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Reirradiation human spinal cord tolerance for stereotactic body radiotherapy

机译:立体定向人体放疗对人体脊髓的再照射耐受性

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Purpose: We reviewed the treatment for patients with spine metastases who initially received conventional external beam radiation (EBRT) and were reirradiated with 1-5 fractions of stereotactic body radiotherapy (SBRT) who did or did not subsequently develop radiation myelopathy (RM). Methods and Materials: Spinal cord dose-volume histograms (DVHs) for 5 RM patients (5 spinal segments) and 14 no-RM patients (16 spine segments) were based on thecal sac contours at retreatment. Dose to a point within the thecal sac that receives the maximum dose (P max), and doses to 0.1-, 1.0-, and 2.0-cc volumes within the thecal sac were reviewed. The biologically effective doses (BED) using α/β = 2 Gy for late spinal cord toxicity were calculated and normalized to a 2-Gy equivalent dose (nBED = Gy 2/2). Results: The initial conventional radiotherapy nBED ranged from ~30 to 50 Gy 2/2 (median ~40 Gy 2/2). The SBRT reirradiation thecal sac mean P max nBED in the no-RM group was 20.0 Gy 2/2 (95% confidence interval [CI], 10.8-29.2), which was significantly lower than the corresponding 67.4 Gy 2/2 (95% CI, 51.0-83.9) in the RM group. The mean total P max nBED in the no-RM group was 62.3 Gy 2/2 (95% CI, 50.3-74.3), which was significantly lower than the corresponding 105.8 Gy 2/2 (95% CI, 84.3-127.4) in the RM group. The fraction of the total P max nBED accounted for by the SBRT P max nBED for the RM patients ranged from 0.54 to 0.78 and that for the no-RM patients ranged from 0.04 to 0.53. Conclusions: SBRT given at least 5 months after conventional palliative radiotherapy with a reirradiation thecal sac P max nBED of 20-25 Gy 2/2 appears to be safe provided the total P max nBED does not exceed approximately 70 Gy 2/2, and the SBRT thecal sac P max nBED comprises no more than approximately 50% of the total nBED.
机译:目的:我们审查了脊柱转移患者的治疗方法,这些患者最初接受常规的体外束放射治疗(EBRT),然后再接受1-5份立体定向放射治疗(SBRT)的放射线治疗,而放射线脊髓病(RM)发生或未发生。方法和材料:5例RM患者(5个脊柱节段)和14例非RM患者(16个脊柱节段)的脊髓剂量-体积直方图(DVHs)基于再治疗时的囊囊轮廓。剂量达到囊囊内的最大剂量(P max),并检查了囊囊内0.1-,1.0-和2.0-cc的剂量。计算使用α/β= 2 Gy治疗晚期脊髓毒性的生物有效剂量(BED),并将其标准化为2 Gy当量剂量(nBED = Gy 2/2)。结果:最初的常规放射治疗nBED的范围为〜30至50 Gy 2/2(中位数为〜40 Gy 2/2)。 no-RM组的SBRT再照射胆囊平均P max nBED为20.0 Gy 2/2(95%置信区间[CI],10.8-29.2),明显低于相应的67.4 Gy 2/2(95%)。 CI,51.0-83.9)。无RM组的平均总P max nBED为62.3 Gy 2/2(95%CI,50.3-74.3),明显低于相应的105.8 Gy 2/2(95%CI,84.3-127.4)。 RM组。对于RM患者,SBRT P max nBED占总P max nBED的比例为0.54至0.78,而对于非RM患者则为0.04至0.53。结论:常规姑息性放疗后至少5个月给予再照射鞘膜囊P max nBED为20-25 Gy 2/2的SBRT似乎是安全的,只要总P max nBED不超过约70 Gy 2/2,并且SBRT囊囊P max nBED不超过总nBED的约50%。

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