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Efficacy, safety and pharmacokinetics of subcutaneous azacitidine in Chinese patients with higher risk myelodysplastic syndromes: Results from a multicenter, single-arm, open-label phase 2 study.

Xin DuYue-Yun LaiZhijian XiaoTing LiuYu HuAining SunXiao LiZhi-Xiang ShenJie JinLi YuEric LailleQian DongStephen SongerC L Beach
Published in: Asia-Pacific journal of clinical oncology (2017)
Azacitidine was safe and effective in Chinese patients with HR-MDS. Clinical outcomes were comparable to those for primarily Caucasian patients in the phase 3 AZA-001 study. Cmax differences between Chinese and North American patients were not associated with differences in TEAE frequency or severity. No initial azacitidine dose adjustment is required for Chinese patients with HR-MDS.
Keyphrases
  • end stage renal disease
  • open label
  • acute myeloid leukemia
  • ejection fraction
  • chronic kidney disease
  • newly diagnosed
  • prognostic factors
  • clinical trial
  • randomized controlled trial
  • rectal cancer
  • placebo controlled