Re-irradiation

再辐照
  • 文章类型: Journal Article
    背景:近年来,已经积累的证据表明,作为治疗的一部分,通过再次照射保护乳腺癌的第二种方法可能是可行和安全的.由于担心晚期并发症,许多肿瘤学家对乳房再照射持怀疑态度。因此,获取乳房再照射并发症发生率的定量数据非常重要。在这个荟萃分析中,我们确定乳房再照射后正常组织并发症的发生率.
    方法:使用EMBASE进行搜索以识别合格的研究,MEDLINE,pubmed,谷歌学者,和科克伦合作图书馆电子数据库,从2000年到2023年。总的来说,在这项荟萃分析中应用了10项主要研究来估计疾病并发症的患病率,皮肤纤维化,和胸痛。使用I2指数和荟萃回归对异质性进行调查,以评估怀疑引起异质性的变量。使用Stata17进行统计分析和合成。
    结果:接受两个阶段放射治疗的患者接受的平均剂量为100.32Gy,在这些患者中,皮肤纤维化和疾病的患病率为47%(95%CI71-22%;I2=96.76%,P<0.001),胸痛的患病率为35%(95%CI68-8%;I2=98.13%,P<0.001)。
    结论:关于乳房再照射治疗并发症发生率的临床信息很少。这项荟萃分析提出了乳房再照射后并发症的发生率,以帮助放射肿瘤学家和物理学家做出更好的决定。
    BACKGROUND: In recent years, evidence has accumulated that a second method of conserving the breast from cancer with re-irradiation as part of treatment may be feasible and safe. Many oncologists are skeptical of breast re-irradiation due to concerns about late complications, so access to quantitative data on the prevalence of breast re-irradiation complications is very important. In this meta-analysis, we determine the prevalence of complications in normal tissue after breast re-irradiation.
    METHODS: A search was done to recognize qualified studies using EMBASE, MEDLINE, PUBMED, Google Scholar, and Cochrane Collaboration Library electronic databases from 2000 to 2023. In total, ten primary studies were applied in this meta-analysis to estimate the prevalence of complications of disorders, skin fibrosis, and chest pain. Heterogeneity was investigated using the I2 index and the meta-regression to evaluate variables suspected of causing heterogeneity. Statistical analysis and synthesis were performed using Stata 17.
    RESULTS: The average dose received by patients who underwent radiation therapy in two stages was 100.32 Gy, and in these patients, the prevalence of skin fibrosis and disorders was 47% (95% CI 71-22%; I2 = 96.76%, P < 0.001) and the prevalence of chest pain was 35% (95% CI 68-8%; I2 = 98.13%, P < 0.001).
    CONCLUSIONS: There is little clinical information about the incidence of complications in breast re-irradiation therapy. This meta-analysis presents the prevalence of complications after breast re-irradiation to help radiation oncologists and physicists make better decisions.
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  • 文章类型: Journal Article
    调强放疗(IMRT)的再照射仍然是无法手术的局部复发性鼻咽癌(NPC)的主要治疗方式。然而,与辐射相关的晚期不良反应的发生率通常很高.因此,我们旨在探讨不能手术的局部复发性NPC的失败模式和再照射的个体化治疗方案.回顾性分析97例接受IMRT的患者。62例患者的临床目标复发体积(rCTV)划定,35例患者仅描绘了大体肿瘤复发体积(rGTV)。29例患者在再次接受IMRT照射后出现第二次局部衰竭(28例可用)。在这些患者中,64.3%(18/28)的患者和35.7%(10/28)的患者发展为场内或场外,分别。目标体积(rGTV或rCTV)与局部复发率之间无统计学相关性,局部故障模式,≥3级毒性,和生存。多因素分析显示,复发T(rT)分期(HR2.62,P=0.019)和rGTV体积(HR1.73,P=0.037)是总生存期(OS)的独立预后因素。基于rT分期和rGTV量的风险分层显示,低风险组的3年OS率更长(66.7%vs.23.4%),较低的总毒性≥3级(P=0.004),再放疗相关死亡率(HR0.45,P=0.03)低于高危人群。这项研究表明,rCTV的轮廓可能不利于在局部复发性NPC中使用IMRT进行再次照射。低风险患者最适合再次照射,最大限度地提高当地的抢救和减少辐射相关的毒性。更精确和个性化的再辐照计划是必要的。
