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Intuitive evaluation of contemporary management strategies in thymoma - the largest Indian experience. 对胸腺瘤当代管理策略的直观评估-印度最大的经验。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0050
Rahul Lal Chowdhary, Kundan Singh Chufal, Mohammed Ismail, Irfan Ahmad, M Jwala, Anjali K Pahuja, Lalit Kumar

Background: The aim was perusal of the treatment strategies, clinical outcomes and factors impacting these outcomes in thymoma.

Materials and methods: A total of 119 patients diagnosed and treated cases of thymoma, at our hospital, were taken for analysis. Thirty-one patients were excluded due to inadequate medical records. Descriptive statistics were used to report demographic and clinical characteristics. Time period between diagnosis and death was defined as overall survival (OS). Multivariate analysis (MVA), using cox regression modelling, was done by including clinicopathological factors in a bid to identify prognostic factors influencing OS. SPSS version 26 was used for statistical analysis.

Results: The mean age of the patients was 52.17 years and 39 (44.3%), 19 (21.6%), 17 (1.3%) and 13 (4.8%) patients presented with Masaoka stage II, IV, III and I, respectively. Surgery was done in 64 (72.7%) of the patients as a part of the treatment strategy. Radiotherapy was administered to a total of 57 patients with a median dose of 50.4 Gy. Early Masaoka stage at presentation and use of surgery in the treatment plan were statistically significant prognostic factors for a better overall survival on multivariate analysis.

Conclusion: Judicious use of radiotherapy and chemotherapy in locally advanced cases may render them resectable. In a bid to gain good survival rates, aggressive multimodality treatment should be offered to the patients.

背景:目的是仔细阅读胸腺瘤的治疗策略、临床结果和影响这些结果的因素。材料与方法:对我院收治的119例胸腺瘤患者进行分析。31名患者因医疗记录不足而被排除在外。描述性统计用于报告人口统计学和临床特征。诊断和死亡之间的时间段被定义为总生存期(OS)。采用cox回归模型进行多变量分析(MVA),包括临床病理因素,以确定影响OS的预后因素。采用SPSS 26进行统计分析。结果:患者的平均年龄为52.17岁,Masaoka II、IV、III和I期患者分别为39例(44.3%)、19例(21.6%)、17例(1.3%)和13例(4.8%)。作为治疗策略的一部分,64名(72.7%)患者接受了手术治疗。共有57名患者接受了放射治疗,中位剂量为50.4 Gy。多变量分析显示,Masaoka早期阶段和治疗计划中手术的使用是提高总生存率的具有统计学意义的预后因素。结论:在局部晚期病例中,正确使用放疗和化疗可以使其切除。为了获得良好的生存率,应该为患者提供积极的多模式治疗。
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引用次数: 0
Upper limit of radiation treatment portals in rectal cancer: is it wise to keep using bony landmarks in the present era of 3D conformal treatment? 癌症放射治疗入口的上限:在目前的3D适形治疗时代,继续使用骨标志是否明智?
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0045
Surya Prakash Vankina, Surekha Goyal, Geeta S Narayanan

Background: This study aimed to compare the levels of L5-S1 interspace and the bifurcation of common iliac vessels on simulation images of rectal cancer patients to evaluate the adequacy of superior borders in conventional 2D planning for covering internal iliac vessels.

Materials and methods: Simulation images of 236 rectal cancer patients who received neoadjuvant chemoradiation and surgery were analyzed. The images were retrieved from the radiation treatment database and included delineations of L5-S1 interspace and common iliac vessel bifurcation. Distances between these landmarks were measured.

Results: Among the 236 patients, the majority had the common iliac artery bifurcation positioned above the L5-S1 interspace. Specifically, 78.3% of patients had the right common iliac bifurcation above L5-S1 interspace, with an average distance of 2.02 cm. For the left common iliac artery, 77.11% of patients had the bifurcation above L5-S1 interspace, with an average distance of 1.99 cm. Notably, there were cases where the bifurcations were not at the same level.

Conclusion: Using the L5-S1 junction as the upper border of the treatment portal may result in missing proximal nodes at risk of metastases. However, further research is needed to determine the significance of failures above the L5-S1 interspace for justifying the inclusion of the common iliac artery bifurcation in the treatment portal.

