帕唑帕尼治疗原发性肺雷米肉瘤:病例报告与文献综述

0 RESPIRATORY SYSTEM Therapeutic advances in pulmonary and critical care medicine Pub Date : 2024-10-21 eCollection Date: 2024-01-01 DOI:10.1177/29768675241279709
Sahar Khosravi, Sana Keshtegar, Ali Tavakoli Pirzaman
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引用次数: 0

摘要

原发性肺平滑肌肉瘤(PPL)来源于肺平滑肌组织,在肺部恶性肿瘤中的发病率不到 0.5%,而在原发性肺肉瘤中的发病率为 30%。在此,我们介绍一例帕唑帕尼治疗的PPL病例。此外,我们还对相关文献进行了简要回顾。一名 65 岁女性患者因慢性咳嗽、体重减轻和反复肺炎就诊,病史包括糖尿病、高血压和高脂血症,既往曾行结肠切除术和子宫切除术(因异常子宫出血,病理检查正常,未发现子宫良性肌瘤)。入院时,她表现出发热、咳嗽、呼吸困难和上肺叶呼吸音减弱。诊断性检查发现了一个巨大的肺部肿块,通过核心针活检和随后的免疫组化染色确诊为子宫肌瘤。患者接受了伊佛酰胺和阿霉素的新辅助治疗,随后接受了化放疗,但无法进行肿瘤切除手术。吉西他滨和多西他赛在伊佛酰胺和阿霉素无效后被选为新的治疗方案。影像学检查显示,肿瘤对最新治疗也没有反应。鉴于病情持续存在,且患者接受化疗的能力减弱,目前患者正在接受帕唑帕尼治疗,并持续监测治疗效果。帕唑帕尼(口服,每次 200 毫克,每天两次)治疗 3 个月后,患者的肿瘤体积明显缩小,从 135 毫米缩小到 80 毫米,约为初始体积的三分之一,显示出积极的治疗效果。本病例报告提供的初步证据表明,帕唑帕尼(一种口服多酪氨酸激酶抑制剂)可能是治疗 PPL 的一种很有前景的治疗选择。然而,要评估这种疗法的临床疗效和优越性,还需要进一步的深入和长期研究。
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Primary Pulmonary Leiomyosarcoma Managed With Pazopanib: A Case Report and Literature Review.

Primary pulmonary leiomyosarcoma (PPL) arises from pulmonary smooth muscle tissue, with less than 0.5% incidence among pulmonary malignancies and 30% among primary pulmonary sarcomas. Here, we present a case of PPL managed with pazopanib. Moreover, a brief review of relevant literature was conducted. A 65-year-old female presented with chronic cough, weight loss, and recurrent pneumonia, with a medical history including diabetes mellitus, hypertension, and hyperlipidemia, as well as past surgical colectomy and hysterectomy (due to abnormal uterine bleeding with normal pathology and no evidence of uterine leiomyosarcoma). Upon admission, she exhibited fever, cough, dyspnea, and decreased breath sounds over the upper lung lobe. Diagnostic workups revealed a large pulmonary mass, diagnosed as leiomyosarcoma via core needle biopsy and subsequent immunohistochemical staining. Neoadjuvant treatment with ifosfamide and adriamycin followed by chemoradiotherapy was attempted, but surgery for tumor resection was not feasible. Then, gemcitabine and docetaxel were chosen as the new treatment after ifosfamide and adriamycin were not effective. Imaging revealed tumor not reacting to latest treatment, either. Given the disease's persistence and the patient's diminished capacity for chemotherapy, the patient is presently undergoing pazopanib treatment, with ongoing monitoring of its effects. After 3 months of treatment with pazopanib (administered orally at 200 mg twice daily), the patient experienced a significant reduction in tumor size, with a notable decrease from 135 mm to 80 mm, approximating one-third of the initial size, indicating a positive therapeutic effect. This case report provides preliminary evidence suggesting that pazopanib, an oral multi-tyrosine kinase inhibitor, may be a promising therapeutic option for the management of PPL. However, further in-depth and long-term studies are warranted to evaluate the clinical efficacy and superiority of this treatment.

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