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Neurocognitive Function and Quality of Life After Multifraction Radiosurgery for Large Resected and Intact Brain Metastases: Results of a Prospective Clinical Trial 一项前瞻性临床试验的结果:大切除和完整脑转移瘤的多重放射治疗后的神经认知功能和生活质量
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-14 DOI: 10.1016/j.adro.2025.101956
James R. Janopaul-Naylor MD , Anny Reyes MS , Yichun Cao MPH , Jeffrey Switchenko PhD, MS , Jeffrey J. Olson MD , Jim Zhong MD , Hui-Kuo Shu MD, PhD , Cady K. Block PhD , Bree R. Eaton MD

Purpose

Stereotactic radiosurgery (SRS) is the standard of care for brain metastases, providing effective local tumor control while avoiding the neurocognitive effects of whole-brain radiation therapy. However, large brain metastases have been excluded from the randomized studies of single-fraction SRS, and there are limited data regarding neurocognitive outcomes with multifraction radiosurgery approaches for large intact or resected brain metastases.

Methods and Materials

We performed a prospective phase 1 dose-escalation study of multifraction SRS for intact or resected brain metastases 3 to 6 cm in diameter from 2012 to 2021. Patients longitudinally completed the Hopkins Verbal Learning Test (HVLT), Mini-Mental State Examination, Functional Assessment of Cancer Therapy—Brain, and Medical Outcomes Cognitive Scale. Reliable Change Index is used to assess HVLT change from baseline to 4 months. Significance is defined as greater than 1 SD change. Analysis of variance comparisons were performed for clinicodemographic characteristics associated with neurocognitive outcomes or quality-of-life metrics.

Results

Of the 24 patients treated in the trial, 15 completed both baseline and 4-month neurocognitive assessments. For the 15 patients with neurocognitive assessments, median age was 57 years (range, 37-74 years), median baseline Karnofsky Performance Status was 80 (range, 70-90), and median volume of radiation target was 15.9 cm3 (range, 7.7-57.2 cm3). At 4 months, 20% of patients had a significant decline in HVLT Total Recall scores, 33% had no significant change, and 47% had significant improvement. Mean neurocognitive function and quality-of-life scores were either stable or improved over time up to the last evaluation at 25 months. There were no clinical or treatment characteristics significantly associated with changes in neurocognitive function or quality-of-life scores.

Conclusions

Of the evaluable patients with large brain metastases treated with dose-escalated, multifraction SRS, the majority of patients demonstrated stable or improved neurocognitive function and quality of life in follow-up.
目的立体定向放射外科(SRS)是脑转移瘤的标准治疗方法,可有效控制局部肿瘤,同时避免全脑放射治疗对神经认知的影响。然而,大的脑转移瘤被排除在单段SRS的随机研究之外,并且关于多段放射手术治疗大的完整或切除的脑转移瘤的神经认知结果的数据有限。方法和材料我们在2012年至2021年期间对直径3至6cm的完整或切除的脑转移瘤进行了多组分SRS的前瞻性1期剂量递增研究。患者纵向完成霍普金斯语言学习测试(HVLT)、迷你精神状态检查、癌症治疗-脑功能评估和医疗结果认知量表。使用可靠变化指数评估HVLT从基线到4个月的变化。显著性定义为大于1个标准差的变化。对与神经认知结果或生活质量指标相关的临床人口学特征进行方差比较分析。结果在试验中接受治疗的24名患者中,15名完成了基线和4个月的神经认知评估。15例接受神经认知评估的患者中位年龄为57岁(范围37-74岁),基线Karnofsky Performance Status中位为80(范围70-90),放射靶中位体积为15.9 cm3(范围7.7-57.2 cm3)。4个月时,20%的患者HVLT总回忆评分显著下降,33%无显著变化,47%有显著改善。平均神经认知功能和生活质量评分在25个月的最后一次评估中保持稳定或有所改善。没有临床或治疗特征与神经认知功能或生活质量评分的变化显著相关。结论在可评估的大脑转移患者中,大多数患者在随访中表现出稳定或改善的神经认知功能和生活质量。
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引用次数: 0
Clinical Outcomes and Institutional Experience of Ultrahypofractionated Radiation Therapy in Patients With Breast Cancer 乳腺癌患者超低分割放射治疗的临床结果和机构经验
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-12 DOI: 10.1016/j.adro.2025.101948
Hiba Othman MD, FRCPC , Aisling Barry MD, FRCPC , Anthony Fyles MD, FRCPC , Danielle Rodin MD, MPH, FRCPC , Ezra Hahn MD, FRCPC , Fei-Fei Liu MD, FRCPC , Joelle Helou MD, FRCPC , Kathy Han MD, MSc, FRCPC , Rachel Glicksman MD, MSc, FRCPC , Naghmeh Isfahanian MD, FRCPC , Zeynep Baskurt MSc, PhD , Michelle Chan , Tom Purdie PhD, MCCPM , Anne Koch MD, FRCPC, PhD , Jennifer Croke MD, MHPE, FRCPC

Purpose

Prompted by COVID-19 and publication of the FAST-Forward study, our institution rapidly implemented ultrahypofractionated radiation therapy (U-HFRT) for patients with early-stage breast cancer. Our objective was to evaluate our early experience and toxicity outcomes for U-HFRT.

Methods and Materials

Patients with consecutive stage 0-II breast cancer treated with adjuvant whole breast radiation therapy (RT) were evaluated. Patient demographics and treatment characteristics were extracted and categorized into 2 cohorts: U-HFRT, 26 Gy/5 fractions (F) and M (moderate)-HFRT, 40.05 Gy/15F. Physician-assessed skin toxicity was evaluated using the Radiation Therapy Oncology Group radiation morbidity scale at baseline/during RT, 1 to 90 days post-RT and >90 days post-RT. Descriptive statistics summarized patient demographics and treatment characteristics and were stratified based on dose fractionation. A multivariable logistic model evaluated associations between toxicity and fractionation.