背景:本研究旨在比较癌症患者模拟图像中L5-S1间隙和髂总血管分叉的水平,以评估传统二维规划中覆盖髂内血管的上边界的充分性。材料与方法:对236例癌症患者接受新辅助放化疗和手术后的仿真图像进行分析。这些图像是从放射治疗数据库中检索的,包括L5-S1间隙和髂总血管分叉的轮廓。测量了这些地标之间的距离。结果:236例患者中,大多数髂总动脉分叉位于L5-S1间隙上方。具体而言,78.3%的患者右髂总动脉分叉位于L5-S1间隙上方,平均距离为2.02cm。对于左髂总动脉,77.11%的患者分叉位于L5-S1间隙以上,平均距离1.99cm。值得注意的是,也有分叉不在同一水平的情况。结论:使用L5-S1交界处作为治疗门的上边界可能导致有转移风险的近端淋巴结缺失。然而,还需要进一步的研究来确定L5-S1间隙以上故障的重要性,以证明在治疗门静脉中包括髂总动脉分叉。
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引用次数: 0
The institutional experience of the implementing 4DCT in NSCLC radiotherapy planning. 非小细胞肺癌放疗计划实施4DCT的机构经验。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0056
Huy Quang Dang, Cong Thanh Nguyen, Hoat Viet Pham, Linh Duc Tran, Cong Duc Nguyen, Dung Vu Manh Truong, Trang Thi Kieu Hoang, Tao Van Chau

Background: The study was to evaluate the effectiveness of dose distribution of four-dimensional computed tomography (4DCT) simulation.

Materials and methods: The gross tumor volume (GTV) and clinical target volume (CTV) were contoured in all 10 respiratory phases of 4DCT in 30 patients with non-small cell lung cancer (NSCLC). Both 3D and 4D treatment plans were made individually for each patient using the planning volume (PTV). The PTV3D was taken from a single CTV plus the recommended margin, and the PTV4D was taken from the 4D internal target volume, including all 10 CTVs plus the setup margins.

Results: The mean PTV was 460 ± 179 (69-820) cm3 for 3DCT and 401 ± 167 (127-854) cm3 for 4DCT (p = 0.0018). The dose distribution (DD) of organs at risk, especially the lungs, was lower for the 4DCT simulation. The V5%, V10%, and V20% of the total lung dose for 4DCT were significantly lower for the 3DCT. However, lung V30% the heart, esophagus, and spinal cord were not significantly different. In addition, the conformity index and the dose heterogeneity index of the PTV were not significantly different. The normal tissue complication probability (NTCP) of the lung and heart was significantly lower for 4DCT than for 3DCT.

Conclusions: The 4DCT simulation gives better results on the NTCP. The organs at risk, especially the lungs, receive a significantly lower DD compared with the 3DCT. The conformity index (CI), heterogeneity index (HI) and the DD to the heart, spinal cord, and esophagus were not significantly different between the two techniques.

背景:本研究旨在评估四维计算机断层扫描(4DCT)模拟剂量分布的有效性。材料与方法:对30例癌症(NSCLC)患者在4DCT的10个呼吸时相的总肿瘤体积(GTV)和临床靶体积(CTV)进行了测量。使用计划容积(PTV)分别为每位患者制定3D和4D治疗计划。PTV3D取自单个CTV加上推荐裕度,PTV4D取自4D内部目标体积,包括所有10个CTV加加上设置裕度。结果:3DCT和4DCT的平均PTV分别为460±179(69-820)cm3和401±167(127-854)cm3(p=0.0018)。4DCT模拟的危险器官,尤其是肺部的剂量分布(DD)较低。4DCT的V5%、V10%和V20%占肺部总剂量的比例显著低于3DCT。然而,肺V30%与心脏、食道和脊髓没有显著差异。此外,PTV的一致性指数和剂量异质性指数没有显著差异。4DCT的肺和心脏的正常组织并发症概率(NTCP)显著低于3DCT。结论:4DCT模拟对NTCP的结果更好。与3DCT相比,处于危险中的器官,尤其是肺部,接受的DD明显更低。两种技术的一致性指数(CI)、异质性指数(HI)和对心脏、脊髓和食道的DD没有显著差异。
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引用次数: 0
GPC3 gene expression and allelic discrimination of FZD7 gene in Egyptian patients with hepatocellular carcinoma. 埃及肝细胞癌患者的GPC3基因表达和FZD7基因的等位基因鉴别。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0049
Amany Ramadan, Hala M Ghanem, Amal A Mohamed, Mohamed Elshobaky, Waleed El Agawy, Eman Al Hussain A Gawad, Hala H Eldeeb, Mohamed R Ezz Al Arab, Maha M Kamal

Background: Hepatocellular carcinoma (HCC) is the second leading cause of cancer-related deaths worldwide, and especially in Egypt. Early diagnosis of HCC greatly improves the survival and prognosis of patients. Low sensitivity and specificity of alpha-fetoprotein (AFP) has led to the demand for novel biomarkers of HCC. The aim of the present study was to evaluate the validity of frizzled-7 (FZD7) and glypican-3 (GPC3) gene expression as potential biomarkers for HCC early diagnosis, and to investigate the association between FZD7 rs2280509 polymorphism and HCC risk.

Materials and methods: Quantification of FZD7 and GPC3 gene expression by real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) assay, and genotyping FZD 7 (rs2280509 SNP) gene polymorphism using RT-PCR.

