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针对体积大于10立方厘米的脑转移瘤,采用不同总肿瘤剂量和不均匀性的十分割立体定向放射外科治疗:治疗反应提示适用于单次分割和十次分割的合适生物等效剂量公式。

Ten-Fraction Stereotactic Radiosurgery With Different Gross Tumor Doses and Inhomogeneities for Brain Metastasis of >10 cc: Treatment Responses Suggesting Suitable Biological Effective Dose Formula for Single and 10 Fractions.

作者信息

Ohtakara Kazuhiro, Nakabayashi Kiyo, Suzuki Kojiro

机构信息

Department of Radiation Oncology, Kainan Hospital Aichi Prefectural Welfare Federation of Agricultural Cooperatives, Yatomi, JPN.

Department of Radiology, Aichi Medical University, Nagakute, JPN.

出版信息

Cureus. 2023 Feb 4;15(2):e34636. doi: 10.7759/cureus.34636. eCollection 2023 Feb.

DOI:10.7759/cureus.34636
PMID:36895545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9989553/
Abstract

Stereotactic radiosurgery (SRS) with >5 fractions (fr) has been increasingly adopted to improve local control and safety for brain metastases (BM) of >10 cm, given the limited brain tolerance of SRS with ≤5 fr. However, the optimal indication and treatment design, including the prescribed dose and distribution for 10 fr SRS, remains uncertain. A single fr of 24 Gy provides approximately 95% of the one-year local tumor control probability. The potential SRS doses in 10 fr that is clinically equivalent to a single fr of 24 Gy regarding anti-tumor effect range from 48.4 to 81.6 Gy as biological effective doses (BED) as a function of the BED model formulas along with the alpha/beta ratios. The most appropriate BED formula in conjunction with an alpha/beta ratio to estimate similar anti-BM effects for single and 10 fr remains controversial. Herein, we describe four cases of symptomatic radiation-naïve BM >10 cm (range, 11 to 26 cm), treated with 10 fr SRS with a standard prescribed dose of 42 Gy, for which modified dynamic conformal arcs were used with forward planning to improve dose conformity. In the first two cases with gross tumor volumes (GTV) of 15.3 and 10.9 cm, 42 Gy was prescribed to 70%-80% isodose, normalized to 100% at the isocenter, which encompasses the boundary of the planning target volume: GTV + isotropic 1 mm margin. The tumor responses were initially marked regression followed by regrowth within three months in case 1 and no shrinkage with subsequent progression within three months in case 2. In the remaining two cases with larger GTVs of 19.1 and 26.2 cm, the GTV boundary and 2-3 mm margin-added object volume was covered by 80% and 56% isodoses with 53 Gy and 37 Gy, respectively, to further increase the marginal and internal doses of GTV and to ensure moderate dose spillage outside the GTV, while >1-1.5 mm outside the GTV was covered by 42 Gy with 63% isodose. According to the BED based on the linear-quadratic (LQ) model with an alpha/beta ratio of 10 (BED), 53 Gy corresponds to approximately 81 Gy in BED and 24 Gy in a single fr. Excellent initial maximum tumor response and subsequently sustained tumor regression (STR) were achieved in both cases. Subsequently, enlarging nodules that could not exclude the possibility of tumor regrowth were disclosed within two years, while late adverse radiation effects remained moderate. These dose-effect relationships suggest that a GTV marginal dose of ≥53 Gy with ≤80% isodose would be preferred to effect ≥1-year STR and that further dose escalation of both marginal and internal GTV may be necessary to achieve ≥2-year STR, while GTV of >25 cm may be unsuitable for 10 fr SRS in terms of long-term brain tolerance. Among LQ, LQ-cubic, and LQ-linear model formulas and alpha/beta ratios of 10-20, BED may be clinically most suitable to estimate a 10 fr SRS dose that provides anti-BM efficacy similar to that for a single fr.