Results

Between May 2020 and March 2021, 320 patients were evaluated: 133 (41.6%) received U-HFRT and 187 (58.4%) received M-HFRT. For the U-HFRT cohort, median age at diagnosis was 65.4 years (range, 57-73), 71% had hormone receptor-positive invasive disease, and 18% had ductal carcinoma in-situ. All patients received whole breast RT, and 33% received a boost. U-HFRT was used more in patients who were older, hormone receptor-positive, and did not receive a boost (P < .001). On multivariable analysis, M-HFRT patients experienced significantly more grade 1+skin toxicity during RT (odds ratio = 32.3, P < .001), while 1 to 90 days post-RT, M-HFRT patients experienced less grade 1+ toxicity (odds ratio = 0.36, P < .014) after adjusting for boost, age, and chemotherapy. Rates of skin toxicity >90 days post-RT were low overall.

Conclusions

This study reports real-world clinical outcomes of patients with stage 0-II breast cancer treated with U-HFRT. We observed low rates of acute skin toxicity compared to M-HFRT, confirming its acceptability as a standard regimen for select patients. Longer term follow-up would be necessary to confirm clinical outcomes in terms of both local control and late normal tissue toxicity.
目的受2019冠状病毒病(COVID-19)和FAST-Forward研究发表的影响,我院迅速对早期乳腺癌患者实施了超低分割放射治疗(U-HFRT)。我们的目的是评估U-HFRT的早期经验和毒性结果。方法与材料对连续0-II期乳腺癌患者进行辅助全乳放射治疗(RT)。提取患者人口统计学和治疗特征并将其分为2组:U-HFRT, 26 Gy/5分数(F)和M(中度)-HFRT, 40.05 Gy/15F。医师评估的皮肤毒性使用放射治疗肿瘤组放射发病率量表在基线/放疗期间,放疗后1至90天和放疗后90天进行评估。描述性统计总结了患者的人口统计学和治疗特征,并根据剂量分级进行分层。一个多变量逻辑模型评估毒性和分馏之间的关系。结果2020年5月至2021年3月期间,对320例患者进行了评估:133例(41.6%)接受了U-HFRT, 187例(58.4%)接受了M-HFRT。在U-HFRT队列中,诊断时的中位年龄为65.4岁(范围57-73岁),71%患有激素受体阳性侵袭性疾病,18%患有导管原位癌。所有患者都接受了全乳放疗,其中33%的患者得到了改善。U-HFRT更多地用于年龄较大、激素受体阳性且未得到提高的患者(P < .001)。在多变量分析中,M-HFRT患者在放疗期间经历了更多的1+级皮肤毒性(优势比= 32.3,P < .001),而在放疗后1至90天,M-HFRT患者经历了更少的1+级毒性(优势比= 0.36,P < .014)。放疗后90天皮肤毒性发生率总体较低。本研究报告了接受U-HFRT治疗的0-II期乳腺癌患者的真实临床结果。我们观察到,与M-HFRT相比,急性皮肤毒性发生率较低,证实了其作为选定患者的标准方案的可接受性。需要长期随访以确认局部控制和晚期正常组织毒性方面的临床结果。
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引用次数: 0
Resident Versus Teaching Faculty Perceptions of Radiation Treatment Plan Education: A National Survey 住院医师与教师对放射治疗计划教育的看法:一项全国调查
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-12 DOI: 10.1016/j.adro.2025.101941
Graham Boyd MD , Derealise Garcia-Almedina BS , Liam Van Benthuysen CMD , Thomas P. Howard MD, PhD , Rachel B. Jimenez MD

Purpose

Radiation treatment plan (RTP) evaluation is a critical, but often undertaught component of radiation oncology training. We hypothesized that radiation oncology residents and attendings would hold different attitudes regarding resident knowledge and comfort with RTP review.

Methods and Materials

A web-based survey was developed and distributed to residents (35 items) and attendings (28 items) at 14 geographically diverse Accreditation Council for Graduate Medical Education (ACGME)-accredited residency programs. The survey consisted of a combination of multiple-choice questions, Likert-style, and free-text responses.

Results

One hundred sixty-nine residents and 71 faculty received the survey (response rate: 43% and 28%, respectively). Approximately half (47%) of residents reported reviewing fewer than half of all treatment plans for their patients. While 20% of residents reported “often” or “always” reviewing treatment plans with an attending, 31% reported “rarely” or “never” doing so. More than half (56%) of residents felt they had inadequate exposure to RTP review. More than half (54%) did not feel confident or competent independently evaluating RTPs. In contrast, 85% of attendings reported reviewing at least half of all treatment plans alongside residents and 90% of faculty agreed or strongly agreed that residents were competent at RTP evaluation by the end of a rotation. Both residents and faculty perceived that challenges in schedule alignment and interest of the other party were common barriers to adequate RTP exposure and both agreed that a systematic approach to RTP review and a dedicated educational resource would improve the ability to evaluate a RTP.

