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A prospective, comparative evaluation of an augmented reality tool (Postural Video™) vs. standard SGRT for efficient patient setup. 增强现实工具(姿势视频™)与标准SGRT的前瞻性比较评估,以提高患者的设置效率。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.104011
Kira Oliver, Nicholas Subick, Torsten Moser

Background: Surface guided radiation therapy (SGRT) for patient positioning and motion management during radiation therapy is used on ~40% of US linear accelerators. Postural Video™ (PV), an augmented reality tool for SGRT, is showing a live patient video feed against an outline of the intended treatment position, at patient setup and intrafraction monitoring. A study was performed to assess any potential additional values of SGRT with PV, versus SGRT alone.

Materials and methods: Two radiation therapy centers, comparable across patient numbers, case mix, treatment times and staff experience, were selected to compare performance difference in SGRT with/without PV, focused on productivity. Site A used SGRT alone for patient setup, while Site B used SGRT with PV. Both sites were proficient in the use of SGRT prior to the study. 250 treatment delivery fractions per site were analyzed, evaluating average patient setup time, average wait time and frequency of repeated radiographic imaging. A qualitative survey completed information of PV impact on setup quality, access, and efficiency.

Results: Average time saving per patient by introducing PV is 28.8% plus additional 60 sec time saving in patient wait time. Repeated radiographic imaging was reduced by 63% (p < 0.05). Qualitative ratings and open comments supported PV being included in standard SGRT.

Conclusions: The scope of this work was to evaluate a feature under economic considerations. This data demonstrates an increase in quality, safety, accuracy and efficiency of patient setup with PV, and allows us to make an objective, business-focused assessment of the investment in PV.

背景:表面引导放射治疗(SGRT)用于放射治疗期间患者的定位和运动管理,约40%的美国线性加速器使用。姿势视频™(PV)是一种用于SGRT的增强现实工具,在患者设置和屈光监测时,根据预期治疗位置的轮廓显示实时患者视频。我们进行了一项研究,以评估SGRT联合PV与单独SGRT相比的潜在附加价值。材料和方法:选择两家在患者数量、病例组合、治疗时间和工作人员经验方面具有可比性的放射治疗中心,比较有/没有PV的SGRT的性能差异,重点是生产力。A区单独使用SGRT进行患者设置,而B区使用SGRT联合PV。两个试验点在研究前都熟练使用SGRT。分析每个部位250个治疗递送分数,评估平均患者准备时间,平均等待时间和重复放射成像频率。一项定性调查完成了光伏对安装质量、接入和效率的影响。结果:引入PV后,每位患者平均节省28.8%的时间,并额外节省60秒的患者等待时间。重复x线影像减少63% (p < 0.05)。定性评级和公开评论支持将PV纳入标准SGRT。结论:这项工作的范围是在经济考虑下评估一个特征。这些数据表明PV患者设置的质量、安全性、准确性和效率都有所提高,并使我们能够对PV投资进行客观的、以业务为中心的评估。
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引用次数: 0
Carcinoma lung with cutaneous metastasis: experience from an Indian institute. 肺癌伴皮肤转移:来自印度研究所的经验。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.103526
Diptajit Paul, Sheeba Bhardwaj, Abhishek Soni, Ashok Chauhan, Rakesh Dhankhar, Paramjeet Kaur

Background: Majority of lung cancer patients are presented with metastatic disease. However, cutaneous metastasis (CM) from lung carcinoma is a rare entity with very few case reports published in the Indian background. Moreover, outcome in these patients is dismal and no standard therapeutic approaches are there. Thus, a long-term analysis from a single institute in this infrequent occurrence holds scientific importance. The purpose of this study was to describe the clinico-demographic profile of patients having CM with lung primary and also to evaluate the survival outcomes in these patients.

Materials and methods: This was a retro-prospective study conducted over 5-year time period in an academic institute of India. Records of all histopathologically confirmed lung cancer patients were reviewed and patients having biopsy-proven CM were included in this analysis. Permission from Institutional Ethics Committee and informed consent from all the patients were taken. Data of these patients were collected and analysed using standard statistical software.

Results: Total of 25 cases of biopsy-proven CM were found in the stipulated time period. Mean age of patients was 57.6 years with high male predominance. Anterior chest wall was the most common site of skin involvement and squamous cell carcinoma was the most common primary histopathology. Overall, median survival was 4.9 months.

Conclusion: Once CM developed, survival of lung carcinoma patients become dismal. Goal of the treatment will be to palliate and to improve quality of life in these patients. Understanding the clinical pattern and demographic profile of these patients will guide a standard treatment approach.

