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日本儿童和青少年血液系统恶性肿瘤的发病率和生存率(2006-2010 年):基于日本小儿血液学会登记数据。

Incidence and survival rates of hematological malignancies in Japanese children and adolescents (2006-2010): based on registry data from the Japanese Society of Pediatric Hematology.

机构信息

Clinical Research Center, National Hospital Organization Nagoya Medical Center, 4-1-1 Sannomaru, Naka-ku, Nagoya, Aichi 460-0001, Japan.

出版信息

Int J Hematol. 2013 Jul;98(1):74-88. doi: 10.1007/s12185-013-1364-2. Epub 2013 May 24.

DOI:10.1007/s12185-013-1364-2
PMID:23702913
Abstract

Neither accurate incidence nor survival data for pediatric patients with hematological malignancies (HM) have been available in Japan to date. Incidence of patients under 20 years of age, who were diagnosed with HM from 2006 to 2010, and their two-year survival rate (2y-OS) were obtained from disease registry data maintained by the Japan Society of Pediatric Hematology (JSPH). A total of 5,287 cases of HM were identified during this period. Acute lymphoblastic leukemia (ALL, 46.6%) showed the highest incidence, followed by acute myeloid leukemia (AML, 16.7%), non-Hodgkin lymphoma (NHL, 11.9%), and histiocytosis (11.8%). ALL, AML and histiocytosis were common in younger patients aged 1-4, while NHL tended to occur more frequently in older patients aged 5-14. The 2y-OS of HM was 91.6%, with that for the most common B-precursor ALL rising to 96.2%. The 2y-OS for M3 AML, lymphoblastic-B-precursor or diffuse large B cell NHL, Hodgkin lymphoma, myeloproliferative disorders, and Langerhans cell histiocytosis was >95%. There were no gender differences in prognosis, while infants (88.0%) and adolescents aged 15-19 (90.6%) tended toward a poorer prognosis. This is the first report to describe incidence and survival times from the nationwide JSPH disease registry. More precise data with longer follow-up is needed.

摘要

目前在日本,尚无儿童血液恶性肿瘤(HM)患者的确切发病率和生存数据。从 2006 年到 2010 年,从疾病登记处获得了年龄在 20 岁以下、被诊断患有 HM 的患者的发病率和他们的两年生存率(2y-OS)。在此期间,共发现 5287 例 HM。急性淋巴细胞白血病(ALL,46.6%)发病率最高,其次是急性髓细胞白血病(AML,16.7%)、非霍奇金淋巴瘤(NHL,11.9%)和组织细胞增生症(11.8%)。ALL、AML 和组织细胞增生症在 1-4 岁的年轻患者中较为常见,而 NHL 则多见于 5-14 岁的老年患者。HM 的 2y-OS 为 91.6%,最常见的 B 前体 ALL 上升至 96.2%。M3 AML、淋巴母细胞-B 前体或弥漫性大 B 细胞 NHL、霍奇金淋巴瘤、骨髓增生性疾病和朗格汉斯细胞组织细胞增生症的 2y-OS >95%。预后无性别差异,而婴儿(88.0%)和 15-19 岁青少年(90.6%)的预后较差。这是首次从全国性 JSPH 疾病登记处报告发病率和生存时间。需要更长时间随访的更精确数据。

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