Department of Gastroenterology and Hepatology, Austin Health, Heidelberg 3084, Victoria, Australia.
Department of Radiation Oncology, Austin Health, Heidelberg 3084, Victoria, Australia.
World J Gastroenterol. 2021 Nov 14;27(42):7387-7401. doi: 10.3748/wjg.v27.i42.7387.
Image-guided radiotherapy (IGRT) has significantly improved the precision in which radiotherapy is delivered in cancer treatment. Typically, IGRT uses bony landmarks and key anatomical structures to locate the tumor. Recent studies have demonstrated the feasibility of peri-tumor fiducials in enabling even more accurate delineation of target and normal tissue. The use of gold coils as fiducials in gastrointestinal tumors has been extensively studied. However, placement requires expertise and specialized endoscopic ultrasound equipment. This article reports the long-term outcomes of using a standard gastroscopy to inject liquid fiducials for the treatment of oesophageal and gastric tumors with IGRT.
To assess the long-term outcomes of liquid fiducial-guided IGRT in a cohort of oesophageal and gastric cancer patients.
A retrospective cohort study of consecutive adults with Oesophagogastric cancers referred for liquid fiducial placement before definitive/neo-adjuvant or palliative IGRT between 2013 and 2021 at a tertiary hospital in Melbourne, Australia was conducted. Up to four liquid fiducials were inserted per patient, each injection consisting of 0.2-0.5mL of a 1:1 mixture of iodized oil (Lipiodol; Aspen Pharmacare) and n-butyl 2-cyanoacrylate (Histoacryl; B. Braun). A 23-gauge injector (Cook Medical) was used for the injection. All procedures were performed by or under the supervision of a gastroenterologist. Liquid fiducial-based IGRT (LF-IGRT) consisted of computer-assisted direct matching of the fiducial region on cone-beam computerised tomography at the time of radiotherapy. Patients received standard-IGRT (S-IGRT) if fiducial visibility was insufficient, consisting of bone match as a surrogate for tumor position. Radiotherapy was delivered to 54Gy in 30 fractions for curative patients and up to 45Gy in 15 fractions for palliative treatments.
52 patients were referred for liquid fiducial placement within the study period. A total of 51 patients underwent liquid fiducial implantation. Of these a total of 31 patients received radiotherapy. Among these, the median age was 77.4 years with a range between 57.5 and 88.8, and 64.5% were male. Twenty-seven out of the 31 patients were able to have LF-IGRT while four had S-IGRT. There were no complications after endoscopic implantation of liquid fiducials in our cohort. The cohort overall survival (OS) post-radiotherapy was 19 mo (range 0 to 87 mo). Whilst the progression-free survival (PFS) post-radiotherapy was 13 mo (range 0 to 74 mo). For those treated with curative intent, the median OS was 22.0 mo (range 0 to 87 mo) with a PFS median of 14.0 mo (range 0 to 74 mo). Grade 3 complication rate post-radiotherapy was 29%.
LF-IGRT is feasible in 87.1% of patients undergoing liquid fiducial placement through standard gastroscopy injection technique. Our cohort has an overall survival of 19 mo and PFS of 13 mo. Further studies are warranted to determine the long-term outcomes of liquid-fiducial based IGRT.
图像引导放疗(IGRT)显著提高了癌症治疗中放疗的精度。通常,IGRT 使用骨性标志和关键解剖结构来定位肿瘤。最近的研究表明,在肿瘤周围放置标记物可以更精确地描绘靶区和正常组织。在胃肠道肿瘤中,使用金线圈作为标记物已经得到了广泛的研究。然而,这种方法的实施需要专业知识和专门的内镜超声设备。本文报告了使用标准胃镜注射液体标记物进行 IGRT 的长期结果,该方法用于治疗食管和胃肿瘤。
评估液体标记物引导 IGRT 在一组食管和胃癌患者中的长期结果。
对 2013 年至 2021 年间在澳大利亚墨尔本一家三级医院接受液体标记物放置以进行确定性/新辅助或姑息性 IGRT 的连续成年食管胃癌症患者进行回顾性队列研究。每位患者最多可插入四个液体标记物,每次注射由 0.2-0.5mL 碘油(Lipiodol;Aspen Pharmacare)和正丁基 2-氰基丙烯酸酯(Histoacryl;B. Braun)的 1:1 混合物组成。使用 23 号注射器(Cook Medical)进行注射。所有程序均由或在胃肠病学家的监督下进行。液体标记物基础的 IGRT(LF-IGRT)包括在放疗时通过计算机辅助直接匹配锥形束计算机断层扫描上的标记区域。如果标记物的可视性不足,则使用标准 IGRT(S-IGRT),即骨匹配作为肿瘤位置的替代物。对于根治性治疗的患者,给予 54Gy 分 30 次治疗,对于姑息性治疗的患者,给予 45Gy 分 15 次治疗。
在研究期间,共有 52 名患者被推荐进行液体标记物放置。共有 51 名患者接受了液体标记物植入。其中,共有 31 名患者接受了放疗。在这些患者中,中位年龄为 77.4 岁,年龄范围为 57.5 至 88.8 岁,64.5%为男性。在我们的队列中,31 名患者中有 27 名能够进行 LF-IGRT,而有 4 名患者需要进行 S-IGRT。在我们的队列中,内镜下植入液体标记物后没有发生任何并发症。总体放疗后生存(OS)为 19 个月(范围为 0 至 87 个月)。放疗后无进展生存(PFS)为 13 个月(范围为 0 至 74 个月)。对于接受根治性治疗的患者,中位 OS 为 22.0 个月(范围为 0 至 87 个月),中位 PFS 为 14.0 个月(范围为 0 至 74 个月)。放疗后 3 级并发症发生率为 29%。
通过标准胃镜注射技术进行液体标记物放置,LF-IGRT 的可行性为 87.1%。我们的队列的总生存时间为 19 个月,无进展生存时间为 13 个月。需要进一步的研究来确定液体标记物基础的 IGRT 的长期结果。