Conclusions

A majority of residents reported inadequate RTP education and a lack of confidence and competence in evaluating RTPs. There was discordance between resident and faculty perceptions of RTP education and resident competence, but both groups agreed that residents would benefit from a dedicated resource on RTP review. Future work should focus on the development of a systematic guideline and accompanying tools for RTP evaluation.
目的:放射治疗计划(RTP)评估是放射肿瘤学培训中一个关键但经常被忽视的组成部分。我们假设放射肿瘤学住院医师和主治医师对住院医师对RTP回顾的了解程度和舒适度持不同的态度。方法和材料一项基于网络的调查被开发并分发给14个地理位置不同的研究生医学教育认证委员会(ACGME)认可的住院医师项目的住院医师(35项)和主治医师(28项)。调查包括多项选择题、李克特式和自由文本回答。结果共有169名住院医师和71名教师接受了调查,回复率分别为43%和28%。大约一半(47%)的住院医生报告说,他们对病人的所有治疗方案的审查不到一半。20%的住院医生表示“经常”或“总是”与主治医生一起审查治疗计划,31%的人表示“很少”或“从不”这样做。超过一半(56%)的居民认为他们对RTP审查的了解不足。超过一半(54%)的人没有信心或能力独立评估rtp。相比之下,85%的主治医生报告说,他们与住院医生一起审查了至少一半的治疗计划,90%的教师同意或强烈同意住院医生在轮转结束时能够胜任RTP评估。住院医生和教师都认为,时间表调整方面的挑战和对方的兴趣是充分接触RTP的常见障碍,双方都同意系统的RTP审查方法和专门的教育资源将提高评估RTP的能力。结论大部分居民对RTP教育程度不高,缺乏评价RTP的信心和能力。住院医生和教师对RTP教育和住院医生能力的看法不一致,但双方都认为住院医生将从RTP审查的专门资源中受益。今后的工作应侧重于为RTP评价制定系统的指导方针和配套的工具。
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引用次数: 0
The Impact of Radiation Dose to Bowel on the Risk of Developing Gastrointestinal Toxicities When Treating Abdominopelvic Soft-Tissue Sarcomas With Preoperative Radiation Therapy 术前放疗治疗腹盆腔软组织肉瘤时,肠道放射剂量对胃肠道毒性风险的影响
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-09 DOI: 10.1016/j.adro.2025.101953
Alison Yoder MD , Tucker Netherton PhD , Xin Wang PhD , Tze Lim PhD , Catherine Wang PhD , Dershan Luo PhD , Congjun Wang PhD , Sara Thrower PhD , Callistus Nguyen PhD , Heather Lyu MD , Christopher Scally MD , Christina Roland MD , Devarati Mitra MD PhD , Andrew Bishop MD , Ahsan Farooqi MD PhD , B Ashleigh Guadagnolo MD

Purpose

Abdominopelvic soft-tissue sarcomas (AP-STS) are selectively treated with radiation therapy (RT) followed by surgery. We investigated dosimetric factors predictive of acute and long-term gastrointestinal (GI) toxicities in patients treated with preoperative RT for AP-STS.

Methods and Materials

We performed a retrospective cohort study of patients treated for nonmetastatic AP-STS with preoperative RT and surgery from 2005 to 2020. Individual loops of small and large bowel, as well as a “Bowel Bag” space, were autocontoured using a clinically validated deep learning-based approach (nnU-Net) and then manually reviewed. Chi-square or Fisher’s exact test was used to assess how bowel dosimetry related to the development of GI toxicities. In particular, the effect on GI toxicity of exceeding bowel constraints as defined in the consensus guidelines was evaluated. Recurrence outcomes were analyzed using the Kaplan-Meier method.

Results

We evaluated 76 patients with a median follow-up of 46 months (IQR, 42-50). Approximately half of the tumors were located in the retroperitoneal space (n = 39, 51%). A total of 60 patients (79%) presented with de novo disease, and 21% (n = 16) were recurrent presentations that had not received prior RT. Fourteen patients (18%) had a local recurrence alone, 23 (30%) a distant recurrence alone, and 3 (4%) combined local and distant recurrence. As a result of RT, 23 patients (30%) had acute grade 1 to 2 diarrhea, and 14 (18%) had grade 1 nausea. There were no acute grade 3 toxicities. Six patients (8%) had any long-term RT-related toxicity, including 1 small bowel obstruction. Patients were more likely to have an acute GI toxicity if bowel bag V45>195 cm3 (P = .05).