    Re-irradiation with intensity-modulated radiotherapy (IMRT) remains the primary treatment modality for inoperable locally recurrent nasopharyngeal carcinoma (NPC). However, the rate of radiation-related late adverse effects is often substantially high. Therefore, we aimed to explore failure patterns and individualized treatment plans of re-irradiation for inoperable locally recurrent NPC. Ninety-seven patients who underwent IMRT were retrospectively analyzed. Sixty-two patients had clinical target volume of recurrence (rCTV) delineated, and thirty-five patients had only gross tumor volume of recurrence (rGTV) delineated. Twenty-nine patients developed second local failures after re-irradiation with IMRT (28 cases available). Among those patients, 64.3% (18/28) of patients and 35.7% (10/28) developed in-field or out-field, respectively. No statistical correlation was observed between target volume (rGTV or rCTV) and the local recurrence rate, local failure patterns, grade ≥ 3 toxicity, and survival. Multivariate analysis showed that recurrent T (rT) stage (HR 2.62, P = 0.019) and rGTV volume (HR 1.73, P = 0.037) were independent prognostic factors for overall survival (OS). Risk stratification based on rT stage and rGTV volume revealed that low risk group had a longer 3-year OS rate (66.7% vs. 23.4%), lower total grade ≥ 3 toxicity (P = 0.004), and lower re-radiation associated mortality rates (HR 0.45, P = 0.03) than high risk group. This study demonstrates that the delineation of rCTV may not be beneficial for re-irradiation using IMRT in locally recurrent NPC. Patients with low risk were most suitable for re-irradiation, with maximizing local salvage and minimizing radiation-related toxicities. More precise and individualized plans of re-irradiation are warranted.
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  • 文章类型: Journal Article
    目的:高级别胶质瘤(HGG)被认为是一种高复发率的致死性疾病。在复发性HGG中没有标准的护理。目前有许多治疗选择,比如复活,全身治疗,和重新辐照。重新辐照似乎是一个有希望的选择。在这项研究中,我们旨在比较两种再照射方案的疗效和毒性.
    方法:将40例复发性HGG患者随机分为两组。A臂收到30Gy/10f/2w,B组接受立体定向放疗(SBRT)30Gy/5f/1w。在两组中同时给予替莫唑胺(TMZ)。计算中位无进展生存期(PFS)和总生存期(OS),放疗后2个月,然后每2个月进行一次脑MRI,使用第5版不良事件通用术语(CTCAE)记录毒性。
    结果:再次照射后的中位随访时间为11个月(范围8-15个月)。复发后的中位PFS为6.4个月(95%CI5.3-7.4),复发后的中位OS为8.6个月(95%CI7.5-8.7),纳入患者的中位总OS诊断日期为18.5个月(95%CI17.3~19.8).有利于B臂的PFS差异有统计学意义,A组的中位PFS为7.3个月,而A组的中位PFS为6.2个月,p值为0.004。中位OS差异无统计学意义(B组9.3个月与A组8.4个月),p值为0.088。所有患者都能很好地耐受他们的治疗,以及急性和亚急性G1-G2毒性,包括头痛,萎靡不振,恶心,在重新照射过程结束期间和之后不久记录。
    结论:两种方案对复发性HGG进行再照射是安全有效的,SBRT臂的PFS有显著改善,但OS没有显著改善。
    OBJECTIVE: High grade glioma (HGG) is considered a lethal disease with a high recurrence rate. There is no standard of care in recurrent HGG. Many treatment options are present, such as resurgery, systemic therapy, and re-irradiation. Re-irradiation seems to be a promising option. In this study, we aimed at comparing the efficacy and toxicity of two re-irradiation protocols.
    METHODS: Forty patients with recurrent HGG were randomized equally into two arms. Arm A received 30 Gy/10f/2w, and arm B received stereotactic body radiotherapy (SBRT) 30 Gy/5f/1w. Concurrent temozolamide (TMZ) was given in both arms. Median progression free survival (PFS) and overall survival (OS) were calculated, and brain MRI was done after 2 months of radiotherapy and then every 2 months, with documented toxicity using the Common Terminology of Adverse Events version 5 (CTCAE).