Results: The current results revealed that FZD7 gene expression had a greater area under the curve (AUC) for identifying HCC than GPC3 gene expression and AFP levels. The combination of the three markers as a panel showed a better diagnostic performance with a greater AUC than any of the single markers alone (p < 0.05). The FZD7 rs2280509 polymorphism (CT) was found to be significantly associated with an increased risk of HCC. The CT genotype and T allele were significantly more prevalent in the HCC group compared to either the cirrhosis (p = 0.03) or control groups (p = 0.0009 and 0.002; respectively).

Conclusion: FZD7 and GPC3 gene expressions have a complementary role in early HCC detection, with a greater diagnostic sensitivity and accuracy than AFP. In addition, FZD7 rs2280509 polymorphism is significantly associated with an increased risk of HCC in the Egyptian population.

背景:肝细胞癌(HCC)是全球癌症相关死亡的第二大原因,尤其是在埃及。HCC的早期诊断大大提高了患者的生存率和预后。甲胎蛋白(AFP)的低敏感性和特异性导致了对HCC新生物标志物的需求。本研究的目的是评估frizzled-7(FZD7)和glypian-3(GPC3)基因表达作为HCC早期诊断的潜在生物标志物的有效性,并研究FZD7 rs2280509多态性与HCC风险之间的关系。材料和方法:通过实时定量逆转录聚合酶链式反应(qRT-PCR)测定FZD7和GPC3基因的表达,并使用RT-PCR对FZD7(rs2280509SNP)基因多态性进行分型。结果:目前的结果显示,FZD7基因表达在鉴定HCC时比GPC3基因表达和AFP水平具有更大的曲线下面积(AUC)。三种标记物的组合显示出比单独任何一种标记物更好的诊断性能,AUC更大(p<0.05)。FZD7 rs2280509多态性(CT)被发现与HCC风险增加显著相关。CT基因型和T等位基因在HCC组的发病率明显高于肝硬化组(p=0.003)或对照组(分别为p=0.0009和0.002)。结论:FZD7和GPC3基因表达在早期HCC检测中具有互补作用,比AFP具有更高的诊断敏感性和准确性。此外,FZD7 rs2280509多态性与埃及人群中HCC风险增加显著相关。
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引用次数: 0
Comparison of pain-relieving effects by number of irradiations, through propensity score matching and the international consensus endpoint. 通过倾向评分匹配和国际共识终点,通过照射次数比较止痛效果。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0054
Yuki Aoki, Michihiro Nakayama, Kaori Nakajima, Masaaki Yamashina, Atsutaka Okizaki

Background: Palliative radiotherapy for bone metastases utilizes various dose fractionation schedules. The pain-relieving effects of a single fraction (SF) and multiple fractions (MF) are largely debated due to the difficulty in matching patients' backgrounds and in assessing the effectiveness of pain relief. This study aimed to compare the pain-relieving effects of SF and MF palliative radiotherapy for bone metastases using propensity score matching and the international consensus endpoint (ICE).

Materials and methods: Our study included 195 patients irradiated for bone metastasis. The primary endpoint was the pain-relieving effects used by ICE. In addition, the evaluation was performed by using responder (complete response/partial response) and non-responder (pain progression/indeterminate response) categorization. The secondary endpoints were the discharge or transfer rate at one month after irradiation and postirradiation pathological fracture rate. Propensity score matching was used to adjust patient's characteristics and reduce selection bias.

Results: After adapting propensity score matching, the total number of patients was 74. There was no significant difference in the pain-relieving effects between SF and MF (p = 0.184). There were no significant differences in them between SF and MF when using responder and non-responder categorization (p = 0.163). Furthermore, there were no differences in the discharge or transfer rates (p = 0.693) and pathological fracture rates (p = 1.00).

Conclusions: The combination of propensity score matching and ICE revealed no significant difference in the pain-relieving effects between SF and MF for bone metastases, thus, SF has no significant disadvantage compared to MF in pain-relieving effects.

