Higashi Jukiya, Miyoshi Kotoko, Hirai Kazuhiro, Kanazawa Fumiaki, Nakaji Hitoshi, Miyagaki Aki
Department of Respiratory Medicine, Toyooka Public Hospital, Toyooka, JPN.
Department of Gastroenterology, Toyooka Public Hospital, Toyooka, JPN.
Cureus. 2025 Apr 1;17(4):e81586. doi: 10.7759/cureus.81586. eCollection 2025 Apr.
Pulmonary pleomorphic carcinoma (PPC) is a rare subtype of non-small cell lung cancer (NSCLC). It has a rapid progression and poor prognosis and is resistant to conventional chemotherapy. The efficacy of molecular-targeted drugs for patients with PPC with targetable driver mutations has been reported. However, most molecular-targeted drugs are administered orally, limiting their application in cases where oral administration is difficult. We report the case of a 78-year-old male patient diagnosed with stage IIA lung cancer. He underwent lobectomy and was pathologically diagnosed with PPC harboring a BRAF-V600E mutation. His lung cancer recurred two months postoperatively with multiple metastases, including those in the small intestine, which caused intussusception and ileus. Because the resected specimen from the small intestinal tumor resembled the histopathological results of the preoperative lung tissue, treatment with dabrafenib and trametinib could be effective. A percutaneous endoscopic gastrojejunostomy (PEG-J) tube was placed on the anal side of the intussusception site to depressurize intragastric pressure, allowing drug administration while decompressing the stomach. Treatment initiated for a few days improved abdominal symptoms, and computed tomography (CT) revealed tumor shrinkage. This is the first reported case of a patient with malignant intestinal obstruction successfully treated with targeted therapy drugs administered via a PEG-J tube, which is a viable method for patients with NSCLC with driver mutations who cannot take oral medications or via a nasogastric tube. Furthermore, therapies targeting driver mutations may be effective for patients with PPC.
肺多形性癌(PPC)是一种罕见的非小细胞肺癌(NSCLC)亚型。它进展迅速,预后较差,对传统化疗耐药。已有报道分子靶向药物对具有可靶向驱动基因突变的PPC患者的疗效。然而,大多数分子靶向药物为口服给药,限制了其在难以口服给药的情况下的应用。我们报告一例78岁男性患者,诊断为IIA期肺癌。他接受了肺叶切除术,病理诊断为携带BRAF-V600E突变的PPC。术后两个月肺癌复发并伴有多处转移,包括小肠转移,导致肠套叠和肠梗阻。由于小肠肿瘤切除标本的组织病理学结果与术前肺组织相似,使用达拉非尼和曲美替尼治疗可能有效。在肠套叠部位的肛门侧放置了经皮内镜下胃空肠造口术(PEG-J)管以降低胃内压力,从而在胃减压的同时允许给药。治疗开始几天后腹部症状改善,计算机断层扫描(CT)显示肿瘤缩小。这是首例报道的通过PEG-J管给予靶向治疗药物成功治疗恶性肠梗阻患者的病例,对于无法口服药物或通过鼻胃管给药的具有驱动基因突变的NSCLC患者而言,这是一种可行的方法。此外,针对驱动基因突变的治疗可能对PPC患者有效。