Preview

Current Pediatrics

Advanced search

Biological Therapy Survivability in Children with Psoriasis: Cohort Study

https://doi.org/10.15690/vsp.v20i5.2323

Abstract

Background. There is a need to study genetically engineered biological therapy (GEBT) survivability and identify any significant risk factors for its ineffectiveness due to the increasing prevalence of psoriasis among children and the spreading GEBT administration. Such information has practical importance, it can be used to predict treatment outcomes and to develop individual therapeutic approaches. Objective. Our aim was to study biological therapy survivability and to identify risk factors for its ineffectiveness in children with moderate and severe forms of psoriasis. Methods. The study included data from 4-17 years old patients with moderate and severe forms of psoriasis vulgaris. Groups were formed according to the biological medication used. Statistical analyses were performed via SPSS Statistics. Biologic therapy survivability was determined via Kaplan-Meier method with the assessment of differences significance using log-rank test. Significant factors affecting cumulative risk growth were determined by Cox multiple regression method. Results. The study analysed data from the medical records of 105 patients. The average survivability of ustekinumab was 28.7 months, etanercept — 23.1, and adalimumab — 18.4. In the group of bio-naive patients, the survivability was higher: 30.8 months for ustekinumab and 24.4 months for ethanercept, while in the group of patients administrated previously with biological medication the survivability was 24.2 and 8.3 months, respectively. No statistically significant difference was revealed for adalimumab therapy. Significant risk factors for therapy ineffectiveness were the following: high body mass index (BMI) at the time of GEBT onset, aggravated family history, and prior use of one or several subsequent GEBT lines. Conclusion. The therapy survivability is inevitably declining over time. The best results were noted in bio-naive patients treated with ustekinumab that allows us to recommend it as the first-line drug in children with severe and moderate forms of psoriasis.

About the Authors

Roman A. Ivanov
National Medical Research Center of Children's Health
Russian Federation

Moscow.


Disclosure of interest:

Roman A. Ivanov confirmed the absence of a reportable conflict of interests.



Nikolay N. Murashkin
National Medical Research Center of Children's Health; Sechenov First Moscow State Medical University (Sechenov University); Central State Medical Academy
Russian Federation

Moscow.


Disclosure of interest:

Nikolay N. Murashkin — receiving research grants from pharmaceutical companies Janssen, Eli Lilly, Novartis. Scientific consultant of Galderma, Pierre Fabre, Bayer, LEO Pharma, Pfizer, AbbVie, Amryt Pharma, Zeldis Pharma.



References

1. Michalek IM, Loring B, John SM. A systematic review of worldwide epidemiology of psoriasis. J Europ Acad Dermatol Venereol. 2016;31(2):205-212. doi:10.1111/jdv.13854

2. Murzina E. Pediatric Psoriasis: Clinical Features and Course. OAJBS. 2020;1(5):207-209. doi: 10.38125/OAJBS.000147

3. Augustin M, Glaeske G, Radtke MA, et al. Epidemiology and comorbidity of psoriasis in children. Br J Dermatol. 2010;162(3):633-636. doi: 10.1111/j.1365-2133.2009.09593.x

4. Gelfand JM, Weinstein R, Porter SB, et al. Prevalence and treatment of psoriasis in the United Kingdom: a population-based study. Arch Dermatol. 2005;141(12):1537-1541. doi: 10.1001/archderm.141.12.1537

5. Kubanov AA, Bogdanova EV. Dermatovenereologic health care delivery management in the Russian Federation. Results of 2018. Vestnik Dermatologii i Venerologii. 2019;95(4):8-23. (In Russ). doi: 10.25208/0042-4609-2019-95-4-8-23

6. Torrelo A. The use of biologics for childhood psoriasis. J Eur Acad Dermatol Venereol. 2019;33(10):1816-1816. doi: 10.1111/jdv.15855

7. Cramer JA, Roy A, Burrell A, et al. Medication Compliance and Persistence: Terminology and Definitions. Value Health. 2008;11(1):44-47. doi: 10.1111/j.1524-4733.2007.00213.x

8. Phan C, Beauchet A, Burztejn A-C, et al. Biological treatments for paediatric psoriasis: A retrospective observational study on biological drug survival in daily practice in childhood psoriasis. J Eur Acad Dermatol Venereol. 2019;33(10):1984-1992. doi: 10.1111/jdv.15579

9. Augustin M, Krger K, Radtke MA, et al. Disease severity, quality of life and health care in plaque-type psoriasis: a multicenter crosssectional study in Germany. Dermatology. 2008;216(4):366-372. doi: 10.1159/000119415

10. Sokolovskiy EV, Kruglova LS, Ponich ES. The flaws of total systems therapy with biological preparations in psoriasis. Russian Journal of Skin and Venereal Diseases (Rossiyskiy zhurnal kozhnykh i venericheskikh bolezney). 2015;18(6):32-38. (In Russ).

11. Lesnaya IN, Frigo NV, Kaganova NL, et al. Molecular markers in forecasting the clinical efficacy of infliximab in psoriasis patients. Vestnik Dermatologii i Venerologii. 2010;86(1):57-66. (In Russ). doi: 10.25208/vdv827


Review

For citations:


Ivanov R.A., Murashkin N.N. Biological Therapy Survivability in Children with Psoriasis: Cohort Study. Current Pediatrics. 2021;20(5):451-458. (In Russ.) https://doi.org/10.15690/vsp.v20i5.2323

Views: 717


ISSN 1682-5527 (Print)
ISSN 1682-5535 (Online)