期刊文献+
共找到160篇文章
< 1 2 8 >
每页显示 20 50 100
Parametric and Non-Parametric Survival Analysis of Patients with Acute Myeloid Leukemia (AML)
1
作者 Aditya Chakraborty Chris P. Tsokos 《Open Journal of Applied Sciences》 2021年第1期126-148,共23页
<strong>Background:</strong> Acute Myeloid leukemia (AML) is the most prominent acute leukemia in adults. In the United States, we experience over 20,000 cases per year. Over the past decade, improvements ... <strong>Background:</strong> Acute Myeloid leukemia (AML) is the most prominent acute leukemia in adults. In the United States, we experience over 20,000 cases per year. Over the past decade, improvements in the diagnosis of subtypes of AML and advances in therapeutic approaches have improved the outlook for patients with AML. However, despite these advancements, the survival rate among patients who are less than 65 years of age is only 40 percent. <strong>Purpose:</strong> The purpose of the paper is to study if there exists any significant difference in the survival probabilities of male and female AML patients. Also, we want to investigate if there is any parametric probability distribution that best fits the male and female patient survival and compare the survival probabilities with the non-parametric Kaplan-Meier (KM) method. <strong>Methods:</strong> We used both parametric and non-parametric statistical methods to perform the survival analysis to assess the survival probabilities of 2015 patients diagnosed with AML.<strong> Results:</strong> We found evidence of a statistically significant difference between the mean survival time of male and female patients diagnosed with AML. We performed parametric survival analysis and found a Generalized Extreme Value (GEV) distribution best fitting the data of the survival time for male and female patients. We then estimated the survival probabilities and compared them with the frequently used non-parametric Kaplan-Meier (KM) survival method. <strong>Conclusion:</strong> The comparison between the survival probability estimates of the two methods revealed a better survival probability estimate by the parametric method than the Kaplan-Meier. We also compared the median survival time of male and female patients individually with descriptive, parametric, and non-parametric methods of analysis. The parametric survival analysis is more robust and efficient because it is based on a well-defined parametric probabilistic distribution, hence preferred over the non-parametric Kaplan-Meier estimate. This study offers therapeutic significance for further enhancement to treat patients with Acute Myeloid Leukemia. 展开更多
关键词 Acute myeloid leukemia (aml) Generalized Extreme Value (GEV) Distribution Probability Weighted Moment (PWM) Method Kaplan-Meier (KM) Estimate
下载PDF
Sunitinib Reduces Acute Myeloid Leukemia Clonogenic Cells in Vitro and Has Potent Inhibitory Effect on Sorted AML ALDH+ Cells
2
作者 Asad M. Ilyas Youssri Ahmed +7 位作者 Mamdooh Gari Mohammed H. Alqahtani Taha A. Kumosani Abdulrahman L. Al-Malki Khalid O. Abualnaja Saad H. S. Albohairi Adeel G. A. Chaudhary Farid Ahmed 《Open Journal of Blood Diseases》 2016年第1期9-16,共8页
