• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一名先前接受过BRAF靶向治疗和免疫治疗的晚期转移性黑色素瘤患者对伊匹木单抗/纳武单抗再激发治疗及BRAF抑制剂/MEK抑制剂再激发治疗的反应

Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy.

作者信息

Myrdal Caitlyn N, Sundararajan Srinath

机构信息

University of Arizona College of Medicine, Tucson, AZ, USA.

Hematology and Oncology, Texas Oncology, Houston, TX, USA.

出版信息

Case Rep Oncol Med. 2020 Jun 25;2020:4392562. doi: 10.1155/2020/4392562. eCollection 2020.

DOI:10.1155/2020/4392562
PMID:32670650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7334770/
Abstract

Little is known about the optimal sequencing of targeted therapy and immunotherapy in the treatment of patients with BRAF-mutated metastatic melanoma. BRAF/MEK inhibition often has the benefit of rapid disease regression; however, resistance is frequently seen with long-term use. Treatment with immune checkpoint inhibitors offers the potential for long-term response but displays a lower rate of objective response. The benefit of synergy between therapies is apparent; however, there is limited data regarding optimal sequencing in the treatment of advanced melanoma. We present the case of a 62-year-old gentleman with advanced BRAF-mutated melanoma who followed an unconventional treatment path. After progressing on single-agent vemurafenib, he had response to multiple modalities of immunotherapy before progression. After, he had a substantial response to multiple BRAF/MEK inhibitor rechallenges before developing resistance. The patient is now stable after a retrial of combination immunotherapy. Our case illustrates that with the right sequencing of therapy, meaningful clinical responses can be elicited with rechallenging of targeted therapy and immunotherapy in metastatic melanoma.

摘要

关于BRAF突变的转移性黑色素瘤患者治疗中靶向治疗和免疫治疗的最佳顺序,人们了解甚少。BRAF/MEK抑制通常具有疾病快速消退的益处;然而,长期使用时耐药很常见。免疫检查点抑制剂治疗具有产生长期反应的潜力,但客观反应率较低。治疗之间协同作用的益处是明显的;然而,关于晚期黑色素瘤治疗中最佳顺序的数据有限。我们报告一例62岁患有晚期BRAF突变黑色素瘤的男性患者,其遵循了非常规的治疗路径。在单药维莫非尼治疗进展后,他在疾病进展前对多种免疫治疗方式有反应。之后,在出现耐药前,他对多种BRAF/MEK抑制剂再次治疗有显著反应。在联合免疫治疗再次试验后,患者目前病情稳定。我们的病例表明,通过正确的治疗顺序,在转移性黑色素瘤中对靶向治疗和免疫治疗进行再次治疗可引发有意义的临床反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d43/7334770/985306f855a2/CRIONM2020-4392562.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d43/7334770/a337ab452b28/CRIONM2020-4392562.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d43/7334770/985306f855a2/CRIONM2020-4392562.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d43/7334770/a337ab452b28/CRIONM2020-4392562.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d43/7334770/985306f855a2/CRIONM2020-4392562.002.jpg

相似文献

1
Response to Ipilimumab/Nivolumab Rechallenge and BRAF Inhibitor/MEK Inhibitor Rechallenge in a Patient with Advanced Metastatic Melanoma Previously Treated with BRAF Targeted Therapy and Immunotherapy.一名先前接受过BRAF靶向治疗和免疫治疗的晚期转移性黑色素瘤患者对伊匹木单抗/纳武单抗再激发治疗及BRAF抑制剂/MEK抑制剂再激发治疗的反应
Case Rep Oncol Med. 2020 Jun 25;2020:4392562. doi: 10.1155/2020/4392562. eCollection 2020.
2
Case Report: Rechallenge With BRAF and MEK Inhibitors in Metastatic Melanoma: A Further Therapeutic Option in Salvage Setting?病例报告:BRAF和MEK抑制剂在转移性黑色素瘤中的再激发:挽救治疗中的另一种治疗选择?
Front Oncol. 2021 May 31;11:645008. doi: 10.3389/fonc.2021.645008. eCollection 2021.
3
A Dramatic Response to Second-Line Nivolumab and Ipilimumab in BRAF-V600-Mutated Metastatic Melanoma.BRAF-V600 突变的转移性黑色素瘤对二线纳武单抗和伊匹单抗的显著反应
Case Rep Oncol. 2024 Jan 29;17(1):161-168. doi: 10.1159/000535902. eCollection 2024 Jan-Dec.
4
Atezolizumab, cobimetinib, and vemurafenib as first-line treatment for unresectable metastatic BRAF V600 mutated melanoma.阿替利珠单抗、考比替尼和维莫非尼作为不可切除的转移性BRAF V600突变黑色素瘤的一线治疗方案。
Expert Rev Anticancer Ther. 2022 Jan;22(1):17-25. doi: 10.1080/14737140.2022.2017286. Epub 2022 Jan 2.
5
Current and future roles of targeted therapy and immunotherapy in advanced melanoma.靶向治疗和免疫疗法在晚期黑色素瘤中的当前和未来作用。
J Manag Care Spec Pharm. 2014 Apr;20(4):346-56. doi: 10.18553/jmcp.2014.20.4.346.
6
Clinical Predictors of Survival in Patients With BRAFV600-Mutated Metastatic Melanoma Treated With Combined BRAF and MEK Inhibitors After Immune Checkpoint Inhibitors.联合 BRAF 和 MEK 抑制剂治疗免疫检查点抑制剂后 BRAFV600 突变转移性黑色素瘤患者的生存临床预测因素。
Oncologist. 2024 Apr 4;29(4):e507-e513. doi: 10.1093/oncolo/oyad300.
7
Systemic treatments for metastatic cutaneous melanoma.转移性皮肤黑色素瘤的全身治疗
Cochrane Database Syst Rev. 2018 Feb 6;2(2):CD011123. doi: 10.1002/14651858.CD011123.pub2.
8
Successful treatment of BRAF/MEK inhibitor-resistant advanced cutaneous melanoma with nivolumab plus ipilimumab combination therapy followed by intensity-modulated radiotherapy.纳武利尤单抗联合伊匹单抗序贯调强放疗治疗 BRAF/MEK 抑制剂耐药的晚期皮肤黑色素瘤的成功治疗。
J Dermatol. 2021 Sep;48(9):1419-1422. doi: 10.1111/1346-8138.15962. Epub 2021 May 18.
9
Controversies in the management of advanced melanoma: "gray" areas amid the "black and blue".晚期黑色素瘤治疗中的争议:“青一块紫一块”中的“灰色地带”
Ann Pharmacother. 2014 Nov;48(11):1456-68. doi: 10.1177/1060028014544165. Epub 2014 Jul 23.
10
Immunotherapy and Targeted Therapy in Patients With Advanced Melanoma and the V600 BRAF Mutation: Which One First?晚期黑色素瘤伴 V600 BRAF 突变患者的免疫治疗与靶向治疗:先选哪个?