背景:大多数肺癌患者表现为转移性疾病。然而,肺癌的皮肤转移(CM)是一种罕见的实体,在印度背景下发表的病例报告很少。此外,这些患者的预后很差,没有标准的治疗方法。因此,对这种不常见的情况,由单一机构进行长期分析具有科学意义。本研究的目的是描述肺原发CM患者的临床人口学特征,并评估这些患者的生存结果。材料和方法:本研究是在印度某学术机构进行的为期5年的回顾性前瞻性研究。我们回顾了所有组织病理学证实的肺癌患者的记录,并将活检证实的CM患者纳入本分析。获得了机构伦理委员会的许可和所有患者的知情同意。采用标准统计软件对患者资料进行收集和分析。结果:在规定时间内共发现活检证实的CM 25例。患者平均年龄57.6岁,男性居多。前胸壁是最常见的皮肤受累部位,鳞状细胞癌是最常见的原发组织病理。总体而言,中位生存期为4.9个月。结论:肺癌患者一旦发生CM,生存期较低。治疗的目标将是缓解和改善这些患者的生活质量。了解这些患者的临床模式和人口统计特征将指导标准的治疗方法。
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引用次数: 0
Stereotactic body radiotherapy results for de-novo extracranial oligometastatic cancer patients. 立体定向放射治疗颅内外少转移癌患者的效果。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.103528
Ipek Pinar Aral, Gonca Altınışık İnan, Suheyla Aytac Arslan, Ali Kerim Aksakal, Huseyin Furkan Ozturk, Yasin Caygın, Havva Beyaz, Muhammet Bülent Akıncı, Yılmaz Tezcan

Background: The aim of study was to evaluate the oncological results of stereotactic body radiotherapy (SBRT) in de-novo oligometastatic (dOM) disease.

Materials and methods: Patients who underwent SBRT for dOM disease in Radiation Oncology Clinic of XXX Hospitals were analyzed retrospectively. The endpoints of the study were overall survival (OS) and disease free survival (DFS).

Results: 84 patients with treated between 08.06.2019-15.11.2022 were analyzed. The median follow up was 26 (range 6-219) months. dOM subgroups were as follows: 37 (44.0%) synchronous dOM (sdOM); 31 (37%) metachronous oligorecurrence (mdOR) and 16 (19.0%) metachronous oligoprogression (mdOP). Grade 1 acute side effects (ASE) were observed in only 1 patient and no grade ≥ 2 a ASE were observed. Progression was observed in 45 (53.6%) of the patients. The median DFS was 8 (range 1-32) mo, 1y DFS was 44.5%; 2y DFS was 26.2%. Significantly higher DFS was obtained in mdOR than sdOM and mdOP [p = 0.020; hazard ratio (HR): 1.6; 95% confidence interval (CI): 0.75-3.68%]. The relationship between response assessment after SBRT and DFS was significant (p < 0.001; HR: 4.8; 95% CI: 1.9-12.2). Twenty-nine (34.5%) patients were ex and 55 (65.5%) were alive. 1y OS was 75.6%; 2y OS -61.2%; 3y OS -57.4% and the median OS value has not yet been reached. Lower OS was observed in sdOM compared to mdOP and mdOR (p = 0.035, HR: 0.45; 95% CI: 0.21-0.96). The relationship between response assessment after SBRT and OS was significant (p = 0.017; HR: 6.6; 95% CI: 1.7-25.7).

Conclusion: Higher DFS was observed in mdOR patients and lower OS was observed in sdOM patients. SBRT response in dOM patients may be a prognostic factor for DFS and OS.

背景研究旨在评估立体定向体放射治疗(SBRT)对去原发寡转移(dOM)疾病的肿瘤学效果:对在XXX医院放射肿瘤科接受SBRT治疗的dOM患者进行回顾性分析。研究终点为总生存期(OS)和无病生存期(DFS):对2019年6月8日至2022年11月15日期间接受治疗的84名患者进行了分析。中位随访时间为 26 个月(6-219 个月):37人(44.0%)为同步dOM(sdOM);31人(37%)为mdOR(metachronous oligorecurrence);16人(19.0%)为mdOP(metachronous oligoprogression)。只有 1 名患者出现了 1 级急性副作用(ASE),没有出现≥2 a 级的急性副作用。45例(53.6%)患者的病情出现进展。中位生存期为 8 个月(1-32 个月),1 年生存期为 44.5%,2 年生存期为 26.2%。mdOR 的 DFS 明显高于 sdOM 和 mdOP [p = 0.020;危险比 (HR):1.6;95% 置信区间 (CI):0.75-3.68%]。SBRT 后的反应评估与 DFS 之间的关系显著(p < 0.001;HR:4.8;95% CI:1.9-12.2)。29例(34.5%)患者出院,55例(65.5%)患者存活。1年的OS为75.6%;2年的OS为-61.2%;3年的OS为-57.4%,中位OS值尚未达到。与 mdOP 和 mdOR 相比,sdOM 的 OS 更低(p = 0.035,HR:0.45;95% CI:0.21-0.96)。SBRT后的反应评估与OS之间的关系显著(p = 0.017;HR:6.6;95% CI:1.7-25.7):结论:在mdOR患者中观察到较高的DFS,而在sdOM患者中观察到较低的OS。dOM患者的SBRT反应可能是DFS和OS的预后因素。
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引用次数: 0
A study to compare the efficacy of neoadjuvant chemotherapy in locally advanced human epidermal growth factor receptor 2 overexpressing breast cancer. 比较新辅助化疗治疗局部晚期人表皮生长因子受体2过表达乳腺癌疗效的研究。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.104019
Dharmendra Singh, Pritanjali Singh, Amiy Arnav, Nishit Ranjan, Ashis Ranjan

