阿法替尼联合立体定向放疗治疗少转移性egfr突变非小细胞肺癌1例报告及文献复习

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
AME Case Reports Pub Date : 2025-04-08 eCollection Date: 2025-01-01 DOI:10.21037/acr-24-174
Lisi Sun, Dan Tao, Yuyu Lv, Chunyu Wang, Yue Xie, Wei Zhou
{"title":"阿法替尼联合立体定向放疗治疗少转移性egfr突变非小细胞肺癌1例报告及文献复习","authors":"Lisi Sun, Dan Tao, Yuyu Lv, Chunyu Wang, Yue Xie, Wei Zhou","doi":"10.21037/acr-24-174","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Epidermal growth factor receptor (<i>EGFR</i>)-mutated patients treated with target therapy are inevitable to develop resistance to tyrosine kinase inhibitors (TKIs). It has been proved that concurrent stereotactic body radiotherapy (SBRT) and the first-generation TKIs can prolong both progression-free survival (PFS) and overall survival (OS) of <i>EGFR</i>-mutated patients with limited metastases. However, the efficacy and safety of concomitant second-generation TKIs and SBRT is still unknown.</p><p><strong>Case description: </strong>We for the first time present a stage IVA patient with mutation of both <i>EGFR</i> G719X and L861Q, who after initial response, had developed intracranial progression during afatinib monotherapy. With local treatment for the brain metastasis, she continued to receive afatinib and then a concurrent consolidative lung SBRT. Until January 2023, the patient had achieved a PFS of 24 months and OS of 32 months without serious adverse events except for a grade 1 radiation pneumonitis after the lung SBRT.</p><p><strong>Conclusions: </strong>With this case and a literature review, we aim to demonstrate that concurrent afatinib and consolidative SBRT can bring prognostic benefits to oligometastatic NSCLC patients with uncommon <i>EGFR</i> mutations with good tolerance. However, larger studies with longer follow-up, including randomized controlled trials, are needed to better define the response rates, survival outcomes, and toxicity profiles of this combined therapy. Additionally, further research is required to determine the optimal timing for introducing SBRT in conjunction with afatinib.</p>","PeriodicalId":29752,"journal":{"name":"AME Case Reports","volume":"9 ","pages":"50"},"PeriodicalIF":0.7000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12053448/pdf/","citationCount":"0","resultStr":"{\"title\":\"Concurrent afatinib and stereotactic body radiotherapy in patient with oligometastatic <i>EGFR</i>-mutated non-small cell lung cancer: a case report and literature review.\",\"authors\":\"Lisi Sun, Dan Tao, Yuyu Lv, Chunyu Wang, Yue Xie, Wei Zhou\",\"doi\":\"10.21037/acr-24-174\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Epidermal growth factor receptor (<i>EGFR</i>)-mutated patients treated with target therapy are inevitable to develop resistance to tyrosine kinase inhibitors (TKIs). It has been proved that concurrent stereotactic body radiotherapy (SBRT) and the first-generation TKIs can prolong both progression-free survival (PFS) and overall survival (OS) of <i>EGFR</i>-mutated patients with limited metastases. However, the efficacy and safety of concomitant second-generation TKIs and SBRT is still unknown.</p><p><strong>Case description: </strong>We for the first time present a stage IVA patient with mutation of both <i>EGFR</i> G719X and L861Q, who after initial response, had developed intracranial progression during afatinib monotherapy. With local treatment for the brain metastasis, she continued to receive afatinib and then a concurrent consolidative lung SBRT. Until January 2023, the patient had achieved a PFS of 24 months and OS of 32 months without serious adverse events except for a grade 1 radiation pneumonitis after the lung SBRT.</p><p><strong>Conclusions: </strong>With this case and a literature review, we aim to demonstrate that concurrent afatinib and consolidative SBRT can bring prognostic benefits to oligometastatic NSCLC patients with uncommon <i>EGFR</i> mutations with good tolerance. However, larger studies with longer follow-up, including randomized controlled trials, are needed to better define the response rates, survival outcomes, and toxicity profiles of this combined therapy. Additionally, further research is required to determine the optimal timing for introducing SBRT in conjunction with afatinib.</p>\",\"PeriodicalId\":29752,\"journal\":{\"name\":\"AME Case Reports\",\"volume\":\"9 \",\"pages\":\"50\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-04-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12053448/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"AME Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21037/acr-24-174\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"AME Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21037/acr-24-174","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

摘要

背景:表皮生长因子受体(EGFR)突变患者接受靶向治疗不可避免地会对酪氨酸激酶抑制剂(TKIs)产生耐药性。已经证明,同步立体定向放疗(SBRT)和第一代TKIs可以延长有限转移的egfr突变患者的无进展生存期(PFS)和总生存期(OS)。然而,伴随第二代TKIs和SBRT的有效性和安全性仍然未知。病例描述:我们首次报道了一例EGFR G719X和L861Q突变的IVA期患者,该患者在初始反应后,在阿法替尼单药治疗期间发生颅内进展。在局部治疗脑转移的同时,她继续接受阿法替尼治疗,然后同时接受巩固性肺SBRT治疗。截至2023年1月,该患者的PFS为24个月,OS为32个月,除肺部SBRT后出现1级放射性肺炎外,无严重不良事件。结论:通过本病例和文献综述,我们旨在证明阿法替尼联合巩固性SBRT可为罕见EGFR突变的少转移性NSCLC患者带来预后益处,且耐受性良好。然而,需要更大规模、随访时间更长的研究,包括随机对照试验,以更好地确定这种联合治疗的反应率、生存结果和毒性特征。此外,需要进一步的研究来确定SBRT与阿法替尼联合应用的最佳时机。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Concurrent afatinib and stereotactic body radiotherapy in patient with oligometastatic <i>EGFR</i>-mutated non-small cell lung cancer: a case report and literature review.

Concurrent afatinib and stereotactic body radiotherapy in patient with oligometastatic <i>EGFR</i>-mutated non-small cell lung cancer: a case report and literature review.

Concurrent afatinib and stereotactic body radiotherapy in patient with oligometastatic EGFR-mutated non-small cell lung cancer: a case report and literature review.

Background: Epidermal growth factor receptor (EGFR)-mutated patients treated with target therapy are inevitable to develop resistance to tyrosine kinase inhibitors (TKIs). It has been proved that concurrent stereotactic body radiotherapy (SBRT) and the first-generation TKIs can prolong both progression-free survival (PFS) and overall survival (OS) of EGFR-mutated patients with limited metastases. However, the efficacy and safety of concomitant second-generation TKIs and SBRT is still unknown.

Case description: We for the first time present a stage IVA patient with mutation of both EGFR G719X and L861Q, who after initial response, had developed intracranial progression during afatinib monotherapy. With local treatment for the brain metastasis, she continued to receive afatinib and then a concurrent consolidative lung SBRT. Until January 2023, the patient had achieved a PFS of 24 months and OS of 32 months without serious adverse events except for a grade 1 radiation pneumonitis after the lung SBRT.

Conclusions: With this case and a literature review, we aim to demonstrate that concurrent afatinib and consolidative SBRT can bring prognostic benefits to oligometastatic NSCLC patients with uncommon EGFR mutations with good tolerance. However, larger studies with longer follow-up, including randomized controlled trials, are needed to better define the response rates, survival outcomes, and toxicity profiles of this combined therapy. Additionally, further research is required to determine the optimal timing for introducing SBRT in conjunction with afatinib.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信