Survival difference among adult and pediatric mediastinal yolk sac tumors cases: A meta-analysis of case reports

• Published in: European journal of surgical oncology 2024-03, Vol.50 (3), p.108019-108019, Article 108019
• Main Authors: Dabsha, Anas, Elkharbotly, Ismail A.M.H., Yaghmour, Mohammad, Badr, Amr, Badie, Fady, Khairallah, Sherif, Esmail, Yomna M., Hossny, Mohamed, Rizk, Amr, El-Demiry, Amr, Ghaly, Galal, Al-Thani, Shaikha, Demetres, Michelle, Mohamed, Abdelrahman, Villena-Vargas, Jonathan, Kamal, Mona, Rahouma, Mohamed
• Format: Article
• Language: English
• Subjects: Adults yolk sac; Mediastinal; Meta-analysis; Pediatrics yolk sac; Yolk sac tumor
• ISSN: 0748-7983; 1532-2157
• DOI: 10.1016/j.ejso.2024.108019

Mediastinal Yolk sac tumors (YST) are rare and highly malignant extragonadal germ cell tumors with rapid growth and early metastases. We sought to conduct a meta-analysis of published case reports/case series to compare differences in survival, demographics, and treatment modalities between adult and pediatric patients with YST. Ovid Embase, Cochrane, and Ovid Medline databases were searched for primary mediastinal pure YST cases. The primary outcome was overall survival (OS). Log-rank and Cox regression were used. This study is registered on PROSPERO (CRD42022367586). Among 846 studies, 87 met our inclusion criteria including 130 patients (Adults: 90 and Pediatrics: 40). About 41.5% of the patients were from the United States. The median age was 23.0 (Q1-Q3: 17.0–30.0), 88.5% were males, and (32.3%) were Asian. Stage II represented almost 40%. AFP was elevated in 96.9%. Respiratory distress was the presenting symptom in 65.4%. Chemotherapy, radiotherapy, and surgery were utilized in 84.6, 23.1, and 64.7% respectively. Median OS was 24 months (Adults: 23 months, Pediatrics: 25 months, P = 0.89). 3- and 5-year OS were 34.4% and 22.9% in adults and 41.5% and 41.5% in pediatrics, respectively. On multivariate analysis, anterior location of tumors, receipt of chemotherapy, and undergoing surgery were associated with better OS. Primary mediastinal YSTs are rare, but lethal neoplasms. Our meta-analysis showed that mediastinal YSTs mimic other non-seminomatous mediastinal GCTs in terms of clinical characteristics and available treatment options. Early diagnosis, neoadjuvant chemotherapy, and surgical resection are the key points for effective management and improved outcomes.