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Testicular cancer: new developments, molecular pathology, and current research keynote
1Department of Morphological Sciences, Cordoba University Medical School, Avda. Menendez-Pidal S/N, 14004, Cordoba, Spain. em1lobea@uco.es.
Abstract:
Germ cell tumors (GCTs) are now considered a curable cancer, with a > 95% cure rate in all patients and about 90% cure rate in patients with metastatic disease. The success of physicians in curing the disease is underpinned by multidisciplinary advances. Of relevance in this regard are the nowadays-applied homogeneous terminology based on pathologically better characterized testicular neoplasms and the development of a widely used risk stratification model for metastatic disease introduced by the International Germ Cell Cancer Collaborative Group in 1997 and updated in 2021. Non-pulmonary visceral metastases, high levels of the serum tumor markers alpha-fetoprotein (AFP) and human chorionic gonadotropin (HCG), and primary mediastinal non-seminoma are currently identified as determinants of poor prognosis. In addition, the presence of distinct microRNA profiles between seminomas and non-seminoma GCTs has opened up important perspectives in terms of noninvasive biomarkers that can be used in diagnosis and treatment monitoring.
Insights
Germ cell tumors (GCTs) are highly curable cancers, with cure rates over 95%. Advances in terminology and risk stratification, alongside novel biomarkers like microRNAs, improve diagnosis and treatment monitoring for testicular neoplasms.
Area of Science:
- Oncology
- Genetics
Background:
- Germ cell tumors (GCTs) represent a curable malignancy with high success rates.
- Multidisciplinary advancements have significantly improved patient outcomes.
- Standardized terminology and risk stratification models are crucial for effective management.
Purpose of the Study:
- To review the current understanding and management of GCTs.
- To highlight key prognostic factors and emerging biomarkers.
- To discuss the impact of recent updates in risk stratification.
Main Methods:
- Literature review focusing on GCTs, terminology, risk stratification, and biomarkers.
- Analysis of prognostic determinants including metastases and serum tumor markers.
- Exploration of microRNA profiles in GCT subtypes.
Main Results:
- GCTs exhibit a >95% cure rate overall and ~90% in metastatic cases.
- Poor prognostic indicators include non-pulmonary visceral metastases, elevated alpha-fetoprotein (AFP) and human chorionic gonadotropin (HCG), and mediastinal non-seminoma.
- Distinct microRNA profiles in seminomas versus non-seminomas offer potential for noninvasive biomarkers.
Conclusions:
- GCT management has benefited from standardized terminology and risk models.
- Prognostic factors and serum tumor markers remain critical for patient stratification.
- MicroRNA research presents promising avenues for noninvasive diagnosis and monitoring of GCTs.
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