15 , 31 , 32 In the global phase III VIALE‐C trial, the addition of venetoclax to LDAC in patients ineligible for intensive chemotherapy improved the median OS from 4.1 months to 7.2 months, but the difference failed to reach statistical significance ( p = 0.11). 32 The CR/CRi rate was significantly improved from 13% with LDAC to 48% with venetoclax plus LDAC ( p < 0.001).
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Glasdegib with intensive/nonintensive chemotherapy in Japanese patients with untreated acute myeloid leukemia or high-risk myelodysplastic syndromes.
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