首页> 外文期刊>Advances in Radiation Oncology >Feasibility of Dose Escalating [ 18F]fluciclovine Positron Emission Tomography Positive Pelvic Lymph Nodes During Moderately Hypofractionated Radiation Therapy for High-Risk Prostate Cancer
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Feasibility of Dose Escalating [ 18F]fluciclovine Positron Emission Tomography Positive Pelvic Lymph Nodes During Moderately Hypofractionated Radiation Therapy for High-Risk Prostate Cancer

机译:在高危前列腺癌的中等低分割放疗过程中,剂量递增[ 18 F]氟西洛韦正电子发射断层扫描阳性盆腔淋巴结的可行性

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PurposeThe aim of this study was to report the treatment planning feasibility of dose escalation to suspicious lymph nodes (LNs) for a series of men who underwent pretreatment [18F]fluciclovine positron emission tomography (PET)/magnetic resonance imaging (MRI).Methods and MaterialsCases of men with prostate cancer who enrolled in a clinical trial of pretreatment [18F]fluciclovine PET who had suspicious LNs were selected. Pelvic LNs <1?cm were defined as positive based on [18F]fluciclovine-PET if their maximum standardized uptake value (SUVmax) was ≥1.3-fold greater than the reference blood pool SUVmean, and LNs ≥1?cm were defined as positive if the SUV was greater than the reference SUV bone marrow reference. For each case, a radiation treatment plan was generated to deliver 70?Gy to the prostate and proximal seminal vesicles, 60.2?Gy to the PET-positive LNs, and 50.4?Gy to the elective nodal regions, simultaneously in 28 fractions of 2.5?Gy, 2.15?Gy, and 1.8?Gy, respectively. Treatment planning goals were defined a priori. The resulting target volume and organ-at-risk dosimetry were compared with the original treatment plan.ResultsFour cases were identified, with between 1 and 5 [18F]fluciclovine PET–positive LNs each. Goals for the prostate and elective nodal target volumes were successfully met in all cases. The goal of covering more than 90% of the positive LN planning target volume by the prescription dose of 60.2?Gy was met in 3 of the 4 cases. This goal was not met in 1 case, but 100% of clinical target volume was covered by 60.2?Gy. The primary organ-at-risk tradeoff was that a small volume (0.5-8.2?cm3) of small bowel would receive ≥54?Gy in each case.ConclusionsThese preliminary results suggest that [18F]fluciclovine PET/MRI directed dose escalation of suspicious pelvic LNs is likely feasible in the setting of definitive radiation therapy. The potential clinical benefit of dose escalating [18F]fluciclovine PET–positive LNs should be investigated in a prospective clinical trial.
机译:目的本研究的目的是报告一系列接受预处理[18F]氟氯乙烯正电子发射断层扫描(PET)/磁共振成像(MRI)的男性的剂量规划,将剂量提升至可疑淋巴结(LNs)的治疗计划可行性。资料选择了参加有可疑LN的[18F]氟氯乙烯预处理的临床试验的前列腺癌男性病例。如果盆腔LNs的最大标准摄取值(SUVmax)比参考血池SUVmean高1.3倍以上,则根据[18F]氟氯乙烯-PET将其定义为阳性,并且将LNs≥1?cm定义为阳性如果SUV大于参考SUV骨髓参考。对于每种情况,都制定了放射治疗计划,分别向前列腺和近端精囊输送70?Gy,向PET阳性LNs输送60.2?Gy,向选择性淋巴结区域输送50.4?Gy,同时分28批2.5? Gy,2.15?Gy和1.8?Gy。事先确定治疗计划目标。将产生的目标体积和危险器官剂量与原始治疗计划进行了比较。结果确定了4例病例,每例中有1至5个[18F]氟氯乙烯PET阳性LN。在所有情况下,前列腺目标和选择性淋巴结目标量的目标均已成功实现。 4例病例中有3例达到了通过60.2?Gy的处方剂量覆盖超过90%的LN规划目标阳性目标的目标。 1例未达到该目标,但60.2?Gy覆盖了100%的临床目标体积。主要的风险器官权衡是在每种情况下小体积小肠(0.5-8.2?cm3)都会接受≥54?Gy。结论这些初步结果表明,[18F]流乳头PET / MRI指导可疑剂量的逐步增加在确定性放射治疗的背景下,骨盆LNs可能是可行的。应在一项前瞻性临床试验中研究剂量递增的[18F]氟氯乙烯PET阳性LN的潜在临床益处。

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