Huang Junting, Tan Yuting, Zhen Zijun, Lu Suying, Sun Feifei, Zhu Jia, Wang Juan, Liao Ru, Sun Xiaofei
Department of Pediatric Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, P. R. China.
Department of Radiation Oncology, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, P. R. China.
PLoS One. 2017 Aug 16;12(8):e0183219. doi: 10.1371/journal.pone.0183219. eCollection 2017.
Primary malignant mediastinal germ cell tumors (MMGCTs) are rare in children and adolescents and have a poorer prognosis than their gonadal counterparts. We report a single institutional experience of a 10-year period of primary advanced MMGCTs treated with chemotherapy, followed by radiotherapy in those who had residual mass.
Children and adolescents with primary advanced MMGCTs between 2005 and 2014 were identified from the Cancer Center, Sun Yat-Sen University. Medical records were reviewed for clinicopathological characteristics, treatments, and outcomes.
Twenty-four children and adolescents with either stage III or IV primary advanced MMGCTs met the inclusion criteria. There were 23 males and one female with a median age of 16 (range 10-18). Seven cases were seminomas (29.2%); four (16.7%) yolk sac tumors (YST); three (12.5%) choriocarcinomas; and ten (41.6%) nonteratomatous combined germ cell tumors (CGCTs). All patients were treated with first-line cisplatin-based chemotherapy regimens (PEB: 19, VIP: 5). Thirteen (54.2%) and Twelve (50%) patients received surgery and radiotherapy, respectively. With a median follow-up of 46.2 months (range 9.6-124.8 months), a total of five (20%) patients died of disease progression; the five-year overall survival (OS) and disease-free survival (DFS) rates were 82.3% and 64.9%, respectively.-Seven patients with seminoma GCTs received post-chemotherapy irradiation were alive with sustained CR (5-year OS and DFS, 100%, respectively). Five patients with NSGCTs were administered irradiation and one relapsed 35 months later and died of metastasis (5-year OS, 100%; 5-year DFS 66.7%). Univariate analysis identified histology and stage were prognostic factors.
Multimodality treatment approach of chemotherapy followed by radiation consolidation ensured long-term survival in primary advanced MMGCTs. Further research is warranted to improve the prognosis of children with primary advanced MMGCTs.
原发性恶性纵隔生殖细胞肿瘤(MMGCTs)在儿童和青少年中较为罕见,且预后比性腺生殖细胞肿瘤更差。我们报告了单一机构在10年期间对原发性晚期MMGCTs进行化疗,对有残留肿块者进行放疗的经验。
从中山大学肿瘤防治中心识别出2005年至2014年间患有原发性晚期MMGCTs的儿童和青少年。回顾病历以了解临床病理特征、治疗方法和结果。
24例患有III期或IV期原发性晚期MMGCTs的儿童和青少年符合纳入标准。其中男性23例,女性1例,中位年龄为16岁(范围10 - 18岁)。7例为精原细胞瘤(29.2%);4例(16.7%)为卵黄囊瘤(YST);3例(12.5%)为绒毛膜癌;10例(41.6%)为非畸胎性混合生殖细胞肿瘤(CGCTs)。所有患者均接受一线含顺铂化疗方案(PEB:19例,VIP:5例)。分别有13例(54.2%)和12例(50%)患者接受了手术和放疗。中位随访时间为46.2个月(范围9.6 - 124.8个月),共有5例(20%)患者死于疾病进展;五年总生存率(OS)和无病生存率(DFS)分别为82.3%和64.9%。7例接受化疗后放疗的精原细胞瘤GCTs患者持续完全缓解存活(五年OS和DFS分别为100%)。5例非精原细胞瘤GCTs患者接受了放疗,其中1例在35个月后复发并死于转移(五年OS为100%;五年DFS为66.7%)。单因素分析确定组织学和分期为预后因素。
化疗后放疗巩固的多模式治疗方法确保了原发性晚期MMGCTs的长期生存。有必要进一步研究以改善原发性晚期MMGCTs患儿的预后。