1.Paradoxical Flare of Psoriasis after Ustekinumab Therapy.
Ho Yeol LEE ; Cheong Ha WOO ; Sik HAW
Annals of Dermatology 2017;29(6):794-795
No abstract available.
Psoriasis*
;
Ustekinumab*
2.Erythrodermic Psoriasis Improved by Ustekinumab: A Report of Two Cases.
Ye Seul KIM ; Hyun Ju KIM ; Sanghoon LEE ; Young Lip PARK
Annals of Dermatology 2016;28(1):121-122
No abstract available.
Psoriasis*
;
Ustekinumab
3.Multiple Lentigines Arising in Sites of Resolving Psoriatic Plaques after Treatment with Ustekinumab.
Jeong Soo KIM ; Seul Ki LEE ; Ha Ryeong RYU ; Chul Hyun YUN ; Jin Ok BAEK ; Joo Young ROH ; Jong Rok LEE
Annals of Dermatology 2018;30(3):371-372
No abstract available.
Lentigo*
;
Ustekinumab*
4.The Phase 3 Trials of Ustekinumab as Induction and Maintenance Therapy for Crohn's Disease.
The Korean Journal of Gastroenterology 2017;69(1):90-91
No abstract available.
Crohn Disease*
;
Ustekinumab*
5.Recalcitrant Pityriasis Rubra Pilaris Treated with Ustekinumab
Myeong Heon CHAE ; Jee Yon SHIN ; Ji Yeoun LEE ; Tae Young YOON
Korean Journal of Dermatology 2019;57(2):101-102
No abstract available.
Pityriasis Rubra Pilaris
;
Pityriasis
;
Ustekinumab
6.Ustekinumab for adult Filipino patients with moderate to severe chronic plaque psoriasis: A clinical series.
Verallo-Rowell Vermen ; Frez Ma. Lorna F. ; Roa Francisca C. ; Salvino Roberto P. ; Benedicto Erwin G.
Journal of the Philippine Dermatological Society 2013;22(2):36-40
BACKGROUND: Psoriasis is a chronic inflammatory disease occurs worldwide. At the Philippine General Hospital dermatology clinic, psoriasis accounted for 2.2% -2.4 % of new consults seen in 2004-2010. Its pathogenesis remains obscure but current studies indicate that activated Thai and Thai response mechanisms mediate inflammation and are implicated as key players in psoriasis genesis. Ustekinumab is a fully human monoclonal antibody that targets two interleukins (IL): IL-12 and IL-23 which influence T-cell differentiation into Thi and Thai, respectively. These naturally occurring proteins help regulate the immune system secondary to their role in linking innate and adaptive immune responses.
CASE SERIES: This is a retrospective chart review on the use of ustekinumab in 22 adult Filipinos (10 males and 12 females) conducted at six (6) dermatologists' clinics in 2010. Included were patients enrolled in the Named Patient Program (NPP) of Janssen Pharmaceutical Companies of Johnson & Johnson Philippines, diagnosed with moderate to severe long-standing plaque psoriasis and contraindicated for, or with inadequate response to, conventional systemic treatment. Patients received ustekinumab subcutaneously at loading doses of 45mg during the initial visit and at four weeks. Subsequently, it was given every twelve weeks. For patients who weighed 100 kg or more, 90mg of ustekinumab was administered. Clinical responses to the drug were assessed using Psoriasis Area and Severity Index (PASI) at initial visit and at the end of the program (52 weeks). At the end of the one-year program period, the median (range) PASI score of patients was 1.50 (0-29.2). Sixteen of the twenty-two subjects (72.73%) were able to achieve ±75% improvement from baseline (PASI 75). There was a significant (94.52%) reduction in median PASI scores of the patients from baseline to end visit (p < 0.0001). Overall, 27% (6/22) of patients with plaque psoriasis achieved complete clearance. Adverse events reported were relatively mild, including increased appetite, weight gain and body weakness/fatigue.
CONCLUSION: Ustekinumab was shown to significantly reduce the median PASI scores of 22 adult Filipino patients with moderate to severe plaque psoriasis. It was also shown to be well tolerated, with relatively mild adverse events.
Human ; Male ; Female ; Ustekinumab ; Psoriasis ; Dermatology ; Philippines
7.Severe Refractory Atopic Dermatitis in an Adolescent Patient Successfully Treated with Ustekinumab.
Anna AGUSTI-MEJIAS ; Francesc MESSEGUER ; Ramon GARCIA ; Isabel FEBRER
Annals of Dermatology 2013;25(3):368-370
No abstract available.
