局部晚期和复发直肠癌患者cea靶向荧光引导手术后的长期局部控制

IF 2.5 4区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Molecular Imaging and Biology Pub Date : 2025-08-01 Epub Date: 2025-06-05 DOI:10.1007/s11307-025-02021-4
Mats I Warmerdam, Davy M J Creemers, Miranda Kusters, Koen C M J Peeters, Fabian A Holman, J Sven D Mieog, Francoise Cailler, Pim J W A Burger, Jacobus Burggraaf, Harm J T Rutten, Cornelis Verhoef, Alexander L Vahrmeijer, Denise E Hilling
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引用次数: 0

摘要

目的:在我们之前的2期试验中,局部晚期(LARC)或局部复发直肠癌(LRRC)患者接受了SGM-101,一种靶向cea的荧光剂,以实现实时近红外荧光(NIRF)引导手术。该研究表明,SGM-101能够在一些患者中进行额外的肿瘤切除,并支持其他患者进行微创手术。尽管术中有这种积极的效果,但对长期肿瘤控制的影响尚不清楚。因此,在这篇文章中,我们报告了所有参与试验的直肠癌患者的长期预后。程序:对参与SGM-101二期试验的所有29例LARC和LRRC患者收集随访数据。主要结局指标为5年局部肿瘤控制。结果:所有患者的中位随访时间为5.0年(IQR 4.5-5.5)。在12例LARC患者中,3例(25%)患者发生局部复发。在nif引导下进行微创手术的两例患者仍然没有局部复发。在17例接受根治性手术治疗的LRRC患者中,11例(65%)患者发生局部复发。在SGM-101引导手术直接导致R0而不是R1的3例患者中,1例患者出现局部复发(33%),而另外2例患者仍然没有局部复发。结论:这是第一个报道肿瘤靶向nif引导手术患者随访数据的研究。尽管SGM-101导致术中手术管理发生了必要的变化,但在整个队列中没有观察到改善的长期益处。然而,基于NIRF修改手术入路的患者子集-通过进行微创手术或切除额外的恶性组织-显示出良好的长期预后。正在进行的大型试验的结果正在等待中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Long-term Local Control Following CEA-targeted Fluorescence-guided Surgery in Patients With Locally Advanced and Recurrent Rectal Cancer.

Long-term Local Control Following CEA-targeted Fluorescence-guided Surgery in Patients With Locally Advanced and Recurrent Rectal Cancer.

Long-term Local Control Following CEA-targeted Fluorescence-guided Surgery in Patients With Locally Advanced and Recurrent Rectal Cancer.

Long-term Local Control Following CEA-targeted Fluorescence-guided Surgery in Patients With Locally Advanced and Recurrent Rectal Cancer.

Purpose: In our previous phase 2 trial, patients with locally advanced (LARC) or locally recurrent rectal cancer (LRRC) received SGM-101, a CEA-targeted fluorescent agent, to enable real-time near-infrared fluorescence (NIRF) guided surgery. This study demonstrated that SGM-101 enabled additional tumor removal in some patients and supported less invasive surgery in others. Despite this positive intraoperative effect, the impact on long-term tumor control is unknown. Therefore, in this article we report the long-term outcomes of all rectal cancer patients that participated to the trial.

Procedures: For all 29 LARC and LRRC patients that participated in the SGM-101 phase 2 trial, follow-up data were collected. Main outcome measure was 5-year local tumor control.

Results: The median follow-up of all patients was 5.0 years (IQR 4.5-5.5). Of the 12 LARC patients, three (25%) patients developed a local recurrence. The two patients in whom NIRF-guided surgery resulted in less invasive surgery remained locally recurrence-free. Among the 17 patients undergoing curative surgery for LRRC, 11 (65%) patients developed a local re-recurrence. Of the three patients who had an R0 instead of R1 as a direct result of SGM-101 guided surgery, one patient developed a local re-recurrence (33%), while the other two remained local recurrence-free.

Conclusions: This is the first study to report follow-up data on patients undergoing tumor-targeted NIRF-guided surgery. Although SGM-101 resulted in warranted changes in surgical management intra-operatively, no improved long-term benefit could be observed for the entire cohort. However, the subset of patients whose surgical approach was modified based on NIRF - either by performing less invasive surgery or removing additional malignant tissue-showed favorable long-term outcomes. Results from ongoing large trials are awaited.

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来源期刊
CiteScore
6.90
自引率
3.20%
发文量
95
审稿时长
3 months
期刊介绍: Molecular Imaging and Biology (MIB) invites original contributions (research articles, review articles, commentaries, etc.) on the utilization of molecular imaging (i.e., nuclear imaging, optical imaging, autoradiography and pathology, MRI, MPI, ultrasound imaging, radiomics/genomics etc.) to investigate questions related to biology and health. The objective of MIB is to provide a forum to the discovery of molecular mechanisms of disease through the use of imaging techniques. We aim to investigate the biological nature of disease in patients and establish new molecular imaging diagnostic and therapy procedures. Some areas that are covered are: Preclinical and clinical imaging of macromolecular targets (e.g., genes, receptors, enzymes) involved in significant biological processes. The design, characterization, and study of new molecular imaging probes and contrast agents for the functional interrogation of macromolecular targets. Development and evaluation of imaging systems including instrumentation, image reconstruction algorithms, image analysis, and display. Development of molecular assay approaches leading to quantification of the biological information obtained in molecular imaging. Study of in vivo animal models of disease for the development of new molecular diagnostics and therapeutics. Extension of in vitro and in vivo discoveries using disease models, into well designed clinical research investigations. Clinical molecular imaging involving clinical investigations, clinical trials and medical management or cost-effectiveness studies.
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