Ricci Riccardo, Chiarello Gaia, Attili Fabia, Fuccio Lorenzo, Alfieri Sergio, Persiani Roberto, Di Pietro Salvatore, Martini Maurizio, Costamagna Guido, Larocca Luigi M, Larghi Alberto
Department of Pathology, Catholic University, Rome, Italy.
Department of Pathology, Catholic University, Rome, Italy.
Dig Liver Dis. 2015 Apr;47(4):291-5. doi: 10.1016/j.dld.2014.12.011. Epub 2014 Dec 25.
Current prognostication of gastrointestinal stromal tumours is validated on/applies to resected tumours, mainly because surgery is recommended whenever possible. However, pre-treatment prognostication is increasingly warranted, considering the follow-up strategy recently admitted for expectedly low-risk tumours and the possible distinctive molecular features/spontaneous regression of some small cases.
To investigate whether endoscopic ultrasound-guided fine-needle tissue acquisition-biopsies reflect prognosticators of resected gastrointestinal stromal tumours, for possibly developing reliable pre-treatment prognostic criteria.
The applicability/reliability of mitotic index/5mm(2) and MIB1 proliferative index/1000 cells were tested in 35 endoscopic ultrasound-guided fine-needle tissue acquisition-biopsies diagnosed as gastrointestinal stromal tumour, subsequently resected without intervening therapy, consecutively collected in thirty months. Size and mitotic/proliferative indexes were compared with resection specimens. The feasibility of bioptic genotyping was also tested.
35 patients were studied (45.7% males; mean age 61.6 years, range 26-83 years). Mitotic/proliferative indexes were determinable in 68.6%/88.6% of biopsies, respectively; they were nevertheless underestimated, as happened with endoscopic ultrasound-determined tumour size. Bioptic genotyping revealed reliable.
Endoscopic ultrasound-guided fine-needle tissue acquisition does not reliably reflect gastrointestinal stromal tumours' proliferation and size. Alternative parameters should be validated for a pre-surgical prognostic classification. Considering the emerging potentially prognostic genetic markers in gastrointestinal stromal tumours, the reliability of bioptic genotyping is a promising result.
目前胃肠道间质瘤的预后评估是基于/适用于已切除的肿瘤,主要是因为只要有可能就建议进行手术。然而,考虑到最近针对预期低风险肿瘤采用的随访策略以及一些小病例可能具有的独特分子特征/自发消退情况,治疗前的预后评估越来越有必要。
研究内镜超声引导下细针组织获取活检是否能反映已切除胃肠道间质瘤的预后因素,以便可能制定可靠的治疗前预后标准。
对35例经内镜超声引导下细针组织获取活检诊断为胃肠道间质瘤且随后未接受介入治疗而直接切除的患者进行了有丝分裂指数/5mm²和MIB1增殖指数/1000个细胞的适用性/可靠性测试,这些病例是在30个月内连续收集的。将活检标本的大小、有丝分裂/增殖指数与切除标本进行比较。还测试了活检基因分型的可行性。
共研究了35例患者(男性占45.7%;平均年龄61.6岁,范围26 - 83岁)。活检标本中分别有68.6%/88.6%可确定有丝分裂/增殖指数;然而,这些指数被低估了,内镜超声测定的肿瘤大小也是如此。活检基因分型显示可靠。
内镜超声引导下细针组织获取不能可靠反映胃肠道间质瘤的增殖情况和大小。应验证其他参数用于术前预后分类。鉴于胃肠道间质瘤中出现的潜在预后基因标志物,活检基因分型的可靠性是一个有前景的结果。