    RESULTS: The median follow-up time after the re-irradiation course was 11 months (range 8-15 months). The median PFS after recurrence was 6.4 months (95% CI 5.3-7.4), the median OS after recurrence was 8.6 months (95% CI 7.5-8.7), and the median total OS form date of diagnosis was 18.5 months (95% CI 17.3-19.8) among the included patients. There was a statistically significant difference in PFS favoring arm B, with a median PFS of 7.3 versus 6.2 months in arm A, with p values of 0.004. There was no statistically significant difference in in median OS (9.3 months in arm B versus 8.4 months in arm A) with p values of 0.088. All patients tolerated their treatment well, and acute and subacute G1-G2 toxicity, consisting of headache, malaise, and nausea, were recorded during and shortly after the end of the re-irradiation course.
    CONCLUSIONS: Re-irradiation in recurrent HGG by both protocols is safe and effective, with a significant improvement in PFS in SBRT arm but no significant improvement in OS.
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  • 文章类型: Journal Article
    在前列腺癌明确放疗后,使用立体定向放疗(SBRT)对前列腺进行再照射的数据越来越多,近年来,越来越多的证据表明使用C臂LINAC或MRLINAC进行前列腺再照射。因此,我们对前列腺再照射进行了系统评价和荟萃分析,包括2020年至2023年发表的研究,以作为现有荟萃分析的更新。
    我们在2023年10月搜索了PubMed和Embase数据库,查询包括“repeat”的组合,“放射治疗”,\"前列腺\",“重新辐照”,\"再辐照\",“重新治疗”,\"SBRT\",“再处理”。出版日期定于2020年至2023年。语言没有限制。我们坚持系统审查和荟萃分析(PRISMA)建议的首选报告项目。数据提取后,通过计算I2进行异质性测试。使用具有受限最大似然估计器的随机效应模型来估计组合效应。目测评估漏斗图的不对称性,并使用Egger测试评估是否存在出版物和/或小的研究偏差。
    14种出版物被纳入系统综述。纳入研究报告的急性≥2级(G2)泌尿生殖系统(GU)和胃肠道(GI)毒性的发生率分别为0.0-30.0%和0.0-25.0%。对于晚期≥G2GU和GI毒性,范围为4.0-51.8%和0.0-25.0%。急性GU和GI毒性≥G2的合并率为13%(95%CI:7-18%)和2%(95%CI:0-4%)。对于晚期GU和GI毒性≥G2,合并率为25%(95%CI:14-35%)和5%(95%CI:1-9%)。合并的2年生化无复发生存率为72%(95%CI:64-92%)。
    SBRT在放射性复发性前列腺癌的再照射中是安全有效的。进一步的前瞻性数据是必要的。
    UNASSIGNED: There is increasing data on re-irradiation to the prostate using stereotactic body radiotherapy (SBRT) after definitive radiotherapy for prostate cancer, with increasing evidence on prostate re-irradiation using a C-arm LINAC or an MR LINAC in recent years. We therefore conducted this systematic review and meta-analysis on prostate re-irradiation including studies published from 2020 to 2023, to serve as an update on existing meta-analysis.
    UNASSIGNED: We searched the PubMed and Embase databases in October 2023 with queries including combinations of \"repeat\", \"radiotherapy\", \"prostate\", \"re-irradiation\", \"reirradiation\", \"re treatment\", \"SBRT\", \"retreatment\". Publication date was set to be from 2020 to 2023. There was no limitation regarding language. We adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) recommendations. After data extraction, heterogeneity testing was done by calculating the I2. A random effects model with a restricted maximum likelihood estimator was used to estimate the combined effect. Funnel plot asymmetry was assessed visually and using Egger\'s test to estimate the presence of publication and/or small study bias.
    UNASSIGNED: 14 publications were included in the systematic review. The rates of acute ≥ grade 2 (G2) genitourinary (GU) and gastrointestinal (GI) toxicities reported in the included studies ranged from 0.0-30.0 % and 0.0-25.0 % respectively. For late ≥ G2 GU and GI toxicity, the ranges are 4.0-51.8 % and 0.0-25.0 %. The pooled rate of acute GU and GI toxicity ≥ G2 were 13 % (95 % CI: 7-18 %) and 2 % (95 % CI: 0-4 %). For late GU and GI toxicity ≥ G2 the pooled rates were 25 % (95 % CI: 14-35 %) and 5 % (95 % CI: 1-9 %). The pooled 2-year biochemical recurrence-free survival was 72 % (95 % CI: 64-92 %).
