Pediatric primary extragonadal choriocarcinoma - A study on male patients at a single tertiary medical institution

IF 2.3 4区 医学 Q2 PEDIATRICS
Jui-Ju Tseng , Chi-Yen Chen , Chiung-Wen Liang , Fang-Liang Huang
{"title":"Pediatric primary extragonadal choriocarcinoma - A study on male patients at a single tertiary medical institution","authors":"Jui-Ju Tseng ,&nbsp;Chi-Yen Chen ,&nbsp;Chiung-Wen Liang ,&nbsp;Fang-Liang Huang","doi":"10.1016/j.pedneo.2024.03.008","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Primary extragonadal choriocarcinoma (PEGCC) in male is rare. It is highly malignant, typically presents with distant metastasis at the time of diagnosis, and responds poorly to treatment. Because of its associated high levels of PD-L1, the PD-1/PD-L1 pathway is a likely therapeutic target. Herein, we report our experience of treating pediatric PEGCC in six boys at a tertiary hospital.</div></div><div><h3>Methods</h3><div>We analyzed the data of six boys with pathologically confirmed PEGCC between 2009 and 2021. Their clinicodemographic and histopathological characteristics as well as treatments and clinical outcomes were retrieved from their medical charts.</div></div><div><h3>Results</h3><div>The patients' median age was 15 (range: 12–17) years. The most common primary tumor site was the mediastinum (67%, 4/6), with one case each in the retroperitoneum (16.7%) and brain (16.7%). Except for the patient with brain PEGCC, all presented with metastasis at the time of diagnosis. The following metastatic sites were observed: the lungs (100%, 5/5), brain (3/5, 60%), liver (3/5, 60%), kidneys (2/5, 40%), and spleen (1/5, 20%). Most patients had dry cough, dyspnea, and hemoptysis at initial presentation, likely due to lung metastasis. Serum human chorionic gonadotropin (HCG) levels were highly elevated in all patients. All patients received platinum-based cytotoxic chemotherapy. The patient with brain choriocarcinoma underwent surgical tumor resection; all others underwent only surgical biopsy. Strong positive PD-L1 immunohistochemical staining was noted for two patients. One patient received the PD-L1 inhibitor pembrolizumab and achieved a good response. Our cohort's 1-year survival rate was 33.3%, with a median survival of 4.34 months. Serum HCG levels remained normal in the two survivors during follow-up visits.</div></div><div><h3>Conclusion</h3><div>The poor response to current platinum-based chemotherapy remains a major challenge in the management of pediatric PEGCC. Adding pembrolizumab to a conventional chemotherapy regimen may improve the outcomes in boys with PEGCC.</div></div>","PeriodicalId":56095,"journal":{"name":"Pediatrics and Neonatology","volume":"66 2","pages":"Pages 152-156"},"PeriodicalIF":2.3000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatrics and Neonatology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1875957224000974","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Primary extragonadal choriocarcinoma (PEGCC) in male is rare. It is highly malignant, typically presents with distant metastasis at the time of diagnosis, and responds poorly to treatment. Because of its associated high levels of PD-L1, the PD-1/PD-L1 pathway is a likely therapeutic target. Herein, we report our experience of treating pediatric PEGCC in six boys at a tertiary hospital.

Methods

We analyzed the data of six boys with pathologically confirmed PEGCC between 2009 and 2021. Their clinicodemographic and histopathological characteristics as well as treatments and clinical outcomes were retrieved from their medical charts.

Results

The patients' median age was 15 (range: 12–17) years. The most common primary tumor site was the mediastinum (67%, 4/6), with one case each in the retroperitoneum (16.7%) and brain (16.7%). Except for the patient with brain PEGCC, all presented with metastasis at the time of diagnosis. The following metastatic sites were observed: the lungs (100%, 5/5), brain (3/5, 60%), liver (3/5, 60%), kidneys (2/5, 40%), and spleen (1/5, 20%). Most patients had dry cough, dyspnea, and hemoptysis at initial presentation, likely due to lung metastasis. Serum human chorionic gonadotropin (HCG) levels were highly elevated in all patients. All patients received platinum-based cytotoxic chemotherapy. The patient with brain choriocarcinoma underwent surgical tumor resection; all others underwent only surgical biopsy. Strong positive PD-L1 immunohistochemical staining was noted for two patients. One patient received the PD-L1 inhibitor pembrolizumab and achieved a good response. Our cohort's 1-year survival rate was 33.3%, with a median survival of 4.34 months. Serum HCG levels remained normal in the two survivors during follow-up visits.

Conclusion

The poor response to current platinum-based chemotherapy remains a major challenge in the management of pediatric PEGCC. Adding pembrolizumab to a conventional chemotherapy regimen may improve the outcomes in boys with PEGCC.
小儿原发性对角线外绒毛膜癌--对一家三级医疗机构男性患者的研究。
背景:男性原发性绒毛膜外癌(PEGCC)非常罕见。它恶性程度高,确诊时通常伴有远处转移,且对治疗反应差。由于其伴有高水平的 PD-L1,PD-1/PD-L1 通路可能是一个治疗靶点。在此,我们报告了一家三甲医院治疗六名男孩小儿 PEGCC 的经验:我们分析了 2009 年至 2021 年期间病理确诊为 PEGCC 的六名男孩的数据。我们从病历中检索了他们的临床人口学和组织病理学特征以及治疗和临床结果:结果:患者的中位年龄为 15 岁(12-17 岁)。最常见的原发肿瘤部位是纵隔(67%,4/6),腹膜后(16.7%)和脑(16.7%)各有一例。除一名脑PEGCC患者外,其他患者在确诊时均已出现转移。转移部位如下:肺(100%,5/5)、脑(3/5,60%)、肝(3/5,60%)、肾(2/5,40%)和脾(1/5,20%)。大多数患者最初出现干咳、呼吸困难和咯血,这可能是由于肺部转移所致。所有患者的血清人绒毛膜促性腺激素(HCG)水平均高度升高。所有患者都接受了以铂类为基础的细胞毒化疗。脑绒毛膜癌患者接受了外科肿瘤切除术,其他患者仅接受了外科活检。两名患者的PD-L1免疫组化染色呈强阳性。一名患者接受了PD-L1抑制剂pembrolizumab治疗,并取得了良好反应。我们队列的 1 年生存率为 33.3%,中位生存期为 4.34 个月。两名幸存者在随访期间血清HCG水平保持正常:结论:目前以铂类为基础的化疗反应不佳仍是治疗小儿PEGCC的一大挑战。在常规化疗方案中加入pembrolizumab可能会改善PEGCC男孩的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.10
自引率
0.00%
发文量
170
审稿时长
48 days
期刊介绍: Pediatrics and Neonatology is the official peer-reviewed publication of the Taiwan Pediatric Association and The Society of Neonatology ROC, and is indexed in EMBASE and SCOPUS. Articles on clinical and laboratory research in pediatrics and related fields are eligible for consideration.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信