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首页> 外文期刊>Oncology letters >Effect of therapy-related acute myeloid leukemia on the outcome of patients with acute myeloid leukemia
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Effect of therapy-related acute myeloid leukemia on the outcome of patients with acute myeloid leukemia

机译:治疗相关的急性髓性白血病对急性髓性白血病患者预后的影响

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摘要

Therapy-related acute myeloid leukemia (t-AML) is a rare and almost always fatal late side effect of antineoplastic treatment involving chemotherapy, radiotherapy or the two combined. The present retrospective study intended to characterize t-AML patients that were diagnosed and treated in a single referral to an oncological institution in North Portugal. Over the past 10 years, 231 cases of AML were diagnosed and treated at the Portuguese Institute of Oncology of Porto, of which 38 t-AML cases were identified. Data regarding the patient demographics, primary diagnosis and treatment, age at onset of therapy-related myeloid neoplasm, latency time of the neoplasm, cytogenetic characteristics, AML therapy and outcome were collected from medical records. A previous diagnosis with solid tumors was present in 28 patients, and 10 patients possessed a history of hematological conditions, all a lymphoproliferative disorder. Breast cancer was the most frequent solid tumor identified (39.5% of all solid tumors diagnosed). The mean latency time was 3 years. In the present study, t-AML patients were older (P<0.001) and more frequently carried cytogenetic abnormalities (P=0.009) compared with denovo AML patients. The overall survival time was observed to be significantly poorer among individuals with t-AML (P<0.001). However, in younger patients (age, <50 years) there was no difference between the overall survival time of patients with t-AML and those with de novo AML (P=0.983). Additionally, patients with promyelocytic leukemia possess a good prognosis, even when AML occurs as a secondary event (P=0.98). To the best of our knowledge, the present study is the first to evaluate t-AML in Portugal and the results are consistent with the data published previously in other populations. The present study concludes that although t-AML demonstrates a poor prognosis, this is not observed among younger patients or promyelocytic leukemia patients.
机译:与治疗有关的急性髓细胞性白血病(t-AML)是一种罕见的且几乎总是致命的抗肿瘤药物,包括化学疗法,放疗或两者结合的晚期副作用。本回顾性研究旨在描述在一次转诊至北葡萄牙一家肿瘤机构后被诊断和治疗的t-AML患者的特征。在过去的10年中,葡萄牙波尔图肿瘤研究所诊断和治疗了231例AML,其中38例t-AML病例被发现。从病历中收集有关患者人口统计学,初步诊断和治疗,与治疗有关的骨髓瘤发作的年龄,肿瘤的潜伏时间,细胞遗传学特征,AML治疗和预后的数据。先前诊断为实体瘤的患者为28例,其中10例具有血液病史,均为淋巴增生性疾病。乳腺癌是最常见的实体瘤(占诊断出的所有实体瘤的39.5%)。平均等待时间为3年。在本研究中,与denovo AML患者相比,t-AML患者年龄更大(P <0.001),且携带细胞遗传学异常的频率更高(P = 0.009)。观察到t-AML患者的总生存时间明显较差(P <0.001)。然而,在年轻患者(年龄<50岁)中,t-AML患者和从头AML患者的总生存时间没有差异(P = 0.983)。另外,即使AML是继发性事件,早幼粒细胞白血病患者也具有良好的预后(P = 0.98)。据我们所知,本研究是第一个在葡萄牙评估t-AML的研究,其结果与先前在其他人群中发表的数据一致。本研究得出结论,尽管t-AML预后较差,但在年轻患者或早幼粒细胞白血病患者中未观察到。

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