背景:骨转移的姑息性放射治疗采用不同的剂量分割方案。由于难以匹配患者的背景和评估疼痛缓解的有效性,单组分(SF)和多组分(MF)的疼痛缓解效果在很大程度上存在争议。本研究旨在使用倾向评分匹配和国际共识终点(ICE)比较SF和MF姑息性放疗治疗骨转移瘤的止痛效果。材料和方法:我们的研究包括195名接受骨转移放射治疗的患者。主要终点是ICE使用的止痛效果。此外,通过使用应答者(完全应答/部分应答)和非应答者(疼痛进展/不确定应答)分类进行评估。次要终点是放疗后一个月的出院率或转移率以及放疗后病理性骨折率。倾向性评分匹配用于调整患者的特征并减少选择偏差。结果:采用倾向评分匹配后,患者总数为74人。SF和MF的止痛效果无显著差异(p=0.184)。使用应答者和非应答者分类时,SF和MF之间的止痛效果没有显著差异(p=0.163)。此外,出院率或转移率(p=0.693)和病理性骨折率(p=1.00)没有差异。结论:倾向评分匹配和ICE相结合显示,SF和MF对骨转移的止痛效果没有显著差异,因此,SF在止痛效果上与MF相比没有显著劣势。
{"title":"Comparison of pain-relieving effects by number of irradiations, through propensity score matching and the international consensus endpoint.","authors":"Yuki Aoki,&nbsp;Michihiro Nakayama,&nbsp;Kaori Nakajima,&nbsp;Masaaki Yamashina,&nbsp;Atsutaka Okizaki","doi":"10.5603/RPOR.a2023.0054","DOIUrl":"10.5603/RPOR.a2023.0054","url":null,"abstract":"<p><strong>Background: </strong>Palliative radiotherapy for bone metastases utilizes various dose fractionation schedules. The pain-relieving effects of a single fraction (SF) and multiple fractions (MF) are largely debated due to the difficulty in matching patients' backgrounds and in assessing the effectiveness of pain relief. This study aimed to compare the pain-relieving effects of SF and MF palliative radiotherapy for bone metastases using propensity score matching and the international consensus endpoint (ICE).</p><p><strong>Materials and methods: </strong>Our study included 195 patients irradiated for bone metastasis. The primary endpoint was the pain-relieving effects used by ICE. In addition, the evaluation was performed by using responder (complete response/partial response) and non-responder (pain progression/indeterminate response) categorization. The secondary endpoints were the discharge or transfer rate at one month after irradiation and postirradiation pathological fracture rate. Propensity score matching was used to adjust patient's characteristics and reduce selection bias.</p><p><strong>Results: </strong>After adapting propensity score matching, the total number of patients was 74. There was no significant difference in the pain-relieving effects between SF and MF (p = 0.184). There were no significant differences in them between SF and MF when using responder and non-responder categorization (p = 0.163). Furthermore, there were no differences in the discharge or transfer rates (p = 0.693) and pathological fracture rates (p = 1.00).</p><p><strong>Conclusions: </strong>The combination of propensity score matching and ICE revealed no significant difference in the pain-relieving effects between SF and MF for bone metastases, thus, SF has no significant disadvantage compared to MF in pain-relieving effects.</p>","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"28 4","pages":"506-513"},"PeriodicalIF":1.2,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b4/11/rpor-28-4-506.PMC10547426.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41153179","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
Tyrosine kinase inhibitors induced thyroid dysfunction: myth or reality? 酪氨酸激酶抑制剂诱导的甲状腺功能障碍:神话还是现实?
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0055
Anjli Malhotra, Rajeev Gupta, Shveta Mahajan

Background: Chronic myelogenous leukemia (CML) is a hematopoietic stem cell disorder. It is associated with acquired genetic changes in the hematopoietic stem cells in the form of BCR-ABL fusion gene also known as Philadelphia chromosome.

Materials and methods: We prospectively studied thyroid function at baseline and at 6 months of imatinib treatment in 26 newly diagnosed BCR-ABL positive CML patients.

Result: The thyroid-stimulating hormone (TSH) levels increased significantly from baseline (3.20 ± 0.978 mIU/L vs. 3.724 ± 1.726 mIU/L, p < 0.05) after 6 months of treatment, 88.4% of the patients remained euthyroid. Only 2 patients had subclinical hypothyroidism, 1 had hypothyroidism after 6 months of tyrosine kinase inhibitors (TKI) therapy.

Conclusion: Imatinib did not have any significant effect on thyroid function in CML patients in this study.