Background: This prospective single institutional study was conducted to compare the efficacy of the two different neoadjuvant chemotherapy (NACT) regimens in human epidermal growth factor receptor 2 (Her2neu) overexpressing non metastatic breast cancer.

Materials and methods: Patients randomly assigned into two arms in a 1:1 ratio. Arm A received NACT containing docetaxel, doxorubicin, and cyclophosphamide (TAC) regimen. Arm B received NACT containing docetaxel, carboplatin, and trastuzumab (TCH) regimen. Patients underwent surgical intervention following completion of 6 cycles of NACT. Postoperative histopathological reports were compared in terms of pathological response.

Results: 122 patients (Arm A = 61; Arm B = 61) analysed. The mean breast tumor size was 7.724 cm and 7.896 cm in Arm A and Arm B, respectively, at diagnosis and clinical staging. After 6 cycles of NACT, the mean breast tumor size in Arm A and Arm B was 3.495 cm and 3.711 cm, respectively. The Arm A and Arm B exhibited 22.9% and 40.9% of pathological complete response (pCR), respectively, with statistically significant difference (p = 0.033). All patients experienced varying degrees of bone marrow suppression. Grade 2 or 3 chemotherapy induced nausea and vomiting was 37.7% and 23% in Arm A and Arm B, respectively, without statistically significant difference (p = 0.076). 14.8% and 4.9% of patients exhibited febrile neutropenia in Arm A and Arm B, respectively, without statistically significant differences (p = 0.067).

Conclusion: TCH exhibited greater pCR with tolerable adverse reactions in Her2neu overexpressing breast cancer compared to TAC regimen as NACT. Therefore, TCH regimen should be considered for node positive Her2neu overexpressing breast cancer.

背景:本前瞻性单机构研究旨在比较两种不同的新辅助化疗(NACT)方案对人表皮生长因子受体2 (Her2neu)过表达的非转移性乳腺癌的疗效。材料与方法:患者按1:1的比例随机分为两组。A组接受含有多西紫杉醇、阿霉素和环磷酰胺(TAC)方案的NACT治疗。B组接受含有多西紫杉醇、卡铂和曲妥珠单抗(TCH)方案的NACT治疗。患者在完成6个NACT周期后接受手术干预。比较术后组织病理学报告的病理反应。结果:122例患者(A组61例;B组= 61)。在诊断和临床分期时,A组和B组的平均乳腺肿瘤大小分别为7.724 cm和7.896 cm。NACT治疗6个周期后,A组和B组乳腺肿瘤平均大小分别为3.495 cm和3.711 cm。A组和B组病理完全缓解率分别为22.9%和40.9%,差异有统计学意义(p = 0.033)。所有患者均出现不同程度的骨髓抑制。2级或3级化疗引起的恶心呕吐在A组和B组分别为37.7%和23%,差异无统计学意义(p = 0.076)。A组发热性中性粒细胞减少14.8%,B组发热性中性粒细胞减少4.9%,差异无统计学意义(p = 0.067)。结论:与TAC方案相比,TCH方案在Her2neu过表达乳腺癌中表现出更大的pCR和可耐受的不良反应。因此,对于淋巴结阳性Her2neu过表达乳腺癌,应考虑TCH方案。
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引用次数: 0
PET/CT-based dose-escalated definitive radiotherapy in cervical cancer: a single-institution series. 基于PET/ ct剂量递增的宫颈癌最终放疗:单一机构系列。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.104018
Samir A Hanna, Alice R N S Silva, Leticia Hernandes de Brito, Gabriela Silva Moreira de Siqueira, Tatiana Midori Martins Teles Alves, Daniela de Freitas, Rudinei Linck, José Carlos Sadalla, Sergio Mancini Nicolau, Carlos Buchpiguel, Jesus Paula Carvalho

Background: The objective was to evaluate clinical outcomes and toxicity of patients with cervical cancer treated by radiotherapy with dose escalation in involved lymph nodes based on positron emission tomography/computed tomography (PET/CT) staging.