Sunitinib is an orally administered, multi-target tyrosine kinase inhibitor that has been approved by the FDA for the treatment of renal cell carcinoma and imatinib resistant gastro-intestinal tumors. Anti-leukemic ac... Sunitinib is an orally administered, multi-target tyrosine kinase inhibitor that has been approved by the FDA for the treatment of renal cell carcinoma and imatinib resistant gastro-intestinal tumors. Anti-leukemic activity of sunitinib has been examined in early clinical trials with limited success. However, recent trials on acute myeloid leukemia (AML) patients carrying FLT3 mutations have shown promising results. Effects of sunitinib on leukemic clonogenic cells and potential leukemic stem cells have not been examined so far. We analyzed the anti-proliferative and apoptotic properties of sunitinib on AML-derived cell lines. We also tested the effect of sunitinib on AML patient derived clonogenic cells (AML-CFC), as well as flow-sorted potential leukemic progenitors. Peripheral blood or bone marrow samples were obtained from newly diagnosed AML patients and flow sorted for CD34+ CD133+ or ALDH+ cells. Umbilical cord blood derived CD34+ cells were used as normal controls. Sunitinib induced growth arrest and apoptosis in AML derived cell lines. In addition, 7 μM sunitinib induced 75% reduction of AML-CFC as compared to DMSO treated control (±6.79%;n = 4). In contrast, 7 μM sunitinib treatment of umbilical cord blood derived normal CD34+ cells showed 29% reduction in AML-CFC (±6.77%;n = 5). Treatment of ALDH+ cells sorted from 2 AML cases and CD34+ CD133+ cells from one patient showed reduction of AML-CFC on treatment with sunitinib. Our study highlighted a potent anti-proliferative and proapoptotic effect of sunitinib on AML cell lines, AML patient derived clonogenic cells and potential leukemic stem cells. 展开更多
关键词 Acute myeloid leukemia SUNITINIB Tyrosine Kinase Inhibitor aml-CFC Leukemic Stem Cells
下载PDF
Resveratrol-downregulated Phosphorylated Liver Kinase B1 Is Involved in Senescence of Acute Myeloid Leukemia Stem Cells 被引量:7
3
作者 彭丹月 宋慧 刘凌波 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2015年第4期485-489,共5页
Summary: Senescence is an important obstacle to cancer development. Engaging a senescent response may be an effective way to cure acute myeloid leukemia (AML). The aim of this study was to examine the effect of res... Summary: Senescence is an important obstacle to cancer development. Engaging a senescent response may be an effective way to cure acute myeloid leukemia (AML). The aim of this study was to examine the effect of resveratrol-downregulated phosphorylated liver kinase B1 (pLKB1) on the senescence of acute myeloid leukemia (AML) stem cells. The protein expressions of pLKB 1 and Sirtuin 1 (SIRT1), a regulator ofpLKB1, were measured in CD34+CD38-KGla cells treated with resveratrol (40 μmol/L) or not by Western blotting. Senescence-related factors were