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Radiosurgery Society Case-Based Guide to Stereotactic Body Radiation Therapy for Challenging Cases of Spinal Metastases. 放射外科协会《针对脊柱转移瘤疑难病例的立体定向体放射治疗病例指南》。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-02 DOI: 10.1016/j.prro.2024.08.004
Khaled Aziz, Daniel Koffler, April Vassantachart, Abbas Rattani, Nii-Kwanchie Ankrah, Emile Gogineni, Therese Y Andraos, Arjun Sahgal, Balamurugan Vellayappan, Emma M Dunne, Shankar Siva, Fabio Y Moraes, Matthias Guckenberger, Daniel Lubelski, Samuel Chao, Stephanie Combs, Eric Chang, Anubhav G Amin, Matthew Foote, Iris Gibbs, Minsun Kim, Joshua Palmer, Simon Lo, Kristin J Redmond

Purpose: Spinal stereotactic body radiation therapy (SBRT) has become the standard of care in management of patients with limited sites of metastatic disease, radio-resistant histologies, painful vertebral metastases with long life expectancy and cases of reirradiation. Our case-based guidelines aim to assist radiation oncologists in the appropriate utilization of SBRT for common, yet challenging, cases of spinal metastases.

Materials and methods: Cases were selected to include scenarios of large volume sacral disease with nerve entrapment, medically inoperable disease abutting the thecal sac, and local failure after prior SBRT. Relevant literature was reviewed, and areas requiring further investigation were discussed to offer a framework for evidence-based clinical practice.

Results: Spinal SBRT can be effectively delivered in challenging cases following multidisciplinary discussion by utilizing a methodical approach to patient selection, appropriate dose selection, and adherence to evidence-based dose constraints.

Conclusions: The Radiosurgery Society's case-based practice review offers guidance to practicing physicians treating technically challenging SBRT candidate patients with spinal metastases.

目的:脊柱立体定向体放射治疗(SBRT)已成为治疗转移性疾病部位有限、放射抗性组织学、预期寿命长的疼痛性椎体转移以及再照射病例的标准治疗方法。我们基于病例的指南旨在帮助放射肿瘤专家在常见但具有挑战性的脊柱转移病例中适当使用 SBRT:我们选择的病例包括神经卡压的大体积骶骨疾病、与椎管囊相邻的医学上无法手术的疾病以及之前SBRT治疗局部失败的病例。对相关文献进行了回顾,并讨论了需要进一步研究的领域,为循证临床实践提供了一个框架:结果:经过多学科讨论,脊柱SBRT可以在具有挑战性的病例中有效实施,方法是有条不紊地选择患者、选择合适的剂量并遵守循证剂量限制:放射外科协会基于病例的实践评论为执业医师治疗具有技术难度的脊柱转移瘤 SBRT 候选患者提供了指导。
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引用次数: 0
Comprehensive Clinical Usability-oriented Contour Quality Evaluation for Deep learning Auto-segmentation: Combining Multiple Quantitative Metrics through Machine Learning. 用于深度学习自动分割的以临床可用性为导向的综合轮廓质量评估:通过机器学习结合多种定量指标。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-02 DOI: 10.1016/j.prro.2024.07.007
Ying Zhang, Asma Amjad, Jie Ding, Christina Sarosiek, Mohammad Zarenia, Renae Conlin, William A Hall, Beth Erickson, Eric Paulson

Purpose: The current commonly-used metrics for evaluating the quality of auto-segmented contours have limitations and do not always reflect the clinical usefulness of the contours. This work aims to develop a novel contour quality classification (CQC) method by combining multiple quantitative metrics for clinical usability-oriented contour quality evaluation for deep learning-based auto-segmentation (DLAS).

Methods: The CQC was designed to categorize contours on slices as acceptable, minor edit, or major edit based on the expected editing effort/time with supervised ensemble tree classification models using seven quantitative metrics. Organ-specific models were trained for five abdominal organs (pancreas, duodenum, stomach, small and large-bowels) using 50 MRI datasets. Twenty additional MRI and nine CT datasets were employed for testing. Inter-observer variation (IOV) was assessed among six observers and consensus labels were established through majority vote for evaluation. The CQC was also compared with a threshold-based baseline approach.