Materials and methods: Retrospective cohort study involving locally advanced cervical neoplasms treated with definitive radiotherapy. Volumetric modulated arc therapy (VMAT), image-guided radiotherapy (IGRT), and registration of PET/CT were employed in all. Involved lymph nodes were given higher doses simultaneously.

Results: Between February 2012 and September 2023, there were 37 patients, with median age of 48 (range 27-91) years. Almost 70% were stages III/IVA. Two-thirds were given retroperitoneal irradiation. The mean delivered doses to primary tumor and to involved lymph nodes were, respectively, 52.5 Gy, and 62.5 Gy. The 10-year rates of overall survival, event-free survival, local-recurrence-free survival, and metastasis-free survival were, respectively, 76%, 50%, 91%, and 82%. There were 13 and 2 cases of gastrointestinal toxicity grades II and III, respectively. Grades II and III of genitourinary toxicity were seen respectively in 7 and 3 patients. On univariate analysis, age was related to local recurrence-free survival (LRFS); standard uptake values (SUV) was related to event-free survival (EFS); lymph node dose was related to overall survival (OS), and EFS; primary tumor dose was directly related to EFS, albeit inversely to the likelihood of grade > II gastrointestinal toxicity. Retroperitoneal irradiation improved LRFS, and rates of grade > II gastrointestinal toxicity. On multivariate analysis, SUV remained an independent predictor of EFS; lymph node dose was an independent predictor of OS, and age was an independent predictor of lymph node recurrence.

Conclusion: Dose escalation radiotherapy (RT) based on PET/CT for cervical cancer may be feasible and safe. Further robust study results are needed.

背景:目的是基于正电子发射断层扫描/计算机断层扫描(PET/CT)分期评估宫颈癌患者在受累淋巴结进行剂量递增放疗的临床结果和毒性。材料和方法:回顾性队列研究涉及局部晚期宫颈肿瘤放疗治疗。所有患者均采用体积调制弧线治疗(VMAT)、图像引导放疗(IGRT)和PET/CT配准。受累淋巴结同时给予较高剂量。结果:2012年2月至2023年9月,37例患者,中位年龄48岁(27-91岁)。近70%为III/IVA期。三分之二给予腹膜后照射。原发肿瘤和受累淋巴结的平均递送剂量分别为52.5 Gy和62.5 Gy。10年总生存率、无事件生存率、局部无复发生存率和无转移生存率分别为76%、50%、91%和82%。II级和III级胃肠道毒性分别为13例和2例。II级和III级泌尿生殖系统毒性分别为7例和3例。单因素分析显示,年龄与局部无复发生存率(LRFS)相关;标准摄取值(SUV)与无事件生存期(EFS)相关;淋巴结剂量与总生存期(OS)和EFS相关;原发肿瘤剂量与EFS直接相关,尽管与bb0级胃肠道毒性的可能性呈负相关。腹膜后照射改善了LRFS,并降低了>级胃肠道毒性发生率。在多变量分析中,SUV仍然是EFS的独立预测因子;淋巴结剂量是OS的独立预测因子,年龄是淋巴结复发的独立预测因子。结论:基于PET/CT的剂量递增放疗(RT)治疗宫颈癌是可行且安全的。需要进一步的可靠研究结果。
{"title":"PET/CT-based dose-escalated definitive radiotherapy in cervical cancer: a single-institution series.","authors":"Samir A Hanna, Alice R N S Silva, Leticia Hernandes de Brito, Gabriela Silva Moreira de Siqueira, Tatiana Midori Martins Teles Alves, Daniela de Freitas, Rudinei Linck, José Carlos Sadalla, Sergio Mancini Nicolau, Carlos Buchpiguel, Jesus Paula Carvalho","doi":"10.5603/rpor.104018","DOIUrl":"10.5603/rpor.104018","url":null,"abstract":"<p><strong>Background: </strong>The objective was to evaluate clinical outcomes and toxicity of patients with cervical cancer treated by radiotherapy with dose escalation in involved lymph nodes based on positron emission tomography/computed tomography (PET/CT) staging.</p><p><strong>Materials and methods: </strong>Retrospective cohort study involving locally advanced cervical neoplasms treated with definitive radiotherapy. Volumetric modulated arc therapy (VMAT), image-guided radiotherapy (IGRT), and registration of PET/CT were employed in all. Involved lymph nodes were given higher doses simultaneously.</p><p><strong>Results: </strong>Between February 2012 and September 2023, there were 37 patients, with median age of 48 (range 27-91) years. Almost 70% were stages III/IVA. Two-thirds were given retroperitoneal irradiation. The mean delivered doses to primary tumor and to involved lymph nodes were, respectively, 52.5 Gy, and 62.5 Gy. The 10-year rates of overall survival, event-free survival, local-recurrence-free survival, and metastasis-free survival were, respectively, 76%, 50%, 91%, and 82%. There were 13 and 2 cases of gastrointestinal toxicity grades II and III, respectively. Grades II and III of genitourinary toxicity were seen respectively in 7 and 3 patients. On univariate analysis, age was related to local recurrence-free survival (LRFS); standard uptake values (SUV) was related to event-free survival (EFS); lymph node dose was related to overall survival (OS), and EFS; primary tumor dose was directly related to EFS, albeit inversely to the likelihood of grade > II gastrointestinal toxicity. Retroperitoneal irradiation improved LRFS, and rates of grade > II gastrointestinal toxicity. On multivariate analysis, SUV remained an independent predictor of EFS; lymph node dose was an independent predictor of OS, and age was an independent predictor of lymph node recurrence.</p><p><strong>Conclusion: </strong>Dose escalation radiotherapy (RT) based on PET/CT for cervical cancer may be feasible and safe. Further robust study results are needed.</p>","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"29 6","pages":"754-763"},"PeriodicalIF":1.2,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11912892/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143658272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Can the daily position of bolus material influence radiotherapy treatment? 每日丸料放置位置是否会影响放射治疗?
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.104013
Ghizela A-M Salagean, Zoltán Bálint, Philip Poortmans, Daniel Portik

