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Association details:
Evidence:
Evidence Level:
Sensitive: D – Preclinical
New
Title:

Identification of IGF2 as genomic driver and actionable therapeutic target in hepatoblastoma

Excerpt:
Xentuzumab, a monoclonal antibody against IGF2, significantly reduced proliferation and clonogenic capacity in IGF2-high HB cell lines, whereas in combination with cisplatin in an IGF2-high organoid model was able to increase cisplatin efficacy by 25-fold and promote apoptosis. In vivo, xentuzumab + cisplatin reduced viable tumor volume and extended time to sacrifice (1500 mm3) compared to cisplatin alone (p = 0.04).
Evidence Level:
Sensitive: D – Preclinical
New
Title:

Identification of IGF2 as genomic driver and actionable therapeutic target in hepatoblastoma

Excerpt:
Xentuzumab, a monoclonal antibody against IGF2, significantly reduced proliferation and clonogenic capacity in IGF2-high HB cell lines, whereas in combination with cisplatin in an IGF2-high organoid model was able to increase cisplatin efficacy by 25-fold and promote apoptosis. In vivo, xentuzumab + cisplatin reduced viable tumor volume and extended time to sacrifice (1500 mm3) compared to cisplatin alone (p = 0.04).
Secondary therapy:
cisplatin