Results: For the five organs, the average AUC was 0.982±0.01 and 0.979±0.01, the mean-accuracy was 95.8±1.7% and 94.3±2.1%, and the mean risk-rate was 0.8±0.4% and 0.7±0.5% for MRI and CT testing dataset, respectively. The CQC results closely matched the IOV results (mean-accuracy of 94.2±0.8% and 94.8±1.7%) and were significantly higher than those obtained using the threshold-based method (mean-accuracy of 80.0±4.7%, 83.8±5.2%, and 77.3±6.6% using one, two, and three metrics).

Conclusion: The CQC models demonstrated high performance in classifying the quality of contour slices. This method can address the limitations of existing metrics and offers an intuitive and comprehensive solution for clinically oriented evaluation and comparison of DLAS systems.

目的:目前常用的自动分割轮廓质量评估指标存在局限性,并不总能反映轮廓的临床实用性。本研究旨在开发一种新颖的轮廓质量分类(CQC)方法,该方法结合了多种定量指标,用于基于深度学习的自动分割(DLAS)中以临床实用性为导向的轮廓质量评估:CQC 的设计目的是根据预期的编辑工作量/时间,利用七个量化指标的监督集合树分类模型,将切片上的轮廓分为可接受、小编辑或大编辑。使用 50 个 MRI 数据集为五个腹部器官(胰腺、十二指肠、胃、小肠和大肠)训练了特定器官模型。另外还使用了 20 个 MRI 数据集和 9 个 CT 数据集进行测试。对六位观察者的观察者间差异(IOV)进行了评估,并通过多数票确定了共识标签进行评估。CQC 还与基于阈值的基线方法进行了比较:对于五个器官,MRI 和 CT 测试数据集的平均 AUC 分别为 0.982±0.01 和 0.979±0.01,平均准确率分别为 95.8±1.7% 和 94.3±2.1%,平均风险率分别为 0.8±0.4% 和 0.7±0.5%。CQC结果与IOV结果(平均准确率为94.2±0.8%和94.8±1.7%)非常接近,并且明显高于使用基于阈值的方法所获得的结果(使用一个、两个和三个指标的平均准确率分别为80.0±4.7%、83.8±5.2%和77.3±6.6%):结论:CQC 模型在轮廓切片质量分类方面表现出很高的性能。这种方法可以解决现有指标的局限性,为临床导向的 DLAS 系统评估和比较提供了直观、全面的解决方案。
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引用次数: 0
Centralized Quality Assurance of Stereotactic Body Radiation Therapy for the Veterans Affairs Cooperative Studies Program Study Number 2005: A Phase 3 Randomized Trial of Lung Cancer Surgery or Stereotactic Radiotherapy for Operable Early-Stage Non-Small Cell Lung Cancer (VALOR). 退伍军人事务合作研究计划研究编号 2005:立体定向体外放射治疗的集中质量保证:肺癌手术或立体定向放疗治疗可手术早期非小细胞肺癌的 3 期随机试验 (VALOR)。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-02 DOI: 10.1016/j.prro.2024.07.010
Timothy A Ritter, Robert D Timmerman, Hena I Hanfi, Hairong Shi, Matthew K Leiner, Hua Feng, Vicki L Skinner, Lisa M Robin, Cheryl Odle, Gabriella Amador, Tom Sindowski, Amanda J Snodgrass, Grant D Huang, Domenic J Reda, Christopher Slatore, Catherine Sears, Lorraine D Cornwell, Tomer Karas, David H Harpole, Jatinder Palta, Drew Moghanaki

Background: The phase III Veterans Affairs Lung cancer surgery Or stereotactic Radiotherapy (VALOR) study implemented centralized quality assurance (QA) to mitigate risks of protocol deviations. This report summarizes quality and compliance for the first 100 participants treated with SBRT in this study.

Methods: A centralized QA program was developed to credential and monitor study sites to ensure standard-of-care lung stereotactic body radiation therapy (SBRT) treatments are delivered to participants. Requirements were adapted from protocols established by the National Cancer Institute's Image and Radiation Oncology Core, which provides oversight for clinical trials sponsored by the NCI's National Clinical Trials Network.