Conclusions

Traditional RT volumetric bowel dose constraints are frequently exceeded, given the large size of AP-STS at presentation and the corresponding large RT volumes. Exceeding the conventional bowel dosimetric constraints should not dissuade the use of RT, but instead signal the need for aggressive prophylactic management of potential toxicities.
目的对腹腔软组织肉瘤(AP-STS)进行选择性放疗后手术治疗。我们研究了预测AP-STS术前放疗患者急性和长期胃肠道(GI)毒性的剂量学因素。方法和材料我们对2005年至2020年接受术前放疗和手术治疗的非转移性aps - sts患者进行了回顾性队列研究。使用临床验证的基于深度学习的方法(nnU-Net)自动绘制小肠和大肠的单个回路以及“肠袋”空间,然后手动检查。卡方检验或费雪精确检验用于评估肠剂量学与胃肠道毒性发展的关系。特别地,评估了超过共识指南中定义的肠道限制对胃肠道毒性的影响。使用Kaplan-Meier法分析复发结果。结果我们评估了76例患者,中位随访时间为46个月(IQR, 42-50)。大约一半的肿瘤位于腹膜后间隙(n = 39, 51%)。总共有60名患者(79%)表现为新发疾病,21% (n = 16)为未接受过术前放疗的复发症状。14名患者(18%)仅局部复发,23名(30%)仅远处复发,3名(4%)局部和远处合并复发。作为RT治疗的结果,23名患者(30%)出现急性1至2级腹泻,14名患者(18%)出现1级恶心。无急性3级毒性反应。6例患者(8%)有任何长期rt相关毒性,包括1例小肠梗阻。当肠袋体积为45& 195 cm3时,患者更容易发生急性胃肠道毒性(P = 0.05)。结论考虑到AP-STS出现时的大体积和相应的大RT体积,传统的RT体积肠剂量限制经常被超越。超过常规肠剂量限制不应阻止RT的使用,而是表明需要积极预防潜在毒性的管理。
{"title":"The Impact of Radiation Dose to Bowel on the Risk of Developing Gastrointestinal Toxicities When Treating Abdominopelvic Soft-Tissue Sarcomas With Preoperative Radiation Therapy","authors":"Alison Yoder MD ,&nbsp;Tucker Netherton PhD ,&nbsp;Xin Wang PhD ,&nbsp;Tze Lim PhD ,&nbsp;Catherine Wang PhD ,&nbsp;Dershan Luo PhD ,&nbsp;Congjun Wang PhD ,&nbsp;Sara Thrower PhD ,&nbsp;Callistus Nguyen PhD ,&nbsp;Heather Lyu MD ,&nbsp;Christopher Scally MD ,&nbsp;Christina Roland MD ,&nbsp;Devarati Mitra MD PhD ,&nbsp;Andrew Bishop MD ,&nbsp;Ahsan Farooqi MD PhD ,&nbsp;B Ashleigh Guadagnolo MD","doi":"10.1016/j.adro.2025.101953","DOIUrl":"10.1016/j.adro.2025.101953","url":null,"abstract":"<div><h3>Purpose</h3><div>Abdominopelvic soft-tissue sarcomas (AP-STS) are selectively treated with radiation therapy (RT) followed by surgery. We investigated dosimetric factors predictive of acute and long-term gastrointestinal (GI) toxicities in patients treated with preoperative RT for AP-STS.</div></div><div><h3>Methods and Materials</h3><div>We performed a retrospective cohort study of patients treated for nonmetastatic AP-STS with preoperative RT and surgery from 2005 to 2020. Individual loops of small and large bowel, as well as a “Bowel Bag” space, were autocontoured using a clinically validated deep learning-based approach (nnU-Net) and then manually reviewed. Chi-square or Fisher’s exact test was used to assess how bowel dosimetry related to the development of GI toxicities. In particular, the effect on GI toxicity of exceeding bowel constraints as defined in the consensus guidelines was evaluated. Recurrence outcomes were analyzed using the Kaplan-Meier method.</div></div><div><h3>Results</h3><div>We evaluated 76 patients with a median follow-up of 46 months (IQR, 42-50). Approximately half of the tumors were located in the retroperitoneal space (n = 39, 51%). A total of 60 patients (79%) presented with <em>de novo</em> disease, and 21% (n = 16) were recurrent presentations that had not received prior RT. Fourteen patients (18%) had a local recurrence alone, 23 (30%) a distant recurrence alone, and 3 (4%) combined local and distant recurrence. As a result of RT, 23 patients (30%) had acute grade 1 to 2 diarrhea, and 14 (18%) had grade 1 nausea. There were no acute grade 3 toxicities. Six patients (8%) had any long-term RT-related toxicity, including 1 small bowel obstruction. Patients were more likely to have an acute GI toxicity if bowel bag V45&gt;195 cm<sup>3</sup> (<em>P</em> = .05).</div></div><div><h3>Conclusions</h3><div>Traditional RT volumetric bowel dose constraints are frequently exceeded, given the large size of AP-STS at presentation and the corresponding large RT volumes. Exceeding the conventional bowel dosimetric constraints should not dissuade the use of RT, but instead signal the need for aggressive prophylactic management of potential toxicities.</div></div>","PeriodicalId":7390,"journal":{"name":"Advances in Radiation Oncology","volume":"11 2","pages":"Article 101953"},"PeriodicalIF":2.7,"publicationDate":"2025-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145735319","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of Injection Technique on Microsphere Distribution During Transarterial Radioembolization in a Successively Bifurcating In Vitro Model 注射技术对连续分叉体外模型经动脉放射栓塞过程中微球分布的影响
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-09 DOI: 10.1016/j.adro.2025.101954
Tess J. Snoeijink MSc , Jan L. van der Hoek MSc , Anne van den Brekel MSc , Gerhard van Wolfswinkel MSc , Marcel J.R. Janssen MD, PhD , Erik Groot Jebbink PhD , J. Frank W. Nijsen PhD

Purpose

This study aimed to experimentally investigate how injection technique affects the distribution of microspheres during transarterial radioembolization in a successively bifurcating in vitro model.

Methods and Materials

A symmetrical phantom, bifurcating 3 times into 8 outlets, was incorporated into a flow circuit. A blood-mimicking fluid was pumped through the phantom using a physiological representative waveform. A microcatheter was placed into the lumen of the phantom, and holmium-165 microspheres were administered with a conventional administration device and a newly designed controlled administration device, containing a rotating syringe to keep the microspheres in suspension during administration. Two clinicians performed manual injections to establish clinically relevant injection rates. Then, different injection profiles were tested using syringe pumps: pulsed vs continuous injections (24 mL/min), and reduced continuous injection rates (10 and 5 mL/min). Microspheres were collected at each outlet and their distribution over the 8 outlets was analyzed.

Results

Continuous high injection rates led to more homogeneous radial distributions of microspheres over the right side of the phantom (outlet 5-8 received 16.5%-23.1% of the microspheres per outlet) compared with the clinically standard used pulsed injections (outlet 5-8 received 11.3%-40.1% of the microspheres per outlet). In contrast, reduced continuous injection rates led to more selective distributions (outlet 5-8 received 2.5%-68.8% of the microspheres at 10 mL/min and 1.0%-80.0% at 5 mL/min).