背景:慢性粒细胞白血病(CML)是一种造血干细胞疾病。它以BCR-ABL融合基因(也称为费城染色体)的形式与造血干细胞的后天遗传变化有关。材料和方法:我们前瞻性研究了26例新诊断的BCR-ABL阳性CML患者在基线和伊马替尼治疗6个月时的甲状腺功能。结果:治疗6个月后,促甲状腺激素(TSH)水平较基线显著升高(3.20±0.978mIU/L对3.724±1.726mIU/L,p<0.05),88.4%的患者保持甲状腺功能正常。只有2名患者患有亚临床甲状腺功能减退症,1名患者在接受酪氨酸激酶抑制剂(TKI)治疗6个月后患有甲状腺功能减退。结论:伊马替尼对慢性粒细胞白血病患者的甲状腺功能无明显影响。
{"title":"Tyrosine kinase inhibitors induced thyroid dysfunction: myth or reality?","authors":"Anjli Malhotra,&nbsp;Rajeev Gupta,&nbsp;Shveta Mahajan","doi":"10.5603/RPOR.a2023.0055","DOIUrl":"https://doi.org/10.5603/RPOR.a2023.0055","url":null,"abstract":"<p><strong>Background: </strong>Chronic myelogenous leukemia (CML) is a hematopoietic stem cell disorder. It is associated with acquired genetic changes in the hematopoietic stem cells in the form of BCR-ABL fusion gene also known as Philadelphia chromosome.</p><p><strong>Materials and methods: </strong>We prospectively studied thyroid function at baseline and at 6 months of imatinib treatment in 26 newly diagnosed BCR-ABL positive CML patients.</p><p><strong>Result: </strong>The thyroid-stimulating hormone (TSH) levels increased significantly from baseline (3.20 ± 0.978 mIU/L <i>vs</i>. 3.724 ± 1.726 mIU/L, p < 0.05) after 6 months of treatment, 88.4% of the patients remained euthyroid. Only 2 patients had subclinical hypothyroidism, 1 had hypothyroidism after 6 months of tyrosine kinase inhibitors (TKI) therapy.</p><p><strong>Conclusion: </strong>Imatinib did not have any significant effect on thyroid function in CML patients in this study.</p>","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"28 4","pages":"463-467"},"PeriodicalIF":1.2,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8d/be/rpor-28-4-463.PMC10547422.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41178726","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
Biological dosimetric impact of dose-delivery time for hypoxic tumour with modified microdosimetric kinetic model. 改良微剂量动力学模型对缺氧肿瘤给药时间的生物剂量测定影响。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0062
Daisuke Kawahara, Yasushi Nagata
Background An improved microdosimetric kinetic model (MKM) can address radiobiological effects with prolonged delivery times. However, these do not consider the effects of oxygen. The current study aimed to evaluate the biological dosimetric effects associated with the dose delivery time in hypoxic tumours with improved MKM for photon radiation therapy. Materials and methods Cell survival was measured under anoxic, hypoxic, and oxic conditions using the Monte Carlo code PHITS. The effect of the dose rate of 0.5–24 Gy/min for the biological dose (Dbio) was estimated using the microdosimetric kinetic model. The dose per fraction and pressure of O2 (pO2) in the tumour varied from 2 to 20 Gy and from 0.01 to 5.0% pO2, respectively. Results The ratio of the Dbio at 1.0–24 Gy/min to that at 0.5 Gy/min (RDR) was higher at higher doses. The maximum RDR was 1.09 at 1.0 Gy/min, 1.12 at 12 Gy/min, and 1.13 at 24 Gy/min. The ratio of the Dbio at 0.01–2.0% of pO2 to that at 5.0% of pO2 (Roxy) was within 0.1 for 2–20 Gy of physical dose. The maximum Roxy was 0.42 at 0.01% pO2, 0.76 at 0.4% pO2, 0.89 at 1% pO2, and 0.96 at 2% pO2. Conclusion Our proposed model can estimate the cell killing and biological dose under hypoxia in a clinical and realistic patient. A shorter dose-delivery time with a higher oxygen distribution increased the radiobiological effect. It was more effective at higher doses per fraction than at lower doses.
背景:改进的微剂量动力学模型(MKM)可以解决延长给药时间的放射生物学效应。然而,这些没有考虑氧气的影响。目前的研究旨在评估使用改进的MKM进行光子辐射治疗的缺氧肿瘤中与剂量递送时间相关的生物剂量测定效果。材料和方法:使用蒙特卡罗程序PHITS测量缺氧、缺氧和有氧条件下的细胞存活率。使用微剂量动力学模型估计0.5-24Gy/min的剂量率对生物剂量(Dbio)的影响。肿瘤中O2(pO2)的每级分剂量和压力分别在2至20Gy和0.01至5.0%pO2之间变化。结果:1.0~24Gy/min的Dbio与0.5Gy/min的比值(RDR)随剂量的增加而增大。在1.0Gy/min时最大RDR为1.09,在12Gy/min时为1.12,在24Gy/min时则为1.13。对于2-20Gy的物理剂量,在0.01-2.0%的pO2下的Dbio与在5.0%的pO2(Roxy)的Dbio的比率在0.1以内。在0.01%pO2时,最大Roxy为0.42,在0.4%pO2时为0.76,在1%pO2时为0.89,在2%pO2下为0.96。结论:我们提出的模型可以估计临床和现实患者在缺氧条件下的细胞杀伤和生物剂量。较短的剂量输送时间和较高的氧气分布增加了放射生物学效应。它在每部分较高的剂量下比在较低的剂量下更有效。
{"title":"Biological dosimetric impact of dose-delivery time for hypoxic tumour with modified microdosimetric kinetic model.","authors":"Daisuke Kawahara,&nbsp;Yasushi Nagata","doi":"10.5603/RPOR.a2023.0062","DOIUrl":"https://doi.org/10.5603/RPOR.a2023.0062","url":null,"abstract":"Background An improved microdosimetric kinetic model (MKM) can address radiobiological effects with prolonged delivery times. However, these do not consider the effects of oxygen. The current study aimed to evaluate the biological dosimetric effects associated with the dose delivery time in hypoxic tumours with improved MKM for photon radiation therapy. Materials and methods Cell survival was measured under anoxic, hypoxic, and oxic conditions using the Monte Carlo code PHITS. The effect of the dose rate of 0.5–24 Gy/min for the biological dose (Dbio) was estimated using the microdosimetric kinetic model. The dose per fraction and pressure of O2 (pO2) in the tumour varied from 2 to 20 Gy and from 0.01 to 5.0% pO2, respectively. Results The ratio of the Dbio at 1.0–24 Gy/min to that at 0.5 Gy/min (RDR) was higher at higher doses. The maximum RDR was 1.09 at 1.0 Gy/min, 1.12 at 12 Gy/min, and 1.13 at 24 Gy/min. The ratio of the Dbio at 0.01–2.0% of pO2 to that at 5.0% of pO2 (Roxy) was within 0.1 for 2–20 Gy of physical dose. The maximum Roxy was 0.42 at 0.01% pO2, 0.76 at 0.4% pO2, 0.89 at 1% pO2, and 0.96 at 2% pO2. Conclusion Our proposed model can estimate the cell killing and biological dose under hypoxia in a clinical and realistic patient. A shorter dose-delivery time with a higher oxygen distribution increased the radiobiological effect. It was more effective at higher doses per fraction than at lower doses.","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"28 4","pages":"514-521"},"PeriodicalIF":1.2,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/3f/38/rpor-28-4-514.PMC10547428.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41147945","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
Stereotactic MR-guided adaptive radiotherapy (SMART) for primary rectal cancer: evaluation of early toxicity and pathological response. 立体定向磁共振导向适应性放疗(SMART)治疗原发性癌症:早期毒性和病理反应的评估。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0051
Alessandra Castelluccia, Domenico Marchesano, Gianmarco Grimaldi, Ivan Annessi, Federico Bianciardi, Cristian Borrazzo, Annamaria Dipalma, Randa El Gawhary, Marica Masi, Maria Rago, Maria Valentino, Laura Verna, Maurizio Portaluri, PierCarlo Gentile

