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  • The efficacy and safety of ...
    Xu, Z F; Qin, T J; Zhang, H L; Fang, L W; Zhang, Y; Pan, L J; Hu, N B; Qu, S Q; Li, B; Xiao, Z J

    Zhōnghuá xuèyèxué zázhì, 2017-Jul-14, 20170714, Letnik: 38, Številka: 7
    Journal Article

    To observe the clinical efficacy and safety of the patients of myelodysplastic syndromes-refractory anemia with excess blasts (MDS-REAB) treated with decitabine alone or based on low dose cytarabine (Ara-C) regimen CAG/HAG aclarubrci (ACR) /homoharring-tonine (HHT) +cytarabine+granulocyte colony stimulating factor (G-CSF) . Totally 121 patients with MDS-REAB were retrospectively analyzed, including 59 patients treated with decitabine alone (20 mg·m(-2)·d(-1) for 5 days) , the rest 62 ones treated with low-dose Ara-C-based regimen CAG/HAG. Overall response rate (ORR) , overall survival (OS) and adverse events of the two groups were analyzed and compared retrospectively. The ORR of decitabine alone or CAG/HAG were 66.2% and 56.4% respectively, with no statistically significant differences ( (2)=1.185, =0.276) . Initial response rate detected by the end of first cycle of CAG/HAG was higher than that of decitabine alone (94.3% 69.2%) , there was statistically significant difference in the overall comparison of