Conclusions

Injection technique strongly influences the distribution of microspheres. During high continuous injections, more mixing between microspheres and blood-mimicking fluid was observed. This led to more uniform radial microsphere distributions, creating a more predictive setting for transarterial radioembolization.
目的通过实验研究注射技术对经动脉放射栓塞过程中微球分布的影响。方法与材料采用对称模体,分岔3次,共8个输出口,组成流动电路。一种模拟血液的液体通过生理代表性波形泵入幻象。将一根微导管置入假体腔内,使用常规给药装置和新设计的可控给药装置给药,其中包含旋转注射器以使微球在给药过程中保持悬浮状态。两名临床医生进行手动注射以确定临床相关的注射率。然后,使用注射泵测试不同的注射轮廓:脉冲注射与连续注射(24 mL/min),以及降低连续注射速率(10和5 mL/min)。在每个出口采集微球,并分析其在8个出口的分布。结果与临床标准使用的脉冲注射(5-8出口每个出口获得11.3%-40.1%的微球)相比,连续高注射率导致微球在幻肢右侧径向分布更均匀(5-8出口每个出口获得16.5%-23.1%的微球)。相比之下,降低连续注射速度导致更强的选择性分布(出口5-8在10 mL/min时获得2.5%-68.8%的微球,在5 mL/min时获得1.0%-80.0%的微球)。结论注射工艺对微球分布有较大影响。在高连续注射期间,观察到微球和模拟血液液体之间的更多混合。这导致了更均匀的径向微球分布,为经动脉放射栓塞创造了更具预测性的设置。
{"title":"Impact of Injection Technique on Microsphere Distribution During Transarterial Radioembolization in a Successively Bifurcating In Vitro Model","authors":"Tess J. Snoeijink MSc ,&nbsp;Jan L. van der Hoek MSc ,&nbsp;Anne van den Brekel MSc ,&nbsp;Gerhard van Wolfswinkel MSc ,&nbsp;Marcel J.R. Janssen MD, PhD ,&nbsp;Erik Groot Jebbink PhD ,&nbsp;J. Frank W. Nijsen PhD","doi":"10.1016/j.adro.2025.101954","DOIUrl":"10.1016/j.adro.2025.101954","url":null,"abstract":"<div><h3>Purpose</h3><div>This study aimed to experimentally investigate how injection technique affects the distribution of microspheres during transarterial radioembolization in a successively bifurcating in vitro model.</div></div><div><h3>Methods and Materials</h3><div>A symmetrical phantom, bifurcating 3 times into 8 outlets, was incorporated into a flow circuit. A blood-mimicking fluid was pumped through the phantom using a physiological representative waveform. A microcatheter was placed into the lumen of the phantom, and holmium-165 microspheres were administered with a conventional administration device and a newly designed controlled administration device, containing a rotating syringe to keep the microspheres in suspension during administration. Two clinicians performed manual injections to establish clinically relevant injection rates. Then, different injection profiles were tested using syringe pumps: pulsed vs continuous injections (24 mL/min), and reduced continuous injection rates (10 and 5 mL/min). Microspheres were collected at each outlet and their distribution over the 8 outlets was analyzed.</div></div><div><h3>Results</h3><div>Continuous high injection rates led to more homogeneous radial distributions of microspheres over the right side of the phantom (outlet 5-8 received 16.5%-23.1% of the microspheres per outlet) compared with the clinically standard used pulsed injections (outlet 5-8 received 11.3%-40.1% of the microspheres per outlet). In contrast, reduced continuous injection rates led to more selective distributions (outlet 5-8 received 2.5%-68.8% of the microspheres at 10 mL/min and 1.0%-80.0% at 5 mL/min).</div></div><div><h3>Conclusions</h3><div>Injection technique strongly influences the distribution of microspheres. During high continuous injections, more mixing between microspheres and blood-mimicking fluid was observed. This led to more uniform radial microsphere distributions, creating a more predictive setting for transarterial radioembolization.</div></div>","PeriodicalId":7390,"journal":{"name":"Advances in Radiation Oncology","volume":"11 2","pages":"Article 101954"},"PeriodicalIF":2.7,"publicationDate":"2025-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145665620","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Can Patients With Recurrent or Primary Squamous Cell Carcinoma of the Anus in a Previously Irradiated Pelvis Receive Definitive Reirradiation? 骨盆放射后复发或原发肛门鳞状细胞癌患者是否可以接受再放射治疗?
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-09 DOI: 10.1016/j.adro.2025.101952
Jordan McDonald MD , Ethan P. Damron MD , Prajnan Das MD, MS, MPH , Eugene J. Koay MD, PhD , Ethan B. Ludmir MD , Bruce D. Minsky MD , Sonal S. Noticewala MD , Grace L. Smith MD, PhD, MPH , Craig Messick MD , Van K. Morris MD , Emma B. Holliday MD

Purpose

Although salvage surgery is the standard of care for locoregionally recurrent anal cancer, few local options exist for inoperable pelvic recurrences. Newly diagnosed anal cancer arising in a previously irradiated field also provides a unique treatment challenge, as delivery of standard doses would result in unsafe cumulative dose to pelvic structures. We aimed to evaluate efficacy and toxicity of a hyperfractionated accelerated reirradiation (reRT) regimen for such patients.

Methods and Materials

Patients treated with hyperfractionated accelerated reRT at a single institution between 2005 and 2024 for nonmetastatic inoperable locoregionally recurrent anal cancer or primary anal cancer in a previously irradiated field were included. The reRT regimen consisted of 1.5 Gy in twice daily fractions separated by 6 hours to a median (range) of 39 (30-51) Gy. Complete clinical response rates, recurrence rates, and toxicities were reported.

Results

The median (IQR) follow-up was 13.4 (7.5-42.2) months. Twenty-six (74.3%) patients were treated with reRT for recurrent anal cancer, and 9 (25.7%) patients were treated with reRT for a new squamous cell carcinoma of the anus (SCCA) primary after prior pelvic radiation. The complete clinical response rate was 46.2% among patients with recurrent anal cancer and 77.8% among patients with a new SCCA primary after prior pelvic radiation. Two-year locoregional recurrence rate was 64.0% among patients with recurrent anal cancer and 22.0% among patients treated with reRT for a new SCCA primary after prior pelvic radiation. Eight patients (22.9%) developed acute grade 3 toxicity and 10 (28.6%) developed late grade 3-4 toxicity.

