索托拉西布治疗KRAS p.G12C突变肺肉瘤样癌:KRAS抑制剂对有症状脑转移瘤的治疗效果

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2024-09-16 eCollection Date: 2024-01-01 DOI:10.1159/000540675
Jonas Frederik Schmidt, Dominik Entz, Frank Brasch, Martin Goerner
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引用次数: 0

摘要

简介肺肉瘤样癌(PSC)是非小细胞肺癌(NSCLC)中的一个罕见亚组。与其他非小细胞肺癌相比,肺肉瘤的预后较差,因为放疗和化疗的疗效有限。因此,需要其他治疗方法。KRAS突变发生在PSC中,比例高达30%,其中大部分为G12C,可选择索拉西布(sotorasib)治疗:在此,我们描述了一例合并胸膜转移的 PSC 患者。一线化疗后,患者出现了新的神经系统症状,如右臂偏瘫和局灶性癫痫发作。在发现新的脑转移灶后,由于存在 KRAS G12C 突变,我们将治疗方案改为索托拉西布。在使用索托拉西布治疗期间,患者的病情逐渐恶化,神经系统症状更加严重。治疗过程中进行的CCT检查显示脑转移灶有所进展。服药 48 天后,由于患者无法口服药物,决定终止索拉西布治疗,并改用最佳支持治疗方案。患者在终止治疗数周后因病情迅速进展而死亡:本病例强调,由于化疗、放疗以及目前的靶向治疗缺乏疗效,PSC 患者的预后较差。我们的病例强调了进一步评估靶向治疗对这种罕见亚型 NSCLC 治疗反应的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sotorasib in KRAS p.G12C-Mutated Pulmonary Sarcomatoid Carcinoma: Therapeutic Efficacy of a KRAS Inhibitor in Symptomatic Brain Metastases.

Introduction: Pulmonary sarcomatoid carcinomas (PSCs) are a rare subgroup of non-small cell lung cancer (NSCLC). In contrast to other NSCLCs, PSCs have a poor prognosis due to limited efficacy of radiation and chemotherapy. Therefore, other therapeutic approaches are needed. KRAS mutations occur in PSC with a significant proportion of 30%, and most of them are G12C with the therapeutic option of sotorasib.

Case report: Here, we describe the case of a patient with PSC and pleural metastases. After first-line chemotherapy, the patient presented with new neurological symptoms such as a hemiparesis of the right arm and focal seizures. Following the detection of new brain metastases, we switched the therapy to sotorasib due to the presence of a KRAS G12C mutation. During treatment with sotorasib, the patient's condition worsened progressively and his neurological symptoms got more severe. A CCT performed during the course of treatment showed progression of the brain metastases. After 48 days being on drug, decision to discontinuate therapy with sotorasib due to patient's inability to take oral medication and change to a best supportive care concept was made. The patient died few weeks after termination of therapy with rapidly progressive disease.

Discussion/conclusion: This case emphasizes the poor prognosis of patients with PSC due to a lack of therapeutic response to chemotherapy, radiation, and, as seen in this case, current targeted therapy as well. Our case emphasizes the need to further evaluate therapeutic responses of targeted therapy in this rare subtype of NSCLC.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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