Durable complete response in a patient with leptomeningeal melanoma after treatment with dabrafenib, trametinib, and nivolumab

IF 3.9 3区 医学 Q2 CELL BIOLOGY Pigment Cell & Melanoma Research Pub Date : 2024-07-03 DOI:10.1111/pcmr.13179
Sarah E. Lochrin, Darren J. Buonocore, Robert J. Young, Thomas J. Kaley, Michael A. Postow, Jedd D. Wolchok, Alexander N. Shoushtari, Parisa Momtaz, Allison S. Betof Warner, Margaret K. Callahan
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Abstract

Leptomeningeal disease (LMD) is a devastating complication of melanoma with a dismal prognosis. We present the case of a young man with stage IV BRAF V600E mutant melanoma with lung, lymph node, and brain metastases initially treated with ipilimumab and nivolumab, who subsequently developed LMD. Upon change to BRAF/MEK targeted therapy with nivolumab, a durable complete response was achieved and remains ongoing, off treatment, 7 years from diagnosis. Management of symptomatic LMD remains a critical unmet clinical challenge, with limited clinical trial data. This exceptional case is instructive, as the first published case of the use of the triplet, and the first durable response with therapy discontinuation, in melanoma LMD. The triple-drug regimen may be considered a viable option in fit patients. This case highlights the potential for long-term disease control and the critical and urgent need to develop clinical trials inclusive of patients with LMD to define the best treatment strategies.

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用达拉菲尼、曲美替尼和尼韦单抗治疗一名脑外膜黑色素瘤患者后获得持久完全应答。
多发性脑膜病(LMD)是黑色素瘤的一种破坏性并发症,预后极差。我们介绍了一例患有 IV 期 BRAF V600E 突变黑色素瘤并伴有肺、淋巴结和脑转移的年轻男性患者的病例,该患者最初接受了伊匹单抗和尼伐单抗治疗,随后出现了 LMD。在改用尼妥珠单抗进行 BRAF/MEK 靶向治疗后,患者获得了持久的完全缓解,并且在确诊 7 年后仍在接受治疗。由于临床试验数据有限,无症状 LMD 的治疗仍是一项严峻的临床挑战。这一特殊病例是黑色素瘤 LMD 首次公开发表的使用三联疗法的病例,也是黑色素瘤 LMD 首次在停止治疗后出现持久应答的病例,因此具有指导意义。三联疗法可被视为适合患者的可行方案。该病例凸显了长期控制疾病的潜力,以及开展包括LMD患者在内的临床试验以确定最佳治疗策略的关键性和紧迫性。
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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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