Yokoi Kimiyoshi, Tanaka Noritake, Shoji Kyono, Ishikawa Noriyuki, Seya Tomoko, Horiba Koji, Kanazawa Yoshikazu, Yamashita Kiyohiko, Ohaki Yoshiharu, Tajiri Takashi
Department of Surgery, Nippon Medical School Chiba Hokusoh Hospital, 1715 Kamagari, Inbamura, Inbagun, Chiba, 270-1694, Japan.
J Gastroenterol. 2005 May;40(5):467-73. doi: 10.1007/s00535-005-1571-6.
As no established histopathological criteria exist for assessing the malignant potential of gastrointestinal stromal tumor (GIST), recurrence or metastasis is occasionally observed in lesions diagnosed histopathologically as benign. The present study aimed to clarify the histopathological criteria for assessing the malignancy of GIST, from a clinical standpoint.
The subjects were 22 patients with GIST expressing CD117 (c-kit) and/or CD34, who were followed up for more than 2 years. Clinically, GIST malignancy was diagnosed if any of the following criteria were met: peripheral invasive growth, lymph node metastasis, metastasis to another organ, peritoneal dissemination, recurrence, or death. GIST was also categorized as either benign or malignant by a new histological malignancy classification system, based on the determination of significant factors indicating malignancy in the clinical classification system above.
Significant factors for malignancy identified in the clinical malignancy classification were: tumor hemorrhage/necrosis (present vs absent; P = 0.0053), tumor size (<5 cm vs > or =5 cm; P = 0.0022), and Ki-67 labeling index (<3% vs > or =3%; P = 0.0002). A new histological malignancy classification, based on a combination of these three factors, was developed. A significant correlation existed between the clinical system and the new histological malignancy classification system (P = 0.0008). The recurrence-free survival rate was 100% in the histologically benign cases and 37.5% in the histologically malignant cases (P = 0.0012).
The new histological malignancy classification for GIST was demonstrated to be useful from a clinical standpoint.
由于目前尚无既定的组织病理学标准来评估胃肠道间质瘤(GIST)的恶性潜能,因此在组织病理学诊断为良性的病变中偶尔会观察到复发或转移。本研究旨在从临床角度阐明评估GIST恶性程度的组织病理学标准。
研究对象为22例表达CD117(c-kit)和/或CD34的GIST患者,随访时间超过2年。临床上,如果符合以下任何一项标准,则诊断为GIST恶性:外周浸润性生长、淋巴结转移、远处器官转移、腹膜播散、复发或死亡。根据上述临床分类系统中表明恶性的重要因素的判定结果,GIST还通过一种新的组织学恶性分类系统分为良性或恶性。
在临床恶性分类中确定的恶性重要因素为:肿瘤出血/坏死(存在与否;P = 0.0053)、肿瘤大小(<5 cm与≥5 cm;P = 0.0022)和Ki-67标记指数(<3%与≥3%;P = 0.0002)。基于这三个因素的组合,制定了一种新的组织学恶性分类。临床系统与新的组织学恶性分类系统之间存在显著相关性(P = 0.0008)。组织学良性病例的无复发生存率为100%,组织学恶性病例为37.5%(P = 0.0012)。
从临床角度来看,新的GIST组织学恶性分类被证明是有用的。