examined, including p21 mRNA tested by real-time PCR, cell morphology by senescence-associated β-galactosidase (SA-β-gal) staining, cell pro- liferation by MTT assay and cell cycle by flow cytometry. Besides, apoptosis was flow cytometrically determined. The results showed that pLKB1 was highly expressed in CD34+CD38- KGla cells, and resveratrol, which could downregulate pLKB1 through activation of SIRT1, induced senescence and apoptosis of CD34+CD38- KGla cells. It was concluded that resveratrol-downregulated pLKB1 is in- volved in the senescence of AML stem cells. 展开更多
关键词 phosphorylated liver kinase B1 (pLKB1) Sirtuin 1 (SIRT1) RESVERATROL acute myeloid leukemia (aml leukemia stem cells (LSCs) cellular senescence
下载PDF
Cutaneous Symptoms Revealing M5 Acute Myeloid Leukemia: A Case Report 被引量:1
4
作者 Sara Anane Ayad Ghanam +2 位作者 Amal Bennani Manal Azizi Noufissa Benajiba 《Journal of Cancer Therapy》 CAS 2022年第11期640-647,共8页
Cutaneous presentation revealing acute myeloid leukemia (AML) is rare, and the prognosis is poor. We report a case of an 11-month-old male who presented with cutaneous lesions present as diffuse purplish papulo-nodula... Cutaneous presentation revealing acute myeloid leukemia (AML) is rare, and the prognosis is poor. We report a case of an 11-month-old male who presented with cutaneous lesions present as diffuse purplish papulo-nodular lesions, revealing M5 acute myeloid leukemia. Skin biopsy and immunohistochemical examination, combined with routine blood analysis and bone marrow examination, contributed to early diagnosis. However, despite intensive chemotherapy treatment, the prognosis was poor and death occurred during the first months of treatment. 展开更多
关键词 Acute myeloid leukemia aml-M5 Skin Nodules Case Report CHILD
下载PDF
Rare myeloid sarcoma/acute myeloid leukemia with adrenal mass after allogeneic mobilization peripheral blood stem cell transplantation
5
作者 Ya-Fei Wang Qian Li +4 位作者 Wen-Gui Xu Jian-Yu Xiao Qing-Song Pang Qing Yang Yi-Zuo Zhang 《Cancer Biology & Medicine》 SCIE CAS CSCD 2013年第4期232-235,共4页
Myeloid sarcoma(MS)is a rare hematological neoplasm that develops either de novo or concurrently with acute myeloid leukemia(AML).This neoplasm can also be an initial manifestation of relapse in a previously treated A... Myeloid sarcoma(MS)is a rare hematological neoplasm that develops either de novo or concurrently with acute myeloid leukemia(AML).This neoplasm can also be an initial manifestation of relapse in a previously treated AML that is in remission.A 44-year-old male patient was diagnosed with testis MS in a local hospital in August 2010.After one month,bone marrow biopsy and aspiration confirmed the diagnosis of AML.Allogeneic mobilization peripheral blood stem cell transplantation was performed,with the sister of the patient as donor,after complete remission(CR)was achieved by chemotherapy.Five months after treatment,an adrenal mass was detected by positron emission tomography-computed tomography(PET-CT).Radiotherapy was performed for the localized mass after a multidisciplinary team(MDT)discussion.The patient is still alive as of May 2013,with no evidence of recurrent MS or leukemia. 展开更多