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/56c4cc3a8dec/cureus-0015-00000034636-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/dc7acd545e5c/cureus-0015-00000034636-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/86810affe4f6/cureus-0015-00000034636-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/76011ffceb55/cureus-0015-00000034636-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/591bb124c4be/cureus-0015-00000034636-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/56c4cc3a8dec/cureus-0015-00000034636-i05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/dc7acd545e5c/cureus-0015-00000034636-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/86810affe4f6/cureus-0015-00000034636-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/76011ffceb55/cureus-0015-00000034636-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/591bb124c4be/cureus-0015-00000034636-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8aca/9989553/56c4cc3a8dec/cureus-0015-00000034636-i05.jpg
摘要

鉴于≤5次分割的立体定向放射外科手术(SRS)对脑的耐受性有限,>5次分割(fr)的SRS已越来越多地被采用,以提高对直径>10 cm的脑转移瘤(BM)的局部控制和安全性。然而,最佳适应证和治疗设计,包括10次分割SRS的处方剂量和剂量分布,仍不确定。单次分割24 Gy可提供约95%的一年局部肿瘤控制概率。就抗肿瘤效果而言,在10次分割中临床上等同于单次分割24 Gy的潜在SRS剂量,作为生物等效剂量(BED),根据BED模型公式以及α/β比值,范围为48.4至81.6 Gy。结合α/β比值来估计单次分割和10次分割类似抗BM效果的最合适BED公式仍存在争议。在此,我们描述4例直径>10 cm(范围为11至26 cm)、未经放疗且有症状的BM患者,采用10次分割SRS治疗,标准处方剂量为42 Gy,使用改良动态适形弧和正向计划以改善剂量适形性。在前两例大体肿瘤体积(GTV)分别为15.3 cm和10.9 cm的病例中,42 Gy处方给70%-80%等剂量线,在等中心归一化为100%,其涵盖计划靶体积的边界:GTV + 各向同性1 mm边界。病例1的肿瘤反应最初为明显退缩,随后在3个月内复发;病例2在3个月内无缩小且随后进展。在其余两例GTV较大(分别为19.1 cm和26.2 cm)的病例中,GTV边界和添加2-3 mm边界的目标体积分别由53 Gy的80%等剂量线和37 Gy的56%等剂量线覆盖,以进一步增加GTV的边缘剂量和内部剂量,并确保GTV外有适度的剂量溢出,而GTV外>1-1.5 mm由42 Gy的63%等剂量线覆盖。根据基于α/β比值为10的线性二次(LQ)模型的BED,53 Gy相当于BED约81 Gy和单次分割24 Gy。两例均实现了出色的初始最大肿瘤反应及随后持续的肿瘤退缩(STR)。随后,在两年内发现了无法排除肿瘤复发可能性的增大结节,而晚期放射不良反应仍较轻微。这些剂量-效应关系表明,为实现≥1年的STR,GTV边缘剂量≥53 Gy且等剂量线≤80%可能更可取;为实现≥2年的STR,GTV边缘和内部可能都需要进一步增加剂量;而就长期脑耐受性而言,>25 cm的GTV可能不适合10次分割SRS。在LQ、LQ-立方和LQ-线性模型公式以及α/β比值为10-20中,BED在临床上可能最适合估计提供与单次分割类似抗BM疗效的10次分割SRS剂量。

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9
Single- and Multifraction Stereotactic Radiosurgery Dose/Volume Tolerances of the Brain.单剂量和多剂量立体定向放射外科治疗脑的剂量/体积耐受量。
Int J Radiat Oncol Biol Phys. 2021 May 1;110(1):68-86. doi: 10.1016/j.ijrobp.2020.08.013. Epub 2020 Sep 11.
10
Changes in Brain Metastasis During Radiosurgical Planning.放射外科计划中的脑转移瘤变化。
Int J Radiat Oncol Biol Phys. 2018 Nov 15;102(4):727-733. doi: 10.1016/j.ijrobp.2018.06.021. Epub 2018 Jun 25.