Haller F
Institut für allgemeine Pathologie und pathologische Anatomie, Universitätsklinikum Freiburg, Breisacher Str. 115a, 79106 Freiburg.
Pathologe. 2010 Oct;31 Suppl 2:161-6. doi: 10.1007/s00292-010-1333-y.
Prognosis evaluation in gastrointestinal stromal tumors (GIST) is currently based on tumor diameter, mitotic counts and anatomic localisation. There are two risk classifications as well as the first ever TNM classification for GISTs, whereby the risk classification according to the Armed Forces Institute of Pathology (AFIP) has the best correlation with clinical follow-up according to own experiences. "Very low/low risk" GISTs are almost benign, while the majority of "high risk" GISTs metastasize and benefit from adjuvant therapy. Careful evaluation of mitotic counts in 50 high-power fields is of particular relevance for correct risk classification. Apart from these classical prognostic factors, many molecular genetic parameters with correlation to follow-up have been evaluated and may help to improve prognosis evaluation of GISTs in the future. Since most of the molecular genetic parameters are associated or even determined by the clinico-pathological parameters, an integrated model for tumor progression of GISTs is helpful to interpret the different factors in correlation to one another. In particular for "intermediate risk" GISTs, additional parameters are needed for improved prognosis evaluation.
胃肠道间质瘤(GIST)的预后评估目前基于肿瘤直径、有丝分裂计数和解剖定位。GIST有两种风险分类以及首个TNM分类,根据自身经验,美国武装部队病理研究所(AFIP)的风险分类与临床随访的相关性最佳。“极低/低风险”GIST几乎是良性的,而大多数“高风险”GIST会发生转移并受益于辅助治疗。在50个高倍视野下仔细评估有丝分裂计数对于正确的风险分类尤为重要。除了这些经典的预后因素外,许多与随访相关的分子遗传学参数也已得到评估,可能有助于未来改善GIST的预后评估。由于大多数分子遗传学参数与临床病理参数相关甚至由其决定,GIST肿瘤进展的综合模型有助于解释不同因素之间的相互关系。特别是对于“中风险”GIST,需要额外的参数来改善预后评估。