• 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

相似文献

1
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.
2
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.
3
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.
4
Combination of dabrafenib plus trametinib for BRAF and MEK inhibitor pretreated patients with advanced BRAF-mutant melanoma: an open-label, single arm, dual-centre, phase 2 clinical trial.达拉非尼联合曲美替尼治疗 BRAF 和 MEK 抑制剂预处理的晚期 BRAF 突变型黑色素瘤患者:一项开放标签、单臂、双中心、Ⅱ期临床研究。
Lancet Oncol. 2017 Apr;18(4):464-472. doi: 10.1016/S1470-2045(17)30171-7. Epub 2017 Mar 4.
5
Spectrum and Frequency of BRAF Mutations in Skin Melanomas in the Dalmatian Region of Croatia.克罗地亚达尔马提亚地区皮肤黑色素瘤中 BRAF 突变的谱和频率。
Acta Dermatovenerol Croat. 2024 Mar;32(1):75-76.
6
Successful retreatment with combined BRAF/MEK inhibition in metastatic BRAFV600-mutated melanoma.转移性 BRAFV600 突变型黑色素瘤中联合 BRAF/MEK 抑制的成功治疗。
J Eur Acad Dermatol Venereol. 2017 Oct;31(10):1638-1640. doi: 10.1111/jdv.14268. Epub 2017 May 8.
7
Recent advances in molecular targeted therapy for unresectable and metastatic BRAF-mutated melanoma.不可切除和转移性 BRAF 突变型黑色素瘤的分子靶向治疗的最新进展。
Jpn J Clin Oncol. 2021 Mar 3;51(3):315-320. doi: 10.1093/jjco/hyaa222.
8
Immunomodulatory Effects of BRAF, MEK, and CDK4/6 Inhibitors: Implications for Combining Targeted Therapy and Immune Checkpoint Blockade for the Treatment of Melanoma.BRAF、MEK 和 CDK4/6 抑制剂的免疫调节作用:对联合靶向治疗和免疫检查点阻断治疗黑色素瘤的意义。
Front Immunol. 2021 May 7;12:661737. doi: 10.3389/fimmu.2021.661737. eCollection 2021.
9
Cautious addition of targeted therapy to PD-1 inhibitors after initial progression of BRAF mutant metastatic melanoma on checkpoint inhibitor therapy.在接受检查点抑制剂治疗后,BRAF 突变转移性黑色素瘤初始进展时谨慎地添加靶向治疗联合 PD-1 抑制剂。
BMC Cancer. 2021 Nov 7;21(1):1187. doi: 10.1186/s12885-021-08906-1.
10
Anti-PD-(L)1 plus BRAF/MEK inhibitors (triplet therapy) after failure of immune checkpoint inhibition and targeted therapy in patients with advanced melanoma.抗 PD-(L)1 联合 BRAF/MEK 抑制剂(三联疗法)治疗晚期黑色素瘤患者免疫检查点抑制剂和靶向治疗失败后的情况。
Eur J Cancer. 2024 May;202:113976. doi: 10.1016/j.ejca.2024.113976. Epub 2024 Mar 1.

引用本文的文献

1
ERK pathway agonism for cancer therapy: evidence, insights, and a target discovery framework.用于癌症治疗的ERK通路激动作用:证据、见解及一个靶点发现框架
NPJ Precis Oncol. 2024 Mar 14;8(1):70. doi: 10.1038/s41698-024-00554-5.
2
Trametinib-Resistant Melanoma Cells Displaying MITF/NGFR/IL-8 Phenotype Are Highly Responsive to Alternating Periods of Drug Withdrawal and Drug Rechallenge.对曲美替尼耐药的黑素瘤细胞表现出 MITF/NGFR/IL-8 表型,对药物撤药和药物再挑战的交替周期高度敏感。
Int J Mol Sci. 2023 Apr 26;24(9):7891. doi: 10.3390/ijms24097891.
3
Intermittent treatment of BRAF melanoma cells delays resistance by adaptive resensitization to drug rechallenge.间歇性治疗 BRAF 黑色素瘤细胞通过对药物再挑战的适应性再敏化来延迟耐药性。
Proc Natl Acad Sci U S A. 2022 Mar 22;119(12):e2113535119. doi: 10.1073/pnas.2113535119. Epub 2022 Mar 15.

