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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Long-term risk for subsequent leukemia after treatment for childhood cancer: a report from the Childhood Cancer Survivor Study.
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Long-term risk for subsequent leukemia after treatment for childhood cancer: a report from the Childhood Cancer Survivor Study.

机译:儿童期癌症幸存者研究报告指出,儿童期癌症治疗后发生白血病的长期风险。

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Previous investigations of cancer survivors report that the cumulative incidence of subsequent leukemia plateaus between 10 and 15 years after primary therapy. Risk beyond 15 years has not been comprehensively assessed, primarily because of lack of long-term follow-up. Among 5-year survivors from the Childhood Cancer Survivor Study cohort, 13 pathologically confirmed cases of subsequent leukemia occurred >/= 15 years after primary malignancy, with a mean latency of 21.6 years (range, 15-32 years). Seven were acute myeloid leukemia (2 acute promyelocytic leukemia with t(15;17), 2 with confirmed preceding myelodysplastic syndrome), 4 acute lymphoblastic leukemia (2 pre-B lineage, 1 T cell, 1 unknown), and 2 other. Two acute myeloid leukemia cases had the 7q- deletion. The standardized incidence ratio was 3.5 (95% confidence interval, 1.9-6.0). Median survival from diagnosis of subsequent leukemia was 2 years. This is the first description of a statistically significant increased risk of subsequent leukemia >/= 15 years from primary diagnosis of childhood cancer.
机译:先前对癌症幸存者的调查报告称,在一级治疗后的10至15年间,随后的白血病高原的累积发生率。尚未对15年以上的风险进行全面评估,这主要是因为缺乏长期随访。在儿童期癌症幸存者研究队列的5年幸存者中,有13例经病理学证实的随后的白血病病例在原发性恶性肿瘤后15年发生,≥15年,平均潜伏期为21.6年(范围为15-32年)。七例为急性髓细胞性白血病(2例t(15; 17)的急性早幼粒细胞白血病,2例确认为先前的骨髓增生异常综合征),4例急性淋巴细胞白血病(2例B前血统,1例T细胞,1例未知)和另外2例。 2例急性髓性白血病病例具有7q-缺失。标准化发生率为3.5(95%置信区间为1.9-6.0)。诊断为随后的白血病的中位生存期为2年。这是对从儿童期癌症初次诊断开始> 15年的随后白血病的统计学显着增加风险的首次描述。

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