Clinical and genomic features in patients with second primary glioblastoma following first primary renal cell carcinoma

To explore the potential pathogenesis and clinical features of second primary glioblastoma (spGBM) following first primary renal cell carcinoma (fpRCC). Patients with spGBM after fpRCC were enrolled from our institution and the SEER dataset. Sanger sequencing, whole genome sequencing, and immunehist...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BMC cancer 2023-01, Vol.23 (1), p.104-104, Article 104
Hauptverfasser: Zhang, Guang-Tao, Liu, Qi, Zuo, Fu-Xing, Liu, Hou-Jie, Wang, Song-Quan, Yuan, Qing, Liu, Ang-Si, Hu, Ke, Meng, Xiao-Li, Wang, Wei-Jia, Qian, Hai-Peng, Wan, Jing-Hai, Cai, Hong-Qing
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:To explore the potential pathogenesis and clinical features of second primary glioblastoma (spGBM) following first primary renal cell carcinoma (fpRCC). Patients with spGBM after fpRCC were enrolled from our institution and the SEER dataset. Sanger sequencing, whole genome sequencing, and immunehistochemistry were used to detect molecular biomarkers. Four and 122 cases from our institution and the SEER dataset, respectively, were collected with an overall median age of 69 years at spGBM diagnosis following fpRCC. The median interval time between fpRCC and spGBM was 50.7 months and 4 years, for the four and 122 cases respectively. The median overall survival time was 11.2 and 6.0 months for the two datasets. In addition, spGBM patients of younger age (
ISSN:1471-2407
1471-2407
DOI:10.1186/s12885-023-10541-x