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水凝胶 spacer 前瞻性多中心随机对照关键试验:经直肠 spacer 应用于接受前列腺图像引导调强放疗的男性患者的剂量学和临床效果。

Hydrogel Spacer Prospective Multicenter Randomized Controlled Pivotal Trial: Dosimetric and Clinical Effects of Perirectal Spacer Application in Men Undergoing Prostate Image Guided Intensity Modulated Radiation Therapy.

机构信息

Associated Medical Professionals of New York, Syracuse, New York.

21st Century Oncology, East Bradenton, Florida.

出版信息

Int J Radiat Oncol Biol Phys. 2015 Aug 1;92(5):971-977. doi: 10.1016/j.ijrobp.2015.04.030. Epub 2015 Apr 23.

Abstract

PURPOSE

Perirectal spacing, whereby biomaterials are placed between the prostate and rectum, shows promise in reducing rectal dose during prostate cancer radiation therapy. A prospective multicenter randomized controlled pivotal trial was performed to assess outcomes following absorbable spacer (SpaceOAR system) implantation.

METHODS AND MATERIALS

Overall, 222 patients with clinical stage T1 or T2 prostate cancer underwent computed tomography (CT) and magnetic resonance imaging (MRI) scans for treatment planning, followed with fiducial marker placement, and were randomized to receive spacer injection or no injection (control). Patients received postprocedure CT and MRI planning scans and underwent image guided intensity modulated radiation therapy (79.2 Gy in 1.8-Gy fractions). Spacer safety and impact on rectal irradiation, toxicity, and quality of life were assessed throughout 15 months.

RESULTS

Spacer application was rated as "easy" or "very easy" 98.7% of the time, with a 99% hydrogel placement success rate. Perirectal spaces were 12.6 ± 3.9 mm and 1.6 ± 2.0 mm in the spacer and control groups, respectively. There were no device-related adverse events, rectal perforations, serious bleeding, or infections within either group. Pre-to postspacer plans had a significant reduction in mean rectal V70 (12.4% to 3.3%, P<.0001). Overall acute rectal adverse event rates were similar between groups, with fewer spacer patients experiencing rectal pain (P=.02). A significant reduction in late (3-15 months) rectal toxicity severity in the spacer group was observed (P=.04), with a 2.0% and 7.0% late rectal toxicity incidence in the spacer and control groups, respectively. There was no late rectal toxicity greater than grade 1 in the spacer group. At 15 months 11.6% and 21.4% of spacer and control patients, respectively, experienced 10-point declines in bowel quality of life. MRI scans at 12 months verified spacer absorption.

CONCLUSIONS

Spacer application was well tolerated. Increased perirectal space reduced rectal irradiation, reduced rectal toxicity severity, and decreased rates of patients experiencing declines in bowel quality of life. The spacer appears to be an effective tool, potentially enabling advanced prostate RT protocols.

摘要

目的

将生物材料置于前列腺和直肠之间的直肠周围间隙(perirectal spacing),有望降低前列腺癌放射治疗过程中的直肠剂量。进行了一项前瞻性多中心随机对照关键试验,以评估可吸收间隔物(SpaceOAR 系统)植入后的结果。

方法和材料

总共 222 名临床 T1 或 T2 期前列腺癌患者接受了计算机断层扫描(CT)和磁共振成像(MRI)扫描以进行治疗计划,随后进行了基准标记放置,并随机接受了间隔物注射或不注射(对照组)。患者接受了术后 CT 和 MRI 计划扫描,并接受了图像引导强度调制放射治疗(79.2Gy,1.8Gy 剂量)。在 15 个月内评估了间隔物的安全性以及对直肠照射、毒性和生活质量的影响。

结果

间隔物应用的评价为“容易”或“非常容易”,占 98.7%,水凝胶放置成功率为 99%。直肠周围间隙在间隔物组和对照组中分别为 12.6±3.9mm 和 1.6±2.0mm。两组均无与器械相关的不良事件、直肠穿孔、严重出血或感染。与术前相比,术后间隔物计划直肠 V70 显著降低(12.4%至 3.3%,P<.0001)。两组之间的总体急性直肠不良事件发生率相似,间隔物组患者的直肠疼痛发生率较低(P=.02)。在间隔物组中观察到晚期(3-15 个月)直肠毒性严重程度的显著降低(P=.04),间隔物组和对照组的晚期直肠毒性发生率分别为 2.0%和 7.0%。间隔物组无 1 级以上的晚期直肠毒性。在 15 个月时,分别有 11.6%和 21.4%的间隔物组和对照组患者的肠道生活质量下降了 10 分。12 个月时的 MRI 扫描证实了间隔物的吸收。

结论

间隔物应用耐受良好。增加的直肠周围间隙减少了直肠照射,降低了直肠毒性严重程度,并降低了生活质量下降的患者比例。间隔物似乎是一种有效的工具,可能使先进的前列腺放射治疗方案成为可能。

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