Background: Daily bolus positioning implies a high degree of variability, which can affect the dose distribution within the planning target volume (PTV) and the organs at risk (OAR). We carried out a retrospective study to evaluate bolus positioning in patients with breast cancer.

Materials and methods: We evaluated 7 cases with left and 5 cases with right chest-wall with comprehensive nodal region irradiation in which bolus material was used to obtain better skin surface coverage. The bolus positioning on the daily cone-beam computed tomography (CBCT) images was compared to the reference image from the treatment planning system. Deviations from the reference position of the bolus were categorized as positive shifts (PosS) or negative shifts (NegS), depending on the material's overlapping with its planned position. Subsequently, a second plan was calculated using the information from the CBCT images for comparison with the original treatment plan. We performed a statistical and dosimetric analysis on the results.

Results: For both the 95% dose coverage for the PTV for the chest wall and for the lymph node regions, about 2% variation between initial and recalculated plans was seen, with a shift of the hotspots' position in some cases. The average mean heart dose was 4.1 ± 0.3 Gy, whereas the values for PosS and NegS mean heart doses were 3.8 ± 0.4 Gy and 4.0 ± 0.6 Gy, respectively. In contrast to the original values for the ipsilateral lung V5 (57.1 ± 12.9%), V20 (30.2 ± 2.7%), and Dmean (15.0 ± 1.7 Gy), the values for PosS were 56.1 ± 4.2% for V5:, 30.1 ± 3.3% for V20, and 14.9 ± 1.2 Gy for Dmean while for NegS we obtained 56.9 ± 8.9% for V5, 30.0 ± 2.3% for V20, and 15.2 ± 1.8 Gy for Dmean.

Conclusion: We observed dosimetric differences between the initial and given treatment plans depending on the position of the bolus for all cases, indifferent of the shift direction. Although the differences were not statistically significant, we identified a few specific instances where the variations might cause uncertainties regarding doses to the organs at risk (OAR). We suggest therefore that strategies for correct daily reproducibility of the bolus need to be implemented on a departmental level.

背景:每日剂量定位意味着高度的可变性,这可能影响计划靶体积(PTV)内的剂量分布和危险器官(OAR)。我们进行了一项回顾性研究,以评估乳腺癌患者的丸剂定位。材料和方法:我们对7例左胸壁和5例右胸壁进行综合淋巴结区照射,其中使用丸状材料获得更好的皮肤表面覆盖。将每日锥形束计算机断层扫描(CBCT)图像上的丸子定位与治疗计划系统中的参考图像进行比较。根据材料与其计划位置的重叠程度,丸子与参考位置的偏差被分类为正偏移(PosS)或负偏移(NegS)。随后,利用CBCT图像信息计算第二种方案,并与原始治疗方案进行比较。我们对结果进行了统计和剂量学分析。结果:对于胸壁和淋巴结区域的PTV 95%的剂量覆盖率,初始计划和重新计算计划之间的差异约为2%,在某些情况下热点位置发生了变化。平均心脏剂量为4.1±0.3 Gy,而PosS和NegS的平均心脏剂量分别为3.8±0.4 Gy和4.0±0.6 Gy。与同侧肺V5(57.1±12.9%)、V20(30.2±2.7%)和Dmean(15.0±1.7 Gy)的原始值相比,PosS的V5值为56.1±4.2%,V20值为30.1±3.3%,Dmean值为14.9±1.2 Gy,而阴性肺V5值为56.9±8.9%,V20值为30.0±2.3%,Dmean值为15.2±1.8 Gy。结论:我们观察到所有病例的初始和给予治疗方案的剂量学差异取决于丸的位置,而与移位方向无关。虽然这些差异在统计上并不显著,但我们确定了一些特定的情况,其中这些差异可能会导致风险器官(OAR)剂量的不确定性。因此,我们建议在部门层面上实施正确的每日药丸再现策略。
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引用次数: 0
A comprehensive site-specific analysis of patient-specific quality assurance based on dose volume histogram of RapidArc treatment delivery. 基于RapidArc治疗递送剂量-体积直方图的患者特异性质量保证的综合位点特异性分析。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.103529
Sumanta Manna, Benoy Kumar Singh, K J Maria Das

