原发性肺腺癌BRAF突变PD-L1阳性转移性肌肉骨骼病变联合vemurafenib和pembrolizumab治疗:病例报告。

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Corazon A Ngelangel, Florge Francis Sy
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引用次数: 0

摘要

背景:B-Raf突变阳性、B-Raf突变阳性伴有程序性死亡配体1过表达以及肌肉骨骼转移在非小细胞肺癌中非常罕见,更罕见的是这些情况都发生在一名患者身上:一位63岁的菲律宾男性患者患有B-Raf突变阳性和程序性死亡配体1过表达的肺腺癌无症状转移性肌肉骨骼病变,他接受了BRAF抑制剂vemurafenib联合免疫检查点抑制剂pembrolizumab的治疗。他的疼痛和肌肉骨骼转移病灶的负担明显减轻:结论:B-Raf突变阳性程序性死亡配体1过度表达的肺腺癌伴有转移性肌肉骨骼病变,这种情况虽然罕见,而且预后较差,但可以对免疫检查点抑制剂和BRAF抑制剂联合用药产生良好反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BRAF mutant PD-L1 positive metastatic musculoskeletal lesions from primary lung adenocarcinoma treated with combination vemurafenib and pembrolizumab: a case report.

Background: B-Raf mutation positivity, B-Raf mutation positivity occurrence with programmed death ligand 1 overexpression, and musculoskeletal metastasis are singly rare in non-small cell lung cancer, and even rarer is all occurring in one patient.

Case presentation: A Filipino 63-year-old male had B-Raf mutation positive and programmed death ligand 1 overexpressed symptomatic metastatic musculoskeletal lesions from lung adenocarcinoma treated with a BRAF inhibitor, vemurafenib, in combination with an immune checkpoint inhibitor, pembrolizumab. He exhibited significant reduction in pain and burden of musculoskeletal metastatic lesions.

Conclusion: Although a rare occurrence and known to have a poor prognosis, B-Raf mutation positive programmed death ligand 1 overexpressed lung adenocarcinoma presenting with metastatic musculoskeletal lesions can respond favorably to a combination immune checkpoint inhibitor and BRAF inhibitor medication.

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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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