引用本文的文献

1
Clinical Implications of Acquired BRAF Inhibitors Resistance in Melanoma.黑色素瘤中获得性 BRAF 抑制剂耐药的临床意义。
Int J Mol Sci. 2020 Dec 20;21(24):9730. doi: 10.3390/ijms21249730.

本文引用的文献

1
The American Cancer Society's Facts & Figures: 2020 Edition.美国癌症协会《2020年事实与数据》版
J Adv Pract Oncol. 2020 Mar;11(2):135-136. doi: 10.6004/jadpro.2020.11.2.1. Epub 2020 Mar 1.
2
Dabrafenib, trametinib and pembrolizumab or placebo in BRAF-mutant melanoma.达拉非尼、曲美替尼联合或不联合 pembrolizumab 治疗 BRAF 突变型黑色素瘤。
Nat Med. 2019 Jun;25(6):941-946. doi: 10.1038/s41591-019-0448-9. Epub 2019 Jun 6.
3
Cutaneous Melanoma, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology.皮肤黑色素瘤临床实践指南(第 2 版).2019,NCCN 肿瘤学临床实践指南。
J Natl Compr Canc Netw. 2019 Apr 1;17(4):367-402. doi: 10.6004/jnccn.2019.0018.
4
Nivolumab plus ipilimumab or nivolumab alone versus ipilimumab alone in advanced melanoma (CheckMate 067): 4-year outcomes of a multicentre, randomised, phase 3 trial.纳武利尤单抗联合伊匹单抗或纳武利尤单抗单药对比伊匹单抗单药治疗晚期黑色素瘤(CheckMate 067):一项多中心、随机、III 期临床试验的 4 年结果。
Lancet Oncol. 2018 Nov;19(11):1480-1492. doi: 10.1016/S1470-2045(18)30700-9. Epub 2018 Oct 22.
5
Encorafenib plus binimetinib versus vemurafenib or encorafenib in patients with BRAF-mutant melanoma (COLUMBUS): a multicentre, open-label, randomised phase 3 trial.恩考芬尼加比美替尼与维莫非尼或恩考芬尼用于治疗 BRAF 突变型黑色素瘤患者(COLUMBUS):一项多中心、开放标签、随机 3 期临床试验。
Lancet Oncol. 2018 May;19(5):603-615. doi: 10.1016/S1470-2045(18)30142-6. Epub 2018 Mar 21.
6
Pembrolizumab versus ipilimumab for advanced melanoma: final overall survival results of a multicentre, randomised, open-label phase 3 study (KEYNOTE-006).帕博利珠单抗对比伊匹单抗用于晚期黑色素瘤:一项多中心、随机、开放标签的 3 期研究(KEYNOTE-006)的最终总生存结果。
Lancet. 2017 Oct 21;390(10105):1853-1862. doi: 10.1016/S0140-6736(17)31601-X. Epub 2017 Aug 16.
7
Heterogeneity and frequency of BRAF mutations in primary melanoma: Comparison between molecular methods and immunohistochemistry.原发性黑色素瘤中BRAF突变的异质性和频率:分子方法与免疫组织化学的比较
Oncotarget. 2017 Jan 31;8(5):8069-8082. doi: 10.18632/oncotarget.14094.
8
Sequencing Treatment in BRAFV600 Mutant Melanoma: Anti-PD-1 Before and After BRAF Inhibition.BRAFV600突变型黑色素瘤的序贯治疗:BRAF抑制前后使用抗PD-1治疗
J Immunother. 2017 Jan;40(1):31-35. doi: 10.1097/CJI.0000000000000148.
9
Genomic Classification of Cutaneous Melanoma.皮肤黑色素瘤的基因组分类
Cell. 2015 Jun 18;161(7):1681-96. doi: 10.1016/j.cell.2015.05.044.
10
Dabrafenib and trametinib versus dabrafenib and placebo for Val600 BRAF-mutant melanoma: a multicentre, double-blind, phase 3 randomised controlled trial.达拉非尼联合曲美替尼与达拉非尼联合安慰剂治疗 Val600BRAF 突变型黑色素瘤:一项多中心、双盲、III 期随机对照临床试验。
Lancet. 2015 Aug 1;386(9992):444-51. doi: 10.1016/S0140-6736(15)60898-4. Epub 2015 May 31.