| Objective:To evaluate the efficacy and safety of epoetin-α to chemotherapy-relatedanemia in cancer.Methods:We retrievaled the randomized controlled trial(RCT) in thefollowing databases as the CBM〠CNKI〠Pubmed〠EMBase〠The CochraneLibrary.Conference papers and relevant dates published by Chinese and English were alsomanually searched.Besides,we traced the references from the literatures we had included.Finally,we screened out the RCTs of chemotherapy-related anemia in solid tumorscomparing epoetin-α group with control group.We assessed the quality of the includedstudies by the Cochrane Handbook5.1.2recommend standard,and meta-analyses wereused on the results under RevMan5.1software.Results:A total of8studies containing2122patients were included.Compared with the control group,epoetin-α could increase theincidence of thrombotic events[RR=1.71,95%CI(1.14,2.58),P=0.009],but it can’t add theserious adverse events rate[RR=1.07,95%CI(0.87,1.32),P=0.50]and patients’ totalmortality[RR=1.06,95%CI(0.94,1.20),P=0.31],besides,epoetin-α could increase the meanchange of hemoglobin[SMD=0.53,95%CI(0.32,0.74),P<0.00001],and cut down the bloodtransfusion rate[RR=0.52,95%CI(0.38,0.70),P<0.0001]and blood transfusions[SMD=-0.41,95%CI(-0.54,-0.28),P<0.00001]of the experimental group.Moreover,it canimprove patients’ hemoglobin response rate and quality of life,but there were no statisticalsignificance(P>0.05)in Median survival time(MST)ã€Progression-free survival rate(PFS)ã€Relapse-free survival rate(RFS)and Time to disease progression(TTP).Conclusions:Evidence indicates that,epoetin-α may raise the incidence of thrombotic events but it wasunable to increase the patients’ total rate of death and the serious adverse event,so weshould use it carefully.However,well-designed RCTs with high-quality and a largersample size are still needed. |