Jones G L, Taylor P R A, Windebank K P, Hoye N A, Lucraft H, Wood K, Angus B, Proctor S J
Newcastle upon Tyne NHS Foundation Trust, Newcastle upon Tyne NE1 4LP, UK.
Br J Cancer. 2007 Jul 2;97(1):29-36. doi: 10.1038/sj.bjc.6603809. Epub 2007 May 29.
The aim was to assess outcome in a population-based cohort of adolescents with Hodgkin's lymphoma (HL) diagnosed in the UK's northern region over a 10-year period. Among a population of 3.09 million, 55 of 676 patients (8%) diagnosed with HL were aged 13-19. Seven had nodular lymphocyte-predominant HL, 48 classical HL (cHL). Of the latter, 36 were >or=16 years. Application of the Scottish and Newcastle Lymphoma Group (SNLG) prognostic index meant 21 patients were considered high risk (index >or=0.5). They received PVACEBOP multi-agent chemotherapy as primary therapy. Standard risk patients (SNLG index <0.5) were treated with standard ChlVPP or ABVD chemotherapy+/-radiotherapy. Scottish and Newcastle Lymphoma Group indexing is not valid for patients under 16. Twelve patients therefore received UKCCSG protocols (n=8), ABVD plus radiotherapy (n=2), or PVACEBOP (n=2). Forty-six patients with cHL (96%) achieved complete remission. Seven patients relapsed but all entered complete remission after salvage therapy. Five patients died: three of HL, one in an accident and one of disseminated varicella complicating cystic fibrosis. Five- and 10-year overall survival was 93 and 86%, respectively; disease-specific survival was 95 and 92%. The data suggest that older adolescents with high-risk HL require intensive protocols as primary therapy to secure optimal outcome.
目的是评估在英国北部地区10年间确诊的霍奇金淋巴瘤(HL)青少年人群队列的预后情况。在309万人口中,676例确诊为HL的患者中有55例(8%)年龄在13 - 19岁。其中7例为结节性淋巴细胞为主型HL,48例为经典型HL(cHL)。后者中,36例年龄≥16岁。应用苏格兰和纽卡斯尔淋巴瘤组(SNLG)预后指数表明,21例患者被认为是高危患者(指数≥0.5)。他们接受PVACEBOP多药联合化疗作为初始治疗。低危患者(SNLG指数<0.5)接受标准的ChlVPP或ABVD化疗及±放疗。SNLG指数对16岁以下患者无效。因此,12例患者接受了英国儿童癌症研究组(UKCCSG)方案(n = 8)、ABVD加放疗(n = 2)或PVACEBOP(n = 2)。46例cHL患者(96%)实现完全缓解。7例患者复发,但所有患者在挽救治疗后均进入完全缓解期。5例患者死亡:3例死于HL,1例死于意外,1例死于播散性水痘并发囊性纤维化。5年和10年总生存率分别为93%和86%;疾病特异性生存率分别为95%和92%。数据表明,高危HL的年长青少年需要强化方案作为初始治疗以确保最佳预后。