Evidence map›Paper›PMID 41675560›Full record

ArticleNeuro-oncology advances

Pre-treatment journey and outcome for children with intracranial non-germinomatous germ cell tumors-the Shanghai experience.

Anan Zhang, Xiang Huang, Yijin Gao, Haiyan Chen, Ibrahim Qaddoumi, Bo Yang, Xiaolong Chen, Anthony Pak-Yin Liu, Rong Zhang

Abstract read
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Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Anan ZhangDepartment of Hematology and Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai.ORCID https://orcid.org/0000-0001-8439-2707
Xiang HuangDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai.
Yijin GaoDepartment of Hematology and Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai.
Haiyan ChenDepartment of Radiation Oncology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai.
Ibrahim QaddoumiDepartment of Oncology, St Jude Children's Research Hospital, Memphis, TN.
Bo YangDepartment of Neurosurgery, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai.
Xiaolong ChenPediatric Translational Medicine Institute, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai.
Anthony Pak-Yin LiuDivision of Hematology and Oncology, Department of Pediatrics, The Hospital for Sick Children, Toronto.ORCID https://orcid.org/0000-0002-8597-9128
Rong ZhangDepartment of Neurosurgery, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Non-germinomatous germ cell tumors (NGGCTs) occur 3.5 times more frequently in Chinese children than in western populations. This study aimed to evaluate treatment outcomes, prognostic factors, and diagnostic challenges in a Chinese cooperative group, with particular focus on the roles of pathology and surgical intervention. Methods: We retrospectively analyzed 62 consecutively diagnosed pediatric patients with NGGCT (September 2018-June 2023) from Shanghai Children's Medical Center and Huashan Hospital. NGGCT was diagnosed by histopathology with/without elevated tumor markers ( Results: The study cohort included 49 males and 13 females (median age, 9.8 year). Primary locations were mainly pineal (58%) and suprasellar (29%). Treatment delays (>6 mo) occurred in 21% of patients, particularly those with non-pineal locations and endocrine symptoms. The 3 years event-free survival and overall survival rates were 81.9 ± 5.4% and 91.3 ± 3.7%, respectively. Univariate analysis identified poor prognostic factors: elevated AFP >200 ng/mL, spinal metastases, and lack of complete/partial response after induction chemotherapy. Surgical resection of small residual tumors (<2 cm) provided no survival benefit. Molecular analysis revealed Conclusions: Standardized multidisciplinary treatment achieves favorable outcomes comparable to international benchmarks. Aggressive surgery does not improve survival when tumor markers normalize. Diagnostic delays remain common, emphasizing the need for improved awareness and referral systems in China.

Indexed as

Chinadelayed diagnosisglobal healthnon-germinomatous germ cell tumors

Identifiers

PMID41675560
PMCPMC12888384

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