关键词 myeloid sarcoma (MS) acute myeloid leukemia (aml allogeneic hematopoietic stem cell transplantation multidisciplinary team (MDT)
下载PDF
Analyses of therapeutic effects using rludarabine and cytarabine on acute myeloid leukemia at different stages during treatment
6
作者 Na Xu Xiaoli Liu +3 位作者 Qjngfeng Du Lingyun Ouyang Zhi Liu Lijun Hou 《The Chinese-German Journal of Clinical Oncology》 CAS 2009年第6期349-352,共4页
Objective: To evaluate the therapeutic effect of the fludarabine and cytarabine (FA) regimen on acute myeloid leukemia (AML) at different phases during treatment. Methods: A total of 185 patients with AML were divided... Objective: To evaluate the therapeutic effect of the fludarabine and cytarabine (FA) regimen on acute myeloid leukemia (AML) at different phases during treatment. Methods: A total of 185 patients with AML were divided into 4 groups based on the outcome of previous treatments. Patients in Group 1 had no remission after the first course of induction chemotherapy (n = 55). Patients in Group 2 had no remission after no less than two courses of induction chemotherapy (n = 41). Patients in Group 3 had early relapse (n = 40). Patients in Group 4 had late relapse (n = 49). Patients in groups 2, 3 and 4 had refractory AML or AML with relapse. We assessed the efficacy and toxicity of FA combination chemotherapy in each of these 4 groups. Results: The complete remission (CR) rates of Groups 1, 2, 3 and 4 were 74.5% (41/55), 45.9% (19/41), 17.5% (7/40) and 38.8% (19/49), respectively. The CR rate was higher in Group 1 than in the other 3 groups (34.6%, 45/130) (P = 0.000). A significant correlation was found between CR rate and the number of chemotherapeutic courses (P = 0.023). The main adverse reactions included bone marrow suppression and secondary infection. Conclusion: FA regimen is a good choice for patients with AML, especially those who have failed to achieve CR after the first course of induction chemotherapy. 展开更多
关键词 acute myeloid leukemia (aml FLUDARABINE CYTARABINE
下载PDF
A Construction of Object Detection Model for Acute Myeloid Leukemia
7
作者 K.Venkatesh S.Pasupathy S.P.Raja 《Intelligent Automation & Soft Computing》 SCIE 2023年第4期543-560,共18页
The evolution of bone marrow morphology is necessary in Acute Mye-loid Leukemia(AML)prediction.It takes an enormous number of times to ana-lyze with the standardization and inter-observer variability.Here,we proposed ... The evolution of bone marrow morphology is necessary in Acute Mye-loid Leukemia(AML)prediction.It takes an enormous number of times to ana-lyze with the standardization and inter-observer variability.Here,we proposed a novel AML detection model using a Deep Convolutional Neural Network(D-CNN).The proposed Faster R-CNN(Faster Region-Based CNN)models are trained with Morphological Dataset.The proposed Faster R-CNN model is trained using the augmented dataset.For overcoming the Imbalanced