The aim of this study is to observe and analyze the clinical efficacy of Venetoclax+HMAs regimen in the treatment of newly diagnosed higher-risk MDS and CMML cases, and to compare the efficacy of venetoclax +HMAs regimen with that of HMAS regimen alone, in order to provide a normative scheme and basis for clinical use.
Study Type
OBSERVATIONAL
Enrollment
224
Previous phase Ib studies have fully demonstrated that venetoclax combined with HMAs is well tolerated in patients with MDS or CMML. Patients treated with VEN/AZA had a higher chance of SCT after remission and a higher survival benefit
Guangdong Provincial People's Hospital
Guangzhou, Guangdong, China
overall response rate
CR+mCR+PR+HI
Time frame: After the first cycles treatment(Day1, Month2)
IWG2023 Composite response rate
CR+CR-L+CRh+CRequ
Time frame: After the first cycles treatment(Day1, Month2 )
overall survival
Refers to the time from the start of treatment to the patient's death or last follow-up.
Time frame: through study completion, an average of 1 year
Blood transfusion dependence
Change in proportion of transfusion dependence from the start of treatment
Time frame: through study completion, an average of 1 year
adaverse event rate
Grade 3-4 adverse events
Time frame: Up to 1 years after the last subject enrolled.
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