Targeting the IL-2 pathway for the treatment of mucosal melanoma

IF 0.8 4区 医学 Q4 PHARMACOLOGY & PHARMACY Expert Opinion on Orphan Drugs Pub Date : 2022-10-10 DOI:10.1080/21678707.2022.2134776
Ann Mercurio, Ashray B Maniar, A. Wei, R. Carvajal
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Abstract

ABSTRACT Introduction Mucosal melanomas are rare and aggressive forms of cancer that have consistently eluded meaningful recovery with various anticancer therapies. Patients with unresectable mucosal melanomas have benefited from prolonged survival with the use of systemic drugs, including immune checkpoint inhibitors, but prognosis for mucosal malignancies remains inferior compared to cutaneous melanomas. FDA breakthrough and orphan drug designations for novel IL-2 formulations bempegaldesleukin and nemvaleukin highlight the potential for restoring cytokine-based therapy as a viable option in treating mucosal melanomas. Areas covered In this review, we discuss the biological and clinical features of mucosal melanomas, the current therapies available to this patient population including anti-PD1 and targeted therapies, and the potential for integrating novel IL-2 formulations into the existing armamentarium. Recently published clinical trial outcomes evaluating IL-2-based drugs are critically evaluated within the context of the existing treatment landscape for mucosal melanomas. Expert Opinion We conclude that clinical trials are a key priority for eligible patients who may stand to benefit from IL-2 therapy. For patients with unresectable and advanced disease who are unable to participate in trials, anti-PD1 and targeted therapies may still be considered as front- and next-line treatments on a case-by-case basis.
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靶向IL-2途径治疗粘膜黑色素瘤
摘要简介粘膜黑色素瘤是一种罕见的侵袭性癌症,通过各种抗癌疗法一直无法有效恢复。不可切除的粘膜黑色素瘤患者通过使用包括免疫检查点抑制剂在内的全身性药物延长了生存期,但与皮肤黑色素瘤相比,粘膜恶性肿瘤的预后仍然较差。美国食品药品监督管理局对新型IL-2制剂的突破性和孤儿药指定贝姆培格尔德白细胞介素和恩伐真细胞介素突出了恢复基于细胞因子的治疗作为治疗粘膜黑色素瘤的可行选择的潜力。涵盖的领域在这篇综述中,我们讨论了粘膜黑色素瘤的生物学和临床特征,该患者群体目前可用的治疗方法,包括抗PD1和靶向治疗,以及将新型IL-2制剂整合到现有药物中的潜力。最近发表的评估基于IL-2的药物的临床试验结果在粘膜黑色素瘤现有治疗环境的背景下进行了严格评估。专家意见我们的结论是,临床试验是符合条件的患者的关键优先事项,这些患者可能会从IL-2治疗中受益。对于无法参加试验的不可切除和晚期疾病患者,抗PD1和靶向治疗仍可能被视为一线和下一步的治疗方法。
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来源期刊
Expert Opinion on Orphan Drugs
Expert Opinion on Orphan Drugs PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
0.00%
发文量
8
期刊介绍: Expert Opinion on Orphan Drugs is an international, peer-reviewed journal that covers all aspects of R&D on rare diseases and orphan drugs.
期刊最新文献
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