Circulating cell free deoxyribonucleic acid for tracking early treatment response and disease progression in advanced cancers

2017 ◽  
Vol 6 (S10) ◽  
pp. S1530-S1540
Author(s):  
Akash Rathod ◽  
Ashley Hopkins ◽  
Andrew Rowland ◽  
Michael J. Sorich
Antibiotics ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 665
Author(s):  
Lena Herrmann ◽  
Aurelia Kimmig ◽  
Jürgen Rödel ◽  
Stefan Hagel ◽  
Norman Rose ◽  
...  

The Gram-negative bacilli Serratia spp., Providencia spp., Morganella morganii, Citrobacter freundii complex, Enterobacter spp. and Klebsiella aerogenes are common Enterobacterales that may harbor inducible chromosomal AmpC beta-lactamase genes. The purpose of the present study was to evaluate treatment outcomes and identify predictors of early treatment response in patients with bloodstream infection caused by potential AmpC beta-lactamase-producing Enterobacterales (SPICE-BSI). This cohort study included adult patients with SPICE-BSI hospitalized between 01/2011 and 02/2019. The primary outcome was early treatment response 72 h after the start of active treatment, defined as survival, hemodynamic stability, improved or stable SOFA score, resolution of fever and leukocytosis and microbiologic resolution. Among 295 included patients, the most common focus was the lower respiratory tract (27.8%), and Enterobacter spp. (n = 155) was the main pathogen. The early treatment response rate was significantly lower (p = 0.006) in the piperacillin/tazobactam group (17/81 patients, 21.0%) than in the carbapenem group (40/82 patients, 48.8%). Independent negative predictors of early treatment response (p < 0.02) included initial SOFA score, liver comorbidity and empiric piperacillin/tazobactam treatment. In vitro piperacillin/tazobactam resistance was detected in three patients with relapsed Enterobacter-BSI and initial treatment with piperacillin/tazobactam. In conclusion, our findings show that piperacillin/tazobactam might be associated with early treatment failure in patients with SPICE-BSI.


2018 ◽  
Vol 67 (2) ◽  
pp. 217-220 ◽  
Author(s):  
Marco Gasparetto ◽  
Vivien Wong-Spracklen ◽  
Franco Torrente ◽  
Kate Howell ◽  
Mary Brennan ◽  
...  

2012 ◽  
Vol 98 (5) ◽  
pp. e122-e125 ◽  
Author(s):  
Daniel Habermehl ◽  
Florian Blachutzik ◽  
Swantje Ecker ◽  
Jan-Oliver Dittmar ◽  
Stefan Rieken ◽  
...  

Blood ◽  
2017 ◽  
Vol 129 (25) ◽  
pp. 3314-3321 ◽  
Author(s):  
Madita Uffmann ◽  
Mareike Rasche ◽  
Martin Zimmermann ◽  
Christine von Neuhoff ◽  
Ursula Creutzig ◽  
...  

Key Points Reducing therapy intensity in the ML-DS 2006 trial did not impair the excellent prognosis in ML-DS compared with the historical control. Early treatment response and gain of chromosome 8 are independent prognostic factors.


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