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本文引用的文献

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Ramipril reduces incidence and prolongates latency time of radiation-induced rat myelopathy after photon and carbon ion irradiation.雷米普利可降低光子和碳离子照射后放射性诱导的大鼠骨髓病的发生率和潜伏期。
J Radiat Res. 2020 Sep 8;61(5):791-798. doi: 10.1093/jrr/rraa042.
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Intensity-modulated radiation therapy administered to a previously irradiated spine is effective and well-tolerated.调强放疗应用于既往放疗过的脊柱是有效且耐受良好的。
Clin Transl Oncol. 2021 Feb;23(2):229-239. doi: 10.1007/s12094-020-02410-x. Epub 2020 Jun 5.
3
Proton Reirradiation: Expert Recommendations for Reducing Toxicities and Offering New Chances of Cure in Patients With Challenging Recurrence Malignancies.质子再放疗:降低挑战性复发性恶性肿瘤患者毒性反应和提供新治愈机会的专家建议。
Semin Radiat Oncol. 2020 Jul;30(3):253-261. doi: 10.1016/j.semradonc.2020.02.007.
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Br J Radiol. 2020 Mar;93(1107):20190516. doi: 10.1259/bjr.20190516. Epub 2019 Nov 12.
5
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6
Role of upper abdominal reirradiation for gastrointestinal malignancies: a systematic review of cumulative dose, toxicity, and outcomes on behalf of the Re-Irradiation Working Group of the Italian Association of Radiotherapy and Clinical Oncology (AIRO).上腹部再放疗治疗胃肠道恶性肿瘤的作用:意大利放射治疗和临床肿瘤学协会(AIRO)再放疗工作组代表的累积剂量、毒性和结局的系统评价。
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Repeat reirradiation of the spinal cord: multi-national expert treatment recommendations.脊髓重复放疗:多国专家治疗建议。
Strahlenther Onkol. 2018 May;194(5):365-374. doi: 10.1007/s00066-018-1266-6. Epub 2018 Jan 23.

新的人类脊髓再照射耐受临床数据。

New clinical data on human spinal cord re-irradiation tolerance.

机构信息

Miyakojima IGRT Clinic, 1-16-22 Miyakojimahondori, 534-0021, Osaka, Miyakojima-ku, Japan.

Department of Radiation Oncology, Kindai University Faculty of Medicine, 377-2 Ohno-Higashi, 589-8511, Osaka, Osaka-Sayama, Japan.

出版信息

Strahlenther Onkol. 2021 Jun;197(6):463-473. doi: 10.1007/s00066-021-01772-7. Epub 2021 May 5.

DOI:10.1007/s00066-021-01772-7
PMID:33950265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8154818/
Abstract

PURPOSE

To provide additional clinical data about the re-irradiation tolerance of the spinal cord.

METHODS

This was a retrospective bi-institutional study of patients re-irradiated to the cervical or thoracic spinal cord with minimum follow-up of 6 months. The maximum dose (Dmax) and dose to 0.1cc (D0.1cc) were determined (magnetic resonance imaging [MRI]-defined cord) and expressed as equivalent dose in 2‑Gy fractions (EQD2) with an α/β value of 2 Gy.

RESULTS

All 32 patients remained free from radiation myelopathy after a median follow-up of 12 months. Re-irradiation was performed after 6-97 months (median 15). In 22 cases (69%) the re-irradiation spinal cord EQD2 Dmax was higher than that of the first treatment course. Forty-eight of 64 treatment courses employed fraction sizes of 2.5 to 4 Gy to the target volume. The median cumulative spinal cord EQD2 Dmax was 80.7 Gy, minimum 61.12 Gy, maximum 114.79 Gy. The median cumulative spinal cord D0.1cc EQD2 was 76.1 Gy, minimum 61.12 Gy, maximum 95.62 Gy. Besides cumulative dose, other risk factors for myelopathy were present (single-course Dmax EQD2 ≥51 Gy in 9 patients, single-course D0.1cc EQD2 ≥51 Gy in 5 patients).

CONCLUSION

Even patients treated to higher cumulative doses than previously recommended, or at a considerable risk of myelopathy according to a published risk score, remained free from this complication, although one must acknowledge the potential for manifestation of damage in patients currently alive, i.e., still at risk. Individualized decisions to re-irradiate after appropriate informed consent are an acceptable strategy, including scenarios where low re-irradiation doses to the spinal cord would compromise target coverage and tumor control probability to an unacceptable degree.

摘要

目的

提供关于脊髓再照射耐受度的额外临床数据。

方法

这是一项回顾性的双机构研究,对接受颈段或胸段脊髓再照射的患者进行研究,随访时间至少为 6 个月。确定最大剂量(Dmax)和 0.1cc 剂量(D0.1cc)(磁共振成像 [MRI] 定义的脊髓),并用 2-Gy 阿尔法/贝塔值为 2 Gy 的等效剂量 2-Gy 分数(EQD2)表示。

结果

在中位随访 12 个月后,所有 32 例患者均未发生放射性脊髓病。再照射时间为首次治疗后 6-97 个月(中位数 15 个月)。在 22 例(69%)中,再照射脊髓的 EQD2 Dmax 高于首次治疗疗程。64 个疗程中有 48 个采用 2.5 至 4 Gy 的靶区分次剂量。中位累积脊髓 EQD2 Dmax 为 80.7 Gy,最小 61.12 Gy,最大 114.79 Gy。中位累积脊髓 D0.1cc EQD2 为 76.1 Gy,最小 61.12 Gy,最大 95.62 Gy。除累积剂量外,还有其他脊髓病的危险因素(9 例患者单疗程 Dmax EQD2≥51 Gy,5 例患者单疗程 D0.1cc EQD2≥51 Gy)。

结论

即使患者接受的累积剂量高于先前推荐的剂量,或者根据已发表的风险评分处于相当大的脊髓病风险中,也没有发生这种并发症,尽管必须承认目前存活的患者存在发生损害的潜在风险,即仍有风险。在适当知情同意的基础上,重新进行个体化的再照射决策是一种可接受的策略,包括在再照射脊髓剂量较低会导致靶区覆盖和肿瘤控制概率不可接受地降低的情况下。