Results: The first 100 lung SBRT treatment plans were reviewed from April 2017 to October 2022. Tumor contours were appropriate in all submissions. PTV expansions were less than the minimum 5 mm requirement in 2% of cases. Critical organ-at-risk (OAR) structures were contoured accurately for the proximal bronchial tree, trachea, esophagus, spinal cord, and brachial plexus in 75%, 92%, 100%, 100%, and 95% of cases. Prescriptions were appropriate in 98% of cases; two central tumors were treated using a peripheral tumor dose prescription while meeting OAR constraints. PTV V100% values were above the protocol-defined minimum of 94% in all but one submission. The median Dmax within the PTV was 125.4% (105.8% - 149.0%, standard deviation ±8.7%). High-dose conformality (<1.2) and intermediate-dose compactness (R50% and D2cm) indices were acceptable or deviation acceptable in 100% and 94% of cases, respectively.

Conclusions: The first 100 participants randomized to SBRT in this study were appropriately treated without safety concerns. A response to the incorrect prescriptions led to preventative measures without further recurrences. The program was developed in a healthcare system without prior experience with a centralized RT QA program and may serve as a reference for other institutions.

背景:退伍军人事务部肺癌手术或立体定向放射治疗(VALOR)III 期研究实施了集中质量保证(QA),以降低方案偏差风险。本报告总结了在该研究中接受 SBRT 治疗的前 100 名参与者的质量和依从性:方法:制定了一项集中质量保证计划,对研究机构进行认证和监督,以确保为参与者提供符合标准的肺部立体定向体放射治疗(SBRT)。这些要求改编自美国国立癌症研究所图像与放射肿瘤学核心制定的协议,该核心负责监督由美国国立癌症研究所国家临床试验网络赞助的临床试验:从2017年4月到2022年10月,对首批100例肺SBRT治疗计划进行了审查。所有提交的肿瘤轮廓均合适。2%的病例的PTV扩展小于最低5毫米的要求。75%、92%、100%、100% 和 95% 的病例中,近端支气管树、气管、食管、脊髓和臂丛的关键风险器官 (OAR) 结构轮廓准确。在 98% 的病例中,处方都是适当的;有两个中心肿瘤在满足 OAR 限制的情况下,使用外周肿瘤剂量处方进行了治疗。除一个病例外,其他所有病例的 PTV V100% 值都高于方案定义的最低值 94%。PTV内Dmax的中位数为125.4%(105.8% - 149.0%,标准偏差±8.7%)。高剂量符合性(结论:本研究中随机接受 SBRT 治疗的前 100 名参与者均接受了适当的治疗,没有出现安全问题。针对错误处方采取了预防措施,没有再发生复发。该计划是在一个没有集中 RT QA 计划经验的医疗系统中制定的,可为其他机构提供参考。
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引用次数: 0
Masthead/Sub page 刊头/分页
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/S1879-8500(24)00168-1
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引用次数: 0
The Impact of Radiation Therapy in Patients with Systemic Sclerosis and Head and Neck Cancer 放疗对全身性硬化症和头颈部癌症患者的影响。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.04.015

Objective

Systemic sclerosis (SSc) is considered a relative, or in some cases, absolute contraindication for radiation therapy for various cancers; however, radiation is the standard of care and the best option for tumor control for locally advanced head and neck (H&N) cancer. We present a case series to document postradiation outcomes in patients with SSc and H&N cancer.

Methods

Patients with SSc and H&N cancer treated with radiation were identified from the Johns Hopkins Scleroderma Center and the University of Pittsburgh Scleroderma Center research registries. Through chart review, we identified whether patients developed predetermined acute and late side effects or changes in SSc activity from radiation. We further describe therapies used to prevent and treat radiation-induced fibrosis.

Results

Thirteen patients with SSc who received radiation therapy for H&N cancer were included. Five-year survival was 54%. Nine patients (69%) developed local radiation-induced skin thickening, and 7 (54%) developed reduced neck range of motion. Two patients required long-term percutaneous endoscopic gastrostomy use due to radiation therapy complications. No patients required respiratory support related to radiation therapy. Regarding SSc disease activity among the patients with established SSc before radiation therapy, none experienced interstitial lung disease progression in the postradiation period. After radiation, one patient had worsening skin disease outside the radiation field; however, this patient was within the first year of SSc, when progressive skin disease is expected. Treatment strategies to prevent radiation fibrosis included pentoxifylline, amifostine, and vitamin E, while intravenous immunoglobulin (IVIG) was used to treat it.

Conclusion

Although some patients with SSc who received radiation for H&N cancer developed localized skin thickening and reduced neck range of motion, systemic flares of SSc were uncommon. This observational study provides evidence to support the use of radiation therapy for H&N cancer in patients with SSc when radiation is the best treatment option.

