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Role of microRNA in predictingclinical efficacy of neoadjuvant chemoradiotherapy for rectal cancer microRNA在预测直肠癌新辅助放化疗临床疗效中的作用
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.016
Wenyan Yao, Q. Peng, Yaqun Zhu, Ye Tian
Neoadjuvant chemoradiotherapy (NCRT) has become the standard treatment for patients with locally advanced rectal cancer (LARC). However, the response to NCRT varies among LARC patients and a subset of patients show resistance to NCRT. NCRT may delay the timing of surgery and even reduce the overall survival. Therefore, it is of significance to identify biomarkers for predicting the clinical efficacy of NCRT, screen patients who are resistant to NCRT and perform surgery as early as possible, eventually establishing an individualized therapeutic strategy. MicroRNAs are a class of small non-coding RNAs that post-transcriptionally regulate gene expression, which areinvolved in multiple signaling pathways and DNA damage repair process and affect the radiosensitivity of rectal cancer cells. Many recent studies have evaluated the role of microRNA in predicting the response to NCRT. The purpose of this article is to review the research progress and validate the role of microRNA in predicting the clinical efficacy of NCRT for rectal cancer. Key words: Rectal neoplasm/neoadjuvant chemoradiotherapy; MicroRNA; Predict
新辅助放化疗(NCRT)已成为局部晚期直肠癌(LARC)患者的标准治疗方法。然而,LARC患者对NCRT的反应各不相同,一部分患者对NCRT有耐药性。NCRT可能会延迟手术时间,甚至降低总生存率。因此,鉴别生物标志物对预测NCRT临床疗效,筛选耐药患者并尽早进行手术治疗,最终制定个体化治疗策略具有重要意义。MicroRNAs是一类转录后调控基因表达的小分子非编码rna,参与多种信号通路和DNA损伤修复过程,影响直肠癌细胞的放射敏感性。最近的许多研究已经评估了microRNA在预测NCRT疗效中的作用。本文旨在综述相关研究进展,验证microRNA在预测直肠癌NCRT临床疗效中的作用。关键词:直肠肿瘤/新辅助放化疗;微rna;预测
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引用次数: 0
Research progress on biomarkers for radiation-induced intestinal injury based on intestinal flora 基于肠道菌群的辐射肠损伤生物标志物研究进展
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.018
Junjun Zhang, S. Cai, Yongqiang Yang, Junyan Li, Ye Tian
Recently, the relationship between intestinal flora and its metabolites and tumorigenesis, inflammatory bowel diseasesas well as radiation-induced intestinal injury has captivated widespread attention from researchers. Accumulated evidence derived from nuclear accident investigation, animal model experiment and clinical research has proven the role of intestinal flora and its metabolites as the biomarkers to evaluate the radiation dose and severity of radiation-induced intestinal injury. This article reviews the relationship between intestinal flora and its metabolites and radiation-induced intestinal injury, aiming to provide theoretical reference for assessing the risk of radiation-induced intestinal injury. Key words: Intestinal flora; Metabolite; Radiation-induced injury; Biomarker
近年来,肠道菌群及其代谢产物与肿瘤发生、炎症性肠病以及放射性肠道损伤之间的关系引起了研究人员的广泛关注。从核事故调查、动物模型实验和临床研究中积累的证据已经证明,肠道菌群及其代谢产物作为评估辐射剂量和放射性肠损伤严重程度的生物标志物的作用。本文综述了肠道菌群及其代谢产物与放射性肠损伤的关系,旨在为评估放射性肠损伤风险提供理论参考。关键词:肠道菌群;代谢物;辐射损伤;生物标志物
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引用次数: 0
Dose-escalation trial of lobaplatin weekly plus concurrent radiotherapy for local-regionally advanced nasopharyngeal carcinoma 洛铂联合放疗治疗局部-区域晚期鼻咽癌的剂量递增试验
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.003
X. Pang, D. Qing, Bin Zhao, D. Ma
