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Prognostic relevance of integrated genetic profiling in acute myeloid leukemia.急性髓系白血病中综合基因分析的预后相关性。
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Chemotherapy compared with autologous or allogeneic bone marrow transplantation in the management of acute myeloid leukemia in first remission.化疗与自体或异基因骨髓移植在初治缓解期急性髓系白血病治疗中的比较。
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对于缓解期≥3 年的年轻急性髓系白血病患者,有很高的治愈可能:ECOG 在超过 1200 例患者中的经验。

Younger adults with acute myeloid leukemia in remission for ≥ 3 years have a high likelihood of cure: The ECOG experience in over 1200 patients.

机构信息

Leukemia Service, Memorial Sloan Kettering Cancer Center, Weill Cornell Medical College, New York, NY, United States.

Dana-Farber Cancer Institute, Boston, MA, United States; Harvard School of Public Health, Boston, MA, United States.

出版信息

Leuk Res. 2014 Aug;38(8):901-6. doi: 10.1016/j.leukres.2014.05.018. Epub 2014 Jun 2.

DOI:10.1016/j.leukres.2014.05.018
PMID:24986381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4326112/
Abstract

We examined 1229 younger patients with acute myeloid leukemia who achieved CR1 on Eastern Cooperative Oncology Group trials. We defined late relapse as occurring after ≥ 3 years of CR1. With median follow-up of 11.3 years, there were 14 late relapses (1.1% of CR1 patients; 3.3% of 3-year CR1 patients). Eight achieved second CR and median overall survival after late relapse was 3.2 years. Most patients tested (9/11) had a normal karyotype at diagnosis; none had new cytogenetic abnormalities at relapse. Late relapse is rare and nearly all 3-year CR1 patients are cured. If late relapse occurs, outcomes are relatively favorable.

摘要

我们研究了在东部肿瘤协作组试验中达到完全缓解 1 期(CR1)的 1229 名年轻急性髓系白血病患者。我们将晚期复发定义为在 CR1 后≥3 年发生。中位随访时间为 11.3 年,有 14 例晚期复发(CR1 患者的 1.1%;3 年 CR1 患者的 3.3%)。8 例患者获得第二次完全缓解,晚期复发后的中位总生存期为 3.2 年。大多数接受检测的患者(11 例中的 9 例)在诊断时核型正常;复发时无新的细胞遗传学异常。晚期复发较为罕见,几乎所有 3 年 CR1 患者都被治愈。如果发生晚期复发,结局相对较好。