Conclusions

Hyperfractionated accelerated reRT results in promising complete clinical response rates that appear to translate into durable pelvic control for patients with recurrent anal cancer or a new SCCA primary after prior pelvic radiation. Acute toxicity appears similar to initial standard chemoradiation, but limiting reRT doses to 39 Gy may reduce the risk of serious late toxicity.
目的:虽然挽救性手术是局部复发性肛门癌的标准治疗方法,但对于无法手术的盆腔复发,很少有局部选择。新诊断的肛门癌发生在以前的辐照场也提供了一个独特的治疗挑战,因为标准剂量的交付将导致骨盆结构的不安全的累积剂量。我们的目的是评估超分割加速再照射(ert)方案对这类患者的疗效和毒性。方法和材料纳入了2005年至2024年间在单一机构接受超分割加速rt治疗的非转移性不能手术的局部区域复发性肛门癌或先前放射场的原发性肛门癌的患者。rt方案包括1.5 Gy,每日两次,间隔6小时,中位数(范围)为39 (30-51)Gy。报告了完全临床缓解率、复发率和毒性。结果中位(IQR)随访时间为13.4(7.5 ~ 42.2)个月。26例(74.3%)复发性肛门癌患者接受了rt治疗,9例(25.7%)患者在既往盆腔放疗后原发性肛门鳞状细胞癌(SCCA)接受了rt治疗。复发性肛门癌患者的完全临床缓解率为46.2%,既往盆腔放疗后新发SCCA患者的完全临床缓解率为77.8%。复发性肛门癌患者的两年局部复发率为64.0%,在既往盆腔放疗后接受rt治疗的新SCCA患者中为22.0%。8例(22.9%)出现急性3级毒性,10例(28.6%)出现晚期3-4级毒性。结论:对于既往盆腔放疗后复发性肛门癌或新发SCCA的患者,分流加速放疗有希望获得完全的临床缓解率,这似乎转化为持久的盆腔控制。急性毒性似乎与最初的标准放化疗相似,但将rt剂量限制在39 Gy可能会降低严重晚期毒性的风险。
{"title":"Can Patients With Recurrent or Primary Squamous Cell Carcinoma of the Anus in a Previously Irradiated Pelvis Receive Definitive Reirradiation?","authors":"Jordan McDonald MD ,&nbsp;Ethan P. Damron MD ,&nbsp;Prajnan Das MD, MS, MPH ,&nbsp;Eugene J. Koay MD, PhD ,&nbsp;Ethan B. Ludmir MD ,&nbsp;Bruce D. Minsky MD ,&nbsp;Sonal S. Noticewala MD ,&nbsp;Grace L. Smith MD, PhD, MPH ,&nbsp;Craig Messick MD ,&nbsp;Van K. Morris MD ,&nbsp;Emma B. Holliday MD","doi":"10.1016/j.adro.2025.101952","DOIUrl":"10.1016/j.adro.2025.101952","url":null,"abstract":"<div><h3>Purpose</h3><div>Although salvage surgery is the standard of care for locoregionally recurrent anal cancer, few local options exist for inoperable pelvic recurrences. Newly diagnosed anal cancer arising in a previously irradiated field also provides a unique treatment challenge, as delivery of standard doses would result in unsafe cumulative dose to pelvic structures. We aimed to evaluate efficacy and toxicity of a hyperfractionated accelerated reirradiation (reRT) regimen for such patients.</div></div><div><h3>Methods and Materials</h3><div>Patients treated with hyperfractionated accelerated reRT at a single institution between 2005 and 2024 for nonmetastatic inoperable locoregionally recurrent anal cancer or primary anal cancer in a previously irradiated field were included. The reRT regimen consisted of 1.5 Gy in twice daily fractions separated by 6 hours to a median (range) of 39 (30-51) Gy. Complete clinical response rates, recurrence rates, and toxicities were reported.</div></div><div><h3>Results</h3><div>The median (IQR) follow-up was 13.4 (7.5-42.2) months. Twenty-six (74.3%) patients were treated with reRT for recurrent anal cancer, and 9 (25.7%) patients were treated with reRT for a new squamous cell carcinoma of the anus (SCCA) primary after prior pelvic radiation. The complete clinical response rate was 46.2% among patients with recurrent anal cancer and 77.8% among patients with a new SCCA primary after prior pelvic radiation. Two-year locoregional recurrence rate was 64.0% among patients with recurrent anal cancer and 22.0% among patients treated with reRT for a new SCCA primary after prior pelvic radiation. Eight patients (22.9%) developed acute grade 3 toxicity and 10 (28.6%) developed late grade 3-4 toxicity.</div></div><div><h3>Conclusions</h3><div>Hyperfractionated accelerated reRT results in promising complete clinical response rates that appear to translate into durable pelvic control for patients with recurrent anal cancer or a new SCCA primary after prior pelvic radiation. Acute toxicity appears similar to initial standard chemoradiation, but limiting reRT doses to 39 Gy may reduce the risk of serious late toxicity.</div></div>","PeriodicalId":7390,"journal":{"name":"Advances in Radiation Oncology","volume":"11 2","pages":"Article 101952"},"PeriodicalIF":2.7,"publicationDate":"2025-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145665621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Preoperative Fractionated Stereotactic Radiosurgery for Brain Metastases: A Prospective Pilot Study at a Single Institution 术前分割立体定向放射手术治疗脑转移瘤:一项单一机构的前瞻性先导研究
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-08 DOI: 10.1016/j.adro.2025.101951
Alexander Marwaha DO , Matthew J. Shepard MD , Yun Liang PhD , Alexander Yu MD , Stephen M. Karlovits MD , Rodney E. Wegner MD

Purpose

Brain metastases are a common occurrence in patients with advanced malignancy. Treatment ranges from surgical resection, stereotactic radiosurgery (SRS), whole-brain radiation therapy (WBRT), or some combination thereof. Traditionally, SRS has followed surgical resection to help reduce the risk of local recurrence. In recent years, interest has arisen in treating these patients in the preoperative setting to help reduce the risk of leptomeningeal disease (LMD) and radiation necrosis while preserving rates of local control. This prospective pilot study, originally planned as a phase 2 protocol, investigated the use of 3-fraction preoperative SRS on the Gamma Knife (GK) Icon with the goal of examining those outcomes.

Methods and Materials

Patients who had symptomatic and a limited number of brain metastases amenable to surgical resection were prospectively enrolled in this study. Patients were treated with fractionated SRS on the GK Icon to 24 to 27 Gy in 3 fractions followed by surgical resection within 2 weeks. Postoperative MRIs were obtained to assess the extent of resection. Patients were then followed up with standard-of-care MRIs every 3 months for the first 2 years. Rates of local control, distant brain failure, LMD, and delivery of WBRT were recorded on follow-up.

