儿童和青少年低风险性腺生殖细胞肿瘤的预后和复发模式

Tiphaine Courtel , Sylvie Chabaud , Daniel Orbach , Hélène Sudour-Bonnange , Cecile Verité , Angelique Rome , Cecile Dumesnil , Brice Fresneau , Estelle Thebaud , Marleen Renard , Aissatou Barry , Frederic Hameury , Frederique Dijoud , Cecile Faure Conter
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引用次数: 0

摘要

儿童低风险性腺生殖细胞肿瘤(lr - gct)通常在手术后进行密切监测。然而,复发的模式和复发的预后因素仍然不够清楚。我们回顾了2014年5月27日至2022年12月31日期间来自tgm13观察站(EudraCT 2013-004039-60)的72例19岁以下诊断为低危卵巢(OGCT)或睾丸(TGCT) GCT的患者。在30例OGCT(中位年龄13岁)中,15例为异常生殖细胞瘤,15例为非异常生殖细胞瘤OGCT (NDOGCT),其中10例患者腹部分期不完全。11例复发,其中9例为局部复发。异常生殖细胞瘤的三年无进展生存率(PFS)为73% (95% CI: 44-89), NDOGCT的三年无进展生存率为53% (95% CI: 26-74) (p = 0.22)。42例睾丸肿瘤(中位年龄3岁)中,除1例外均为nsgct。10例复发,1例死亡。睾丸gct的三年PFS为76% (95% CI: 59-86)。复发模式因年龄而异:在幼儿中,复发主要发生在肺部,而在青少年中,复发主要发生在主动脉旁淋巴结。复发的中位时间为6个月。未发现复发的显著预后因素,包括年龄较大(11岁)、OGCT分期不完整、TGCT存在淋巴血管浸润或胚胎癌。复发后的生存率仍然很好,需要进一步研究更大的儿童样本,以更好地确定儿童lr - gct复发的危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Outcome and recurrence patterns of low-risk gonadal germ cell tumors in children and adolescents
Pediatric low-risk gonadal germ cell tumors (LR-GCTs) are typically managed with close surveillance following surgery alone. However, the patterns of relapse and prognostic factors for relapse remain insufficiently understood. We reviewed 72 patients under 19 years old diagnosed with low-risk ovarian (OGCT) or testicular (TGCT) GCT between May 27, 2014, and December 31, 2022, from the TGM13-observatory (EudraCT 2013-004039-60). Among 30 OGCT (median age 13 years), 15 were dysgerminomas and 15 were non-dysgerminomatous OGCT (NDOGCT), with 10 patients having incomplete abdominal staging. Eleven relapses were observed, nine of which were locoregional. The three-year progression-free survival (PFS) was 73 % (95 % CI: 44–89) for dysgerminomas and 53 % (95 % CI: 26–74) for NDOGCT (p = 0.22). Among the 42 testicular tumors (median age 3 years), all but one were NSGCTs. Ten relapses occurred, resulting in one death. The three-year PFS for testicular GCTs was 76 % (95 % CI:59–86). Relapse patterns differed by age: in toddlers, relapses predominantly occurred in the lungs, while in adolescents, relapses were primarily in the para-aortic lymph nodes. The median time to relapse was six months. No significant prognostic factors for relapse were identified, including older age (>11 years), incomplete staging for OGCT, and the presence of lymphovascular invasion or embryonal carcinoma for TGCT. Survival after relapse remains excellent, and further research with a larger sample of children is needed to better identify risk factors for relapse in pediatric LR-GCTs.
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