Background: The purpose of this study is to measure the effects of stereotactic MR-guided adaptive radiotherapy (SMART) for rectal cancer patients in terms of early toxicity and pathological response.

Materials and methods: For this prospective pilot study, patients diagnosed with locally advanced rectal cancer (LARC) with positive lymph node clinical staging underwent SMART on rectal lesion and mesorectum using hybrid MR-Linac (MRIdian ViewRay). Dose prescription at 80% isodose for the rectal lesion and mesorectum was 40 Gy (8 Gy/fr) and 25 Gy (5 Gy/fr), respectively, delivered on 5 days (3 fr/week). Response assessment by MRI was performed 3 weeks after SMART, then patients fit for surgery underwent total mesorectal excision. Primary endpoint was evaluation of adverse effect of radiotherapy. Secondary endpoint was pathological complete response rate. Early toxicity was graded according to the Common Terminology Criteria for Adverse Events (CTCAE v5.0).

Results: From October 2020 to January 2022, twenty patients underwent rectal SMART. No grade 3-5 toxicity was recorded. Twelve patients were eligible for total mesorectal excision (TME). Mean interval between the completion of SMART and surgery was 4 weeks. Pathological downstaging occurred in all patients; rate of pathological complete response (pCR) was 17%. pCR occurred with a prolonged time to surgery (> 7 weeks).

Conclusion: To our knowledge, this is the first study to use stereotactic radiotherapy for primary rectal cancer. SMART for rectal cancer is well tolerated and effective in terms of tumor regression, especially if followed by delayed surgery.