Results

Twenty patients were prospectively enrolled in the trial, and an additional 11 were treated off study using 1 to 3 fractions between April 2021 and June 2024. The median age was 64 (31-81), and 55% were females. Primary malignancies were mainly non-small cell lung cancer, melanoma, and esophageal cancer. The median prescription dose was 27 Gy (15-27 Gy) in 3 (1-3) fractions. Surgery was performed at a median of 1 day post-SRS (0-11). All available postoperative MRIs showed gross total resection. Median follow-up was 9 months. One patient experienced a local failure, yielding a 1-year local control rate of 95%. The rate of distant brain failure at 6 and 12 months was 38% at each time point. Three patients (9.6%) developed LMD in follow-up. Six patients ultimately received WBRT, yielding a 1-year WBRT-free survival of 78%. Overall survival at 1 year was 52%. There were no predictors of overall survival, local failure, or distant brain failure on Cox regression. Two patients experienced short-term toxicity, including grade 2 intracranial swelling and one grade 5 hemorrhagic stroke related to a hypertensive crisis. There was no recorded radionecrosis in follow-up.

Conclusions

Fractionated preoperative SRS appears to be safe and effective with high rates of local control and low rates of LMD and radionecrosis. Results of ongoing phase 3 studies directly comparing preoperative to postoperative SRS will help further define the appropriate sequencing of therapies.
目的脑转移是晚期恶性肿瘤患者的常见病。治疗范围包括手术切除、立体定向放射外科(SRS)、全脑放射治疗(WBRT)或其组合。传统上,SRS是在手术切除后进行的,以帮助降低局部复发的风险。近年来,人们对在术前治疗这些患者产生了兴趣,以帮助降低发生轻脑膜病(LMD)和放射性坏死的风险,同时保持局部控制率。这项前瞻性先导研究,最初计划作为第二阶段方案,研究了在伽玛刀(GK)图标上使用3分数术前SRS的目的是检查这些结果。方法和材料有症状且数量有限的可手术切除的脑转移患者被前瞻性纳入本研究。患者在GK Icon上分3次接受24 ~ 27 Gy的SRS治疗,2周内手术切除。术后mri评估切除程度。然后在前两年每3个月对患者进行标准护理mri随访。在随访中记录局部控制、远端脑衰竭、LMD和WBRT的递送率。结果在2021年4月至2024年6月期间,20名患者前瞻性地纳入了该试验,另外11名患者接受了1至3组分的治疗。中位年龄为64岁(31-81岁),55%为女性。原发恶性肿瘤主要为非小细胞肺癌、黑色素瘤和食管癌。处方中位剂量为27 Gy (15-27 Gy),分3(1-3)组。手术中位时间为srs后1天(0-11)。所有可用的术后mri显示大体全切除。中位随访为9个月。1例患者局部失败,1年局部控制率为95%。6个月和12个月时远端脑衰竭的发生率分别为38%。随访中3例(9.6%)发生LMD。6名患者最终接受了WBRT治疗,1年无WBRT生存率为78%。1年总生存率为52%。Cox回归分析没有总生存、局部衰竭或远端脑衰竭的预测因子。2例患者出现短期毒性,包括2级颅内肿胀和1例与高血压危象相关的5级出血性卒中。随访无放射性坏死记录。结论术前分级SRS安全有效,局部控制率高,LMD和放射性坏死发生率低。正在进行的3期研究结果将直接比较术前和术后SRS,这将有助于进一步确定适当的治疗顺序。
{"title":"Preoperative Fractionated Stereotactic Radiosurgery for Brain Metastases: A Prospective Pilot Study at a Single Institution","authors":"Alexander Marwaha DO ,&nbsp;Matthew J. Shepard MD ,&nbsp;Yun Liang PhD ,&nbsp;Alexander Yu MD ,&nbsp;Stephen M. Karlovits MD ,&nbsp;Rodney E. Wegner MD","doi":"10.1016/j.adro.2025.101951","DOIUrl":"10.1016/j.adro.2025.101951","url":null,"abstract":"<div><h3>Purpose</h3><div>Brain metastases are a common occurrence in patients with advanced malignancy. Treatment ranges from surgical resection, stereotactic radiosurgery (SRS), whole-brain radiation therapy (WBRT), or some combination thereof. Traditionally, SRS has followed surgical resection to help reduce the risk of local recurrence. In recent years, interest has arisen in treating these patients in the preoperative setting to help reduce the risk of leptomeningeal disease (LMD) and radiation necrosis while preserving rates of local control. This prospective pilot study, originally planned as a phase 2 protocol, investigated the use of 3-fraction preoperative SRS on the Gamma Knife (GK) Icon with the goal of examining those outcomes.</div></div><div><h3>Methods and Materials</h3><div>Patients who had symptomatic and a limited number of brain metastases amenable to surgical resection were prospectively enrolled in this study. Patients were treated with fractionated SRS on the GK Icon to 24 to 27 Gy in 3 fractions followed by surgical resection within 2 weeks. Postoperative MRIs were obtained to assess the extent of resection. Patients were then followed up with standard-of-care MRIs every 3 months for the first 2 years. Rates of local control, distant brain failure, LMD, and delivery of WBRT were recorded on follow-up.</div></div><div><h3>Results</h3><div>Twenty patients were prospectively enrolled in the trial, and an additional 11 were treated off study using 1 to 3 fractions between April 2021 and June 2024. The median age was 64 (31-81), and 55% were females. Primary malignancies were mainly non-small cell lung cancer, melanoma, and esophageal cancer. The median prescription dose was 27 Gy (15-27 Gy) in 3 (1-3) fractions. Surgery was performed at a median of 1 day post-SRS (0-11). All available postoperative MRIs showed gross total resection. Median follow-up was 9 months. One patient experienced a local failure, yielding a 1-year local control rate of 95%. The rate of distant brain failure at 6 and 12 months was 38% at each time point. Three patients (9.6%) developed LMD in follow-up. Six patients ultimately received WBRT, yielding a 1-year WBRT-free survival of 78%. Overall survival at 1 year was 52%. There were no predictors of overall survival, local failure, or distant brain failure on Cox regression. Two patients experienced short-term toxicity, including grade 2 intracranial swelling and one grade 5 hemorrhagic stroke related to a hypertensive crisis. There was no recorded radionecrosis in follow-up.</div></div><div><h3>Conclusions</h3><div>Fractionated preoperative SRS appears to be safe and effective with high rates of local control and low rates of LMD and radionecrosis. Results of ongoing phase 3 studies directly comparing preoperative to postoperative SRS will help further define the appropriate sequencing of therapies.</div></div>","PeriodicalId":7390,"journal":{"name":"Advances in Radiation Oncology","volume":"11 2","pages":"Article 101951"},"PeriodicalIF":2.7,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145788097","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Is Ultrahigh Dose Rate Critical for the Effectiveness of Microbeam Radiation Therapy in a Broad-Beam Combined Treatment? 在宽束联合治疗中,超高剂量率对微束放射治疗的有效性至关重要吗?
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-07 DOI: 10.1016/j.adro.2025.101949
Elette Engels PhD , Helen B. Forrester PhD , Verdiana Trappetti PhD , Kellie Mouchemore PhD , Mitzi Klein VMD , Alice H. Sprung , Kirsty Brunt , Micah J. Barnes PhD , Matthew Cameron PhD , Vincent de Rover BSc , Bettina de Breuyn Dietler BSc , Anatoly B. Rosenfeld PhD , Michael L.F. Lerch PhD , Robin L. Anderson PhD , Olga A. Martin PhD , Valentin G. Djonov MD