    UNASSIGNED: SBRT in the re-irradiation of radiorecurrent prostate cancer is safe and effective. Further prospective data are warranted.
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  • 文章类型: Journal Article
    明确照射后局部复发性前列腺癌的最佳治疗仍不清楚,但局部挽救治疗正在引起人们的兴趣。回顾,我们在综合癌症中心对抢救I-125低剂量率(LDR)近距离放射治疗(BT)治疗局部复发性前列腺癌后的临床结局和治疗相关毒性进行了单机构分析.
    共纳入了2006年至2021年间接受挽救性LDR-BT治疗的94例患者。目标体积是整个腺体+/-GTV上的提升,半边天,或者只有GTV。处方剂量范围为90至145Gy。毒性按照不良事件通用术语标准(CTCAE)5.0版进行分级。
    中位随访时间为34个月。初始放射治疗是73例患者(78%)的外部放射治疗,中位剂量为76Gy,而21例患者(22%)的I-125BT的处方剂量为145Gy。抢救时的PSA中位数为3.75ng/ml,首次和抢救之间的间隔中位数为9.4年。对于32%的患者,挽救近距离放射治疗与雄激素剥夺治疗有关。只有4%的患者对去势耐药。2年无失败生存率为82%,3年为66%。在多变量分析中,与无失败生存相关的唯一因素是复发时的激素敏感性和欧洲泌尿外科协会(EAU)预后组。晚期3级尿和直肠毒性分别发生在12%和1%的患者中。在三个植入物体积组之间没有观察到毒性或功效的显著差异。
    疗效和毒性结果与MASTER荟萃分析的LDR组中的结果一致。挽救BT被证实是局部复发性前列腺癌的有效和安全的选择。一个集中的方法可能是有趣的减少晚期严重毒性,尤其是泌尿。
    UNASSIGNED: The optimal management of locally recurrent prostate cancer after definitive irradiation is still unclear but local salvage treatments are gaining interest. A retrospective, single-institution analysis of clinical outcomes and treatment-related toxicity after salvage I-125 low-dose-rate (LDR) brachytherapy (BT) for locally-recurrent prostate cancer was conducted in a Comprehensive Cancer Center.
    UNASSIGNED: A total of 94 patients treated with salvage LDR-BT between 2006 and 2021 were included. The target volume was either the whole-gland +/- a boost on the GTV, the hemigland, or only the GTV. The prescribed dose ranged from 90 to 145 Gy. Toxicity was graded by Common Terminology Criteria for Adverse Events (CTCAE) v5.0.
    UNASSIGNED: Median follow-up was 34 months. Initial radiotherapy was external beam radiotherapy in 73 patients (78 %) with a median dose of 76 Gy and I-125 BT in 21 patients (22 %) with a prescribed dose of 145 Gy. Median PSA at salvage was 3.75 ng/ml with a median interval between first and salvage irradiation of 9.4 years. Salvage brachytherapy was associated with androgen deprivation therapy for 32 % of the patients. Only 4 % of the patients were castrate-resistant. Failure free survival was 82 % at 2 years and 66 % at 3 years. The only factors associated with failure-free survival on multivariate analysis were hormonosensitivity at relapse and European Association of Urology (EAU) prognostic group. Late grade 3 urinary and rectal toxicities occurred in 12 % and 1 % of the patients respectively.No significant difference in toxicity or efficacy was observed between the three implant volume groups.
    UNASSIGNED: The efficacy and toxicity results are consistent with those in the LDR group of the MASTER meta-analysis. Salvage BT confirms to be an effective and safe option for locally recurrent prostate cancer. A focal approach could be interesting to reduce late severe toxicities, especially urinary.
