首页> 美国卫生研究院文献>Oncology Letters >Second-line chemotherapy for refractory small cell neuroendocrine carcinoma of the esophagus that relapsed after complete remission with irinotecan plus cisplatin therapy: Case report and review of the literature
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Second-line chemotherapy for refractory small cell neuroendocrine carcinoma of the esophagus that relapsed after complete remission with irinotecan plus cisplatin therapy: Case report and review of the literature

机译:伊立替康联合顺铂治疗完全缓解后食管难治性食管小细胞神经内分泌癌的二线化疗:病例报告及文献复习

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摘要

Small cell esophageal carcinoma is a type of small cell neuroendocrine carcinoma (SCNEC). SCNEC follows an aggressive clinical course and has a poor prognosis despite multidisciplinary therapies. A standard therapeutic strategy, including surgery, radiation and first-/second-line chemotherapy, has not yet been established for SCNEC. We present a case of SCNEC of the esophagus. A 66-year-old male with SCNEC as extensive disease was treated with 60 mg/m2 cisplatin on day 1 plus 60 mg/m2 irinotecan on days 1, 8 and 15 every 4 weeks (IP) with successful complete remission. After the sixth course of IP, increasing pro-gastrin-releasing peptide (ProGRP) and nonspecific enolase (NSE) levels and intense fluorodeoxyglucose (FDG) avidity in a lymph node around the celiac artery (SUVmax, 8.3) indicated a refractory relapse of the disease. The patient was treated with three courses of amrubicin (AMR, 35 mg/m2) administered intravenously for 3 consecutive days every 3 weeks as a second-line chemotherapy. The ProGRP and NSE levels returned to the normal range 1 month after the initiation of second-line chemotherapy. However, the ProGRP and NSE levels were elevated after the third course of AMR, and PET-CT revealed progressive disease with liver metastasis and extended lymph node metastasis. As the patient remained asymptomatic, paclitaxel (100 mg/m2) was started as third-line chemotherapy. Patients with SCNEC of the esophagus with extensive disease should be treated with aggressive chemotherapy rather than surgery or radiation monotherapy. In the present case, tumor markers such as ProGRP and NSE were predictive of relapse and PET-CT was used to detect relapse. Further research is required to identify and exploit promising agents for resistant SCNEC.
机译:小细胞食管癌是一种小细胞神经内分泌癌(SCNEC)。 SCNEC遵循积极的临床过程,尽管采用了多学科治疗,但预后较差。 SCNEC尚未建立包括手术,放疗和一线/二线化疗在内的标准治疗策略。我们提出一例食管SCNEC。一位患有SCNEC广泛性疾病的66岁男性在第1天接受60 mg / m 2 顺铂治疗,并在第1、8天接受60 mg / m 2 伊立替康治疗每4周(IP)成功完成15次。腹膜内注射第六个疗程后,腹腔动脉周围淋巴结中的促胃泌素释放肽(ProGRP)和非特异性烯醇酶(NSE)水平升高,以及强烈的氟脱氧葡萄糖(FDG)亲合力(SUVmax,8.3)提示顽固性复发疾病。该患者接受了三疗程的氨柔比星(AMR,35 mg / m 2 )治疗,每三周连续三天静脉注射,作为二线化疗。开始二线化疗后1个月,ProGRP和NSE水平恢复到正常范围。然而,在第三次AMR疗程后,ProGRP和NSE水平升高,PET-CT显示进展性疾病伴肝转移和淋巴结转移延长。当患者无症状时,紫杉醇(100 mg / m 2 )开始作为三线化疗。食道SCNEC广泛性疾病的患者应采用积极的化学疗法而非手术或放射线单药治疗。在本例中,诸如ProGRP和NSE之类的肿瘤标志物可预示复发,而PET-CT可用于检测复发。需要进一步的研究来鉴定和开发有前景的抗SCNEC药物。

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