Objective To define the maximum-tolerated dose (MTD) of lobaplatin (LBP) in a weekly regimen combined with concurrent radiotherapy in the treatment of locally advanced nasopharyngeal carcinoma (NPC). Methods A total of 18 cases with stage Ⅲ/IV A NPC were enrolled. Concurrent chemoradiotherapy was given to all the patients with a dose escalation of LBP. The initial dose of LBP was 15 mg/m2 with an escalating dose of 5 mg/m2. At least 3 patients were assigned into each group. Patients were proceeded into the next dose group if no dose-limiting toxicity (DLT) occurred until the MTD was achieved. Efficacy and toxicity were evaluated regularly. Results Three patients were assigned into the 10 mg/m2, 3 into the 15 mg/m2, and 6 into the 20 mg/m2 and 25 mg/m2 groups, respectively. Two patients experienced DLT in the 25 mg/m2 group. Hence, the MTD was determined as 20 mg/m2. At 3 months after corresponding treatment, the remission rate of nasopharyngeal tumors and neck-positive lymph nodes of the patients was 100%. The most common toxicity was reversible bone marrow suppression. Conclusions The MTD of weekly lobaplatin plus concurrent IMRT is 20 mg/m2 for locally advanced NPC. This regimen is reliable and safe, which is worthy of further clinical study. Key words: Nasopharyngeal neoplasm/concurrent chemoradiotherapy; Lobaplatin; Dose-limiting toxicity; Maximum tolerated dose
目的探讨洛铂联合放射治疗局部晚期鼻咽癌(NPC)的最大耐受剂量(MTD)。方法选取18例Ⅲ/IV期鼻咽癌患者。所有LBP剂量增加的患者均给予同步放化疗。LBP的初始剂量为15mg /m2,逐渐增加至5mg /m2。每组至少3例。如果在达到MTD之前没有发生剂量限制性毒性(DLT),则患者进入下一剂量组。定期评价疗效和毒性。结果10 mg/m2组3例,15 mg/m2组3例,20 mg/m2组和25 mg/m2组6例。25 mg/m2组2例患者出现DLT。因此,测定MTD为20 mg/m2。相应治疗3个月后,患者鼻咽肿瘤及颈阳性淋巴结的缓解率为100%。最常见的毒性是可逆的骨髓抑制。结论局部晚期鼻咽癌患者每周洛铂联合IMRT的MTD为20 mg/m2。该方案可靠、安全,值得进一步临床研究。关键词:鼻咽肿瘤/同步放化疗;Lobaplatin;Dose-limiting毒性;最大耐受剂量
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引用次数: 0
Analysis of recurrence pattern of neoadjuvant therapy combined with surgical treatment for esophageal squamous cell carcinoma 食管鳞状细胞癌新辅助治疗联合手术治疗的复发模式分析
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.005
C. Fan, Zhu Feng, H. Ge, K. Ye, Hao Wang, Xiao-li Zheng, Yougai Zhang, Hui Luo
Objective To evaluate the recurrence pattern and identify the risk factors of esophageal squamous cell carcinoma after neoadjuvant therapy combined with surgery. Methods Clinical data of 275 patients with thoracic esophageal squamous cell carcinoma treated with neoadjuvant therapy combined with surgery from December 2011 to December 2015 were retrospectively analyzed. The follow-up data of the enrolled patients were complete and analyzable. The recurrence pattern, recurrence time, recurrence location and influencing factors after neoadjuvant therapy in combination with surgery were analyzed. The recurrence rate was calculated by Kaplan-Meier method. The multivariate analysis was performed by Cox regression model. Results The median follow-up time was 32(3-84) months, and the median time of the first recurrence was 10.6(2.0-69.1) months. The 1-, 2-and 3-year recurrence rates were 32.0%, 45.1% and 52.3%, respectively. A total of 152 cases (55.3%) had recurrence. Among them, 77 cases (50.6%) had local-regional recurrence (LRR), 34 cases (23.4%) had distant metastasis (DM), 33 cases (21.7%) had LRR+ DM and 8 cases (6.0%) had recurrence in unknown site. Among the patients with LRR, lymph node recurrence was the most common (n=98, 89.1%). For DM patients, lung metastasis (n=33, 49.3%), liver metastasis (n=16, 23.9%), bone metastasis (n=14, 20.9%) and non-regional lymph node metastasis (n=14, 20.9%) were commonly observed. The multivariate analysis showed that postoperative T stage (P=0.008), N stage (P<0.001) and the number of lymph node dissection (P<0.001) were the independent risk factors for recurrence after treatment. Conclusions The recurrence rate after neoadjuvant therapy remains relatively high for esophageal squamous cell carcinoma, and the regional lymph node is the most common site of recurrence. Postoperative pathological T staging, N staging and the number of lymph node dissection are the independent risk factors for recurrence after treatment. Key words: Esophageal neoplasm/neoadjuvant treatment; Recurrence pattern; Risk factor