本文引用的文献

1
Continuous versus intermittent BRAF and MEK inhibition in patients with BRAF-mutated melanoma: a randomized phase 2 trial.BRAF 突变型黑色素瘤患者中连续与间断 BRAF 和 MEK 抑制:一项随机 2 期试验。
Nat Med. 2020 Oct;26(10):1564-1568. doi: 10.1038/s41591-020-1060-8. Epub 2020 Oct 5.
2
Application of Circulating Cell-Free Tumor DNA Profiles for Therapeutic Monitoring and Outcome Prediction in Genetically Heterogeneous Metastatic Melanoma.循环游离肿瘤DNA图谱在基因异质性转移性黑色素瘤治疗监测和预后预测中的应用
JCO Precis Oncol. 2019 Feb 15;3. doi: 10.1200/PO.18.00229. eCollection 2020.
3
Atezolizumab, vemurafenib, and cobimetinib as first-line treatment for unresectable advanced BRAF mutation-positive melanoma (IMspire150): primary analysis of the randomised, double-blind, placebo-controlled, phase 3 trial.阿替利珠单抗、维莫非尼和考比替尼作为不可切除的晚期 BRAF 突变阳性黑色素瘤的一线治疗药物(IMspire150):随机、双盲、安慰剂对照、III 期临床试验的主要分析。
Lancet. 2020 Jun 13;395(10240):1835-1844. doi: 10.1016/S0140-6736(20)30934-X.
4
BRAF and MEK inhibitors rechallenge as effective treatment for patients with metastatic melanoma.BRAF和MEK抑制剂再次挑战作为转移性黑色素瘤患者的有效治疗方法。
Melanoma Res. 2020 Oct;30(5):465-471. doi: 10.1097/CMR.0000000000000662.
5
Survival of patients with advanced metastatic melanoma: The impact of MAP kinase pathway inhibition and immune checkpoint inhibition - Update 2019.晚期转移性黑色素瘤患者的生存:MAP 激酶通路抑制和免疫检查点抑制的影响-2019 年更新。
Eur J Cancer. 2020 May;130:126-138. doi: 10.1016/j.ejca.2020.02.021. Epub 2020 Mar 13.
6
The Management of Oligoprogression in the Landscape of New Therapies for Metastatic Melanoma.转移性黑色素瘤新疗法背景下的寡进展管理
Cancers (Basel). 2019 Oct 14;11(10):1559. doi: 10.3390/cancers11101559.
7
Undetectable circulating tumor DNA (ctDNA) levels correlate with favorable outcome in metastatic melanoma patients treated with anti-PD1 therapy.抗 PD-1 治疗转移性黑色素瘤患者中,无法检测到的循环肿瘤 DNA(ctDNA)水平与良好的预后相关。
J Transl Med. 2019 Sep 5;17(1):303. doi: 10.1186/s12967-019-2051-8.
8
Drug resistance of BRAF-mutant melanoma: Review of up-to-date mechanisms of action and promising targeted agents.BRAF 突变型黑色素瘤的耐药性:最新作用机制及有前途的靶向药物综述。
Eur J Pharmacol. 2019 Nov 5;862:172621. doi: 10.1016/j.ejphar.2019.172621. Epub 2019 Aug 22.
9
Constitutive Expression of NRAS with Q61R Driver Mutation Activates Processes of Epithelial-Mesenchymal Transition and Leads to Substantial Transcriptome Change of Nthy-ori 3-1 Thyroid Epithelial Cells.具有Q61R驱动突变的NRAS组成型表达激活上皮-间质转化过程,并导致Nthy-ori 3-1甲状腺上皮细胞的大量转录组变化。
Biochemistry (Mosc). 2019 Apr;84(4):416-425. doi: 10.1134/S0006297919040096.
10
Five-Year Outcomes with Dabrafenib plus Trametinib in Metastatic Melanoma.达拉非尼联合曲美替尼治疗转移性黑色素瘤的 5 年结果。
N Engl J Med. 2019 Aug 15;381(7):626-636. doi: 10.1056/NEJMoa1904059. Epub 2019 Jun 4.