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  • 文章类型: Journal Article
    目的:再照射(reRT)是复发性胶质瘤患者的有效治疗方法。剂量递增数据,使用模拟的综合增强和伴随治疗进行reRT仍然很少.在这个n=223例患者的单中心队列中,我们研究了reRT剂量递增以及伴随使用贝伐单抗(BEV)对复发后生存率(PRS)和放射性坏死风险(RN)的影响。
    方法:在2008年7月至2022年8月期间接受BEV治疗的复发性神经胶质瘤患者,回顾性分析替莫唑胺(TMZ)的reRT和不伴随全身治疗的reRT.使用Kaplan-Meier估计器计算所有患者的PRS和无RN生存期(RNFS)。对PRS和RNFS进行单变量和多变量cox回归。计算所有患者的reRT风险评分(RRRS)。
    结果:好,RRRS的中差风险转换为11个月,9个月和7个月的中位数PRS(单变量:p=0.008,多变量:p=0.013)。应用剂量≤36Gy(n=140)或>36Gy(n=83)的ReRT。n=122例患者同时进行贝伐单抗(BEV)治疗,n=32例患者同时进行替莫唑胺(TMZ)治疗。PRS中位数>36Gy的患者为10个月,≤36Gy的患者为8个月(单变量:p=0.032,多变量:p=0.576)。关于伴随TMZ治疗,中位PRS为14个月vs.使用或不使用TMZ治疗的患者为9个月(单变量:p=0.041,多变量:p=0.019)。在本系列中,伴随BEV治疗对PRS无统计学意义。伴随BEV的reRT频率较低,(17/122;13.9%)比没有BEV的reRT(30/101;29.7%)。关于RNFS,用BEV进行reRT的危险比为0.436(单变量;p=0.006)和0.479(多变量;p=0.023),分别。ReRT剂量对RN没有统计学意义(单变量:p=0.073,多变量:p=0.404)。同时接受BEV治疗的患者的RNFS比仅接受reRT治疗的患者更长(平均31.7vs.30.9个月,p=0.004)。
    结论:在这个队列中,在合并BEV治疗的患者中,检测到RN的频率较低,而在合并TMZ治疗的患者中,检测到的PRS时间较长.基于这些结果,最佳合并治疗和最佳剂量应根据患者而定.
    OBJECTIVE: Re-irradiation (reRT) is an effective treatment modality for patients with recurrent glioma. Data on dose escalation, the use of simulated integrated boost and concomitant therapy to reRT are still scarce. In this monocentric cohort of n = 223 patients we investigated the influence of reRT dose escalation as well as the concomitant use of bevacizumab (BEV) with regard to post-recurrence survival (PRS) and risk of radionecrosis (RN).
    METHODS: Patients with recurrent glioma treated between July 2008 and August 2022 with reRT with BEV, reRT with temozolomide (TMZ) and reRT without concomitant systemic therapy were retrospectively analyzed. PRS and RN-free survival (RNFS) were calculated for all patients using the Kaplan-Meier estimator. Univariable and multivariable cox regression was performed for PRS and for RNFS. The reRT Risk Score (RRRS) was calculated for all patients.
    RESULTS: Good, intermediate and poor risk of the RRRS translated into 11 months, 9 months and 7 months of median PRS (univariable: p = 0.008, multivariable: p = 0.013). ReRT was applied with a dose of ≤36 Gy (n = 140) or >36 Gy (n = 83). Concomitant bevacizumab (BEV) therapy was performed in n = 122 and concomitant temozolomide (TMZ) therapy in n = 32 patients. Median PRS was 10 months in patients treated with >36 Gy and 8 months in patients treated with ≤36 Gy (univariable: p = 0.032, multivariable: p = 0.576). Regarding concomitant TMZ therapy, median PRS was 14 months vs. 9 months for patients treated with or without TMZ (univariable: p = 0.041, multivariable: p = 0.019). No statistically significant influence on PRS was seen for concomitant BEV therapy in this series. RN was less frequent for reRT with concomitant BEV, (17/122; 13.9 %) than for reRT without BEV (30/101; 29.7 %). Regarding RNFS, the hazard ratio for reRT with BEV was 0.436 (univariable; p = 0.006) and 0.479 (multivariable; p = 0.023), respectively. ReRT dose did not show statistical significance in regards to RN (univariable: p = 0.073, multivariable: p = 0.404). RNFS was longer for patients receiving concomitant BEV to reRT than for patients treated with reRT only (mean 31.7 vs. 30.9 months, p = 0.004).
