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联合靶向治疗和同期放疗治疗转移性黑色素瘤患者的毒性:单中心回顾性分析。

Toxicity of combined targeted therapy and concurrent radiotherapy in metastatic melanoma patients: a single-center retrospective analysis.

机构信息

Department of Dermatology, University Hospital of Zurich, University of Zurich, Gloriastrasse.

Department of Radiation Oncology, University Hospital of Zurich, University of Zurich, Rämistrasse, Zürich, Switzerland.

出版信息

Melanoma Res. 2020 Dec;30(6):552-561. doi: 10.1097/CMR.0000000000000682.

DOI:10.1097/CMR.0000000000000682
PMID:32658050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7643789/
Abstract

The Eastern Cooperative Oncology Group consensus guidelines from 2016 recommend interruption of targeted therapy with BRAF- and MEK-inhibitors during radiotherapy with data being based mostly on BRAF monotherapy. The aim of this study is to provide data on the safety of concurrent radiotherapy and combination targeted therapy with BRAF- and MEK-inhibitors. A total of 32 patients with 51 sessions of radiotherapy from one center receiving concurrent radiotherapy and BRAF- and MEK- inhibitors were included. Radiotherapy-associated toxicities were retrospectively collected. Incidence was compared between three groups: (A) targeted therapy during radiotherapy with and, (B) without interruption, and (C) radiotherapy before the start of targeted therapy. Survival and local disease control were examined. Targeted therapy was interrupted during radiotherapy in 16, not interrupted in 14, and only started after radiotherapy in 21 sessions. Stereotactic radiotherapy was applied in 28 sessions, conventionally fractionated radiotherapy in 23. The brain was the most common site of irradiation (n = 36). Radiotherapy-associated toxicities occurred in 41.2% (n = 21) of sessions and did not differ significantly among the groups. Overall survival was 11.7 months and progression-free survival was 8.4 months. No increase in radiotherapy-associated toxicity was seen where combination targeted therapy was not interrupted during radiotherapy. Prospective clinical trials are warranted to support our findings.

摘要

2016 年,东部肿瘤协作组(ECOG)共识指南建议在放疗期间中断 BRAF 和 MEK 抑制剂的靶向治疗,这些数据主要基于 BRAF 单药治疗。本研究旨在提供关于同时接受放疗和 BRAF 和 MEK 抑制剂联合靶向治疗的安全性数据。共纳入来自一个中心的 32 例患者,共 51 例接受同步放化疗,包括放疗联合 BRAF 和 MEK 抑制剂治疗、BRAF 和 MEK 抑制剂治疗期间不停药、BRAF 和 MEK 抑制剂治疗开始前放疗三种情况。回顾性收集放疗相关毒性反应。比较三组的发生率:(A)放疗期间中断靶向治疗与不停药,(B)不停药,(C)放疗开始前靶向治疗。检查生存和局部疾病控制情况。有 16 例患者在放疗期间中断靶向治疗,14 例患者未中断,21 例患者在放疗后开始靶向治疗。28 例患者接受立体定向放疗,23 例患者接受常规分割放疗。脑是照射最常见的部位(n=36)。41.2%(n=21)的放疗期间发生放疗相关毒性反应,三组之间无显著差异。总生存期为 11.7 个月,无进展生存期为 8.4 个月。在放疗期间不停药的情况下,联合靶向治疗并未增加放疗相关毒性。需要进行前瞻性临床试验来支持我们的研究结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/8752e8d350cf/mr-30-552-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/43105228c03a/mr-30-552-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/4d9687ada110/mr-30-552-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/8752e8d350cf/mr-30-552-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/43105228c03a/mr-30-552-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/4d9687ada110/mr-30-552-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68ee/7643789/8752e8d350cf/mr-30-552-g003.jpg

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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。
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