目的探讨食管鳞状细胞癌术后新辅助治疗的复发模式及危险因素。方法回顾性分析2011年12月至2015年12月275例胸段食管鳞状细胞癌新辅助治疗联合手术治疗的临床资料。入选患者的随访数据是完整和可分析的。分析新辅助治疗结合手术后的复发模式、复发时间、复发部位及影响因素。复发率采用Kaplan-Meier法计算。采用Cox回归模型进行多元分析。结果中位随访时间为32(3-84)个月,中位首次复发时间为10.6(2.0-69.1)个月。1、2和3年复发率分别为32.0%、45.1%和52.3%。复发152例(55.3%)。其中77例(50.6%)局部复发,34例(23.4%)远处转移,33例(21.7%)LRR+DM,8例(6.0%)不明部位复发。在LRR患者中,淋巴结复发最为常见(n=98,89.1%)。DM患者中,肺转移(n=33,49.3%)、肝转移(n=16,23.9%)、骨转移(n=14,20.9%)和非区域淋巴结转移(n=14,209%)最为常见。多因素分析显示,术后T分期(P=0.008)、N分期(P<0.001)和淋巴结清扫次数(P<0.001。结论食管鳞状细胞癌新辅助治疗后复发率较高,局部淋巴结是最常见的复发部位。术后病理T分期、N分期和淋巴结清扫次数是治疗后复发的独立危险因素。关键词:食管肿瘤/新辅助治疗;复发模式;风险因素
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引用次数: 0
Partial research progress on precision hyperthermia for malignant tumors 恶性肿瘤精准热疗的部分研究进展
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.017
Jianing Qian, Zhi-bing Wu
Since the 21st century, with the changes of people′s living habits and the aggravation ofenvironmental pollution, the incidence of tumors has been increasing day by day, which has become the main deathcauseof human diseases. Atpresent, in addition to the three major conventional treatments of tumors, the emergence of hyperthermia provides a safer and more effective solution for the prevention and treatment of tumors. Attributed to the rapid development of mechanical manufacturing, computertechnology, molecularbiology, materials science and other disciplines, precision hyperthermia presented by radiofrequency and ultrasonic focusing hyperthermia guided by magnetic resonance imaging (MRI) non-invasive temperature measure technology, as well as molecular level targeted hyperthermia have provided a broader perspective for the treatment of tumors. This article reviews the partial research progress on precision hyperthermia to understand the current general situation of precision hyperthermia for tumors. Key words: Neoplasm/hyperthermia; Research progress
21世纪以来,随着人们生活习惯的改变和环境污染的加剧,肿瘤的发病率日益增加,已成为人类疾病的主要致死原因。目前,除了肿瘤的三大常规治疗方法外,热疗的出现为肿瘤的防治提供了更安全、更有效的解决方案。由于机械制造、计算机技术、分子生物学、材料科学等学科的快速发展,以磁共振成像(MRI)无创测温技术为指导的射频和超声聚焦热疗所呈现的精密热疗,以及分子水平的靶向热疗,为肿瘤的治疗提供了更广阔的前景。本文就精密热疗的部分研究进展进行综述,了解肿瘤精密热疗的现状。关键词:肿瘤/热疗;研究进展
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引用次数: 0
Effect of lncRNA MEG3 on radiosensitivity of nasopharyngeal carcinoma cells by down-regulating miR-7-5p expression lncRNA MEG3下调miR-7-5p表达对鼻咽癌细胞放射敏感性的影响
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.011
Xujuan Sun, Lifang Sun, M. Yu, Ying Li, Mingyan Li, Ke Yang, Yujie Li, G. Xing, Q. Han
Objective To investigate the effect and underlying mechanism of lncRNA MEG3 on the radiosensitivity of nasopharyngeal carcinoma cells. Methods this experiment, overexpression control group, MEG3 overexpression group, miR-NC inhibition group, miR-7-5p inhibition group, overexpression control+ 4 Gy group, MEG3 overexpression+ 4 Gygroup, miR-NC inhibition+ 4 Gy group, miR-7-5p inhibition+ 4 Gy group, MEG3 overexpression+ miR-NC overexpression group, MEG3 overexpression+ miR-7-5p overexpression group were established. The expression of miR-7-5p and MEG3 was detected by qRT-PCR. The radiosensitivity of nasopharyngeal carcinoma cells was measured by clone formation assay. Cell apoptosis was assessed by flow cytometry. The fluorescence activity was evaluated by