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1.
J Dermatol ; 50(6): 753-765, 2023 Jun.
Article in English | MEDLINE | ID: mdl-36786158

ABSTRACT

Psoriasis affects approximately 0.3% of the Japanese population. Recently, various effective systemic drugs have become available, and the continuation of a given treatment has become critical because of the chronic nature of psoriasis. Factors affecting drug survival (the time until treatment discontinuation) in psoriasis treatment include efficacy, safety, ease of use, and patient preference. In the present study, the authors retrospectively surveyed a multifacility patient registry to determine the real-world evidence of the survival rate of systemic interventions for psoriasis treatment. Patients with psoriasis who visited 20 facilities in the Western Japan area between January 2019 and May 2020 and gave written consent were registered as study participants, and their medical history of systemic interventions for psoriasis (starting from 2010) was retrospectively collected and analyzed. The drugs investigated were adalimumab, infliximab, ustekinumab, secukinumab, ixekizumab, brodalumab, guselkumab, risankizumab, cyclosporine, and apremilast. When drugs were discontinued, the reasons were also recorded. A total of 1003 patients with psoriasis including 268 with psoriatic arthritis (PsA) were enrolled. In biologics, more recently released drugs such as interleukin 17 inhibitors showed a numerically higher survival rate in the overall (post-2010) analysis. However, in the subset of patients who began treatment after 2017, the difference in the survival rate among the drugs was smaller. The reasons for discontinuing drugs varied, but a loss of efficacy against dermatological or joint symptoms were relatively frequently seen with some biologics and cyclosporine. The stratification of drug survival rates based on patient characteristics such as bio-naive or experienced, normal weight or obese, and with or without PsA, revealed that bio-experienced, obese, and PsA groups had poorer survival rates for most drugs. No notable safety issues were identified in this study. Overall, the present study revealed that the biologics show differences in their tendency to develop a loss of efficacy, and the factors that negatively impact the survival rate of biologics include the previous use of biologics, obesity, and PsA.


Subject(s)
Arthritis, Psoriatic , Biological Products , Psoriasis , Humans , Arthritis, Psoriatic/drug therapy , Retrospective Studies , Survival Rate , Japan/epidemiology , Psoriasis/drug therapy , Psoriasis/diagnosis , Biological Products/therapeutic use , Cyclosporine/therapeutic use , Registries
2.
J Dermatol ; 46(3): 193-198, 2019 Mar.
Article in English | MEDLINE | ID: mdl-30628100

ABSTRACT

Psoriatic arthritis (PsA) is an inflammatory arthritis with as yet unclear pathophysiology. This retrospective, multicenter, cross-sectional study was conducted in 19 facilities in western Japan and aimed to identify patients' characteristics and factors that affect the results of treatment with biologic agents. Of 2116 patients with psoriasis, 285 (13.5%) had PsA. Skin manifestations preceded joint manifestations in 69.8%, the onset was simultaneous in 17.2%, whereas PsA preceded skin manifestations in 2.5%. Peripheral arthritis was most common, occurring in 73.7%, compared with axial disease in 21.8%, enthesitis in 23.5% and dactylitis in 35.4%. Patients with severe skin manifestations were significantly younger at onset (P = 0.02) and more frequently had axial disease (P < 0.01). Biologic agents were used in 206 patients (72.3%), anti-tumor necrosis factor (TNF)-α antibodies being prescribed first to 157 of them. Anti-TNF-α antibodies were continued by 105 participants and discontinued by 47, the remaining five patients being lost to follow up. Patients who discontinued anti-TNF-α antibodies were significantly older than those who continued (55 vs 51 years, P = 0.04) and significantly older at onset of joint manifestations (50 vs 44 years, P = 0.01). Multivariate analysis revealed that patients over 50 years significantly more frequently terminated anti-TNF-α antibodies (P < 0.01). In conclusion, patients with PsA and severe skin manifestations have earlier onset and axial disease, which seriously impacts on quality of life. Anti-TNF-α antibodies were generally effective enough to continue but less so in patients aged over 50 years. Further detailed research is needed.


Subject(s)
Arthritis, Psoriatic/drug therapy , Biological Products/therapeutic use , Immunologic Factors/therapeutic use , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Adult , Age Factors , Age of Onset , Arthritis, Psoriatic/diagnosis , Arthritis, Psoriatic/immunology , Biological Products/pharmacology , Cross-Sectional Studies , Female , Humans , Immunologic Factors/pharmacology , Japan , Male , Middle Aged , Quality of Life , Retrospective Studies , Severity of Illness Index , Skin/drug effects , Skin/pathology , Treatment Outcome , Tumor Necrosis Factor-alpha/immunology
3.
J Dermatol ; 42(6): 616-20, 2015 Jun.
Article in English | MEDLINE | ID: mdl-25808307

ABSTRACT

We report two cases of sebaceous carcinoma associated with actinic keratosis (AK) with an immunohistochemical study, which suggests the possibility that sebaceous carcinoma really does develop within AK. Case 1 had sebaceous carcinoma arising within the atrophic type AK and case 2 had sebaceous carcinoma associated with bowenoid AK in the periphery and some parts of the overlying epidermis of the lesion.


Subject(s)
Adenocarcinoma, Sebaceous/complications , Keratosis, Actinic/complications , Skin Neoplasms/complications , Adenocarcinoma, Sebaceous/chemistry , Adenocarcinoma, Sebaceous/pathology , Aged, 80 and over , Female , Humans , Keratosis, Actinic/metabolism , Keratosis, Actinic/pathology , Skin Neoplasms/chemistry , Skin Neoplasms/pathology
4.
J Dermatol ; 41(7): 631-3, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24942776

ABSTRACT

Malignant peripheral nerve sheath tumors (MPNST) are regarded as sarcomas that arise from peripheral nerves or that display differentiation along the lines of the various elements of the nerve sheath. These tumors occur in deep soft tissues, but superficial primary MPNST with a cutaneous or subcutaneous origin have rarely been reported. A 70-year-old woman presented with a 3-4-year history of a slowly enlarging soft nodule on the left side of her neck. The histopathological diagnosis of the nodule was low-grade MPNST arising from diffuse neurofibroma. There was increased cellularity, but no necrosis or mitotic activity. These histopathological findings pose difficulties in differential diagnosis from a neurofibroma with atypical histological features. We report a rare case of superficial MPNST arising from diffuse neurofibroma associated with underlying occipital bone dysplasia in a neurofibromatosis type 1 patient.


Subject(s)
Neurilemmoma/complications , Neurofibroma/complications , Neurofibromatosis 1/complications , Skin Neoplasms/complications , Aged , Bone Diseases, Developmental/complications , Bone Diseases, Developmental/pathology , Female , Humans , Neurilemmoma/pathology , Neurofibroma/pathology , Neurofibromatosis 1/pathology , Occipital Bone , Skin Neoplasms/pathology
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