目的:系统性硬化症(SSc)被认为是各种癌症放射治疗的相对禁忌症,在某些情况下甚至是绝对禁忌症;然而,放射治疗是局部晚期头颈部癌症(H&N)的标准治疗方法和控制肿瘤的最佳选择。我们提供了一个病例系列,记录了 SSc 和 H&N 癌症患者放疗后的疗效:方法:我们从两个大型硬皮病中心研究登记处找到了接受放射治疗的 SSc 和 H&N 癌症患者。通过病历审查,我们确定了患者是否因放射治疗而出现预先确定的急性和晚期副作用或 SSc 活性变化。我们进一步描述了用于预防和治疗辐射诱导的纤维化的疗法:共纳入了 13 名接受 H&N 癌症放射治疗的 SSc 患者。五年生存率为 54%。九名患者(69%)出现了局部放射引起的皮肤增厚,七名患者(54%)出现了颈部活动范围减小。两名患者因放疗并发症而需要长期使用经皮内镜胃造瘘术。没有患者因放疗而需要呼吸支持。关于放疗前已确诊的 SSc 患者的 SSc 疾病活动情况,没有人在放疗后出现间质性肺病进展。放射治疗后,一名患者在放射野外的皮肤病恶化,但这名患者是在 SSc 第一年内,皮肤病进展是意料之中的。预防放射性纤维化的治疗策略包括喷托维林、阿米福星和维生素E,而静脉注射免疫球蛋白(IVIG)则用于治疗放射性纤维化:虽然一些接受 H&N 癌症放射治疗的 SSc 患者会出现局部皮肤增厚和颈部活动范围减小的情况,但 SSc 全身性复发的情况并不常见。这项观察性研究为SSc患者使用放射治疗H&N癌提供了证据,如果放射治疗是最佳治疗方案的话。
{"title":"The Impact of Radiation Therapy in Patients with Systemic Sclerosis and Head and Neck Cancer","authors":"","doi":"10.1016/j.prro.2024.04.015","DOIUrl":"10.1016/j.prro.2024.04.015","url":null,"abstract":"<div><h3>Objective</h3><p>Systemic sclerosis (SSc) is considered a relative, or in some cases, absolute contraindication for radiation therapy for various cancers; however, radiation is the standard of care and the best option for tumor control for locally advanced head and neck (H&amp;N) cancer. We present a case series to document postradiation outcomes in patients with SSc and H&amp;N cancer.</p></div><div><h3>Methods</h3><p>Patients with SSc and H&amp;N cancer treated with radiation were identified from the Johns Hopkins Scleroderma<span><span> Center and the University of Pittsburgh Scleroderma Center research registries. Through chart review, we identified whether patients developed predetermined acute and late side effects or changes in SSc activity from radiation. We further describe therapies used to prevent and treat radiation-induced </span>fibrosis.</span></p></div><div><h3>Results</h3><p><span>Thirteen patients with SSc who received radiation therapy for H&amp;N cancer were included. Five-year survival was 54%. Nine patients (69%) developed local radiation-induced skin thickening, and 7 (54%) developed reduced neck range of motion. Two patients required long-term percutaneous endoscopic gastrostomy<span> use due to radiation therapy complications. No patients required respiratory support<span> related to radiation therapy. Regarding SSc disease activity among the patients with established SSc before radiation therapy, none experienced interstitial lung </span></span></span>disease progression<span><span><span> in the postradiation period. After radiation, one patient had worsening skin disease outside the radiation field; however, this patient was within the first year of SSc, when progressive skin disease is expected. Treatment strategies to prevent radiation fibrosis included </span>pentoxifylline<span>, amifostine, and </span></span>vitamin E, while intravenous immunoglobulin (IVIG) was used to treat it.</span></p></div><div><h3>Conclusion</h3><p>Although some patients with SSc who received radiation for H&amp;N cancer developed localized skin thickening and reduced neck range of motion, systemic flares of SSc were uncommon. This observational study provides evidence to support the use of radiation therapy for H&amp;N cancer in patients with SSc when radiation is the best treatment option.</p></div>","PeriodicalId":54245,"journal":{"name":"Practical Radiation Oncology","volume":null,"pages":null},"PeriodicalIF":3.4,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140864403","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Radiation Therapy Contouring Atlas for Delineation of the Level I and II Axillae in the Prone Position: A Single-Institution Experience 用于在俯卧位划定 I-II 级腋窝的放射治疗轮廓图:单个机构的经验。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.04.016

Purpose

With transition from supine to prone position, tenting of the pectoralis major occurs, displacing the muscle from the chest wall and shifting the level I and II axillary spaces. For patients for whom we aim to treat the level I and II axillae using the prone technique, accurate delineation of these nodal regions is necessary. Although different consensus guidelines exist for delineation of nodal anatomy in supine position, to our knowledge, there are no contouring guidelines in the prone position that account for this change in nodal anatomy.

