Feasibility of Stereotactic Body Radiation Therapy for Pancreatic Tumors Abutting Organs at Risk Using Magnetic Resonance Guided Adaptive Radiation Therapy.

IF 6.4 1区 医学 Q1 ONCOLOGY
Alden D'Souza, Kylie H Kang, John E Lattin, Bita Kalaghchi, John S Ginn, Alex T Price, David S Lakomy, Michael R Waters, Joshua P Schiff, Yi Huang, Richard Tsai, Pamela P Samson, Carl J DeSelm, Lauren E Henke, Farnoush Forghani, Xiaodong Zhao, Eric Morris, Geoffrey D Hugo, Tong Zhu, Allen Mo, Eric Laugeman, Hyun Kim
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引用次数: 0

Abstract

Purpose: Stereotactic body radiation therapy (SBRT) has historically been contraindicated in patients with tumors abutting gastrointestinal (GI) organs due to risk of toxicity. Adaptive magnetic resonance (MR) guided SBRT (MRgSBRT) is an increasingly used treatment paradigm to prescribe ablative doses to pancreatic tumors. Here we present our institutional experience of adaptive MRgSBRT for pancreatic tumors abutting or invading GI organs at risk (OARs).

Methods and materials: Forty-eight patients with pancreatic adenocarcinoma tumors abutting or invading GI OARs who received MRgSBRT to 50 Gy in 5 fractions at our institution between 2018-2019 were reviewed. Dosimetric variables were compared pre- and postadaptation to determine adequacy of target coverage, reasons for online adaptation, and resulting changes in GI OAR and constraints.

Results: Patients' mean age was 67 years, 50% female, 63% with ECOG 0-1, and with majority of tumors being locally advanced (52%) and located in the pancreatic head, uncinate process, or neck (92%). Tumors abutted or invaded GI OARs in 100% and 21% of cases, respectively. Of the 240 fractions evaluated, 99% required online adaptation and 77% underwent normalization. The mean PTV_opt (PTV minus a 5mm-expansion of GI OAR contours as the plan optimization structure) receiving prescription dose was 93%. The predicted and adapted critical volume (V36Gy ≤0.5 cc) for OARs were found to be statistically significantly different (P < .001). The duodenum had the highest volume receiving 36 Gy for both preadapted (mean 3.4 cc) and postadapted (mean 0.33 cc) plans. Plans for pancreatic head, uncinate process, or neck tumors frequently exceeded duodenum dose constraints and plans for pancreatic body or tail tumors more often exceeded stomach constraints (P < .001).

Conclusions: Adaptive MR guidance may permit SBRT for pancreatic tumors abutting or invading OARs with minimal toxicity.

磁共振引导下适应性放射治疗胰腺肿瘤邻近危险器官的可行性
目的:立体定向全身放射治疗(SBRT)历来被禁止用于肿瘤邻近胃肠道(GI)器官的患者,因为存在毒性风险。自适应磁共振引导的SBRT (MRgSBRT)是一种越来越多地用于胰腺肿瘤消融剂量的治疗范例。在这里,我们介绍了适应性MRgSBRT治疗胰腺肿瘤邻近或侵袭危险的胃肠道器官(OARs)的机构经验。方法/材料:回顾性分析2018-2019年我院48例邻近或侵袭胃肠道OARs的胰腺腺癌肿瘤患者,分5组接受50 Gy的MRgSBRT治疗。比较了适应前后的剂量学变量,以确定目标覆盖的充分性、在线适应的原因以及由此导致的GI OAR变化和限制因素。结果:患者平均年龄为67岁,50%为女性,63% ECOG为0-1,大多数肿瘤为局部晚期(52%),位于胰腺头、钩突或颈部(92%)。肿瘤毗邻或侵犯胃肠道桨的病例分别为100%和21%。在评估的240个分数中,99%需要在线适应,77%需要规范化。接受处方剂量的平均PTV_opt (PTV减去5mm的胃肠道桨叶轮廓扩张作为计划优化结构)为93%。OARs的预测临界体积(V36Gy≤0.5 cc)与适应临界体积(V36Gy≤0.5 cc)差异有统计学意义(p< 0.001)。预适应组(平均3.4 cc)和后适应组(平均0.33 cc)十二指肠容积最高,接受36 Gy。胰腺头部、钩突或颈部肿瘤的计划经常超过十二指肠的剂量限制,胰腺体或尾部肿瘤的计划经常超过胃的剂量限制(p< 0.001)。结论:适应性磁共振引导可使SBRT治疗临近或侵袭桨叶的胰腺肿瘤,且毒性最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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