    CONCLUSIONS: In this cohort, in patients treated with concomitant BEV therapy RN was less frequently detected and in patients treated with concomitant TMZ longer PRS was observed. Based on these results, the best concomitant therapy and the optimal dose should be decided on a patient-by-patient basis.
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  • 文章类型: Journal Article
    目的:局部复发的鼻咽癌(NPC)在临床治疗中提出了巨大的挑战。虽然术后再放疗(re-RT)已被认为是一种潜在的治疗选择,在这种情况下,缺乏关于使用re-RT的标准化指南和共识。本文提供了有关可能可切除的局部复发性NPC的术后管理的国际建议的全面回顾和总结。特别关注术后再RT。
    方法:进行了彻底的搜索,以确定有关局部复发NPC的术后再RT的相关研究。有争议的问题,包括可切除性标准,保证金评估,术后重新RT的适应症,以及再RT的最佳剂量和方法,是通过德尔菲共识过程解决的。
    结果:共识建议强调需要对可切除性进行更清晰和更广泛的定义,强调实现明确手术切缘的重要性,最好是通过整体方法进行冻结部分边缘评估。此外,这些指南建议对于切缘阳性或接近的患者考虑重新RT.术后最佳再RT剂量通常在60Gy左右,超分馏在降低毒性方面显示出了希望。
    结论:这些指南旨在帮助临床医生做出循证决策,并改善患者治疗可能可切除的局部复发性NPC的结果。通过解决争议的关键领域并提供有关可切除性的建议,保证金评估,和重新RT参数,这些指南为参与局部复发NPC治疗的临床专家提供了宝贵的资源.
    结论:本文为可能可切除的局部复发性鼻咽癌(NPC)的术后管理提供了国际建议,特别关注术后再照射(re-RT)。共识指南强调了实现明确手术切缘的重要性,建议考虑对边缘阳性或接近的患者进行重新RT,推荐60Gy左右的最佳再RT剂量,并建议使用超分馏来减少毒性。目的是改善可切除的局部复发性NPC的治疗结果。
    Locally recurrent nasopharyngeal carcinoma (NPC) presents substantial challenges in clinical management. Although postoperative re-irradiation (re-RT) has been acknowledged as a potential treatment option, standardized guidelines and consensus regarding the use of re-RT in this context are lacking. This article provides a comprehensive review and summary of international recommendations on postoperative management for potentially resectable locally recurrent NPC, with a special focus on postoperative re-RT. A thorough search was conducted to identify relevant studies on postoperative re-RT for locally recurrent NPC. Controversial issues, including resectability criteria, margin assessment, indications for postoperative re-RT, and the optimal dose and method of re-RT, were addressed through a Delphi consensus process. The consensus recommendations emphasize the need for a clearer and broader definition of resectability, highlighting the importance of achieving clear surgical margins, preferably through an en bloc approach with frozen section margin assessment. Furthermore, these guidelines suggest considering re-RT for patients with positive or close margins. Optimal postoperative re-RT doses typically range around 60 Gy, and hyperfractionation has shown promise in reducing toxicity. These guidelines aim to assist clinicians in making evidence-based decisions and improving patient outcomes in the management of potentially resectable locally recurrent NPC. By addressing key areas of controversy and providing recommendations on resectability, margin assessment, and re-RT parameters, these guidelines serve as a valuable resource for clinical experts involved in the treatment of locally recurrent NPC.
