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Complete remission in leptomeningeal metastasis of NSCLC with rare EGFR-SEPT14 fusion treated with osimertinib combined with intrathecal chemotherapy with pemetrexed.
Author: FengJie, JiangCheng, LiHuiying, LinYongjuan, QianXiaoping, XieYu, YinZhenyu, YuTingting, ZhengShengnan
Original Abstract of the Article :
Leptomeningeal metastasis (LM) is one of the most serious complications of non-small cell lung cancer (NSCLC) without standard treatment guidelines and is always accompanied by poor prognosis. Identifying the types of gene mutations is essential to improve the outcome, and an increasing number of ra...See full text at original site
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ラクダ博士は、Health Journal が論文の内容を分かりやすく解説するために作成した架空のキャラクターです。
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引用元:
https://pubmed.ncbi.nlm.nih.gov/34486539
データ提供:米国国立医学図書館(NLM)
A Rare EGFR-SEPT14 Fusion: A Case Study in NSCLC-LM Treatment
This fascinating case study delves into the complex realm of [oncology], specifically focusing on [leptomeningeal metastasis (LM)] in [non-small cell lung cancer (NSCLC)]. The research utilizes [NGS] to identify a rare [EGFR-SEPT14 fusion] and explores its implications for treatment. The study focuses on a 56-year-old male patient diagnosed with [lung adenocarcinoma] and subsequently developed [LM]. The researchers investigated the effectiveness of [osimertinib] combined with [intrathecal chemotherapy with pemetrexed] as a treatment option for this rare mutation.
A Beacon of Hope for Patients with Rare Mutations
This case study, the first of its kind, demonstrates the successful treatment of [NSCLC-LM] harboring a specific [EGFR-SEPT14 fusion]. The patient achieved [complete remission] with [osimertinib] and [intrathecal pemetrexed], offering a potential therapeutic strategy for patients with this uncommon mutation. This discovery holds promise for future treatment approaches, offering a ray of hope for individuals facing this challenging diagnosis.
Precision Medicine: Tailoring Treatment to Unique Needs
This study emphasizes the growing importance of [precision medicine], where treatments are tailored to individual patient needs and genetic variations. Just as a camel adapts to the diverse landscape of the desert, understanding the unique characteristics of each patient's condition allows for more targeted and effective treatments. This case study demonstrates the power of precision medicine in achieving remarkable outcomes for patients with rare mutations.
Dr.Camel's Conclusion
This case study exemplifies the power of [precision medicine], highlighting the importance of identifying rare genetic mutations in patients with [NSCLC-LM]. It offers a glimmer of hope for individuals with this specific [EGFR-SEPT14 fusion], demonstrating that personalized treatment strategies can lead to impressive clinical outcomes. This study encourages further exploration of precision medicine approaches to optimize cancer treatment and improve patient outcomes.
Date :
- Date Completed 2022-03-04
- Date Revised 2023-09-02
Further Info :
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