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他扎罗汀与骨化三醇单用及序贯治疗中重度银屑病的头对头比较:一项随机开放标签研究

Head-to-Head Comparison of Tazarotene and Calcitriol with or without Sequential Therapy in Mild-to-Moderate Psoriasis: A Randomized Open-label Study.

作者信息

Sidhu Jaspreet Kaur, Matreja Prithpal Singh, Gupta Ashwani Kumar, Singh Amandeep, Singh Surjit

机构信息

Department of Pharmacology, Government Institute of Medical Sciences, Greater Noida, Uttar Pradesh, India.

Department of Pharmacology, Teerthanker Mahaveer Medical College and Research Center, Moradabad, Uttar Pradesh, India.

出版信息

J Res Pharm Pract. 2024 Jan 31;12(2):44-48. doi: 10.4103/jrpp.jrpp_10_23. eCollection 2023 Apr-Jun.

Abstract

OBJECTIVE

Psoriasis is an autoimmune disease that causes rapid turnover of skin cells. It is a chronic disease that affects a patient's quality of life significantly and frequently requires long-term treatment. The study on sequential therapy with tazarotene 0.1% and calcitriol 0.0003% has not been tried so far; hence, we designed this study to compare the safety and efficacy of sequential therapy with tazarotene 0.1% cream and calcitriol 0.0003% ointment versus monotherapy in mild-to-moderate stable plaque psoriasis (SPP). The objective of this study was to compare the safety and efficacy of topical sequential treatment with tazarotene followed by calcitriol, topical calcitriol followed by tazarotene, tazarotene monotherapy, calcitriol monotherapy, and compare the safety and efficacy of the sequential therapies with monotherapies.

METHODS

The study was a single center, prospective parallel-group, active control, randomized study of 16 weeks duration (treatment for 8 weeks and follow-up for 16 weeks), randomized to either of the four groups, i.e., tazarotene 0.1% for 4 weeks followed by calcitriol 0.0003% for 4 weeks or calcitriol 0.0003% for 4 weeks followed by tazarotene 0.1% for 4 weeks or tazarotene 0.1% for 8 weeks or calcitriol 0.0003% for 8 weeks. Both tazarotene and calcitriol were applied once daily in all the groups.

FINDINGS

There was no significant difference with regard to age and duration of illness among the four treatment groups. Statistically significant improvement was observed in erythema, scaling, and induration scores, and Physician`s global assessment scale at 8 weeks and 16 weeks as compared to baseline in tazarotene - calcitriol, calcitriol - tazarotene, and calcitriol versus tazarotene groups.

CONCLUSION

This study concluded that topical treatment with tazarotene 0.1% and calcitriol 0.003% was efficacious in treating mild-to-moderate SPP as both sequential and monotherapy. However, topical treatment with tazarotene as monotherapy was the least efficacious.

摘要

目的

银屑病是一种自身免疫性疾病,会导致皮肤细胞快速更替。它是一种慢性疾病,严重影响患者的生活质量,且常常需要长期治疗。目前尚未尝试过关于0.1%他扎罗汀和0.0003%骨化三醇序贯治疗的研究;因此,我们设计了本研究,以比较0.1%他扎罗汀乳膏和0.0003%骨化三醇软膏序贯治疗与单一疗法治疗轻度至中度稳定斑块状银屑病(SPP)的安全性和有效性。本研究的目的是比较他扎罗汀后接骨化三醇的局部序贯治疗、骨化三醇后接他扎罗汀的局部序贯治疗、他扎罗汀单一疗法、骨化三醇单一疗法的安全性和有效性,并比较序贯疗法与单一疗法的安全性和有效性。

方法

该研究为单中心、前瞻性平行组、活性对照、为期16周(治疗8周,随访16周)的随机研究,随机分为四组,即0.1%他扎罗汀治疗4周后接0.0003%骨化三醇治疗4周,或0.0003%骨化三醇治疗4周后接0.1%他扎罗汀治疗4周,或0.1%他扎罗汀治疗8周,或0.0003%骨化三醇治疗8周。所有组中他扎罗汀和骨化三醇均每日给药一次。

结果

四个治疗组在年龄和病程方面无显著差异。与基线相比,在8周和16周时,他扎罗汀-骨化三醇组、骨化三醇-他扎罗汀组以及骨化三醇组与他扎罗汀组在红斑、鳞屑和硬结评分以及医生整体评估量表方面均观察到具有统计学意义的改善。

结论

本研究得出结论,0.1%他扎罗汀和0.003%骨化三醇局部治疗作为序贯治疗和单一疗法治疗轻度至中度SPP均有效。然而,他扎罗汀单一疗法的局部治疗效果最差。

相似文献

本文引用的文献

1
Psoriasis Pathogenesis and Treatment.银屑病发病机制与治疗。
Int J Mol Sci. 2019 Mar 23;20(6):1475. doi: 10.3390/ijms20061475.
3
Genetic Epidemiology of Psoriasis.银屑病的遗传流行病学
Curr Dermatol Rep. 2014 Mar;3(1):61-78. doi: 10.1007/s13671-013-0066-6.
6
The clinical spectrum of psoriasis.银屑病的临床谱
Clin Dermatol. 2007 Nov-Dec;25(6):510-8. doi: 10.1016/j.clindermatol.2007.08.003.
9
A classification of psoriasis vulgaris according to phenotype.寻常型银屑病的表型分类。
Br J Dermatol. 2007 Feb;156(2):258-62. doi: 10.1111/j.1365-2133.2006.07675.x.

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