Methods and Materials

The level I and II nodal contours from the Radiation Therapy Oncology Group (RTOG) breast cancer supine atlas were adapted for prone position by 2 radiation oncologists and a breast radiologist based on anatomic changes observed from supine to prone positioning on preoperative diagnostic imaging. Forty-three patients from a single institution treated with prone high tangents from 2012 to 2018 were identified as representative cases to delineate the revised level I and II axillae on noncontrast computed tomography (CT) scans obtained during radiation simulation. The revised nodal contours were reviewed by an expanded expert multidisciplinary panel including breast radiologists, radiation oncologists, and surgical oncologists for consistency and reproducibility.

Results

Consensus was achieved among the panel in order to create modifications from the RTOG breast atlas for CT–based contouring of the level I and II axillae in prone position using bone, muscle, and skin as landmarks. This atlas provides representative examples and accompanying descriptions for the changes described to the caudal and anterior borders of level II and the anterior, posterior, medial, and lateral borders of level I. A step-by-step guide is provided for properly identifying the revised anterior border of the level I axilla.

Conclusions

The adaptations to the RTOG breast cancer atlas for prone positioning will enable radiation oncologists to more accurately target the level I and II axillae when the axillae are targets in addition to the breast.

目的:从仰卧位转为俯卧位时,胸大肌会出现帐篷,使肌肉从胸壁移位,并移动 I-II 级腋窝间隙。对于我们打算使用俯卧位技术治疗 I-II 级腋窝的患者来说,准确划分这些结节区域是非常必要的。虽然仰卧位结节解剖的划定有不同的共识指南,但据我们所知,还没有俯卧位的轮廓划定指南考虑到结节解剖的这种变化:两位放射肿瘤专家和一位乳腺放射专家根据术前诊断成像中观察到的从仰卧位到俯卧位的解剖变化,对乳腺癌放射治疗肿瘤学组(RTOG)仰卧位图谱中的 I-II 级结节轮廓进行了调整,使其适用于俯卧位。从 2012 年到 2018 年,来自一家机构的 43 例采用俯卧位高切线治疗的患者被确定为代表性病例,以便在放射模拟期间获得的非对比计算机断层扫描(CT)上划定修订后的 I-II 级腋窝。包括乳腺放射科医生、放射肿瘤科医生和肿瘤外科医生在内的多学科扩大专家小组对修订后的结节轮廓进行了审查,以确保一致性和可重复性:结果:专家小组达成共识,对 RTOG 乳腺图谱进行修改,以骨骼、肌肉和皮肤为地标,绘制出基于 CT 的 I-II 级腋窝俯卧轮廓图。该图谱为 II 级腋窝的尾缘和前缘以及 I 级腋窝的前缘、后缘、内侧缘和外侧缘所作的修改提供了代表性示例和附带说明:对 RTOG 乳腺癌图谱进行俯卧位调整后,当腋窝是乳房以外的目标时,放射肿瘤学家就能更准确地瞄准 I-II 级腋窝。
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引用次数: 0
To pass away on leap day 在闰日去世。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.01.008
{"title":"To pass away on leap day","authors":"","doi":"10.1016/j.prro.2024.01.008","DOIUrl":"10.1016/j.prro.2024.01.008","url":null,"abstract":"","PeriodicalId":54245,"journal":{"name":"Practical Radiation Oncology","volume":null,"pages":null},"PeriodicalIF":3.4,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140121335","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
PROshot: Immunotherapy for Cervical Cancer, Epidermal Growth Factor Receptor-Mutated Stage III Lung Cancer, Perioperative Chemotherapy for Esophageal Cancer, Salvage Postprostatectomy Radiation and Androgen Deprivation Therapy, and Immunotherapy for Head and Neck Cancer 专业摄影宫颈癌免疫疗法、表皮生长因子受体突变的 III 期肺癌、食道癌围手术期化疗、前列腺切除术后挽救性放疗和雄激素剥夺疗法以及头颈癌免疫疗法
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.06.001
{"title":"PROshot: Immunotherapy for Cervical Cancer, Epidermal Growth Factor Receptor-Mutated Stage III Lung Cancer, Perioperative Chemotherapy for Esophageal Cancer, Salvage Postprostatectomy Radiation and Androgen Deprivation Therapy, and Immunotherapy for Head and Neck Cancer","authors":"","doi":"10.1016/j.prro.2024.06.001","DOIUrl":"10.1016/j.prro.2024.06.001","url":null,"abstract":"","PeriodicalId":54245,"journal":{"name":"Practical Radiation Oncology","volume":null,"pages":null},"PeriodicalIF":3.4,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142096505","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Radiation Therapy Dose Response in Bulky Relapsed/Refractory Large B-Cell Lymphoma 大块复发/难治性大B细胞淋巴瘤的放疗剂量反应。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.06.003