背景:本研究的目的是从早期毒性和病理反应两个方面来衡量立体定向磁共振引导适应性放疗(SMART)对癌症直肠患者的影响。材料和方法:在这项前瞻性试点研究中,被诊断为淋巴结临床分期阳性的局部晚期癌症(LARC)患者使用混合MR-Linac(MRIdian ViewRay)对直肠病变和直缝进行了SMART检查。直肠病变和直肠系膜80%等剂量的剂量处方分别为40Gy(8Gy/fr)和25Gy(5Gy/fr。SMART术后3周进行MRI反应评估,然后适合手术的患者接受全直肠系膜切除术。主要终点是评估放疗的不良反应。次要终点为病理完全缓解率。根据不良事件通用术语标准(CTCAE v5.0)对早期毒性进行分级。结果:从2020年10月到2022年1月,20名患者接受了直肠SMART。未记录到3-5级毒性。12名患者符合全直肠系膜切除术(TME)的条件。SMART完成与手术之间的平均间隔时间为4周。所有患者均出现病理性降阶;病理完全缓解率(pCR)为17%。pCR发生时间延长(>7周)。结论:据我们所知,这是首次应用立体定向放射治疗原发性癌症。SMART治疗直肠癌症在肿瘤消退方面具有良好的耐受性和有效性,尤其是在延迟手术后。
{"title":"Stereotactic MR-guided adaptive radiotherapy (SMART) for primary rectal cancer: evaluation of early toxicity and pathological response.","authors":"Alessandra Castelluccia,&nbsp;Domenico Marchesano,&nbsp;Gianmarco Grimaldi,&nbsp;Ivan Annessi,&nbsp;Federico Bianciardi,&nbsp;Cristian Borrazzo,&nbsp;Annamaria Dipalma,&nbsp;Randa El Gawhary,&nbsp;Marica Masi,&nbsp;Maria Rago,&nbsp;Maria Valentino,&nbsp;Laura Verna,&nbsp;Maurizio Portaluri,&nbsp;PierCarlo Gentile","doi":"10.5603/RPOR.a2023.0051","DOIUrl":"https://doi.org/10.5603/RPOR.a2023.0051","url":null,"abstract":"<p><strong>Background: </strong>The purpose of this study is to measure the effects of stereotactic MR-guided adaptive radiotherapy (SMART) for rectal cancer patients in terms of early toxicity and pathological response.</p><p><strong>Materials and methods: </strong>For this prospective pilot study, patients diagnosed with locally advanced rectal cancer (LARC) with positive lymph node clinical staging underwent SMART on rectal lesion and mesorectum using hybrid MR-Linac (MRIdian ViewRay). Dose prescription at 80% isodose for the rectal lesion and mesorectum was 40 Gy (8 Gy/fr) and 25 Gy (5 Gy/fr), respectively, delivered on 5 days (3 fr/week). Response assessment by MRI was performed 3 weeks after SMART, then patients fit for surgery underwent total mesorectal excision. Primary endpoint was evaluation of adverse effect of radiotherapy. Secondary endpoint was pathological complete response rate. Early toxicity was graded according to the Common Terminology Criteria for Adverse Events (CTCAE v5.0).</p><p><strong>Results: </strong>From October 2020 to January 2022, twenty patients underwent rectal SMART. No grade 3-5 toxicity was recorded. Twelve patients were eligible for total mesorectal excision (TME). Mean interval between the completion of SMART and surgery was 4 weeks. Pathological downstaging occurred in all patients; rate of pathological complete response (pCR) was 17%. pCR occurred with a prolonged time to surgery (> 7 weeks).</p><p><strong>Conclusion: </strong>To our knowledge, this is the first study to use stereotactic radiotherapy for primary rectal cancer. SMART for rectal cancer is well tolerated and effective in terms of tumor regression, especially if followed by delayed surgery.</p>","PeriodicalId":47283,"journal":{"name":"Reports of Practical Oncology and Radiotherapy","volume":"28 4","pages":"437-444"},"PeriodicalIF":1.2,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/8e/33/rpor-28-4-437.PMC10547417.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41167729","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
Biological dosimetric impact of dose-delivery time for hypoxic tumour with modified microdosimetric kinetic model 用改进的微剂量动力学模型研究给药时间对缺氧肿瘤的生物剂量学影响
Q4 ONCOLOGY Pub Date : 2023-08-28 DOI: 10.5603/rpor.96868
Daisuke Kawahara, Yasushi Nagata
Background: An improved microdosimetric kinetic model (MKM) can address radiobiological effects with prolonged delivery times. However, these do not consider the effects of oxygen. The current study aimed to evaluate the biological dosimetric effects associated with the dose delivery time in hypoxic tumours with improved MKM for photon radiation therapy. Materials and methods: Cell survival was measured under anoxic, hypoxic, and oxic conditions using the Monte Carlo code PHITS. The effect of the dose rate of 0.5–24 Gy/min for the biological dose (Dbio) was estimated using the microdosimetric kinetic model. The dose per fraction and pressure of O2 (pO2) in the tumour varied from 2 to 20 Gy and from 0.01 to 5.0% pO 2 , respectively. Results: The ratio of the Dbio at 1.0–24 Gy/min to that at 0.5 Gy/min (RDR) was higher at higher doses. The maximum RDR was 1.09 at 1.0 Gy/min, 1.12 at 12 Gy/min, and 1.13 at 24 Gy/min. The ratio of the Dbio at 0.01–2.0% of pO2 to that at 5.0% of pO 2 (Roxy) was within 0.1 for 2–20 Gy of physical dose. The maximum Roxy was 0.42 at 0.01% pO2, 0.76 at 0.4% pO2, 0.89 at 1% pO 2 , and 0.96 at 2% pO2. Conclusion: Our proposed model can estimate the cell killing and biological dose under hypoxia in a clinical and realistic patient. A shorter dose-delivery time with a higher oxygen distribution increased the radiobiological effect. It was more effective at higher doses per fraction than at lower doses.
背景:一种改进的微剂量动力学模型(MKM)可以解决延长递送时间的放射生物学效应。然而,这些都没有考虑到氧气的影响。本研究旨在评估缺氧肿瘤改良MKM光子放射治疗中与剂量传递时间相关的生物剂量学效应。材料和方法:使用蒙特卡洛代码PHITS在缺氧、缺氧和缺氧条件下测量细胞存活率。利用微剂量动力学模型估计了0.5 ~ 24 Gy/min剂量率对生物剂量(Dbio)的影响。肿瘤中每分数O2 (pO2)的剂量和压力分别为2 ~ 20gy和0.01 ~ 5.0% pO2。结果:1.0 ~ 24 Gy/min的Dbio与0.5 Gy/min的Dbio之比(RDR)随剂量增大而增大。1.0 Gy/min时最大RDR为1.09,12 Gy/min时为1.12,24 Gy/min时为1.13。物理剂量为2 ~ 20 Gy时,0.01 ~ 2.0% pO2与5.0% pO2 (Roxy)的Dbio比值在0.1以内。0.01% pO2、0.4% pO2、1% pO2和2% pO2的最大Roxy分别为0.42、0.76、0.89和0.96。结论:该模型能较好地估计临床和现实患者在缺氧条件下的细胞杀伤和生物剂量。较短的给药时间和较高的氧分布增加了放射生物学效应。高剂量时比低剂量时更有效。
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引用次数: 0
Comparison of helical and TomoDirect techniques with simultaneous integrated boost in early breast cancer patients. 螺旋和TomoDirect技术与癌症早期患者同时综合强化的比较。
IF 1.2 Q4 ONCOLOGY Pub Date : 2023-08-28 eCollection Date: 2023-01-01 DOI: 10.5603/RPOR.a2023.0058
Cem Onal, Recep Bozca, Ezgi Oymak, Ozan Cem Guler

