NRG Oncology International Consensus Contouring Atlas on Target Volumes and Dosing Strategies for Dose-Escalated Pancreatic Cancer Radiotherapy.

Nina N Sanford, Amol K Narang, Todd A Aguilera, Michael F Bassetti, Michael D Chuong, Beth A Erickson, Karyn A Goodman, Joseph M Herman, Martijn Intven, Aoife Kilcoyne, Hyun Kim, Eric Paulson, Marsha Reyngold, Susan Tsai, Leila T Tchelebi, Richard Tuli, Eva Versteijne, Alice Wei, Jennifer Y Wo, Ying Zhang, Theodore S Hong, William A Hall
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Abstract

Purpose/objective(s): Dose-escalated radiotherapy is increasingly used in the treatment of pancreatic cancer, however approaches to target delineation vary widely. We present the first North American cooperative group consensus contouring atlas for dose-escalated pancreatic cancer radiotherapy.

Materials/methods: An expert international panel comprising 15 radiation oncologists, 2 surgeons and 1 radiologist were recruited. Participants used MimCloud software to contour high and low risk clinical target volumes (CTV) on three pancreatic cancer cases: a borderline resectable head tumor, a locally advanced head tumor, and a medically inoperable tail tumor. Simultaneous truth and performance level estimation (STAPLE) volumes were created, and contours were analyzed using Dice similarity coefficients.

Results: The contoured gross tumor volume (GTV) for the borderline head, locally advanced head, and unresectable tail tumor cases were 156.7, 58.2 and 9.0 cc, respectively, and the Dice similarity coefficients (SD) for the high- and low-risk CTV ranged from 0.45 to 0.82. Consensus volumes were agreed upon by authors. High-risk CTVs comprised the tumor plus abutting vessels. Low-risk CTVs started superiorly at (tail tumors) or 1 cm above (head tumors) the celiac takeoff and extended inferiorly to the superior mesenteric artery (SMA) at the level of the first jejunal takeoff. For head, neck, and proximal body tumors, the lateral volume encompassed the entire pancreas head and 5-10 mm around the celiac, superior mesenteric artery (SMA), superior mesenteric vein (SMV), including the common hepatic artery and medial portal vein, consistent with a "Triangle" volume-based approach. For distal body and tail tumors, the entire tail was included, along with the splenic vessels and the takeoffs of celiac artery.

Conclusion: Through multidisciplinary collaboration, we created consensus contouring guidelines for dose-escalated pancreatic cancer radiotherapy. These volumes include not only gross disease, but also routine elective coverage, and can be used to standardize practice for future trials seeking to define the role of dose escalated radiotherapy in pancreatic cancer.

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NRG 肿瘤学国际共识图谱:胰腺癌放射治疗剂量分级的靶体积和剂量策略。
目的/目标:剂量递增放疗越来越多地应用于胰腺癌的治疗,然而靶区划分的方法却千差万别。我们为剂量递增胰腺癌放疗提供了第一份北美合作组共识轮廓图谱:材料/方法:我们招募了由 15 名放射肿瘤专家、2 名外科医生和 1 名放射科医生组成的国际专家小组。参与者使用 MimCloud 软件对三个胰腺癌病例的高风险和低风险临床靶体积(CTV)进行轮廓分析:一个边缘可切除的头部肿瘤、一个局部晚期头部肿瘤和一个医学上无法手术的尾部肿瘤。创建了同步真实和性能水平估计(STAPLE)体积,并使用 Dice 相似性系数对轮廓进行了分析:结果:边缘性头部肿瘤、局部晚期头部肿瘤和无法切除的尾部肿瘤病例的等高线肿瘤总体积(GTV)分别为 156.7、58.2 和 9.0 cc,高风险和低风险 CTV 的 Dice 相似系数(SD)在 0.45 至 0.82 之间。作者就共识体积达成一致。高风险CTV包括肿瘤和邻近血管。低风险 CTV 从腹腔起始点上方(尾部肿瘤)或上方 1 厘米(头部肿瘤)开始,向下延伸至第一空肠起始点水平的肠系膜上动脉 (SMA)。对于头颈部和胰体近端肿瘤,外侧容积包括整个胰头和腹腔、肠系膜上动脉(SMA)、肠系膜上静脉(SMV)周围 5-10 mm,包括肝总动脉和内侧门静脉,这与基于 "三角 "容积的方法一致。对于远端体部和尾部肿瘤,则包括整个尾部以及脾脏血管和腹腔动脉分支:通过多学科合作,我们为剂量递增胰腺癌放疗制定了一致的轮廓指引。这些体积不仅包括大体病变,还包括常规选择性覆盖,可用于规范未来试验的实践,以确定剂量递增放疗在胰腺癌中的作用。
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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