Evidence map›Paper›PMID 41329297›Full record

ArticleDiscover oncology2025

A retrospective and comparative analysis of survival in testicular non-germ cell tumors.

Lin Yang, Congcong Li, Yuanyuan Mi, Ning Shao

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Article in Discover oncology, 2025. 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

4 authors.

Lin Yang *Department of Clinical Laboratory, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Congcong Li *Department of Clinical Laboratory, Jinan Shizhong District People's Hospital Laboratory, Jinan, China.
Yuanyuan MiDepartment of Urology, Affiliated Hospital of Jiangnan University, Wuxi, China.
Ning ShaoDepartment of Urology, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, 1665 Kongjiang Road, Shanghai, 200092, People's Republic of China. urologysn@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTesticular cancer is the most frequently diagnosed malignancy in men aged 15–35, predominantly comprising Testicular germ cell tumors (TGCTs). However, less than 5% are classified as testicular non-germ cell tumors (TNGCTs), which are often overlooked despite their aggressive nature and poorer outcomes. The present study aimed to assess the prognosis of TNGCTs and assess the risks of death due to TNGCTs vs. non-cancer causes to provide an in-depth understanding of TNGCTs.

methodsWe used The Surveillance, Epidemiology, and End Results (SEER) database as our source of data for analysis. Overall survival (OS) and cancer-specific survival were assessed using the Kaplan–Meier method.

resultsA total of 1826 patients were identified. Our results suggested that TNGCTs had a significantly worse OS compared to TGCTs, with a hazard ratio of 7.85(95% CI 7.26–8.50). The five-year survival rate for patients with TNGCTs was approximately 50%, particularly for hematolymphoid tumors compared to the other tumor category in TNGCTs, with a HR of 1.79(95% CI 1.55–2.06). Hazards of TNGCTs-related death peaked at the beginning and diminished onward. Additionally, the risk of dying from other causes surpassed cancer-specific deaths approximately 4.5 years after diagnosis.

conclusionsTNGCTs bring great challenges in prognosis and management, emphasizing the need for awareness, appropriate follow-up strategies, and the development of effective treatment, especially for hematolymphoid tumors with the worst prognosis in TNGCTs.

Indexed as

Follow-upNon-germ cell tumorsTesticular cancer

Identifiers

PMID41329297
PMCPMC12775183

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.