Data problem,data augmentation techniques are imposed.The Faster R-CNN performance was com-pared with existing transfer learning techniques.The results show that the Faster R-CNN performance was significant than other techniques.The number of images in each class is different.For example,the Neutrophil(segmented)class consists of 8,486 images,and Lymphocyte(atypical)class consists of eleven images.The dataset is used to train the CNN for single-cell morphology classification.The proposed work implies the high-class performance server called Nvidia Tesla V100 GPU(Graphics processing unit). 展开更多
关键词 Acute myeloid leukemia(aml) convolutional neural network(CNN) and nvidia tesla v100 gpu
下载PDF
地西他滨联合改良CAG方案治疗AML1-ETO阳性复发、难治急性髓系白血病的临床研究 被引量:32
8
作者 靖彧 朱成英 +5 位作者 张琪 牛建花 杨华 刘世研 朱海燕 于力 《中国实验血液学杂志》 CAS CSCD 北大核心 2014年第5期1245-1250,共6页
本研究旨在分析AML1-ETO阳性复发、难治急性髓系白血病的临床特点及地西他滨联合改良CAG方案对该类白血病患者的治疗效果及副作用。回顾性分析2013年1月至8月5例AML1-ETO阳性复发、难治急性髓系白血病,并分析临床特点,包括年龄、性别、... 本研究旨在分析AML1-ETO阳性复发、难治急性髓系白血病的临床特点及地西他滨联合改良CAG方案对该类白血病患者的治疗效果及副作用。回顾性分析2013年1月至8月5例AML1-ETO阳性复发、难治急性髓系白血病,并分析临床特点,包括年龄、性别、初诊时伴随症状、外周血和骨髓特点等;同时分析地西他滨联合改良的CAG方案对该类患者的治疗效果和副作用。5例患者中复发2例,难治合并复发3例,初治时白细胞中位数12.55(7.8-66.55)×109/L、血小板中位数44(20-72)×109/L,血红蛋白中位数110(77-128)g/L、乳酸脱氢酶中位数312.9(123.6-877.8)μ/L。治疗结果表明:经过1个疗程地西他滨联合改良的CAG方案治疗后4例完全缓解,1例未缓解,总缓解率为80%;治疗的副作用主要为骨髓抑制,1例未缓解经FLAG方案治疗后在移植动员过程中突发心衰死亡。结论:初步结果表明AML1-ETO阳性复发、难治急性髓系白血病经本方案治疗后,其缓解率比较高、并发症较少,值得进一步研究和在临床推广应用。 展开更多
关键词 急性髓系白血病 复发难治急性髓系白血病 aml-ETO阳性急性髓系白血病 地西他滨 改良的CAG方案
下载PDF
AML-1/ETO基因相关的AML-M_2型白血病免疫表型分析 被引量:9
9
作者 张建军 杜欣 +2 位作者 黄志新 苏健华 周茂华 《中国实验血液学杂志》 CAS CSCD 2007年第2期378-381,共4页
本研究探讨AML/ETO基因重排的FAB分型为AML-M2患者的骨髓免疫表型的特征和预测性,以及与急性早幼粒白血病(APL)的区别。应用流式细胞术分析17例经荧光原位杂交(FISH)检测AML-1/ETO融合基因阳性、FAB分型为AML-M2(M2/ETO+)患者骨髓的免... 本研究探讨AML/ETO基因重排的FAB分型为AML-M2患者的骨髓免疫表型的特征和预测性,以及与急性早幼粒白血病(APL)的区别。应用流式细胞术分析17例经荧光原位杂交(FISH)检测AML-1/ETO融合基因阳性、FAB分型为AML-M2(M2/ETO+)患者骨髓的免疫表型,并与34例AML-1/ETO阴性、FAB分型AML-M3、临床诊断为APL患者进行了比较。结果发现,17例M2/ETO+患者骨髓中均可见一群(15.89%-68.53%)原始细胞和一群SSC较高异质性的粒细胞。原始细胞表达干细胞相关抗原CD34、HLA-DR和髓系抗原CD33、CD13、MPO。在M2/ETO+患者中CD33表达强度显著低于APL患者(P<0.001),HLA-DR、CD19和CD34+CD56+共表达的阳性率均显著高于APL患者(P<0.001),而CD9的表达率则显著低于APL患者(P<0.001)。M2/ETO+患者粒细胞表达分化的髓系抗原CD11b和CD15,并可分为CD15+CD11b-和CD15+CD11b+两群,而成熟的粒细胞标志CD10均为阴性,与早幼粒细胞的表达图形相似。17例(100%)M2/ETO+患者的粒细胞均表达CD56,显著高于M3患者(6/34例,17.56%)。结论:AML-1/ETO基因重排的AML-M2型(FAB分型)白血病具有独特的免疫表型,对其基因重排有较高的预测性。应用多参数免疫分型技术可较容易地将M2/ETO+亚型白血病与APL鉴别。 展开更多
关键词 aml一1/ETO融合基因 急性髓性白血病 aml—M2型白血病 免疫表型
下载PDF
地西他滨联合CAG方案治疗AML1-ETO^+ AML的临床效果 被引量:16
10
作者 刘强 费小明 《中国实验血液学杂志》 CAS CSCD 北大核心 2016年第5期1334-1338,共5页
目的:观察AML1-ETO^+复发/难治急性髓系白血病患者经地西他滨联合CAG方案治疗的临床治疗效果。方法:收集2015年6月至2016年1月我院收治的8例AML1-ETO+复发/难治急性髓系白血病患者临床资料,分析患者入院一般资料及初诊伴随症状、骨髓特... 目的:观察AML1-ETO^+复发/难治急性髓系白血病患者经地西他滨联合CAG方案治疗的临床治疗效果。方法:收集2015年6月至2016年1月我院收治的8例AML1-ETO+复发/难治急性髓系白血病患者临床资料,分析患者入院一般资料及初诊伴随症状、骨髓特点等,同时分析患者经地西他滨联合CAG方案治疗的临床观察指标及不良反应。结果:8例患者中复发1例,难治合并复发7例,初治时白细胞23.57(7.5-65.29)×10~9/L、血小板40(19-69)×10~9/L,血红蛋白107(79-131)g/L、乳酸脱氢酶313.5(124.1-865.9)U/L。8例患者经地西他滨联合CAG方案1个疗程治疗后7例症状完全缓解,1例症状未缓解,总缓解率为87.5%;本方案的不良反应为骨髓抑制,1例症状未缓解患者经FLAG方案治疗后突发心衰死亡。结论:AML1-ETO^+复发/难治急性髓系白血病患者经地西他滨联合CAG方案治疗后,各临床观察指标较理想,缓解率较高,并发症较少。 展开更多
