early breast cancer patient
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PLoS ONE ◽  
2018 ◽  
Vol 13 (9) ◽  
pp. e0204123 ◽  
Author(s):  
Inna Y. Gong ◽  
Natalie S. Fox ◽  
Vincent Huang ◽  
Paul C. Boutros


2017 ◽  
Author(s):  
Inna Y. Gong ◽  
Natalie S. Fox ◽  
Paul C. Boutros

AbstractBackgroundBiomarkers are a key component of precision medicine. However, full clinical integration of biomarkers has been met with challenges, partly attributed to analytical difficulties. It has been shown that biomarker reproducibility is susceptible to data preprocessing approaches. Here, we systematically evaluated machine-learning ensembles of preprocessing methods as a general strategy to improve biomarker performance for prediction of survival from early breast cancer.ResultsWe risk stratified breast cancer patients into either low-risk or high-risk groups based on four published hypoxia signatures (Buffa, Winter, Hu, and Sorensen), using 24 different preprocessing approaches for microarray normalization. The 24 binary risk profiles determined for each hypoxia signature were combined using a random forest to evaluate the efficacy of a preprocessing ensemble classifier. We demonstrate that the best way of merging preprocessing methods varies from signature to signature, and that there is likely no ‘best’ preprocessing pipeline that is universal across datasets, highlighting the need to evaluate ensembles of preprocessing algorithms. Further, we developed novel signatures for each preprocessing method and the risk classifications from each were incorporated in a meta-random forest model. Interestingly, the classification of these biomarkers and its ensemble show striking consistency, demonstrating that similar intrinsic biological information are being faithfully represented. As such, these classification patterns further confirm that there is a subset of patients whose prognosis is consistently challenging to predict.ConclusionsPerformance of different prognostic signatures varies with pre-processing method. A simple classifier by unanimous voting of classifications is a reliable way of improving on single preprocessing methods. Future signatures will likely require integration of intrinsic and extrinsic clinico-pathological variables to better predict disease-related outcomes.AbbreviationsAUCarea under the receiver operating characteristic curveGCRMAGeneChip Robust Multi-array AverageHG-U133AAffymetrix Human Genome U133AHG-U133 Plus 2.0Affymetrix Human Genome Plus 2.0HRhazard ratioMAS5MicroArray Suite 5.0MBEIModel-base Expression IndexNSCLCNon-small cell lung cancerRFRandom forestROCreceiver operator characteristicRMARobust Multi-array Average







2016 ◽  
Vol 56 ◽  
pp. 85-92 ◽  
Author(s):  
Kathrin Strasser-Weippl ◽  
Nora Horick ◽  
Ian E. Smith ◽  
Joyce O'Shaughnessy ◽  
Bent Ejlertsen ◽  
...  


2011 ◽  
Vol 22 (9) ◽  
pp. 2150-2151 ◽  
Author(s):  
M.J. Serrano ◽  
R. Nadal ◽  
J.A. Lorente ◽  
M. Salido ◽  
R. Rodríguez ◽  
...  


2011 ◽  
Vol 1 (2) ◽  
pp. 33 ◽  
Author(s):  
Alessandro Marco Minisini ◽  
Jessica Menis ◽  
Alessandro Follador ◽  
Claudio Avellini ◽  
Gianpiero Fasola

Anaerobic bacteraemia could be a lifethreatening condition in neutropenic patients receiving chemotherapy. Taxane therapy is associated with necrotising inflammation of the caecum (named also typhlitis) that could be a potential source for bacteraemia. We report the case of a sudden onset of septic shock by Clostridium perfringens in a young patient treated with docetaxel as adjuvant chemotherapy for early breast cancer. A minireview of the literature has been performed.



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