Purpose

To assess whether a radiation therapy (RT) dose affects response in bulky tumors in relapsed/refractory (r/r) diffuse large B-cell lymphoma (DLBCL).

Methods and Materials

Data from patients with r/r DLBCL treated with salvage- or palliative-intent RT (2008-2020) at a single institution were examined. Index lesion size ≥7.5 cm was defined as bulky. Equivalent doses in 2-Gy fractions (EQD2) were calculated to compare doses between conventional and hypofractionated (≥2.5 Gy/fraction) schemes. Objective response rates (ORRs) were compared using nonparametric Mann-Whitney U test or Kruskal-Wallis test with Dunn's multiple comparison corrections. Freedom from local progression (FFLP) was assessed using Kaplan-Meier and Cox proportional hazard regression analyses.

Results

One hundred eighty-three courses of 151 unique patients were included (salvage: 37% and palliative: 63%). Nonbulky and bulky tumors were irradiated in 109 (60%) and 74 (40%) courses, respectively. Median EQD2 was 33 Gy (IQR, 23-39 Gy) with hypofractionation in 84 (46%) cases. Of those with post-RT imaging (80%), the ORR was 59%, with a trend toward worsened ORR in bulky tumors (50% vs 65%, P = .077). For bulky tumors, RT regimens with EQD2s >30 Gy were associated with better ORR (≤30 Gy vs >30 Gy: 27% vs 64%, P = .0073), whereas a lower EQD2 cutoff was sufficient for nonbulky tumors (≤20 Gy vs >20 Gy: 38% vs 75%, P = .0011). On multivariable regression analysis, bulky tumor size was associated with worsened FFLP (hazard ratio, 2.07; 95% CI, 1.16-3.68; P = .014), whereas high EQD2s >30 Gy were associated with better FFLP (hazard ratio, 0.48; 95% CI, 0.25-0.93; P = .031). Bulky tumors treated with EQD2s ≤30 Gy had the lowest median FFLP (4.0 months), whereas EQD2s >30 Gy had an unreached median FFLP (P = .0047).

Conclusions

Bulky r/r DLBCL tumors were associated with less favorable tumor control outcomes in the salvage and palliative settings. RT regimens with higher EQD2s (>30 Gy) should be considered if durable local control of bulky tumors is desired.

