Ann Dermatol.  2016 Apr;28(2):222-231. 10.5021/ad.2016.28.2.222.

The MARCOPOLO Study of Ustekinumab Utilization and Efficacy in a Real-World Setting: Treatment of Patients with Plaque Psoriasis in Asia-Pacific Countries

Affiliations
  • 1Department of Dermatology, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • 2Department of Dermatology, National Taiwan University Hospital, Taipei, Taiwan.
  • 3National Skin Centre, Singapore.
  • 4Department of Dermatology, Hospital Sultanah Aminah, Johor Bahru, Malaysia.
  • 5Private Practice, Jakarta, Indonesia.
  • 6Janssen Asia Pacific, Medical Affairs, Melbourne, Australia.
  • 7Janssen China, Biostatistics, Beijing, China.
  • 8Department of Dermatology and Cutaneous Biology Research Institute, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea. mglee@yuhs.ac

Abstract

BACKGROUND
Ustekinumab is a fully human monoclonal antibody approved for the treatment of chronic moderate-to-severe plaque psoriasis in adults. However, factors including efficacy, tolerability, ease of use, and cost burden may affect ustekinumab utilization. Noncompliance may, in turn, affect treatment response.
OBJECTIVE
To evaluate ustekinumab utilization in the real-world setting in Asia-Pacific countries.
METHODS
In this phase 4 observational study conducted in Indonesia, Malaysia, Singapore, Korea, and Taiwan, adults with plaque psoriasis receiving ustekinumab were followed for up to 52 weeks. Study endpoints were the proportion of all patients using ustekinumab according to label-recommended intervals and the proportion of Korean patients who achieved a psoriasis area severity index 75 response at week 16. Safety was assessed by monitoring adverse events.
RESULTS
Overall, 169 patients received ustekinumab (Korea, n=102; other countries, n=67). Just over half (56.2%) of patients used ustekinumab with the label-recommended interval from baseline to week 40; the proportion was higher in Korea (73.5%) than in other countries (29.9%), probably because ustekinumab was provided without charge for Korean patients up to week 40. Noncompliance increased after week 40 in Korea and from week 28 in other Asia-Pacific countries, with cost cited as the most common reason. At week 16, 56.9% of Korean patients achieved a Psoriasis Area Severity Index 75 response. Safety results were in line with those seen in previous studies.
CONCLUSION
More than half of all patients in Asia-Pacific countries used ustekinumab as per the label-recommended dose interval, but reimbursement variations between countries may have confounded overall results.

Keyword

Asia-Pacific; Compliance; Plaque psoriasis; Reimbursement; Ustekinumab

MeSH Terms

Adult
Compliance
Humans
Indonesia
Korea
Malaysia
Observational Study
Psoriasis*
Singapore
Taiwan
Ustekinumab

Figure

  • Fig. 1 Study design.

  • Fig. 2 Patient disposition. Values are presented number (%).

  • Fig. 3 Change in median PASI scores from baseline. (A) Korea. (B) Other Asia-Pacific countries. Compliant=taking ustekinumab in line with the recommended dosing (week 0, week 4, and every 12 weeks thereafter; dose to be taken within ±10 days). PASI: psoriasis area severity index.


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