Watanabe Jun, Suwa Yusuke, Ota Mitsuyoshi, Ishibe Atsushi, Masui Hidenobu, Nagahori Kaoru, Tsuura Yukio, Endo Itaru
1 Department of Surgery, Yokosuka Kyosai Hospital, Yokosuka, Japan 2 Department of Surgery, Gastroenterological Center, Yokohama City University, Yokohama, Japan 3 Department of Gastroenterological Surgery, Yokohama City University Graduate School of Medicine, Yokohama, Japan 4 Department of Pathology, Yokosuka Kyosai Hospital, Yokosuka, Japan.
Dis Colon Rectum. 2016 Dec;59(12):1160-1167. doi: 10.1097/DCR.0000000000000702.
Mixed adenoneuroendocrine carcinoma of the colon and rectum is a very rare type of tumor.
The aim of the present study was to evaluate the clinicopathological characteristics and prognosis of mixed adenoneuroendocrine carcinomas of the colon and rectum.
This was a retrospective case-matched analysis (from March 2007 to December 2013).
This study was conducted at Yokosuka Kyosai Hospital.
One thousand three hundred six consecutive patients with a preoperative diagnosis of colorectal cancer and who underwent tumor resection were enrolled in the present study. Each patient diagnosed with mixed adenoneuroendocrine carcinoma was 1:2 matched with 2 counterparts who had been diagnosed with adenocarcinoma.
Immunohistochemical staining for neuroendocrine markers (chromogranin A, synaptophysin, and CD56) was performed. Cases in which the neuroendocrine component accounted for >30% of the tumor were diagnosed as mixed adenoneuroendocrine carcinomas.
Among 1306 patients, 42 patients (3.2%) were diagnosed with mixed adenoneuroendocrine carcinoma and were compared with 84 patients with adenocarcinoma who had been randomly case matched. The average Ki-67-labeling index value was 78.0% (range, 30.0%-99.0%). Chromogranin A, synaptophysin, and CD56 positivity were observed in 42.9% (18/42), 81.0% (34/42), and 33.3% (14/42) of the tumors. Both the disease-free survival and overall survival were significantly worse for mixed adenoneuroendocrine carcinoma than for adenocarcinoma. Ten patients underwent treatment with oxaliplatin-based chemotherapy. The response rate was 40.0%; the median progression-free survival and overall survival were 6.3 months and 18.1 months.
This was a retrospective single-institution study that included a limited number of cases. The treatment regimens used included different types of oxaliplatin-based chemotherapy.
Mixed adenoneuroendocrine carcinoma of the colon and rectum has a poor prognosis after curative resection and should be distinguished from adenocarcinoma.
结直肠癌混合性腺神经内分泌癌是一种非常罕见的肿瘤类型。
本研究旨在评估结直肠癌混合性腺神经内分泌癌的临床病理特征及预后。
这是一项回顾性病例对照分析(2007年3月至2013年12月)。
本研究在横须贺共済医院开展。
1306例术前诊断为结直肠癌并接受肿瘤切除术的连续患者纳入本研究。每例诊断为混合性腺神经内分泌癌的患者与2例诊断为腺癌的对照患者进行1:2匹配。
进行神经内分泌标志物(嗜铬粒蛋白A、突触素和CD56)的免疫组化染色。神经内分泌成分占肿瘤>30%的病例诊断为混合性腺神经内分泌癌。
1306例患者中,42例(3.2%)诊断为混合性腺神经内分泌癌,并与84例随机病例匹配的腺癌患者进行比较。Ki-67标记指数平均值为78.0%(范围30.0%-99.0%)。42.9%(18/42)、81.0%(34/42)和33.3%(14/42)的肿瘤观察到嗜铬粒蛋白A、突触素和CD56阳性。混合性腺神经内分泌癌的无病生存期和总生存期均显著差于腺癌。10例患者接受了基于奥沙利铂的化疗。缓解率为40.0%;中位无进展生存期和总生存期分别为6.3个月和18.1个月。
这是一项回顾性单机构研究,病例数量有限。使用的治疗方案包括不同类型的基于奥沙利铂的化疗。
结直肠癌混合性腺神经内分泌癌根治性切除术后预后较差,应与腺癌相鉴别。