dual luciferase reporter assay. Results MEG3 was lowly expressed in nasopharyngeal carcinoma tissues and cells. Overexpression of MEG3 and inhibition of miR-7-5p expression increased the radiosensitivity of nasopharyngeal carcinoma cells and promoted radiation-induced cell apoptosis. MEG3 could targetedly regulate the miR-7-5p expression. Overexpression of miR-7-5p reversed the effect of overexpression of MEG3 on the sensitization of nasopharyngeal carcinoma cells and the promotion of apoptosis induced by radiation exposure. Conclusions Overexpression of MEG3 increases the radiosensitivity of nasopharyngeal carcinoma cells and promotes radiation-induced cell apoptosis. The mechanism may be related to the down-regulation of miR-7-5p expression. Key words: lncRNA MEG3; miR-7-5p; Nasopharyngeal carcinoma cell line; Radiosensitivity; Apoptosis
目的探讨lncRNA MEG3对鼻咽癌细胞放射敏感性的影响及其机制。方法本实验设过表达对照组、MEG3过表达组、miR-NC抑制组、miR-7-5p抑制组、过表达控制+ 4gy组、MEG3过表达+ 4gy组、miR-NC抑制+ 4gy组、miR-7-5p抑制+ 4gy组、MEG3过表达+ miR-NC过表达组、MEG3过表达+ miR-7-5p过表达组。采用qRT-PCR检测miR-7-5p和MEG3的表达。用克隆形成法测定鼻咽癌细胞的放射敏感性。流式细胞术检测细胞凋亡情况。采用双荧光素酶报告基因法测定其荧光活性。结果MEG3在鼻咽癌组织和细胞中低表达。MEG3过表达和miR-7-5p表达抑制增加鼻咽癌细胞的放射敏感性,促进辐射诱导的细胞凋亡。MEG3可靶向调控miR-7-5p的表达。miR-7-5p过表达逆转了MEG3过表达对鼻咽癌细胞致敏和促进辐射暴露诱导的细胞凋亡的作用。结论MEG3过表达增加鼻咽癌细胞的放射敏感性,促进辐射诱导的细胞凋亡。其机制可能与miR-7-5p表达下调有关。关键词:lncRNA MEG3;miR-7-5p;鼻咽癌细胞系;辐射敏感度;细胞凋亡
{"title":"Effect of lncRNA MEG3 on radiosensitivity of nasopharyngeal carcinoma cells by down-regulating miR-7-5p expression","authors":"Xujuan Sun, Lifang Sun, M. Yu, Ying Li, Mingyan Li, Ke Yang, Yujie Li, G. Xing, Q. Han","doi":"10.3760/CMA.J.ISSN.1004-4221.2020.03.011","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1004-4221.2020.03.011","url":null,"abstract":"Objective \u0000To investigate the effect and underlying mechanism of lncRNA MEG3 on the radiosensitivity of nasopharyngeal carcinoma cells. \u0000 \u0000 \u0000Methods \u0000this experiment, overexpression control group, MEG3 overexpression group, miR-NC inhibition group, miR-7-5p inhibition group, overexpression control+ 4 Gy group, MEG3 overexpression+ 4 Gygroup, miR-NC inhibition+ 4 Gy group, miR-7-5p inhibition+ 4 Gy group, MEG3 overexpression+ miR-NC overexpression group, MEG3 overexpression+ miR-7-5p overexpression group were established. The expression of miR-7-5p and MEG3 was detected by qRT-PCR. The radiosensitivity of nasopharyngeal carcinoma cells was measured by clone formation assay. Cell apoptosis was assessed by flow cytometry. The fluorescence activity was evaluated by dual luciferase reporter assay. \u0000 \u0000 \u0000Results \u0000MEG3 was lowly expressed in nasopharyngeal carcinoma tissues and cells. Overexpression of MEG3 and inhibition of miR-7-5p expression increased the radiosensitivity of nasopharyngeal carcinoma cells and promoted radiation-induced cell apoptosis. MEG3 could targetedly regulate the miR-7-5p expression. Overexpression of miR-7-5p reversed the effect of overexpression of MEG3 on the sensitization of nasopharyngeal carcinoma cells and the promotion of apoptosis induced by radiation exposure. \u0000 \u0000 \u0000Conclusions \u0000Overexpression of MEG3 increases the radiosensitivity of nasopharyngeal carcinoma cells and promotes radiation-induced cell apoptosis. The mechanism may be related to the down-regulation of miR-7-5p expression. \u0000 \u0000 \u0000Key words: \u0000lncRNA MEG3; miR-7-5p; Nasopharyngeal carcinoma cell line; Radiosensitivity; Apoptosis","PeriodicalId":10288,"journal":{"name":"Chinese Journal of Radiation Oncology","volume":"29 1","pages":"207-210"},"PeriodicalIF":0.0,"publicationDate":"2020-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46671389","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
