them survived 18.6 and 28 months on maintenance therapy, the third 16.5 months without it. Very elderly AML patients without EMD appear to represent a favorable prognostic biological category (single-lineage AML) that show a good response to standard dose chemotherapy.

摘要

不建议对大多数80岁以上的急性髓系白血病(AML)患者进行化疗,因为他们的中位生存期约为1个月。我们研究的目的是确定该年龄组中可能通过标准剂量化疗实现完全缓解的患者。我们报告了1992年至2008年连续诊断和治疗的9例初发AML患者。所有骨髓样本细胞增多,2例分类为FAB M2型,6例为M4型,1例为M5型。3例患者选择支持治疗或姑息治疗,存活1至4个月。6例患者接受标准剂量化疗。2例核型正常的患者患有难治性AML,存活1.0个月和2.7个月;1例核型复杂的患者在治疗第10天死于感染性休克。这3例患者在初诊时均表现为红系和/或巨核系发育异常(EMD)(2例红系原始细胞超过26%,3例巨核细胞半数或更多出现异常)。其余3例AML M4患者,核型正常但无EMD,尽管存在合并症和较差的体能状态仍实现了完全缓解。其中2例在维持治疗下存活18.6个月和28个月,第3例未接受维持治疗存活16.5个月。无EMD的高龄AML患者似乎代表了一个预后良好的生物学类别(单系AML),对标准剂量化疗反应良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验