Background: The current study aims to evaluate the use of dose-volume histogram (DVH) metrics as part of a comprehensive pre-treatment quality assurance (PSQA) protocol for RapidArc treatment delivery.

Materials and methods: A total of ninety patients were included in this study, with the patient population divided into four groups: Brain (n = 15), Head and Neck (H & N) (n = 30), Thorax (n = 15), and Pelvis (n = 30) RapidArc plans. The delivered dose was assessed using the Octavius 4D 1500 detector array and the Verisoft DVH application, focusing on DVH-related errors pertaining to targets and organ-at-risk (OARs). Additionally, three-dimensional local and global gamma passing rates were analyzed in the axial, coronal, and sagittal planes using various gamma criteria, including 3 mm/3%, 3 mm/2%, 2 mm/3%, and 2 mm/2%.

Results: All treatment plans met the action level requirement, achieving a gamma acceptance rate exceeding 95% with a 3%/3 mm criterion. Among the anatomical planes, the transverse plane consistently exhibited the highest passing rates for various global gamma criteria across all treatment sites. Local gamma analysis revealed that the coronal plane had the highest passing rates for thorax and pelvis sites compared to other planes. DVH analysis indicated that doses to target volumes remained within specified tolerances for all cases. The most significant OAR dose discrepancies were observed in the H&N region.

Conclusion: Integrating DVH metrics into the RapidArc PSQA protocol can yield clinically significant results closely aligned with the gamma index. It was observed that a single action-level approach cannot be universally applied to DVH metrics across different anatomical sites.

背景:目前的研究旨在评估剂量-体积直方图(DVH)指标作为RapidArc治疗递送的综合治疗前质量保证(PSQA)方案的一部分的使用。材料和方法:本研究共纳入90例患者,患者人群分为四组:脑(n = 15)、头颈部(H & n) (n = 30)、胸腔(n = 15)和骨盆(n = 30)。使用Octavius 4D 1500探测器阵列和Verisoft DVH应用程序评估给药剂量,重点关注与靶标和危险器官(OARs)相关的DVH相关误差。此外,在轴位、冠状面和矢状面使用各种伽马标准(包括3mm /3%、3mm /2%、2mm /3%和2mm /2%)分析三维局部和全局伽马通过率。结果:所有治疗方案均达到行动水平要求,以3%/ 3mm为标准,伽玛满意率超过95%。在解剖平面中,横切面在所有治疗部位的各种全局伽玛标准中始终表现出最高的通过率。局部伽玛分析显示,冠状面与其他平面相比,胸部和骨盆部位的通过率最高。DVH分析表明,所有病例的靶量剂量均在规定的耐受范围内。在H&N地区观察到最显著的OAR剂量差异。结论:将DVH指标整合到RapidArc PSQA方案中可以产生与gamma指数密切相关的临床显著结果。我们观察到,单一的行动水平方法不能普遍适用于不同解剖部位的DVH指标。
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引用次数: 0
A cross-sectional study using the Surveillance, Epidemiology, and End Results Program database to estimate the prevalence of Myelodysplastic syndrome (MDS) in the United States. 一项利用监测、流行病学和最终结果项目数据库估计骨髓增生异常综合征(MDS)在美国患病率的横断面研究。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.103137
Shangyi Fu, Michel Adeniran, Zachrieh Alhaj, Diana Bonila, Melissa Marchan-Martinez, Ibeth Caceres, Danny Huynh

Myelodysplastic syndrome (MDS) is a hematologic disorder characterized by ineffective blood cell production leading to cytopenias and a propensity for progression to acute myeloid leukemia (AML). In this study, we aimed to assess the prevalence of MDS in the United States population using data from the Surveillance, Epidemiology, and End Results (SEER) database. Our analysis revealed that the highest prevalence of MDS was observed in the over 85 age group, with an overall prevalence rate of 0.02%. Furthermore, our findings indicated that the White race had the highest prevalence rate compared to other racial groups. However, it should be noted that the SEER database, most likely due to sampling biases, has a potential underestimation of minority populations, but SEER and the US population are statistically similar enough for comparison. These results suggest a need for further research on the underlying factors contributing to the prevalence of MDS in the United States population; factors such as genetic, environmental, comorbidities, and racial disparities should be explored. Early diagnosis and treatment of MDS are crucial for improving outcomes for patients with this condition.