关键词 复发/难治急性髓系白血病 aml-ETO+急性髓系白血病 地西他滨 CAG方案
下载PDF
CD56表达对伴有AML/ETO的急性髓系白血病患者预后影响的分析 被引量:6
11
作者 赵娟 张海涛 《中国实验血液学杂志》 CAS CSCD 北大核心 2020年第1期63-67,共5页
目的:探讨CD56表达对伴有AML/ETO的急性髓系白血病患者的预后影响。方法:回顾性分析西安交通大学第一附属医院2012年1月至2016年12月60例伴有AML/ETO的初发AML患者临床资料,比较CD56^+阳性与阴性组的临床特征。结果:CD56^+与CD56^-2组... 目的:探讨CD56表达对伴有AML/ETO的急性髓系白血病患者的预后影响。方法:回顾性分析西安交通大学第一附属医院2012年1月至2016年12月60例伴有AML/ETO的初发AML患者临床资料,比较CD56^+阳性与阴性组的临床特征。结果:CD56^+与CD56^-2组患者在1个疗程诱导缓解治疗后CR率、1年复发率和基因突变率方面有明显的差异(P<0.05);CD56^+患者RFS和OS均低于CD56^-患者,差异有统计学意义(P<0.05)。结论:CD56^+可能是伴有AML/ETO的AML患者预后差的重要因素。 展开更多
关键词 CD56 急性髓细胞白血病 aml/ETO 临床预后
下载PDF
地西他滨联合CAG化疗方案对AML老年患者IGF-1和VEGF水平及免疫功能的影响 被引量:4
12
作者 雷丽华 张开基 +4 位作者 任丽蓉 任倩 费晓莉 侯铮 林娟 《贵州医科大学学报》 CAS 2020年第12期1469-1473,共5页
目的:分析地西他滨联合CAG化疗方案对急性髓细胞性白血病(AML)老年患者胰岛素样生长因子-1(IGF-1)、血管内皮生长因子(VEGF)水平及免疫功能的影响。方法:选取血液科收治的AML老年患者120例,随机均分为对照组(CAG化疗方案)和观察组(地西... 目的:分析地西他滨联合CAG化疗方案对急性髓细胞性白血病(AML)老年患者胰岛素样生长因子-1(IGF-1)、血管内皮生长因子(VEGF)水平及免疫功能的影响。方法:选取血液科收治的AML老年患者120例,随机均分为对照组(CAG化疗方案)和观察组(地西他滨联合CAG化疗方案),分别抽取2组患者治疗前和治疗14 d时的空腹清晨静脉血5 mL,采用流式细胞仪检测全血CD3+、CD4+及CD8+,并计算CD4+/CD8+比值;采用酶联免疫吸附法检测血清IGF-1和VEGF水平,比较2组患者治疗14 d时血液学、肝肾功能、胃肠道及感染发生情况和治疗疗效。结果:治疗14 d时,2组患者全血CD3+、CD4+、CD4+/CD8+I及IGF-1均较治疗前升高、且观察组高于对照组(P<0.05),血清VEGF均较治疗前较低、且观察组低于对照组(P<0.05);观察组患者治疗后血液学不良反应、肝肾功能、胃肠道不良反应及感染发生率与对照组比较差异均无统计学意义(P>0.05);观察组患者治疗后总有效率高于对照组(P<0.05)。结论:地西他滨联合CAG化疗方案可更好地降低AML老年患者血清VEGF水平,升高血清IGF-1水平,抑制疾病进展,改善患者免疫功能,同时不会增加用药后的不良反应。 展开更多
关键词 T淋巴细胞 血管内皮生长因子类 胰岛素样生长因子Ⅰ 急性髓细胞性白血病 地西他滨 CAG化疗方案 免疫功能
下载PDF
一例AML-M2患者初发和缓解期转录组测序SNV结果比较分析 被引量:1
13
作者 高攀科 曹祥山 刘琰 《中国实验血液学杂志》 CAS CSCD 北大核心 2014年第3期666-670,共5页
本研究旨在进一步阐明急性髓系白血病的发病机制,筛选新的肿瘤特异性突变。利用高通量测序的方法对1例初诊的部分分化型急性髓系白血病(AML-M2)患者发病期及缓解期外周血样本进行转录组测序,通过对初诊时和缓解后表达基因的比较,筛选可... 本研究旨在进一步阐明急性髓系白血病的发病机制,筛选新的肿瘤特异性突变。利用高通量测序的方法对1例初诊的部分分化型急性髓系白血病(AML-M2)患者发病期及缓解期外周血样本进行转录组测序,通过对初诊时和缓解后表达基因的比较,筛选可能与白血病发生相关的单核苷酸变异(SNV)。结果表明:Reads在基因上分布均匀,覆盖完整,检测到大部分基因的表达。通过对SNV的筛选,共检测到29881个基因突变,包括28113个种系突变和752个体突变,其中编码区获得性突变11个(P<0.05),包括ZRSR1、MLXIP、TLN1、LAP3、HK3。结论:高通量测序作为一种无偏的检测基因突变的新方法,可以发现肿瘤相关新突变。MLXIP可能是AML M2新的分子标志物。 展开更多
关键词 高通量测序 单核苷酸变异 急性髓系白血病 aml—M2 转录组测序技术
下载PDF
CCLG-AML-2015方案治疗儿童急性髓系白血病的临床分析 被引量:9
14
作者 王平 熊昊 +7 位作者 李建新 王卓 杨李 陶芳 陈智 杜宇 张爱萍 罗琳琳 《中国实验血液学杂志》 CAS CSCD 北大核心 2022年第2期373-380,共8页
目的:分析CCLG-AML-2015方案治疗初诊儿童急性髓系白血病(AML)的临床效果。方法:总结2015年8月至2019年9月武汉儿童医院血液肿瘤科60例初诊AML患儿的临床资料,回顾性分析使用CCLG-AML-2015方案(以下简称2015方案)化疗的效果,对照组为本... 目的:分析CCLG-AML-2015方案治疗初诊儿童急性髓系白血病(AML)的临床效果。方法:总结2015年8月至2019年9月武汉儿童医院血液肿瘤科60例初诊AML患儿的临床资料,回顾性分析使用CCLG-AML-2015方案(以下简称2015方案)化疗的效果,对照组为本中心2010年2月-2015年7月使用AML-2006方案(以下简称2006方案)治疗的42例AML患儿。结果:2015方案组与2006方案组患者在性别、初诊年龄、危险度分层均无统计学差异(P>0.05)。2015方案组诱导1个疗程化疗后骨髓细胞学完全缓解率(CR,84.7%vs 73.1%,P=0.155)、微小残留病灶检测(MRD)阴性(42.3%vs 41.4%,P=0.928)与2006方案组比较无统计学差异,诱导2个疗程后骨髓细胞学CR(98.1%vs 80.6%,P=0.004)及MRD阴性(83.3%vs 52.8%,P=0.002)高于AML-2006方案组。2015方案组5年总生存(OS)率(62.3%±6.4%vs 20.6%±6.4%,P=0.001),5年无病生存(EFS)率(61.0%±6.4%vs 21.0%±6.4%,P=0.001)均优于2006方案组。2015方案组高危患儿接受移植5年OS、EFS均明显优于高危非移植患儿(86.6%±9.0%vs 26.7%±11.4%,P=0.000;86.6%±9%vs 26.7%±11.4%,P=0.000)。结论:2015方案较2006方案可提高诱导2个疗程后CR率,高危患儿接受造血干细胞移植可显著改善预后。 展开更多
