The purpose is to explore the efficacy and safety of the SYSUCC-RMS regimen for pediatric RMS patients and to explore the impact of concurrent radiotherapy and chemotherapy on the survival rate of low-risk, medium risk, high-risk, and extremely high-risk patients in children.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
300
Low risk: VAC Intermediate risk: VAC/VII High risk: CAV/IE Very high risk: CAV/VIP
Suying Lu
Guangzhou, Guangdong, China
RECRUITINGThe objective response rate (ORR)
The ORR was calculated based on the best overall response.
Time frame: Up to 1 year
disease control rate (DCR)
Time frame: Up to 1 year
progression-free survival (PFS)
Furthermore, we provided Kaplan-Meier plots for PFS
Time frame: Up to 10 years
overall survival (OS)
Furthermore, we provided Kaplan-Meier plots for OS.
Time frame: Up to 10 years
The safety of the SYSUCC-RMS regimen for pediatric RMS patients.
Toxicity will be evaluated according to the Common Terminology Criteria for Adverse Event (CTC AE) scale, version 4.0.
Time frame: Up to 10 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.