Adolescent
;
Antibodies, Monoclonal, Humanized
;
Dermatitis, Atopic
;
Humans
;
Ustekinumab
8.Severe Refractory Atopic Dermatitis in an Adolescent Patient Successfully Treated with Ustekinumab.
Anna AGUSTI-MEJIAS ; Francesc MESSEGUER ; Ramon GARCIA ; Isabel FEBRER
Annals of Dermatology 2013;25(3):368-370
No abstract available.
Adolescent
;
Antibodies, Monoclonal, Humanized
;
Dermatitis, Atopic
;
Humans
;
Ustekinumab
9.Therapeutic effect and safety of ustekinumab for plaque psoriasis: a meta-analysis.
Yi LIU ; Jian-ping GONG ; Wen-fang LI
Chinese Medical Sciences Journal 2014;29(3):131-138
OBJECTIVETo evaluate the efficacy and safety of ustekinumab in the therapy of plaque psoriasis.
METHODSLiteratures published up to November 2013 were collected from Cochrane library, MEDLINE, and PubMed which were related with ustekinumab for plaque psoriasis. The efficacy was estimated using relative risk of Psoriasis Area and Severity Index (PASI) 75 response rate at the week 12 endpoint in clinical trials, and adverse effects were also analyzed. Meta-analysis was carried out by using Review Manager 5.1.
RESULTSSix randomized control trials consistent with the inclusion criteria were selected and reviewed. Ustekinumab 45 mg group and 90 mg group could get better therapeutic effect compared with the placebo group (all P<0.00001). Furthermore, ustekinumab 90 mg group was more effective than ustekinumab 45 mg group (P=0.01). Adverse effects in the 6 trials were mentioned including headache, upper respiratory tract infection, nasopharyngtis, infection, serious infection, cardiovascular events, and malignant tumors. There were no statistically significant differences of these adverse effects among three groups (all P>0.05), except that infection rate in ustekinumab 45 mg group was higher than the placebo group (P=0.02).
CONCLUSIONSUstekinumab is an effective and safe therapeutic method for plaque psoriasis. However, further longer time analysis of safety is needed.
Antibodies, Monoclonal, Humanized ; adverse effects ; therapeutic use ; Humans ; Psoriasis ; drug therapy ; Randomized Controlled Trials as Topic ; Ustekinumab
10.The Effect of Combination Treatment with Ustekinumab and Topical Agents in Korean Patients with Moderate-to-severe Psoriasis: A Retrospective Study of 30 Patients through 5 Years of Follow Up.
Jihong LIM ; Yuri WOO ; Miri KIM ; Hyun Jeong PARK
Korean Journal of Dermatology 2017;55(3):171-177
BACKGROUND: Psoriasis is a chronic inflammatory skin disorder affecting approximately 1~3% of the general population. Ustekinumab is a recently developed human monoclonal antibody for psoriasis that binds to the p40 subunit shared by the interleukins IL-12 and IL-23. OBJECTIVE: The purpose of this study was to evaluate the effect of combination treatment with ustekinumab and topical agents in 30 Korean patients with psoriasis regarding different clinical parameters. METHODS: We retrospectively searched to identify patients with moderate-to-severe plaque-type psoriasis who had initiated treatment with ustekinumab between January 2012 and January 2016. Among them, our study was conducted in 30 patients with psoriasis who were treated with ustekinumab and topical agents for at least 16 weeks by analyzing their clinical charts and photographs. RESULTS: Overall, 16.7%, 93.3%, and 96.2% patients achieved PASI 75 response rates at weeks 4, 16, and 40, respectively. Furthermore, fifteen patients achieved 90% improvement in their PASI score at 100 weeks and five patients maintained their PASI score at 160 weeks. The efficacy of treatment with ustekinumab was different in sub-group analysis. Non-smokers enjoyed a higher therapeutic effect than did smokers. In addition, the therapeutic effect of ustekinumab was lower in the groups with psoriatic arthritis and nail psoriasis. However, it was not statistically significant. None of the patients experienced serious adverse events requiring the interruption of treatment. CONCLUSION: Combination treatment with ustekinumab and topical agents provides effective treatment results for Korean patients with psoriasis.
Arthritis, Psoriatic
;
Follow-Up Studies*
;
Humans
;
Interleukin-12
;
Interleukin-23
;
Interleukins
;
Psoriasis*
;
Retrospective Studies*
;
Skin
;
Ustekinumab*