关键词 急性髓系白血病 儿童 CCLG-aml-2015 造血干细胞移植 预后
下载PDF
NPM1突变阳性AML患者化疗后早期微小残留病水平与预后的关系 被引量:5
15
作者 王丽娟 李弹弹 +2 位作者 孙玲 吴希锋 宋强 《中国实验血液学杂志》 CAS CSCD 北大核心 2020年第1期93-97,共5页
目的:分析NPM1基因突变阳性的急性髓系白血病(AML)患者经化疗后,早期微小残留病水平与患者预后状况的相关性。方法:收集本院112例NPM1基因突变阳性的初诊成人AML患者的临床资料,分析患者化疗后NPM1基因突变转录本水平与患者预后状况的... 目的:分析NPM1基因突变阳性的急性髓系白血病(AML)患者经化疗后,早期微小残留病水平与患者预后状况的相关性。方法:收集本院112例NPM1基因突变阳性的初诊成人AML患者的临床资料,分析患者化疗后NPM1基因突变转录本水平与患者预后状况的相关性。结果:在112例AML患者中,初诊时NPM1基因突变转录本中位水平为83.68%(5.86%-486.57%),FLT3-ITD突变阳性44例(39.29%),染色体核型异常22例(19.64%),完全缓解96例(85.71%);多因素Logistic回归分析结果发现,初始诱导治疗方案和白细胞计数(WBC)与完全缓解密切相关(P<0.05)。在112例患者中,中位随访时间为22(3-36)个月,3年总生存率为66.07%;多因素Logistic回归分析发现,在初次获得完全缓解时微小残留病高水平、巩固治疗后微小残留病高水平是患者总生存期的独立危险因素(P<0.05)。结论:在NPM1基因突变阳性的成人AML患者中,化疗后微小残留病早期高水平与患者预后不良密切相关。 展开更多
关键词 急性髓系白血病 微小残留病 NPM1基因突变 化疗 预后
下载PDF
非血缘脐血移植治疗高危难治AML1-ETO阳性急性髓细胞白血病的疗效分析 被引量:2
16
作者 任佳荣 朱小玉 +9 位作者 汤宝林 皖湘 童娟 张磊 张旭涵 宋闿迪 姚雯 孙光宇 刘会兰 孙自敏 《中国实验血液学杂志》 CAS CSCD 北大核心 2019年第4期1246-1252,共7页
目的:分析非血缘脐血移植(UCBT)治疗AML1-ETO^+急性髓系白血病(AML)患者中的植入、移植物抗宿主病(GVHD)及生存等临床结果。方法:2010年7月-2018年4月,单中心进行单份UCBT治疗高危难治性AML1-ETO+AML患者45例。对所有患者均采用清髓性... 目的:分析非血缘脐血移植(UCBT)治疗AML1-ETO^+急性髓系白血病(AML)患者中的植入、移植物抗宿主病(GVHD)及生存等临床结果。方法:2010年7月-2018年4月,单中心进行单份UCBT治疗高危难治性AML1-ETO+AML患者45例。对所有患者均采用清髓性预处理方案,应用环孢素A(CSA)联合吗替麦考酚酯(MMF)预防GVHD。结果:输注脐血总有核细胞(TNC)中位值为5.21(1.96-12.68)×10^7/kg受者体重,CD34+细胞数为5.61(0.56-15.4)×105/kg受者体重。42d中性粒细胞及120d血小板植入率分别为95.6%及86.7%,中性粒细胞绝对计数(ANC)>0.5×10^9/L和血小板≥20×10^9/L的中位时间分别为移植后16(12-18)d和37(17-140)d。移植后100dⅠ-Ⅳ度急性GVHD(aGVHD)的累积发生率为48.9%(95%CI33.5%-62.6%),Ⅱ-Ⅳ度aGVHD12例(33.3%)(95%CI20%-47.2%),Ⅲ-Ⅳ度aGVHD8例(20%)(95%CI9.8%-32.8%)。40例患者中5例于移植后100d出现慢性GVHD(cGVHD),其中4例为局限性,1例为广泛性。3例复发,2年累积复发率为9.5%(95%CI2.4%-22.8%)。中位随访时间23.5(0.9-89.67)个月,死亡10例,2年无病生存率(DFS)及总生存率(OS)分别72.7%和75.5%,多因素分析结果显示Ⅲ-Ⅳ度急性GVHD影响总生存。结论:UCBT是高危难治性AML1-ETO+AML的一种有效解救治疗措施。 展开更多
关键词 非血缘脐血移植 急性髓细胞白血病 aml1-ETO阳性
下载PDF
FLT3^-的AML细胞对PKC412体外敏感性的初步研究
17
作者 王胤颖 刘聪艳 +3 位作者 张维 贺景娟 苏力 孙婉玲 《中国实验血液学杂志》 CAS CSCD 北大核心 2017年第5期1350-1355,共6页
目的:探索PKC412(midostaurin,米哚妥林)在FLT3^-AM L患者治疗中的价值。方法:无菌采集21例FLT3^-的初治AML患者骨髓血或外周血肝素抗凝,应用密度梯度离心法分离单个核细胞,采用三磷酸腺苷生物荧光肿瘤体外药敏检测技术(ATP bioluminesc... 目的:探索PKC412(midostaurin,米哚妥林)在FLT3^-AM L患者治疗中的价值。方法:无菌采集21例FLT3^-的初治AML患者骨髓血或外周血肝素抗凝,应用密度梯度离心法分离单个核细胞,采用三磷酸腺苷生物荧光肿瘤体外药敏检测技术(ATP bioluminescence-tumor chemosensitivity assay,ATP-TCA)测定白血病细胞体外对8种浓度PKC412的敏感性,并分析其体外药敏结果、危险度分层及临床疗效三者之间的关系。结果:21例AML患者的白血病细胞在体外对PKC412的反应不相同,体外敏感率为42.9%,体外敏感浓度为1-5μmol/L。PKC412体外药敏结果与患者危险度分层之间无相关性,与临床疗效之间也无相关性。低、中危组患者的存活率著优于高危组患者(P=0.015)。结论:PKC412可能是FLT3^-初治AML的有效治疗手段之一;白血病细胞对PKC412的敏感性有可能成为判断PKC421疗效的独立预测指标。 展开更多
关键词 急性髓系白血病 FLT3-急性髓系白血病 PKC412 药敏检测
下载PDF
抗AML特异性T细胞的诱导、扩增及功能研究
18
作者 刘念 秦效英 江滨 《中国免疫学杂志》 CAS CSCD 北大核心 2009年第10期912-915,共4页
目的:体外培养抗急性髓性白血病(AML)细胞的特异性T细胞,并研究其生物学特性和功能。方法:取12例AML患者的外周血或骨髓,分离单个核细胞(MNCs)后接种于96孔板,加入组合细胞因子,诱导AML细胞来源的树突细胞(DC)生成,培养过程中用倒置显... 目的:体外培养抗急性髓性白血病(AML)细胞的特异性T细胞,并研究其生物学特性和功能。方法:取12例AML患者的外周血或骨髓,分离单个核细胞(MNCs)后接种于96孔板,加入组合细胞因子,诱导AML细胞来源的树突细胞(DC)生成,培养过程中用倒置显微镜进行形态学观察,并在7天后用流式细胞术检测免疫学表型。培养第7天时将组合细胞因子培养液换为高IL-2因子培养液,促进抗AML细胞的特异性T细胞生长,培养4~5周后测定T细胞表型,并采用乳酸脱氢酶(LDH)释放法进行T细胞杀伤活性测定。结果:AML细胞经组合细胞因子诱导后,大部分细胞呈现树突状细胞的典型形态,而且CD80、CD86和HLA-DR较培养前明显上调(P<0.01);高IL-2因子培养液培养4~5周后,82.5%的培养孔内CD3+ T细胞占孔内细胞总数99%以上;LDH释放法进行T细胞杀伤试验表明培养出的T细胞对自体AML有较强的杀伤作用,而对异体AML细胞杀伤力弱。结论:在体外可以成功诱导出抗AML细胞的特异性T细胞,且培养出的T细胞对自体AML细胞有特异性杀伤作用。 展开更多