目的:评估放疗(RT)剂量是否会影响复发/难治(r/r)弥漫大B细胞淋巴瘤(DLBCL)巨大肿瘤的反应:方法:研究了在一家机构接受挽救性或姑息性RT治疗的r/r DLBCL患者的数据(2008-2020年)。指标病灶大小≥7.5厘米定义为大块病灶。计算了2格雷(Gy)分次的等效剂量(EQD2),以比较常规和低分次(HF,≥2.5 Gy/分次)方案的剂量。客观反应率(ORR)的比较采用非参数 Mann-Whitney U 检验或 Kruskal-Wallis 检验,并进行 Dunn's 多重比较校正。采用 Kaplan-Meier 和 Cox 比例危险回归分析评估局部进展自由度(FFLP):结果:共纳入了 151 名患者的 183 个疗程(挽救性疗程:37%,姑息性疗程:63%)。109个疗程(60%)和74个疗程(40%)分别对非肿块和肿块肿瘤进行了照射。EQD2中位数为33 Gy(IQR=23-39 Gy),其中84例(46%)为高频。在进行 RT 后成像的病例中(80%),ORR 为 59%,体积大的肿瘤的 ORR 有恶化趋势(50% 对 65%,P=0.077)。对于体积较大的肿瘤,EQD2大于30 Gy的RT方案与较好的ORR相关(≤30 Gy vs. >30 Gy:27% vs. 64%,p=0.0073),而对于非体积较大的肿瘤,较低的EQD2临界值就足够了(≤20 Gy vs. >20 Gy:38% vs. 75%,p=0.0011)。在多变量回归中,体积大的肿瘤与FFLP恶化相关(HR=2.07,95% CI=1.16-3.68,p=0.014),而EQD2>30 Gy的高EQD2与FFLP改善相关(HR=0.48,95% CI=0.25-0.93,p=0.031)。EQD2≤30Gy治疗的大块肿瘤的中位FFLP最低(4.0个月),而EQD2>30Gy的中位FFLP未达到(P=0.0047):结论:大体积r/r DLBCL肿瘤与挽救和姑息治疗中较低的肿瘤控制结果有关。如果希望对体积较大的肿瘤进行持久的局部控制,应考虑采用EQD2较高(>30 Gy)的RT方案。
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引用次数: 0
A Phase II Trial of Stereotactic Body Radiation Therapy and Androgen Deprivation for Oligometastases in Prostate Cancer (SBRT-SG 05) 立体定向体放射治疗和雄激素剥夺治疗前列腺癌寡转移灶的 II 期试验(SBRT-SG 05)。
IF 3.4 3区 医学 Q2 ONCOLOGY Pub Date : 2024-09-01 DOI: 10.1016/j.prro.2024.04.022

Purpose

SBRT-Spanish Group-05 (ClinicalTrials.gov.Identifier: NCT02192788) is a collaborative (SBRT-SG, Grupo de Investigación Clínica en Oncología Radioterápica, and Sociedad Española de Oncología Radioterápica) prospective multicenter phase II trial testing stereotactic body radiation therapy (SBRT) and androgen deprivation therapy (ADT) in patients with oligorecurrent prostate cancer.

Methods and Materials

Two cohorts of patients with prostate cancer in an oligorecurrent stage (hormone-sensitive in the principal cohort and castration-resistant in the exploratory cohort) were assigned to receive ADT and SBRT for at least 24 months from the time of the enrollment. Concomitant treatment with chemotherapy, abiraterone, or enzalutamide was not allowed. Oncologic outcomes were assessed in both cohorts. Toxicity was prospectively analyzed.

Results

From 2014 to 2019, 81 patients with a total of 126 lesions from 14 centers met the inclusion criteria, 14 of whom were castration-resistant. With a median follow-up of 40 months (12-58 months), 3-year local recurrence-free survival was 92.5% (95% CI, 79.9%-96.3%) and 85.7% (95% CI, 48.2%-95.6%) in the principal and exploratory cohorts, respectively. In the principal cohort, biochemical relapse-free survival and metastasis progression-free survival at 1, 2, and 3 years were 91% (95% CI, 81%-95.8%), 73.7% (95% CI, 61.1%-82.8%), 50.6% (95% CI, 36.2%-63.3%), and 92% (95% CI, 83%-97%), 81% (95% CI, 70%-89%), and 67% (95% CI, 53%-77%), respectively. In the exploratory cohort, metastasis progression-free survival at 1, 2, and 3 years was 64% (95% CI, 34%-83%), 43% (95% CI, 18%-66%), and 26% (95% CI, 7%-51%), respectively. None of the patients developed grade III or higher toxicity or symptoms related to local progression, and only 2 (2.4%) patients developed grade II toxicity.

Conclusions

The combination of SBRT and ADT is safe and shows favorable clinical outcomes in patients with hormone-sensitive and castration-resistant prostate cancer. Validation studies are needed in patients with castration-resistant prostate cancer.

