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典型文献
Platinum is essential in neoadjuvant treatment of triple-negative breast cancer: a network meta-analysis
文献摘要:
Objective: This study aimed to assess the efficacy and safety of various neoadjuvant regimens for patients diagnosed with early-stage or locally advanced triple-negative breast cancer (TNBC). Methods: Medline, EMBASE, Cochrane Library, and Web of Science were searched in May 2020 to identify randomized controlled trials (RCTs). Bayesian network meta-analysis (NMA) was performed (Registration: PROSPERO CRD42020223012). Results: A total of 35 RCTs involving 8,424 participants were reviewed, of which 22 RCTs with 5,203 patients were included in this NMA focusing on pathologic complete response (pCR). An anthracycline-taxane-based (AT) regimen combined with a platinum (ATPt) [odds ratio (OR) = 2.04, 95% credible interval (CrI): 1.69, 2.48] regimen, and a docetaxel regimen combined with a carboplatin (TCb; OR = 2.16, 95% CrI: 1.20, 3.91) regimen improved pCR beyond that with AT only. AT and ATPt combined with targeted therapy [including bevacizumab (Bev), veliparib, atezolizumab, or pembrolizumab] also improved pCR. Five RCTs included in this NMA reported serious adverse events (SAEs) or grade ≥ 3 AEs. TCb was associated with fewer grade ≥ 3 AEs than was AT (OR = 0.66, 95% CrI: 0.23, 1.72) alone. In contrast, ATPt, AT + Bev, ATPt + Bev, ATPt + veliparib, and ATPt + pembrolizumab were associated with more SAEs than was AT alone. Conclusions: In patients with TNBC, platinum-based neoadjuvant regimens ATPt and TCb increase pCR beyond that with AT alone, but TCb appears to be better tolerated than either AT or ATPt. Platinum-based regimens combined with targeted therapies (Bev, PARPi, and PD-1/PD-L1 inhibitor) also improve the pCR rate beyond that with AT alone, but this benefit is accompanied by greater toxicity.
文献关键词:
作者姓名:
Junjie Li;Li Chen;Wei Tan;Fang Qi;Yang Zhang;Zhonghua Wang;Zhimin Shao
作者机构:
Key Laboratory of Breast Cancer in Shanghai,Department of Breast Surgery,Fudan University Shanghai Cancer Center,Shanghai 200032,China;Department of Oncology,Shanghai Medical College,Fudan University,Shanghai 200032,China;Nottingham Clinical Trials Unit,University of Nottingham,Nottingham NG72RD,UK;Academic Department,Systematic Review Solutions Ltd,Shanghai 201400,China
引用格式:
[1]Junjie Li;Li Chen;Wei Tan;Fang Qi;Yang Zhang;Zhonghua Wang;Zhimin Shao-.Platinum is essential in neoadjuvant treatment of triple-negative breast cancer: a network meta-analysis)[J].癌症生物学与医学(英文版),2022(05):742-754
A类:
CRD42020223012,ATPt,carboplatin,TCb,veliparib
B类:
Platinum,essential,neoadjuvant,treatment,triple,negative,breast,cancer,network,meta,analysis,Objective,This,study,aimed,assess,efficacy,safety,various,regimens,patients,diagnosed,early,stage,locally,advanced,TNBC,Methods,Medline,EMBASE,Cochrane,Library,were,searched,May,identify,randomized,controlled,trials,RCTs,Bayesian,NMA,was,performed,Registration,PROSPERO,Results,total,involving,participants,reviewed,which,included,this,focusing,pathologic,complete,response,pCR,An,anthracycline,taxane,combined,platinum,odds,credible,interval,CrI,docetaxel,improved,beyond,that,only,targeted,therapy,including,bevacizumab,Bev,atezolizumab,pembrolizumab,also,Five,reported,serious,adverse,events,SAEs,grade,associated,fewer,than,alone,In,contrast,more,Conclusions,increase,but,appears,better,tolerated,either,therapies,PARPi,L1,inhibitor,benefit,accompanied,by,greater,toxicity
AB值:
0.447072
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