HyBryte™ use in early-stage cutaneous T-cell lymphoma

B. Poligone, Carolina V Alexander-Savino, Ellen J. Kim, Aaron R. Mangold, Jennifer Desimone, Henry K. Wong, A. Rumage, O. Donini, Andrea M. Haulenbeek, Christopher J. Schaber, Richard Straube, C. Pullion, A. Rook
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Abstract

Cutaneous T-cell lymphoma (CTCL) is a rare type of non-Hodgkin lymphoma of the skin, where at later stages skin-homing malignant T-cells affect lymph nodes, blood, and visceral organs. Even though early CTCL does not affect survival, it can progress to more advanced stages of disease and have a significant effect on the quality of life of patients. Although expectant management is a treatment consideration in early disease stages, most patients cycle through different skin-directed therapies throughout their lifetime. It can become a challenge to manage the serious and accumulating risk of side effects of these therapies, including various skin cancers and skin damage. Adverse effects from topical therapies limit their long-term utility. Thus, there is an unmet need for well-characterized therapies that have a rapid onset of action and minimal long-term/cumulative side effect profile. Most recently, the results of a Phase 3 study of topical HyBryte™ as a potential treatment for CTCL demonstrated its efficacy and safety profile. This article summarizes what is known about HyBryte™, focuses on its mechanism of action, and highlights its effectiveness, safety, and tolerability in the context of other current FDA-approved topical therapies for CTCL.
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HyBryte™ 用于早期皮肤 T 细胞淋巴瘤
皮肤 T 细胞淋巴瘤(CTCL)是一种罕见的皮肤非霍奇金淋巴瘤,晚期皮肤上的恶性 T 细胞会影响淋巴结、血液和内脏器官。尽管早期的 CTCL 不会影响患者的生存,但它会发展到晚期,对患者的生活质量产生重大影响。虽然在疾病的早期阶段,预期管理是治疗的一个考虑因素,但大多数患者在其一生中会循环使用不同的皮肤导向疗法。管理这些疗法的副作用(包括各种皮肤癌和皮肤损伤)所带来的严重且不断累积的风险是一项挑战。局部疗法产生的不良反应限制了这些疗法的长期使用。因此,对于起效迅速、长期/累积副作用最小的特性良好的疗法的需求尚未得到满足。最近,一项关于外用 HyBryte™ 作为 CTCL 潜在疗法的 3 期研究结果表明了它的疗效和安全性。本文总结了目前对 HyBryte™ 的了解,重点介绍了其作用机制,并结合目前其他经 FDA 批准的 CTCL 外用疗法,强调了其有效性、安全性和耐受性。
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