Objective Good drug survival of tumour necrosis factor inhibitors (TNFi) has been shown in axial spondyloarthritis (axSpA) patients treated in real-life setting. However, few studies have compared drug survival of the first TNF inhibitor between radiographic axSpA (r-axSpA) and non-radiographic axSpA (nr-axSpA) patients in real-world clinical practice. The aim of this work was to evaluate the effectiveness by assessing the retention rate of first-line TNFi in r-axSpA and nr-axSpA patients. Baseline predictive factors for TNFi discontinuation were also evaluated. Methods We retrospectively assessed axSpA patients, who underwent first line therapy with TNFi. Demographic and clinical data was obtained through structured interview, rev...
Objective. To investigate the possibility of achieving partial remission (PR) in patients with non-r...
Objective. To evaluate the 8-year survival of the first TNF inhibitor (TNFi) in patients with axial ...
OBJECTIVE: To investigate the possibility of achieving partial remission (PR) in patients with nonra...
Objective Good drug survival of tumour necrosis factor inhibitors (TNFi) has been shown in axial ...
Objectives: To evaluate the efficacy and drug survival of anti-tumour necrosis factor (anti-TNF) the...
Objectives: To analyse long-term survival and efficacy of TNFi, reasons for switching or discontinui...
To compare the impact of meeting specific classification criteria [modified New York (mNY), European...
To compare the impact of meeting specific classification criteria [modified New York (mNY), European...
OBJECTIVE To compare effectiveness of treatment with secukinumab (SEC) with that of alternative t...
OBJECTIVE To study drug retention and response rates in patients with axial spondyloarthritis (ax...
OBJECTIVE To compare effectiveness of treatment with secukinumab (SEC) with that of alternative t...
none9noObjective. To investigate the possibility of achieving partial remission (PR) in patients wit...
Objective To study drug retention and response rates in patients with axial spondyloarthritis (axSpA...
Objective To evaluate the baseline characteristics of patients with radiographic axial spondyloarthr...
OBJECTIVE To evaluate the initiation of and response to tumor necrosis factor (TNF) inhibitors for ...
Objective. To investigate the possibility of achieving partial remission (PR) in patients with non-r...
Objective. To evaluate the 8-year survival of the first TNF inhibitor (TNFi) in patients with axial ...
OBJECTIVE: To investigate the possibility of achieving partial remission (PR) in patients with nonra...
Objective Good drug survival of tumour necrosis factor inhibitors (TNFi) has been shown in axial ...
Objectives: To evaluate the efficacy and drug survival of anti-tumour necrosis factor (anti-TNF) the...
Objectives: To analyse long-term survival and efficacy of TNFi, reasons for switching or discontinui...
To compare the impact of meeting specific classification criteria [modified New York (mNY), European...
To compare the impact of meeting specific classification criteria [modified New York (mNY), European...
OBJECTIVE To compare effectiveness of treatment with secukinumab (SEC) with that of alternative t...
OBJECTIVE To study drug retention and response rates in patients with axial spondyloarthritis (ax...
OBJECTIVE To compare effectiveness of treatment with secukinumab (SEC) with that of alternative t...
none9noObjective. To investigate the possibility of achieving partial remission (PR) in patients wit...
Objective To study drug retention and response rates in patients with axial spondyloarthritis (axSpA...
Objective To evaluate the baseline characteristics of patients with radiographic axial spondyloarthr...
OBJECTIVE To evaluate the initiation of and response to tumor necrosis factor (TNF) inhibitors for ...
Objective. To investigate the possibility of achieving partial remission (PR) in patients with non-r...
Objective. To evaluate the 8-year survival of the first TNF inhibitor (TNFi) in patients with axial ...
OBJECTIVE: To investigate the possibility of achieving partial remission (PR) in patients with nonra...