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  • 文章类型: Journal Article
    目的:本研究旨在探讨三维打印非共面模板(3D-PNCT)辅助计算机断层扫描(CT)引导的高剂量率间质近距离放射治疗(HDR-ISBT)治疗外照射后盆腔复发性宫颈癌的疗效和安全性。
    方法:从2019年1月至2023年8月,45名符合条件的患者被纳入该前瞻性队列。所有患者均接受3D-PNCT辅助CT引导的HDR-ISBT,规定剂量为4-7Gy/分数,达到3-8分以上的高危临床目标体积(HR-CTV),用于治疗或姑息目的。主要终点是局部无进展生存期(LPFS)和肿瘤缓解率(TRR)。次要结局指标包括总生存期(OS),毒性,和症状解决。
    结果:45例患者接受了261份3D-PNCT辅助的HDR-ISBT。29例患者有孤立的盆腔复发,16例患者同时出现盆腔外或远处复发。TRR为66.7%。2年和5年LPFS率分别为30.0%和25.7%,分别。中位OS为23.2个月,2年和5年OS率分别为49.5%和34.0%,分别。多变量分析表明鳞状细胞癌,根治性手术,无复发间隔≥12个月,肿瘤直径,盆腔复发类型,HR-CTVD90≥45Gy是影响LPFS的独立因素(均p<0.05)。D100≥21Gy,V100≥83%,V150≥45%与较好的LPFS相关(均p<0.05)。肿瘤直径和转移是OS的独立预测因素(均p<0.05)。疼痛缓解率为66.7%(10/15)。20.0%的患者出现3-4级毒性。
    结论:3D-PNCT辅助的HDR-ISBT用于复发性宫颈癌的再照射被证明是根治性手术的有效和安全的替代方案。
    OBJECTIVE: This study aimed to investigate the efficacy and safety of 3-dimensional printing noncoplanar template (3D-PNCT)-assisted computed tomography (CT)-guided high-dose-rate interstitial brachytherapy (HDR-ISBT) for reirradiation of pelvic recurrent cervical carcinoma after external beam radiotherapy.
    METHODS: From January 2019 to August 2023, 45 eligible patients were enrolled in this prospective cohort. All patients underwent 3D-PNCT-assisted CT-guided HDR-ISBT with a prescribed dose of 4-7 Gy/fraction to the high-risk clinical target volume (HR-CTV) over 3-8 fractions, either for curative or palliative purposes. The primary endpoints were local progression-free survival (LPFS) and tumor response rate (TRR). The secondary outcome measures included overall survival (OS), toxicities, and symptom resolution.
    RESULTS: Forty-five patients received 261 fractions of 3D-PNCT-assisted HDR-ISBT. Twenty-nine patients had isolated pelvic recurrence, and 16 patients had simultaneous extra-pelvic or distant recurrences. The TRR was 66.7%. The 2- and 5-year LPFS rates were 30.0% and 25.7%, respectively. The median OS was 23.2 months, and 2- and 5-year OS rates were 49.5% and 34.0%, respectively. The multivariate analysis indicated that squamous cell carcinoma, radical surgery, recurrence-free interval≥12 months, tumor diameter, pelvic recurrence type, and HR-CTV D90≥45 Gy were independent factors influencing LPFS (all p<0.05). D100≥21 Gy, V100≥83%, and V150≥45% were associated with better LPFS (all p<0.05). Tumor diameter and metastasis were independent predictive factors for OS (all p<0.05). The pain relief rate was 66.7% (10/15). Grade 3-4 toxicities occurred in 20.0% of patients.
    CONCLUSIONS: 3D-PNCT-assisted HDR-ISBT for reirradiation of recurrent cervical cancer proved to be an effective and safe alternative to radical surgery.