关键词 急性髓性白血病 树突细胞 T淋巴细胞 免疫治疗
下载PDF
Time Elapsed from AML Diagnosis to Induction Chemotherapy Affects Overall Survival
19
作者 Luis Arthur Flores Pelloso Sandra Serson Rohr +1 位作者 Mihoko Yamamoto Maria de Lourdes LFerrari Chauffaille 《Journal of Cancer Therapy》 2013年第5期957-960,共4页
We aimed to study the effect of elapsed time from AML diagnosis to treatment (TDT) on OS in a group of patients from public Hospital in Brazil. 41 AML (23 M, 18 F, 41 yrs, 18 - 84 yrs, from 2001 to 2004). There were 3... We aimed to study the effect of elapsed time from AML diagnosis to treatment (TDT) on OS in a group of patients from public Hospital in Brazil. 41 AML (23 M, 18 F, 41 yrs, 18 - 84 yrs, from 2001 to 2004). There were 38 de novo AML and 3 secondary, median TDT was 6 days (range 1 - 82 d);the young ones?were treated earlier than old ones (TDT 4 days vs 11, p = 0.07). Longer TDT (>10 d) was associated with worse CR rates (p = 0.02) and OS (p = 0.04). When patients were categorized into TDT from 1 - 4 d (I) vs >5 (II), those from I presented better OS than II (p = 0.004). When TDT was longer than 7 days OS decreased even more. Hb was higher in patients with TDT I vs II (8.3 vs 7.5 g/dL, p = 0.03) but WBC (p = 0.34) and platelet count (p = 0.75) were not different. Patients with TDT of 10 d were younger than TDT > 10 d (median age 41 vs 70 yrs, p = 0.001). The OS was 15.1% in 2 yrs and 8.6% in 7 yrs. Our data suggest longer TDT, when analyzed continuously, predicted for lower CR rates and OS rates. 展开更多
关键词 Acute myeloid leukemia KARYOTYPE Time to Induction Elderly aml Prognostic Factors
下载PDF
维奈克拉方案治疗复发/难治性急性髓系白血病的临床研究
20
作者 雷芳 费小明 +3 位作者 杨元林 季艳萍 余先球 汤郁 《中国肿瘤临床》 CAS CSCD 北大核心 2024年第7期348-353,共6页
目的:评价维奈克拉(venetoclax,VEN)快速剂量递增、最长治疗时间为14天,联合低剂量阿糖胞苷(low-dose cytarabine,LDAC)方案挽救治疗复发/难治性急性髓系白血病(relapsed/refractory acute myeloid leukemia,R/RAML)的安全性和有效性。... 目的:评价维奈克拉(venetoclax,VEN)快速剂量递增、最长治疗时间为14天,联合低剂量阿糖胞苷(low-dose cytarabine,LDAC)方案挽救治疗复发/难治性急性髓系白血病(relapsed/refractory acute myeloid leukemia,R/RAML)的安全性和有效性。方法:回顾性分析2018年10月至2023年11月于江苏大学附属医院接受VEN+LDAC方案挽救治疗的16例R/R AML患者,所有患者既往均未接受过含VEN方案治疗。该方案VEN的剂量第1天为200 mg,其后均为400 mg固定剂量;LDAC 20 mg/m^(2)/d皮下注射。患者在治疗第8天复查骨髓,根据骨髓增生情况决定总疗程为10天还是14天。所有患者均不给予VEN单药治疗。有治疗反应的患者采用相同方案维持直到疾病进展或移植。结果:本研究纳入的R/R AML患者,中位随诊时间为27.5个月。治疗期间未发生有临床表现的肿瘤溶解综合症(tumor lysis syndrome,TLS)。治疗后总反应率(overall response rate,ORR)为68.75%,其中4例达完全缓解(complete response,CR),1例达血液学未恢复的完全缓解(CR with incomplete hematologic recovery,CRi),6例达部分缓解(partial response,PR)。达最佳疗效的治疗周期中位数为1个周期。中位总生存期(overall survival,OS)为5.8(0.5~47.2)个月,中位无进展生存期(progression-free survival,PFS)为22.2(7.3~42.9)个月。发生的不良反应主要为3~4级的血液学不良事件和感染。结论:本研究根据治疗第8天骨髓复查结果调整用药天数的VEN+LDAC方案,对于既往没有接受过含VEN方案治疗的R/R AML患者有较好的安全性和有效率。即使14天的VEN+LDAC治疗也是安全的。 展开更多
关键词 维奈克拉 低剂量 阿糖胞苷 复发/难治性急性髓系白血病
下载PDF
上一页 1 2 8 下一页 到第
使用帮助 返回顶部