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?

Case Report: Rechallenge With BRAF and MEK Inhibitors in Metastatic Melanoma: A Further Therapeutic Option in Salvage Setting?

作者信息

Stagno Anna, Vari Sabrina, Annovazzi Alessio, Anelli Vincenzo, Russillo Michelangelo, Cognetti Francesco, Ferraresi Virginia

机构信息

Department of Medical Oncology 1, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.

Nuclear Medicine Unit, IRCCS-Regina Elena National Cancer Institute, Rome, Italy.

出版信息

Front Oncol. 2021 May 31;11:645008. doi: 10.3389/fonc.2021.645008. eCollection 2021.

DOI:10.3389/fonc.2021.645008
PMID:34136385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8202400/
Abstract

BACKGROUND

The combination of BRAF and MEK inhibitors represents the standard of care treatment for patients with metastatic -mutated melanoma, notwithstanding the high frequency of emergent resistance. Moreover, therapeutic options outside clinical trials are scarce when patients have progressed after both targeted therapy and therapy with immune checkpoint inhibitors. In this article, we report our experience with targeted therapy rechallenging with BRAF and MEK inhibitors in patients with metastatic -mutated melanoma after progression with kinase inhibitors and immunotherapy.

METHODS

Four patients with metastatic -mutated melanoma were rechallenged with BRAF and MEK inhibitors after progression with targeted therapy and subsequent immunotherapy (checkpoint inhibitors).

RESULTS

Two patients (one of them was heavily pretreated) had partial response over 36 months (with local treatment on oligoprogression disease) and 10 months, respectively. A third patient with multisite visceral disease and high serum levels of lactate dehydrogenase had a short-lived clinical benefit rapidly followed by massive progression of disease (early progressor). The fourth patient, currently on treatment with BRAF/MEK inhibitors, is showing a clinical benefit and radiological stable disease over 3 months of therapy. Adverse events were manageable, similar to those reported during the first targeted therapy; the treatment was better tolerated at rechallenge compared with the first treatment by two out of four patients.

摘要

背景

BRAF和MEK抑制剂联合使用是转移性BRAF突变型黑色素瘤患者的标准治疗方案,尽管出现耐药的频率很高。此外,当患者在靶向治疗和免疫检查点抑制剂治疗后病情进展时,临床试验之外的治疗选择很少。在本文中,我们报告了转移性BRAF突变型黑色素瘤患者在激酶抑制剂和免疫治疗进展后,再次使用BRAF和MEK抑制剂进行靶向治疗的经验。

方法

4例转移性BRAF突变型黑色素瘤患者在靶向治疗和随后的免疫治疗(检查点抑制剂)进展后,再次接受BRAF和MEK抑制剂治疗。

结果

2例患者(其中1例接受过大量预处理)分别在36个月(对寡进展性疾病进行局部治疗)和10个月时出现部分缓解。第3例患有多部位内脏疾病且血清乳酸脱氢酶水平高的患者有短暂的临床获益,随后迅速出现疾病大量进展(早期进展者)。第4例患者目前正在接受BRAF/MEK抑制剂治疗,在3个月的治疗中显示出临床获益且影像学疾病稳定。不良事件可控,与首次靶向治疗期间报告的不良事件相似;4例患者中有2例在再次治疗时比首次治疗耐受性更好。