scholarly journals PBI6 Stringent Thresholds of Disease Control Are Associated with Reduced Burden on Paid and Household Work Productivity in Patients with Psoriatic Arthritis during LONG-TERM Treatment with Certolizumab Pegol

2020 ◽  
Vol 23 ◽  
pp. S411
Author(s):  
W. Tillett ◽  
L.C. Coates ◽  
T. Nurminen ◽  
S. Kiri ◽  
P. Mease
2016 ◽  
Vol 14 (12) ◽  
pp. 1753-1762 ◽  
Author(s):  
Edward V. Loftus ◽  
Jean-Frederic Colombel ◽  
Stefan Schreiber ◽  
Charles W. Randall ◽  
Miguel Regueiro ◽  
...  

2017 ◽  
Vol 35 (5) ◽  
pp. 423-432 ◽  
Author(s):  
Stephan R. Vavricka ◽  
Milos Spasojevic ◽  
Gerhard Rogler ◽  
Alain M. Schoepfer ◽  
Frank Seibold ◽  
...  

Background: Long-term data of certolizumab pegol (CZP) in Crohn's disease (CD) from pivotal registry trials are limited. We therefore aimed to evaluate the long-term efficacy of CZP in clinical practice in Switzerland. Methods: In the First Approved Certolizumab Therapeutic Experience in Switzerland-III phase IV multicenter cohort, patients receiving CZP were prospectively included all over Switzerland in (non-) academic hospitals and private practice. Results: We included 104 CD patients (52 male; only 22.1% anti-tumor necrosis factor (TNF) naïve, CZP as third anti-TNF agent in 46.2%) with follow-up time between 6 weeks up to 5 years. During treatment with CZP, we observed a significant decrease of the Harvey Bradshaw Index from a median of 7 at baseline (interquartile range 4-11) to 4, 5, 4, 3, 3, and 2 at weeks 6, 26, 52, 78, 104, and 156, respectively. While anti-TNF naïve patients showed a significantly better response at the end of induction, during CZP maintenance therapy response was similar as compared to anti-TNF experienced patients as well as between patients with a short (0-5 years) vs. long duration of disease (>5 years). Conclusions: CZP is an effective long-term treatment option, including CD patients with long disease duration and prior treatment with 1 or 2 anti-TNF agents.


2007 ◽  
Vol 56 (2) ◽  
pp. 476-488 ◽  
Author(s):  
Dafna D. Gladman ◽  
Philip J. Mease ◽  
Christopher T. Ritchlin ◽  
Ernest H. S. Choy ◽  
John T. Sharp ◽  
...  

2017 ◽  
Vol 69 (3) ◽  
pp. 347-355 ◽  
Author(s):  
Arthur Kavanaugh ◽  
Philip J. Mease ◽  
Andreas M. Reimold ◽  
Hasan Tahir ◽  
Jürgen Rech ◽  
...  

2021 ◽  
pp. 1-8
Author(s):  
Robert Seifert ◽  
Alina Küper ◽  
Mitra Tewes ◽  
Martin Heuschmid ◽  
Anja Welt ◽  
...  

<b><i>Introduction:</i></b> Addition of cyclin-dependent 4/6 kinase (CDK4/6) inhibitors to endocrine therapy is standard of care in the treatment of women with advanced hormone receptor-positive HER2-negative breast cancer. However, the predictive factors for the treatment response to CDK4/6 inhibitor therapy are poorly elucidated. Early changes in the by [<sup>18</sup>F]-fluorodeoxyglucose positron emission tomography (FDG-PET) uptake of tumors receiving different kinds of therapy have proven to reliably predict treatment outcomes in a variety of malignancies. Therefore, the feasibility of early metabolic response assessment to predict the long-term treatment response to CDK4/6 inhibitor therapy was evaluated in the present study. <b><i>Methods:</i></b> Eight patients underwent FDG-PET/CT before and after the initiation of CDK4/6 inhibitor therapy (ribociclib, palbociclib or abemcaciclib). CDK4/6 inhibitor therapy was combined with either aromatase inhibition or fulvestrant. The median interval between the treatment start (including baseline PET) and the follow-up PET examination was 14 days. Conventional radiographic staging was performed 3 months after the start of CDK4/6 inhibitor therapy. The percentual changes in molecular tumor volume, SUV<sub>peak</sub>, the summed SUV<sub>peak</sub> of up to 5 metastases (PERCIST-5), and total lesion glycolysis (TLG) were calculated for each patient. <b><i>Results:</i></b> Three patients showed progressive disease after 3 months of CDK4/6 inhibitor therapy, whereas 5 patients showed disease control (3 stable disease and 2 partial remission). Disease control was maintained in these patients (follow-up range 7–22 months). Patients with disease control had a significantly greater decline in TLG (–55.3 vs. 16.7%; <i>p</i> &#x3c; 0.05). The same was true for the PERCIST-5 (–21.9 vs. 11.3%, <i>p</i> &#x3c; 0.05). All patients with progressive TLG showed treatment failure and/or a poor outcome. <b><i>Conclusion:</i></b> Elevated TLG on early FDG-PET seems to be associated with long-term treatment failure and a poor outcome in patients undergoing CDK4/6 inhibitor therapy for metastatic breast cancer. Early findings indicate a potential prognostic value of early FDG-PET in this setting and warrant a prospective evaluation.


1986 ◽  
Vol 5 (1) ◽  
pp. 124-125 ◽  
Author(s):  
B. Tumiati ◽  
R. Baricchi ◽  
A. Bellelli

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