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评价阿利维 A 酸治疗蕈样肉芽肿和赛泽里综合征。

Evaluation of Alitretinoin for the Treatment of Mycosis Fungoides and Sézary Syndrome.

机构信息

Department of Dermatology, University of Toronto, Toronto, Ontario, Canada,

Sunnybrook Research Institute, University of Toronto, Toronto, Ontario, Canada,

出版信息

Dermatology. 2021;237(3):479-485. doi: 10.1159/000512484. Epub 2021 Jan 11.

DOI:10.1159/000512484
PMID:33429396
Abstract

BACKGROUND

Mycosis fungoides (MF) and Sézary syndrome (SS) are the most common subtypes of cutaneous T-cell lymphoma (CTCL). There is currently no cure for CTCL, and treatment is aimed at limiting disease progression. This study evaluated the efficacy and tolerability of alitretinoin in CTCL management.

METHODS

A retrospective, multicenter study was conducted on CTCL patients treated with alitretinoin as a primary agent or in combination with standard therapies.

RESULTS

Forty-eight patients with MF (n = 40) and SS (n = 8) with a median age of 59.7 years (±14.3) were eligible for study inclusion. Treatment response data were evaluated in 40 patients and safety in 42 patients. 40.0% of the patients had early-stage, 43.8% had advanced-stage CTCL, and in 16.7% of patients there was insufficient information for staging. 40.0% (16/40) of the patients achieved a complete or partial response, whereas 47.5% (19/40) achieved stable disease, 12.5% (5/40) had progressive disease, and there were no cases of disease relapses in responders. Both early and advanced stages of CTCL were responsive to alitretinoin as a primary or combined modality. Alitretinoin was well tolerated, and 64.3% (27/42) of patients did not report any side effects. The most commonly observed side effect was hypertriglyceridemia.

CONCLUSIONS

This retrospective analysis supports the efficacy and safety of alitretinoin in clearing skin disease and preventing disease progression in CTCL as a monotherapy or in combination with standard therapies.

摘要

背景

蕈样真菌病(MF)和塞扎里综合征(SS)是最常见的皮肤 T 细胞淋巴瘤(CTCL)亚型。目前 CTCL 尚无治愈方法,治疗旨在限制疾病进展。本研究评估了阿利维 A 酯在 CTCL 治疗中的疗效和耐受性。

方法

对接受阿利维 A 酯作为单一药物或联合标准疗法治疗的 CTCL 患者进行了回顾性、多中心研究。

结果

48 例 MF(n=40)和 SS(n=8)患者符合研究纳入标准,中位年龄为 59.7 岁(±14.3)。对 40 例患者进行了治疗反应数据评估,对 42 例患者进行了安全性评估。40.0%的患者为早期 CTCL,43.8%为晚期 CTCL,16.7%的患者分期信息不足。40.0%(16/40)的患者获得完全或部分缓解,47.5%(19/40)的患者获得疾病稳定,12.5%(5/40)的患者疾病进展,缓解患者无疾病复发。阿利维 A 酯作为单一或联合治疗对早期和晚期 CTCL 均有效。阿利维 A 酯耐受性良好,64.3%(27/42)的患者未报告任何副作用。最常见的不良反应是高甘油三酯血症。

结论

本回顾性分析支持阿利维 A 酯作为单一药物或联合标准疗法治疗 CTCL 清除皮肤疾病和预防疾病进展的疗效和安全性。

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