Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

The long-term impact of biologic therapy on malignancy risk in patients with psoriasis remains unclear. Given the chronic nature of psoriasis and the increasing use of biologics, understanding their long-term safety profile is crucial. This study aimed to compare the incidence of malignancy between patients receiving continuous biologic therapy and those treated with topical monotherapy. We retrospectively analyzed 446 patients with psoriasis treated at a single center between May 2010 and March 2023 (biologic therapy: n = 226; topical monotherapy: n = 220). Malignancy incidence was estimated using the Kaplan-Meier method. Multivariable Cox proportional hazards regression with propensity score adjustment was employed to control for confounding variables. Subgroup analysis was performed within the biologic-treated cohort to identify additional malignancy risk factors. Malignancies occurred in 11.2% (50/446) of patients, with rates of 4.4% (10/226) in the biologic therapy group and 18.2% (40/220) in the topical therapy group (p < 0.0001). Kaplan-Meier analysis demonstrated a significantly lower cumulative incidence of malignancy in the biologic group (p = 0.0035, log-rank test). Cox regression confirmed that biologic therapy was associated with a significantly reduced malignancy risk (hazard ratio [HR]: 0.316; 95% confidence interval [CI]: 0.119-0.841; p = 0.0211). Notably, subgroup analysis using Cox regression within the biologic-treated cohort revealed that family history of malignancy was significantly associated with an increased risk of malignancy (HR: 9.01; 95% CI: 1.69-4.87; p < 0.05). In conclusion, biologic therapy was associated with a significantly lower risk of malignancy in patients with psoriasis compared to topical monotherapy. Furthermore, family history of malignancy may represent an independent risk factor for malignancy among biologic-treated patients. These findings underscore the importance of individualized cancer risk assessment when selecting treatment strategies and highlight the need for further prospective studies.

Download full-text PDF

Source
http://dx.doi.org/10.1111/1346-8138.17950DOI Listing

Publication Analysis

Top Keywords

biologic therapy
20
malignancy risk
12
therapy malignancy
8
patients psoriasis
8
topical monotherapy
8
therapy group
8
biologic
5
malignancy
5
therapy
5
psoriasis
4

Similar Publications

Background: Recent advances in high-throughput sequencing technologies have enabled the collection and sharing of a massive amount of omics data, along with its associated metadata-descriptive information that contextualizes the data, including phenotypic traits and experimental design. Enhancing metadata availability is critical to ensure data reusability and reproducibility and to facilitate novel biomedical discoveries through effective data reuse. Yet, incomplete metadata accompanying public omics data may hinder reproducibility and reusability and limit secondary analyses.

View Article and Find Full Text PDF

Background: Red blood cell (RBC) transfusion is a common intervention for anemia in preterm infants; however, its association with bronchopulmonary dysplasia (BPD) remains debated. While biological mechanisms suggest potential harm, the clinical impact of transfusion frequency on BPD incidence and severity remains unclear.

Objective: To investigate whether RBC transfusion frequency is independently associated with the risk and severity of BPD in preterm infants born before 32 weeks of gestation.

View Article and Find Full Text PDF

The stress urinary incontinence (SUI) is a difficulty in urology and current sub-urethral sling treatments are associated with inflamation and recurrence. In this study, we developed a novel tissue-engineered sling with myogenic induced adiposederived stem cells (MI-ADSCs) sheets induced by 5-Aza and combined with electrospun scaffolds of silk fibroin and poly(lactide-co-glycolide) (SF/PLGA) for the treatment of stress urinary incontinence. MI-ADSCs increased α-SMA, MyoD and Desmin the mRNA and protein expression.

View Article and Find Full Text PDF

The global surge in the population of people 60 years and older, including that in China, challenges healthcare systems with rising age-related diseases. To address this demographic change, the Aging Biomarker Consortium (ABC) has launched the X-Age Project to develop a comprehensive aging evaluation system tailored to the Chinese population. Our goal is to identify robust biomarkers and construct composite aging clocks that capture biological age, defined as an individual's physiological and molecular state, across diverse Chinese cohorts.

View Article and Find Full Text PDF

Antibody-drug conjugates (ADCs) are effective targeted therapeutics but are limited in their ability to incorporate less-potent payloads, varied drug mechanisms of action, different drug release mechanisms and tunable drug-to-antibody ratios. Here we introduce a technology to overcome these limitations called 'antibody-bottlebrush prodrug conjugates' (ABCs). An ABC consists of an IgG1 monoclonal antibody covalently conjugated to the terminus of a compact bivalent bottlebrush prodrug that has payloads bound through cleavable linkers and polyethylene glycol branches.

View Article and Find Full Text PDF