骨髓增生异常综合征(MDS)是一种血液学疾病,其特征是血细胞产生无效导致细胞减少,并倾向于进展为急性髓性白血病(AML)。在这项研究中,我们旨在利用来自监测、流行病学和最终结果(SEER)数据库的数据评估MDS在美国人群中的患病率。我们的分析显示,MDS的最高患病率在85岁以上年龄组,总患病率为0.02%。此外,我们的研究结果表明,与其他种族相比,白人的患病率最高。然而,应该指出的是,SEER数据库很可能由于抽样偏差,对少数民族人口有潜在的低估,但SEER和美国人口在统计上足够相似,可以进行比较。这些结果表明,需要进一步研究导致MDS在美国人群中流行的潜在因素;应探讨遗传、环境、合并症和种族差异等因素。早期诊断和治疗MDS对于改善患者的预后至关重要。
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引用次数: 0
Clinical and epidemiological characteristics of Ukrainian breast cancer patients in a regional cancer center in Poland after the start of the war in Ukraine. 乌克兰战争开始后,波兰地区癌症中心乌克兰乳腺癌患者的临床和流行病学特征。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.103530
Piotr Radomyski, Maciej Trojanowski, Magdalena Fundowicz, Maria Litwiniuk, Witold Kycler

Background: This study performs an analysis of clinical and epidemiological characteristics of Ukrainian patients with breast cancer (BC) who presented to a regional cancer center in western Poland in 2022.

Materials and methods: Date and country of BC diagnosis, age at diagnosis, age at first visit to the Greater Poland Cancer Centre (GPCC), and clinical staging were collected from hospital records. Multidisciplinary team (MDT) data for all BC cases reviewed at the GPCC in 2022 served as a comparison for the study population.

Results: All 106 patients presented to the GPCC after the outbreak of the full-scale war in Ukraine in February 2022. The year of BC diagnosis ranged from 1993 to 2022. Median age at diagnosis was 47. The majority of cases were diagnosed (76%) and treated (76%) in Ukraine. Treatment at the GPCC was performed for 65% of cases - mostly continued oncological care for patients initially treated in Ukraine. Moreover, the majority of cases treated in Ukraine (55%) have received continued treatment at the GPCC. Cases with stage II BC were most numerous (36%), followed by stage IV BC (26%) and stage III BC (21%). Only 15% of cases were diagnosed with stage I BC and 1% with stage 0 BC.

Conclusions: The study population was characterized by relatively young age at diagnosis and advanced disease when compared with MDT data. Cases initially treated in Ukraine that required continued oncological care constituted the majority of all cases treated at the GPCC.

背景:本研究分析了2022年在波兰西部地区癌症中心就诊的乌克兰乳腺癌(BC)患者的临床和流行病学特征。材料和方法:从医院记录中收集BC诊断的日期和国家、诊断时的年龄、第一次到大波兰癌症中心(GPCC)就诊的年龄和临床分期。2022年GPCC审查的所有BC病例的多学科团队(MDT)数据作为研究人群的比较。结果:106例患者均于2022年2月乌克兰全面战争爆发后向GPCC就诊。BC诊断年份从1993年到2022年不等。诊断时的中位年龄为47岁。大多数病例在乌克兰得到诊断(76%)和治疗(76%)。65%的病例在GPCC接受了治疗,其中大多数是最初在乌克兰接受治疗的患者继续接受肿瘤治疗。此外,在乌克兰接受治疗的大多数病例(55%)在GPCC继续接受治疗。II期BC病例最多(36%),其次是IV期(26%)和III期(21%)。只有15%的病例被诊断为I期BC, 1%被诊断为0期BC。结论:与MDT数据相比,研究人群的特点是诊断时相对年轻,疾病晚期。最初在乌克兰接受治疗但需要继续接受肿瘤治疗的病例占GPCC治疗的所有病例的大多数。
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引用次数: 0
Soft-tissue metastasis in esophageal cancer managed by dose escalation radiation therapy: a clinical case and review of literature. 剂量递增放疗治疗食管癌软组织转移一例及文献复习。
IF 1.2 Q4 ONCOLOGY Pub Date : 2025-02-19 eCollection Date: 2024-01-01 DOI: 10.5603/rpor.104012
Alexander Bennassi, Shaïma El Chammah, Emanuela Salati, Thomas Breuneval, Anna Durigova

