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Details

Autor(en) / Beteiligte
Titel
Neoadjuvant chemotherapy for triple-negative breast cancer: a meta-analysis with 7168 cases
Ist Teil von
  • 中德临床肿瘤学杂志(英文版), 2014 (2), p.58-62
Ort / Verlag
Department of 0ncology, The General Hospital of Shenyang Military Region, Shenyang 110840, China%Molecular Biology Laboratory of Traditional Chinese Medicine, The Basic Medical College of Liaoning University of Traditional Chinese Medicine, Shengyang 110032, China%Department of Gynaecology and 0bstetrics, Zhejiang Chinese Medical University Affiliated Hospital of Wenzhou Traditional Chinese Medicine, Wenzhou 325000, China%Cardiovascular Disease Institute, General Hospital of Shenyang Military Region, Shenyang 110840, China
Erscheinungsjahr
2014
Link zum Volltext
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Objective: The pathological complete response (pCR) rates of neoadjuvant chemotherapy (NAC) in triple-nega- tive breast cancer (TNBC) was reported higher than that in non-TNBC but ranged from 12% to 48%. pCR was reported to be a predictor of long overall survival and exact pCR rate of NAC in TNBC would give us some hints on how to improve outcomes of TNBC patients. The meta-analysis was conducted to estimate the pCR rate of NAC for TNBC through contrasting the pCR rates of TNBC and non-TNBC tumors in NAC. Methods: Studies were selected from the PubMed database and Cochrane Collaboration Library. pCR rates were collected in groups of TNBC and non-TNBC tumors. Review Manager 4.2 was used to perform forest plots and funnel plots. Results: The analysis included 22 studies with 7168 patients, the aggregate pCR rate was 29.5% in TNBC group, which was 17.7% higher than non-TNBC. The summary relative risk (RR) for pCR rate of TNBC group with that of non-TNBC group was 2.55. No obvious statistical heterogeneity and publication bias was detected. Conclu- sion: This meta-analysis demonstrated that NAC showed a higher pCR rate in TNBC than non-TNBC.
Sprache
Englisch
Identifikatoren
ISSN: 1610-1979
eISSN: 1613-9089
DOI: 10.1007/s10330-013-1265-0
Titel-ID: cdi_wanfang_journals_dgyx201402002

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