Department of Melanoma Medical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Exp Dermatol. 2022 Jan;31(1):74-81. doi: 10.1111/exd.14413. Epub 2021 Jul 3.
There has been unprecedented progress in the development of systemic therapies for patients with metastatic melanoma over the last decade. There is now tremendous potential and momentum to further and markedly reduce the impact of this disease. However, developing more effective treatments for metastases to the CNS remains a critical challenge for patients with melanoma. Melanoma patients with active CNS metastases have largely been excluded from both early-phase and registration trials for all currently approved targeted and immune therapies for this disease. While this exclusion has generally been justified in clinical research due to concerns about poor prognosis, lack of CNS penetration of agents and/or risk of toxicities, recent post-approval trials have shown the feasibility, safety and clinical benefit of clinical investigation in these patients. These trials have also identified key areas for which more effective strategies are needed. In parallel, recent translational and preclinical research has provided insights into novel immune, molecular and metabolic features of melanoma brain metastases that may mediate the aggressive biology and therapeutic resistance of these tumors. Together, these advances suggest the need for new paradigms for therapeutic development for melanoma patients with CNS metastasis.
在过去的十年中,转移性黑色素瘤的系统性治疗取得了前所未有的进展。现在有巨大的潜力和动力进一步显著降低这种疾病的影响。然而,开发针对 CNS 转移的更有效治疗方法仍然是黑色素瘤患者面临的一个关键挑战。患有活动性 CNS 转移的黑色素瘤患者基本上被排除在所有目前批准的针对该疾病的靶向和免疫治疗的早期和注册试验之外。虽然由于对预后不良、药物对 CNS 的穿透性差和/或毒性风险的担忧,这种排除在临床研究中通常是合理的,但最近的批准后试验表明了在这些患者中进行临床研究的可行性、安全性和临床获益。这些试验还确定了需要更有效策略的关键领域。与此同时,最近的转化和临床前研究为黑色素瘤脑转移的新型免疫、分子和代谢特征提供了深入了解,这些特征可能介导这些肿瘤的侵袭性生物学和治疗耐药性。总之,这些进展表明需要为患有 CNS 转移的黑色素瘤患者制定新的治疗开发范例。