MTAP deletion frequently occurs in osteosarcoma, and PRMT5 has been identified as a synthetic lethal target for cancers with homozygous deletion of the MTAP gene, making it a promising target for anti-tumor drug development.This study aims to evaluate the overall status of MTAP deficiency in the tissues of osteosarcoma patients and its correlation with clinical features such as metastasis and immune subtypes by examining the MTAP protein expression levels in previous histological samples of the patients and combining this with their clinicopathological data.
Study Type
OBSERVATIONAL
Enrollment
100
Peking University People's Hospital
Beijing, Beijing Municipality, China
Progression free survival
from the start of target treatment until disease progression or death, whichever came first.
Time frame: 2 years
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