Durable complete response in a patient with BRAF-mutated advanced melanoma with ocular and skin toxicities from BRAF/MEK targeted therapy after immune checkpoint inhibitor treatment: a case report.

IF 1.3 Q2 DERMATOLOGY
Carlotta Bertolina, Marinella Bertolotti, Claudia Leporati, Antonina Maria De Angelis, Sara Delfanti, Luigi Cerbone, Marco Ghiglione, Federica Grosso
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引用次数: 0

Abstract

Here we report the case of a woman suffering from advanced melanoma who developed severe toxicities with BRAF and MEK inhibitors (BRAFis, MEKis), given as second-line therapy after failure of immunotherapy, who achieved a complete and durable response lasting for over 5 years. Significant progress has been achieved in the treatment of advanced melanoma with immune checkpoint inhibitors (ICIs) and targeted therapies using BRAFis and MEKis. While these treatments improve survival, they also pose risks of severe toxicities. Notably, when targeted therapy follows immunotherapy, immune-mediated toxicities may emerge months later due to tumor microenvironment modulation. Despite these risks, both approaches offer a durable response in eligible patients. Further understanding is needed to determine how prior immunotherapy may influence subsequent toxicity risks of target therapy. Understanding these factors could optimize treatment strategies and improve patient outcomes.

免疫检查点抑制剂治疗后BRAF突变晚期黑色素瘤伴眼部和皮肤毒性的持久完全缓解:1例报告
在这里,我们报告了一名患有晚期黑色素瘤的女性,她在免疫治疗失败后使用BRAF和MEK抑制剂(BRAFis, MEKis)作为二线治疗,产生了严重的毒性,并获得了持续超过5年的完全和持久的反应。在使用免疫检查点抑制剂(ICIs)治疗晚期黑色素瘤以及使用BRAFis和MEKis靶向治疗方面取得了重大进展。虽然这些治疗方法提高了生存率,但它们也带来了严重毒性的风险。值得注意的是,当免疫治疗之后进行靶向治疗时,由于肿瘤微环境调节,免疫介导的毒性可能在几个月后出现。尽管存在这些风险,但这两种方法都能在符合条件的患者中提供持久的反应。需要进一步了解先前的免疫治疗如何影响后续靶向治疗的毒性风险。了解这些因素可以优化治疗策略,改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Dermatology Reports
Dermatology Reports DERMATOLOGY-
CiteScore
1.40
自引率
0.00%
发文量
74
审稿时长
10 weeks
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