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黑色素瘤治疗中与BRAF和MEK抑制剂相关的口腔不良事件:一项叙述性文献综述

Oral Adverse Events Associated with BRAF and MEK Inhibitors in Melanoma Treatment: A Narrative Literature Review.

作者信息

Basilicata Michele, Terrano Vincenzo, D'Aurelio Alessandro, Bruno Giovanni, Troiani Teresa, Bollero Patrizio, Napolitano Stefania

机构信息

UOSD Special Care Dentistry, Department of Experimental Medicine and Surgery, University of Roma Tor Vergata, 00133 Rome, Italy.

UniCamillus-Saint Camillus, International University of Health Sciences, 00131 Rome, Italy.

出版信息

Healthcare (Basel). 2024 Jan 2;12(1):105. doi: 10.3390/healthcare12010105.

DOI:10.3390/healthcare12010105
PMID:38201012
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10778825/
Abstract

BACKGROUND

Melanoma cancer represents the most lethal type of skin cancer originating from the malignant transformation of melanocyte cells. Almost 50% of melanomas show the activation of BRAF mutations. The identification and characterization of BRAF mutations led to the development of specific drugs that radically changed the therapeutic approach to melanoma.

METHODS

We conducted a narrative review of the literature according to a written protocol before conducting the study. This article is based on previously conducted studies. We identified articles by searching electronic databases (Medline, Google Scholar and PubMed). We used a combination of "melanoma", "Braf-Mek inhibitors", " targeted therapy" and "oral side effects".

RESULTS

Eighteen studies were reported in this article showing the relationship between the use of targeted therapy in melanoma cancer and the development of oral side effects, such as mucositis, hyperkeratosis and cellular proliferation.

CONCLUSION

Targeted therapy plays an important role in the treatment of melanoma cancer, showing a notable increase in response rate, prolonged progression-free survival and overall survival in BRAF-mutated melanoma patients. Oral side effects represent a common finding over the course of treatment. However, these adverse effects can be easily managed in a multidisciplinary approach involving collaboration between medical oncologists and dental doctors.

摘要

背景

黑色素瘤是源自黑素细胞恶性转化的最致命的皮肤癌类型。几乎50%的黑色素瘤显示BRAF突变激活。BRAF突变的鉴定和特征分析促成了特定药物的开发,这些药物从根本上改变了黑色素瘤的治疗方法。

方法

在开展本研究之前,我们根据书面方案对文献进行了叙述性综述。本文基于先前开展的研究。我们通过检索电子数据库(Medline、谷歌学术和PubMed)来确定文章。我们使用了“黑色素瘤”“BRAF - MEK抑制剂”“靶向治疗”和“口腔副作用”的组合词进行检索。

结果

本文报道了18项研究,这些研究表明黑色素瘤靶向治疗的使用与口腔副作用(如黏膜炎、角化过度和细胞增殖)的发生之间的关系。

结论

靶向治疗在黑色素瘤治疗中发挥着重要作用,在BRAF突变的黑色素瘤患者中显示出缓解率显著提高、无进展生存期和总生存期延长。口腔副作用是治疗过程中的常见现象。然而,通过肿瘤内科医生和牙科医生合作的多学科方法可以轻松管理这些不良反应。

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Oral Adverse Events Associated with BRAF and MEK Inhibitors in Melanoma Treatment: A Narrative Literature Review.黑色素瘤治疗中与BRAF和MEK抑制剂相关的口腔不良事件:一项叙述性文献综述
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本文引用的文献

1
Targeting RAS-RAF-MEK-ERK signaling pathway in human cancer: Current status in clinical trials.靶向人类癌症中的RAS-RAF-MEK-ERK信号通路:临床试验现状
Genes Dis. 2022 May 20;10(1):76-88. doi: 10.1016/j.gendis.2022.05.006. eCollection 2023 Jan.
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Neoadjuvant-Adjuvant or Adjuvant-Only Pembrolizumab in Advanced Melanoma.新辅助-辅助或仅辅助派姆单抗治疗晚期黑色素瘤。
N Engl J Med. 2023 Mar 2;388(9):813-823. doi: 10.1056/NEJMoa2211437.
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Neoadjuvant relatlimab and nivolumab in resectable melanoma.新辅助雷利度胺和纳武利尤单抗治疗可切除黑色素瘤。
Nature. 2022 Nov;611(7934):155-160. doi: 10.1038/s41586-022-05368-8. Epub 2022 Oct 26.
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COLUMBUS 5-Year Update: A Randomized, Open-Label, Phase III Trial of Encorafenib Plus Binimetinib Versus Vemurafenib or Encorafenib in Patients With V600-Mutant Melanoma.COLUMBUS 5 年更新:依维莫司或恩考芬尼联合比尼替尼对比维莫非尼用于 V600 突变型黑色素瘤患者的随机、开放标签、III 期试验。
J Clin Oncol. 2022 Dec 20;40(36):4178-4188. doi: 10.1200/JCO.21.02659. Epub 2022 Jul 21.
5
Personalized response-directed surgery and adjuvant therapy after neoadjuvant ipilimumab and nivolumab in high-risk stage III melanoma: the PRADO trial.新辅助伊匹单抗和纳武利尤单抗治疗高危 III 期黑色素瘤后的个体化反应导向手术和辅助治疗:PRADO 试验。
Nat Med. 2022 Jun;28(6):1178-1188. doi: 10.1038/s41591-022-01851-x. Epub 2022 Jun 5.
6
Pembrolizumab versus placebo as adjuvant therapy in completely resected stage IIB or IIC melanoma (KEYNOTE-716): a randomised, double-blind, phase 3 trial.帕博利珠单抗对比安慰剂作为完全切除的IIB期或IIC期黑色素瘤辅助治疗(KEYNOTE-716):一项随机、双盲、3期试验
Lancet. 2022 Apr 30;399(10336):1718-1729. doi: 10.1016/S0140-6736(22)00562-1. Epub 2022 Apr 1.
7
Relatlimab and Nivolumab versus Nivolumab in Untreated Advanced Melanoma.Relatlimab 和 Nivolumab 对比 Nivolumab 用于未经治疗的晚期黑色素瘤。
N Engl J Med. 2022 Jan 6;386(1):24-34. doi: 10.1056/NEJMoa2109970.
8
Signal pathways of melanoma and targeted therapy.黑色素瘤的信号通路与靶向治疗。
Signal Transduct Target Ther. 2021 Dec 20;6(1):424. doi: 10.1038/s41392-021-00827-6.
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Long-Term Outcomes With Nivolumab Plus Ipilimumab or Nivolumab Alone Versus Ipilimumab in Patients With Advanced Melanoma.纳武利尤单抗联合伊匹单抗或纳武利尤单抗对比伊匹单抗治疗晚期黑色素瘤患者的长期结局。
J Clin Oncol. 2022 Jan 10;40(2):127-137. doi: 10.1200/JCO.21.02229. Epub 2021 Nov 24.
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5-Year Outcomes with Cobimetinib plus Vemurafenib in BRAFV600 Mutation-Positive Advanced Melanoma: Extended Follow-up of the coBRIM Study.考比替尼联合威罗非尼治疗 BRAFV600 突变阳性晚期黑色素瘤的 5 年结果:coBRIM 研究的扩展随访。
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