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  • 文章类型: Journal Article
    :随着转移性恶性肿瘤患者生存率的提高,尽管缺乏标准化指南,但姑息性再照射和再照射的要求仍在继续增长.关于颅外第三疗程姑息性放射的数据有限,许多放射肿瘤学家对同一部位进行第三道照射可能会感到不舒服。该评论探讨了有关再辐照的可用现代数据。文献综述确定了四项现代同行评议研究,调查姑息治疗,外束辐射的颅外第三道照射。这些研究是回顾性的,小,和异质。虽然他们报告了与第一疗程照射相当的疼痛缓解率和较低的急性毒性率,由于治疗参数不均匀以及累积剂量当量和时间间隔报告不足,解释变得复杂.可用数据有限,在姑息性放疗中,优先考虑患者安全和生活质量至关重要.患者选择要细致,考虑初始治疗反应和预期寿命等因素。适形辐射技术,严格固定,应采用每日图像指导,以最大程度地减少对危险器官(OAR)的毒性。长期随访对于有效识别和管理晚期毒性至关重要。尽管数据匮乏,回顾性系列研究表明,颅外第三疗程照射可提供与第一疗程照射相当的有效疼痛缓解,且毒性反应可耐受.然而,仔细考虑患者预后和遵守姑息性放疗的既定原则在决策中至关重要.需要进一步的研究和长期随访来完善治疗策略,并确保在这种复杂的临床情况下提供安全有效的护理。
    With improving rates of survival among patients with metastatic malignancies, the request for palliative re-irradiation and re-re-irradiation continues to grow despite an absence of standardized guidelines. With only limited data regarding extra-cranial third-course palliative radiation, many radiation oncologists may feel uncomfortable proceeding with third-course irradiation of the same site. The review explores the available modern data regarding re-re-irradiation. A literature review identified four modern peer-reviewed studies investigating palliative, extra-cranial third-course irradiation with external beam radiation. These studies were retrospective, small, and heterogenous. While they reported comparable rates of pain palliation to first course irradiation and low rates of acute toxicity, interpretation is complicated by heterogeneous treatment parameters and insufficient reporting of cumulative dose equivalents and time intervals. With limited data available, it is critical to prioritize patient safety and quality of life in palliative radiotherapy. Patient selection should be meticulous, considering factors such as initial treatment response and predicted life expectancy. Conformal radiation techniques, strict immobilization, and daily image guidance should be employed to minimize toxicity to organs at risk (OARs). Long-term follow-up is essential for identifying and managing late toxicities effectively. Despite the scarcity of data, retrospective series suggest that extra-cranial third course irradiation can provide effective pain palliation comparable to first-course irradiation with tolerable rates of toxicity. However, careful consideration of patient prognosis and adherence to established principles of palliative radiotherapy are essential in decision-making. Further research and long-term follow-up are needed to refine treatment strategies and ensure safe and efficacious care delivery in this complex clinical scenario.
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  • 文章类型: Journal Article
    背景:在过去的十年中,头颈癌(HNC)的再照射变得越来越容易,由于现代辐照技术提供了减少治疗相关的毒性。本文的目的是比较评估从强度调制光子与再次照射的HNC患者的质子治疗计划。
    方法:本回顾性研究纳入6例复发性HNC患者。对于每个患者,创建两个治疗计划:一个IMRT/VMAT和一个IMPT计划。第二次照射的规定剂量为50至70GyRBE。该研究比较分析了CTV的覆盖率,危险器官(OAR)的剂量和健康组织(OAR除外)接受的低剂量。
    结果:光子与质子计划的CTV覆盖率相似,后者在四种情况下表现出更好的同质性。对于光子计划,CTV的最大剂量通常较高,差异在0.3%至1.9%之间。对于腮腺和身体,质子计划的平均剂量较低。使用质子可以实现低剂量对健康组织(OAR除外)的显着减少,D10%和Dmean的平均值分别为60%和64%,分别。
    结论:光子和质子再照射HNC的剂量学比较表明,对治疗个体化的需求很大,结论认为质子应考虑在个体基础上进行再辐照。
    BACKGROUND: Reirradiation of head and neck cancer (HNC) became more accessible in the last decade, owing to modern irradiation techniques which offer a reduction in treatment related toxicities. The aim of this paper was to comparatively evaluate the dosimetric aspects derived from intensity modulated photon vs. proton treatment planning in reirradiated HNC patients.
    METHODS: Six recurrent HNC patients were enrolled in this retrospective study. For each patient two treatment plans were created: one IMRT/VMAT and one IMPT plan. The prescribed dose for the second irradiation was between 50 and 70 Gy RBE. The study comparatively analyzed the CTV coverage, doses to organs at risk (OARs) and low doses received by the healthy tissue (other than OAR).
    RESULTS: Similar CTV coverage was achieved for photon vs proton plans, with the latter presenting better homogeneity in four cases. Maximum dose to CTV was generally higher for photon plans, with differences ranging from 0.3 to 1.9%. For parotid glands and body, the mean dose was lower for proton plans. A notable reduction of low dose to healthy tissue (other than OARs) could be achieved with protons, with an average of 60% and 64% for D10% and Dmean, respectively.
    CONCLUSIONS: The dosimetric comparison between photon and proton reirradiation of HNC showed a great need for treatment individualization, concluding that protons should be considered for reirradiation on an individual basis.
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