Purpose

The superior therapeutic index of preclinical synchrotron microbeam radiation therapy (MRT) over conventional broad-beam (BB) radiation therapy (RT) has been clearly established. Published data demonstrate that a combination of 1 MRT session with 2 consecutive daily BB-RT sessions effectively controls the primary tumor and triggers an antitumor immune response. Here, we aimed to establish whether an ultrahigh dose rate of MRT, available exclusively on the synchrotron, is essential for effective treatment of murine triple-negative mammary carcinoma.

Methods and Materials

The in vitro response of mammary tumor cells was investigated using a clonogenic survival assay at different MRT dose rates (∼1000, 100, or 10 Gy/s). The in vivo tumor responses at the same dose rates, with an MRT/BB/BB treatment schedule, were evaluated by measuring tumor volume and the induced immune response. Animal survival and normal skin reactions were also assessed.

Results

Clonogenic survival decreased with decreasing MRT dose rate, with most cell sparing at the highest dose rate (1000 Gy/s), indicating that lower dose rates could be more effective against tumors. However, no significant differences in in vivo tumor growth delay were observed in response to dose-rate variations. Decreased infiltration of irradiated tumors with leucocytes and their subpopulations was observed at the lower dose rates, including decreased expression of immune checkpoints PD-1/PD-L1 and prognostic marker CD103, which could impact the overall tumor response in vivo. The higher dose rates were associated with increased antitumor immunity. Early euthanasia of mice, as dictated by ethical endpoints, prevented long-term observation of differences in animal survival. Skin toxicity in the vicinity of irradiated tumors was mild and developed later at the highest MRT dose rate. Overall, MRT at 10 to 1000 Gy/s was tolerated similarly, despite dramatic changes in the dose rate.

Conclusions

These findings are promising for the clinical translation of MRT in combination with conventional RT, using emerging compact x-ray MRT sources with dose rates lower than those delivered by synchrotron sources.
目的明确了同步微束放射治疗(MRT)优于常规宽束放射治疗(RT)的临床前治疗指标。已发表的数据表明,1次MRT和连续2次每日BB-RT的组合有效地控制了原发肿瘤,并引发了抗肿瘤免疫反应。在这里,我们的目的是确定超高剂量率的MRT,仅在同步加速器上可用,是否对有效治疗小鼠三阴性乳腺癌至关重要。方法和材料采用克隆生存实验研究了不同剂量率(~ 1000、100或10 Gy/s)的MRT对乳腺肿瘤细胞的体外反应。在相同剂量率下,采用MRT/BB/BB治疗方案,通过测量肿瘤体积和诱导免疫反应来评估体内肿瘤反应。还评估了动物存活率和正常皮肤反应。结果随着MRT剂量率的降低,克隆存活率降低,在最高剂量率(1000 Gy/s)下,大多数细胞保留,表明较低剂量率对肿瘤更有效。然而,体内肿瘤生长延迟对剂量率变化的反应没有显著差异。在较低剂量率下,观察到照射肿瘤的白细胞及其亚群浸润减少,包括免疫检查点PD-1/PD-L1和预后标志物CD103的表达减少,这可能影响体内整体肿瘤反应。较高的剂量率与增强的抗肿瘤免疫有关。按照伦理终点的要求,对小鼠进行早期安乐死,阻止了对动物存活率差异的长期观察。放射肿瘤附近的皮肤毒性较轻,在最高MRT剂量率时较晚发生。总体而言,尽管剂量率发生了巨大变化,但10至1000 Gy/s的MRT耐受性相似。结论这些发现为MRT与传统RT联合的临床转化提供了希望,使用新出现的致密x射线MRT源,其剂量率低于同步加速器源。
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引用次数: 0
In Reply to Sengul and Sengul 在对Sengul和Sengul的回复中
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.adro.2025.101841
Rong-Tse Hsu MD, Ting-Chun Lin MD
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引用次数: 0
In Regard to Hsu et al 关于Hsu等人
IF 2.7 Q3 ONCOLOGY Pub Date : 2025-11-01 DOI: 10.1016/j.adro.2025.101840
Ilker Sengul MD , Demet Sengul MD
{"title":"In Regard to Hsu et al","authors":"Ilker Sengul MD ,&nbsp;Demet Sengul MD","doi":"10.1016/j.adro.2025.101840","DOIUrl":"10.1016/j.adro.2025.101840","url":null,"abstract":"","PeriodicalId":7390,"journal":{"name":"Advances in Radiation Oncology","volume":"10 11","pages":"Article 101840"},"PeriodicalIF":2.7,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145517067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Advances in Radiation Oncology
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