Real-World Effectiveness of Biologic Agents Used to Treat Moderate-to-Severe Plaque Psoriasis in Poland: Between Treatment Comparison
Speaker(s)
Owczarek W1, Walecka-Herniczek I2, Pochopien M3, Koziara K4, Łanecka A5, Górecki M4, Wojciechowski P6, Clay E7, Aballea S8, Toumi M8
1Military Institute of Medicine, Warsaw, Poland, 2Państwowy Instytut Medyczny MSWiA, Warsaw, Poland, 3Assignity, Paris, France, 4Assignity, Krakow, Poland, 5Assignity, Kraków, MA, Poland, 6Assignity, Żory, SL, Poland, 7Clever-Access, Paris, France, 8InovIntell, Paris, France
Presentation Documents
OBJECTIVES: The objective of this study was to compare the real-world effectiveness of biologic agents used in treating moderate-to-severe plaque psoriasis in Poland.
METHODS: The analysis of treatment effectiveness was conducted using data from approximately 5,000 patients with moderate-to-severe plaque psoriasis treated with biologic agents, enrolled in . The dataset provides details about patients, including demographic information, previous therapies, and qualification dates. It also tracks checkpoint dates and types, patient weight, medications, and current health indices. Eleven biologic agents is available in the program , however one was removed from the analysis as too recently introduced. The Psoriasis Area and Severity Index (PASI) was used to assess the effectiveness of treatment, with PASI75, used as the primary measure of treatment efficacy. The percentage of patients achieving PASI75 was assessed between the 12th and 16th weeks, as well as between the 36th and 40th weeks of treatment.
RESULTS: Between 69% and 93% patients achieved PASI75 between the 12th and 16th weeks of treatment. The After 36 to 40 weeks of treatment, the effectiveness of all but two biologic agents increased, with the percentage of patients reaching PASI75 ranging between 70 and 100.
CONCLUSIONS: ologic agents demonstrated high real-world effectiveness in PASI reduction in patients with moderate-to-severe plaque psoriasis in Poland. The effectiveness of the treatment was relatively stable between the 12th and 40th week of treatment.
Code
CO150
Topic
Clinical Outcomes
Topic Subcategory
Clinician Reported Outcomes, Comparative Effectiveness or Efficacy
Disease
Biologics & Biosimilars, Drugs, Systemic Disorders/Conditions (Anesthesia, Auto-Immune Disorders (n.e.c.), Hematological Disorders (non-oncologic), Pain)