目的:SBRT-西班牙组-05(ClinicalTrials.gov.Identifier:NCT02192788)是一项合作性(SBRT-SG、Grupo de Investigación Clínica en Oncología Radioterápica和Sociedad Española de Oncología Radioterápica)前瞻性多中心II期试验,测试立体定向体放射疗法(SBRT)和雄激素剥夺疗法(ADT)在少流期前列腺癌患者中的应用:两组处于少发期的前列腺癌患者(主要组别为激素敏感型,探索组别为阉割耐药型)被分配接受 ADT 和 SBRT 治疗,治疗时间自注册时算起至少 24 个月。不允许同时接受化疗、阿比特龙或恩杂鲁胺治疗。两组患者均接受了肿瘤学结果评估。对毒性进行了前瞻性分析:2014年至2019年,来自14个中心的81名患者共126个病灶符合纳入标准,其中14名患者为阉割耐药。中位随访时间为40个月(12-58个月),主要队列和探索队列的3年无局部复发生存率分别为92.5%(95% CI,79.9%-96.3%)和85.7%(95% CI,48.2%-95.6%)。在主要队列中,1年、2年和3年的无生化复发生存率和无转移进展生存率分别为91%(95% CI,81%-95.8%)、73.7%(95% CI,61.1%-82.8%)、50.6%(95% CI,36.2%-63.3%)和92%(95% CI,83%-97%)、81%(95% CI,70%-89%)和67%(95% CI,53%-77%)。在探索性队列中,1年、2年和3年的无转移进展生存率分别为64%(95% CI,34%-83%)、43%(95% CI,18%-66%)和26%(95% CI,7%-51%)。没有一名患者出现III级或以上毒性或与局部进展相关的症状,只有2名(2.4%)患者出现II级毒性:结论:SBRT和ADT联合治疗对激素敏感型和阉割耐药型前列腺癌患者是安全的,并显示出良好的临床效果。需要对阉割耐药前列腺癌患者进行验证研究。
{"title":"A Phase II Trial of Stereotactic Body Radiation Therapy and Androgen Deprivation for Oligometastases in Prostate Cancer (SBRT-SG 05)","authors":"","doi":"10.1016/j.prro.2024.04.022","DOIUrl":"10.1016/j.prro.2024.04.022","url":null,"abstract":"<div><h3>Purpose</h3><p><span>SBRT-Spanish Group-05 (ClinicalTrials.gov.Identifier: NCT02192788) is a collaborative (SBRT-SG, Grupo de Investigación Clínica en Oncología Radioterápica, and Sociedad Española de Oncología Radioterápica) prospective multicenter phase II trial testing stereotactic body radiation therapy (SBRT) and androgen deprivation therapy (ADT) in patients with oligorecurrent </span>prostate cancer.</p></div><div><h3>Methods and Materials</h3><p><span><span><span>Two cohorts of patients with prostate cancer in an oligorecurrent stage (hormone-sensitive in the principal cohort and castration-resistant in the exploratory cohort) were assigned to receive ADT and </span>SBRT for at least 24 months from the time of the enrollment. Concomitant treatment with chemotherapy, </span>abiraterone, or </span>enzalutamide was not allowed. Oncologic outcomes were assessed in both cohorts. Toxicity was prospectively analyzed.</p></div><div><h3>Results</h3><p>From 2014 to 2019, 81 patients with a total of 126 lesions from 14 centers met the inclusion criteria, 14 of whom were castration-resistant. With a median follow-up of 40 months (12-58 months), 3-year local recurrence-free survival was 92.5% (95% CI, 79.9%-96.3%) and 85.7% (95% CI, 48.2%-95.6%) in the principal and exploratory cohorts, respectively. In the principal cohort, biochemical relapse-free survival and metastasis progression-free survival at 1, 2, and 3 years were 91% (95% CI, 81%-95.8%), 73.7% (95% CI, 61.1%-82.8%), 50.6% (95% CI, 36.2%-63.3%), and 92% (95% CI, 83%-97%), 81% (95% CI, 70%-89%), and 67% (95% CI, 53%-77%), respectively. In the exploratory cohort, metastasis progression-free survival at 1, 2, and 3 years was 64% (95% CI, 34%-83%), 43% (95% CI, 18%-66%), and 26% (95% CI, 7%-51%), respectively. None of the patients developed grade III or higher toxicity or symptoms related to local progression, and only 2 (2.4%) patients developed grade II toxicity.</p></div><div><h3>Conclusions</h3><p>The combination of SBRT and ADT is safe and shows favorable clinical outcomes in patients with hormone-sensitive and castration-resistant prostate cancer. Validation studies are needed in patients with castration-resistant prostate cancer.</p></div>","PeriodicalId":54245,"journal":{"name":"Practical Radiation Oncology","volume":null,"pages":null},"PeriodicalIF":3.4,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141472584","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Practical Radiation Oncology
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