Background: The aim of the study was to perform dosimetric comparisons of helical (H) and TomoDirect (TD) plans for whole-breast irradiation (WBI) with simultaneous integrated boost (SIB) in early-stage breast cancer patients undergoing breast conserving surgery.

Materials and methods: Fifty patients, 25 with left-side and 25 with right-side tumors, were determined for a treatment planning system for a total dose of 50.4Gy in 1.8Gy per fraction to WBI, with a SIB of 2.3Gy per fraction delivered to the tumor bed. The planning target volume (PTV) doses and the conformity (CI) and homogeneity indices (HI) for PTVbreast and PTVboost, as well as organ-at-risk (OAR) doses and treatment times, were compared between the H and TD plans.

Results: All plans met the PTV coverage criteria for the H plan, except for mean V107 of PTVbreast for TD plan. The H plan yielded better homogeneity and conformity of dose distribution compared to the TD plan. The ipsilateral mean lung doses were not significantly different between the two plans. The TD plans is advantageous for mean doses to the heart, contralateral breast and lung, spinal cord, and esophagus than the H plans. In both the H and TD plans, the right-sided breast patients had lower heart dose parameters than the left-sided breast patients. The TD plan is superior to the H plan in sparing the contralateral breast and lung by decreasing low-dose volumes.

Conclusions: While the OAR dose advantages of TD are appealing, shorter treatment times or improved dose homogeneity and conformity for target volume may be advantageous for H plan.

背景:本研究的目的是对正在接受保乳手术的早期癌症患者进行全乳照射(WBI)和同时综合增强(SIB)的螺旋(H)和TomoDirect(TD)计划的剂量测定比较。材料和方法:50名患者,其中25名为左侧肿瘤,25名为右侧肿瘤,被确定为治疗计划系统,WBI的总剂量为50.4Gy,1.8Gy/分,SIB为2.3Gy/分。比较H计划和TD计划的计划目标体积(PTV)剂量、PTVbreast和PTVboost的一致性(CI)和同质性指数(HI),以及器官风险(OAR)剂量和治疗时间。结果:所有计划均符合H计划的PTV覆盖标准,但TD计划的PTVbreast平均V107除外。与TD方案相比,H方案产生了更好的剂量分布均匀性和一致性。两种方案的同侧平均肺剂量没有显著差异。TD方案对心脏、对侧乳腺和肺、脊髓和食道的平均剂量比H方案有利。在H和TD方案中,右侧乳腺患者的心脏剂量参数均低于左侧乳腺患者。在通过减少低剂量体积来保护对侧乳腺和肺方面,TD方案优于H方案。结论:虽然TD的OAR剂量优势很有吸引力,但缩短治疗时间或改善剂量均匀性和目标体积的一致性可能有利于H计划。
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Reports of Practical Oncology and Radiotherapy
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