Singh S, Hallet J, Rowsell C, Law C H L
Department of Medical Oncology, Sunnybrook Health Sciences Centre, Odette Cancer Centre, Toronto, Ontario, Canada.
Division of General Surgery, University of Toronto, Toronto, Ontario, Canada; Division of General Surgery, Sunnybrook Health Sciences Centre, Odette Cancer Centre, Toronto, Ontario, Canada.
Eur J Surg Oncol. 2014 Nov;40(11):1517-22. doi: 10.1016/j.ejso.2014.06.016. Epub 2014 Jul 24.
The Ki67-LI is a valid surrogate for biologic behavior of neuroendocrine tumors (NETs), with higher levels associated with aggressive behavior. The World Health Organization (WHO) classifies NETs according to Ki67-LI (G1: <3%; G2 : 3-20%; G3: >20%). Little is known about the evolution of NETs histologic characteristics over the disease course. We sought to evaluate variations in Ki67-LI throughout NETs disease course.
We retrospectively reviewed the Sunnybrook Odette Cancer Center NET database for patients with multiple pathology specimens. Primary outcome was the WHO NET class based on Ki67-LI for each specimen. We assessed change in WHO class between specimens.
Forty-three patients were retrieved, of which 39 had specimens from the primary tumor and a metastatic focus, and 4 had specimens from multiple metastatic foci. Sixteen (37.0%) were identified with Ki67-LI falling in different WHO classes on distinct biopsies. For 12 (75.0%) of those 16 patients, Ki67-LI showed enough variability for WHO class to be upstaged: 5 (31%) from G1 to G2, 2 (13%) from G2 to G3, and 5 (31%) from G1 to G3.
When multiple pathology specimens were available, Ki67-LI varied throughout NETs disease course, with a majority of cases upgraded to a higher WHO class. If confirmed, this finding may have implications in how neuroendocrine tumors are monitored and treated. Further research is warranted to confirm these findings, understand better the underlying mechanisms of Ki67 variability, and define its relationship to prognosis.
Ki67标记指数是神经内分泌肿瘤(NETs)生物学行为的有效替代指标,水平越高与侵袭性行为相关。世界卫生组织(WHO)根据Ki67标记指数对NETs进行分类(G1:<3%;G2:3 - 20%;G3:>20%)。关于NETs组织学特征在疾病过程中的演变知之甚少。我们试图评估Ki67标记指数在NETs疾病过程中的变化。
我们回顾性分析了桑尼布鲁克奥德特癌症中心NET数据库中具有多个病理标本的患者。主要结局是基于每个标本的Ki67标记指数的WHO NET分类。我们评估了不同标本之间WHO分类的变化。
共检索到43例患者,其中39例有来自原发性肿瘤和转移灶的标本,4例有来自多个转移灶的标本。16例(37.0%)在不同活检中Ki67标记指数属于不同的WHO分类。在这16例患者中的12例(75.0%)中,Ki67标记指数显示出足够的变异性,使得WHO分类被上调:5例(31%)从G1升至G2,2例(13%)从G2升至G3,5例(31%)从G1升至G3。
当有多个病理标本时,Ki67标记指数在NETs疾病过程中会发生变化,大多数病例会升级到更高的WHO分类。如果得到证实,这一发现可能对神经内分泌肿瘤的监测和治疗方式产生影响。有必要进行进一步研究以证实这些发现,更好地理解Ki67变异性的潜在机制,并确定其与预后的关系。