Suppr超能文献

非霍奇金淋巴瘤治疗后的第二恶性肿瘤:189 例儿童和青少年的回顾性跨国研究。

Second malignant neoplasms after treatment of non-Hodgkin's lymphoma-a retrospective multinational study of 189 children and adolescents.

机构信息

Department of Pediatric Hematology and Oncology, St. Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.

Department of Pediatric Hematology and Oncology, University of Padova, Padova, Italy.

出版信息

Leukemia. 2021 Feb;35(2):534-549. doi: 10.1038/s41375-020-0841-x. Epub 2020 May 11.

Abstract

Data on the spectrum of second malignant neoplasms (SMNs) after primary childhood non-Hodgkin's lymphoma (NHL) are scarce. One-hundred-and-eighty-nine NHL patients diagnosed in a 30 years period of 1980-2010 developing an SMN were retrieved from 19 members of the European Intergroup for Childhood NHL and/or the international Berlin-Frankfurt-Münster Study Group. Five subgroups of SMNs were identified: (1) myeloid neoplasms (n = 43; 23%), (2) lymphoid neoplasms (n = 51; 27%), (3) carcinomas (n = 48; 25%), (4) central nervous system (CNS) tumors (n = 19; 10%), and (5) "other" SMNs (n = 28; 15%). In 37 patients (20%) preexisting disorders were reported with 90% having any kind of cancer predisposition syndrome (CPS). For the 189 primary NHL patients, 5-year overall survival (OS) after diagnosis of an SMN was 56 ± 4%, being worst for patients with preexisting disorders at 28 ± 8%. Five-year OS rates were 38 ± 8%, 59 ± 7%, 79 ± 8%, 34 ± 12%, and 62 ± 11%, respectively, for patients with myeloid and lymphoid neoplasms, carcinomas, CNS tumors, and "other" SMNs (p < 0.0001). Patients with SMNs after childhood NHL having a reported CPS, mostly mismatch repair disorders, carried a very poor prognosis. Moreover, although outcome was favorable in some subtypes of SMNs after childhood NHL (carcinomas, lymphoid neoplasms), other SMNs such as myeloid neoplasms and CNS tumors had a dismal prognosis.

摘要

儿童期非霍奇金淋巴瘤(NHL)后第二恶性肿瘤(SMN)的谱数据很少。从 1980 年至 2010 年的 30 年期间,19 个欧洲儿童 NHL 分组和/或国际柏林-法兰克福-明斯特研究小组的成员中检索到 189 例 NHL 患者,这些患者在诊断后发生了 SMN。确定了 5 种 SMN 亚组:(1)髓样肿瘤(n=43;23%),(2)淋巴样肿瘤(n=51;27%),(3)癌(n=48;25%),(4)中枢神经系统(CNS)肿瘤(n=19;10%)和(5)“其他”SMN(n=28;15%)。在 37 例患者(20%)中报告了先前存在的疾病,其中 90%有任何类型的癌症易感性综合征(CPS)。对于 189 例原发性 NHL 患者,诊断为 SMN 后的 5 年总生存率(OS)为 56±4%,先前存在疾病的患者最差,为 28±8%。5 年 OS 率分别为 38±8%,59±7%,79±8%,34±12%和 62±11%,分别为患有髓样和淋巴样肿瘤,癌,CNS 肿瘤和“其他”SMN 的患者(p<0.0001)。患有 SMN 的儿童 NHL 患者报告了 CPS,主要是错配修复障碍,预后非常差。此外,尽管某些类型的 SMN 后儿童 NHL(癌,淋巴样肿瘤)的预后良好,但其他 SMN,例如髓样肿瘤和 CNS 肿瘤,预后则较差。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验