Soft tissue metastasis in esophageal cancer is a very rare entity. A 76-year-old man was referred for a week's history of dysphagia. Upper gastrointestinal endoscopy was performed, and biopsies were consistent with an adenocarcinoma of the lower esophagus. The patient was free of metastasis on 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT). The patient was treated with pre-operative chemoradiation, followed by surgery. Intravenous carboplatin [area under the curve of 2 mg/mL/min (AUC2)] and intravenous paclitaxel 50 mg/m2 with concurrent radiotherapy (RT) (45 Gy delivered in 25 fractions of 1.8 Gy per fraction) were introduced from May 31st, 2021, to July 2nd, 2021. Lewis-Santy subtotal esophagectomy was performed, and pathology revealed a ypT3 ypN0 (0/26) L0 V1 Pn1 G3 R0. Adjuvant nivolumab was introduced for a total of 12 months. After five months of nivolumab, the patient complained of a painful left shoulder subcutaneous tumefaction in routine evaluation. Biopsy of the deltoid muscle demonstrated a poorly differentiated adenocarcinoma consistent with esophageal metastasis. Additional skeletal muscle (one) and bone metastases (two) were revealed on 18F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT). After multidisciplinary team approach, palliative radiation therapy to all metastases, denosumab and FOLFOX were introduced. Despite initial excellent clinical outcomes, patient presented avascular necrosis of left femoral head managed by surgery but died after post-operative complications. To the best of our knowledge, it is the first reported case with rare soft-tissue metastasis occurring during adjuvant nivolumab in esophageal cancer.

食管癌软组织转移是一种非常罕见的肿瘤。一位76岁的男性因一周的吞咽困难病史被转诊。进行上消化道内镜检查,活检符合下食道腺癌。18f -氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(PET/CT)显示患者无转移。患者接受术前放化疗,随后进行手术。从2021年5月31日至2021年7月2日,静脉注射卡铂[曲线下面积2 mg/mL/min (AUC2)]和静脉注射紫杉醇50 mg/m2,同时放疗(RT) (45 Gy,分25次递送,每次1.8 Gy)。行Lewis-Santy食管次全切除术,病理显示为ypT3, ypN0 (0/26) L0 V1 Pn1 G3 R0。辅助用药纳武单抗总共使用了12个月。使用纳武单抗5个月后,患者在常规评估中抱怨左肩皮下肿大疼痛。三角肌活检显示为低分化腺癌,符合食管转移。18f -氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(PET/CT)显示额外的骨骼肌(1)和骨转移(2)。在多学科团队的方法下,所有转移的姑息性放疗,地诺单抗和FOLFOX被引入。尽管最初的临床结果很好,但患者出现左股骨头缺血性坏死,手术治疗,但死于术后并发症。据我们所知,这是第一例在食管癌辅助纳武单抗治疗期间发生罕见软组织转移的报道。
{"title":"Soft-tissue metastasis in esophageal cancer managed by dose escalation radiation therapy: a clinical case and review of literature.","authors":"Alexander Bennassi, Shaïma El Chammah, Emanuela Salati, Thomas Breuneval, Anna Durigova","doi":"10.5603/rpor.104012","DOIUrl":"10.5603/rpor.104012","url":null,"abstract":"<p><p>Soft tissue metastasis in esophageal cancer is a very rare entity. A 76-year-old man was referred for a week's history of dysphagia. Upper gastrointestinal endoscopy was performed, and biopsies were consistent with an adenocarcinoma of the lower esophagus. The patient was free of metastasis on <sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT). The patient was treated with pre-operative chemoradiation, followed by surgery. Intravenous carboplatin [area under the curve of 2 mg/mL/min (AUC2)] and intravenous paclitaxel 50 mg/m<sup>2</sup> with concurrent radiotherapy (RT) (45 Gy delivered in 25 fractions of 1.8 Gy per fraction) were introduced from May 31<sup>st</sup>, 2021, to July 2<sup>nd</sup>, 2021. Lewis-Santy subtotal esophagectomy was performed, and pathology revealed a ypT3 ypN0 (0/26) L0 V1 Pn1 G3 R0. Adjuvant nivolumab was introduced for a total of 12 months. After five months of nivolumab, the patient complained of a painful left shoulder subcutaneous tumefaction in routine evaluation. Biopsy of the deltoid muscle demonstrated a poorly differentiated adenocarcinoma consistent with esophageal metastasis. Additional skeletal muscle (one) and bone metastases (two) were revealed on <sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography (PET/CT). After multidisciplinary team approach, palliative radiation therapy to all metastases, denosumab and FOLFOX were introduced. Despite initial excellent clinical outcomes, patient presented avascular necrosis of left femoral head managed by surgery but died after post-operative complications. To the best of our knowledge, it is the first reported case with rare soft-tissue metastasis occurring during adjuvant nivolumab in esophageal cancer.</p>","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"29 6","pages":"799-804"},"PeriodicalIF":1.2,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11912882/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143658748","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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Reports of Practical Oncology and Radiotherapy
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