Study of the feasibility of needle path optimization in 3D brachytherapy for cervical cancer 宫颈癌三维近距离放射治疗中针路优化可行性研究
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.013
Xiang Chen, Jianliang Zhou, Xiang-hua Zhang, Binbing Wang
Objective To compare the dosimetric differences between free-hand method and virtually optimized method for implanting needles in intracavitary and interstitial combined brachytherapy (IC/IS BT) of cervical cancer, and to explore the improvement space of the existing interstitial brahcytherapy plan. Methods High-dose-rate cervical cancer IC/IS BT plans (short for Treatment-Plan) of 18 cases were retrospectively analyzed. For each treatment plan, Nucletron Oncentra 3D brachytherapy planning system was utilized to redesign the virtually optimized insertion method IC/IS BT plan (short for Optimized-Plan). Dose volume histogram was adopted to evaluate the dose distribution in high-risk clinical target areas and exposure dose to organ at risk (OAR). The plan execution efficiency between two plans was also assessed. Results Comparing these two plans, the differences in conformity and uniformity of dose distribution of the target area were statistically significant (P=0.000, 0.008). The differences of D0.01 cm3, D1 cm3, D2 cm3 and D5 cm3 in bladder, rectum, sigmoid and small bowel were all statistically significant (all P<0.05). Optimized-Plan could reduce the D2 cm3 of bladder, rectum, sigmoid and small bowel by 60.41, 36.43, 27.53 and 12.43 cGy, respectively. The execution time for the Treatment-Plan and Optimized-Plan were (857.92±243.39) s and (804.53±239.13) s with statistical significance (P<0.001). Conclusions Compared with the free-hand method, virtually optimized method yields more conformable coverage of the target area and more uniform dose distribution. At the same time, the doses of each OAR are reduced to different degrees and the execution time of the plan is also shortened. Key words: Cervical neoplasm/brachytherapy; Interstitial implant; Intracavitary irradiation
目的比较癌症腔内和间质联合近距离放射治疗(IC/IS-BT)中自由手法与虚拟优化法的剂量差异,探讨现有间质内放疗方案的改进空间。方法回顾性分析18例癌症高部位IC/IS BT方案(简称治疗方案)的临床资料。对于每个治疗计划,Nucletron Oncentra 3D近距离放射治疗计划系统被用于重新设计虚拟优化的插入方法IC/IS BT计划(优化计划的缩写)。采用剂量-体积直方图评估高危临床靶区的剂量分布和对危险器官的暴露剂量(OAR)。还评估了两个计划之间的计划执行效率。结果比较两种方案,靶区剂量分布的一致性和均匀性差异有统计学意义(P=0.000,0.008)。膀胱、直肠、乙状结肠和小肠D0.01 cm3、D1 cm3、D2 cm3和D5 cm3的差异均有统计学意义(均P<0.05),乙状结肠和小肠分别增加60.41、36.43、27.53和12.43cGy。治疗方案和优化方案的执行时间分别为(857.92±243.39)s和(804.53±239.13)s,具有统计学意义(P<0.001)。同时,每个OAR的剂量都不同程度地减少,计划的执行时间也缩短了。关键词:宫颈肿瘤/近距离放射治疗;间质植入物;腔内照射
{"title":"Study of the feasibility of needle path optimization in 3D brachytherapy for cervical cancer","authors":"Xiang Chen, Jianliang Zhou, Xiang-hua Zhang, Binbing Wang","doi":"10.3760/CMA.J.ISSN.1004-4221.2020.03.013","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1004-4221.2020.03.013","url":null,"abstract":"Objective \u0000To compare the dosimetric differences between free-hand method and virtually optimized method for implanting needles in intracavitary and interstitial combined brachytherapy (IC/IS BT) of cervical cancer, and to explore the improvement space of the existing interstitial brahcytherapy plan. \u0000 \u0000 \u0000Methods \u0000High-dose-rate cervical cancer IC/IS BT plans (short for Treatment-Plan) of 18 cases were retrospectively analyzed. For each treatment plan, Nucletron Oncentra 3D brachytherapy planning system was utilized to redesign the virtually optimized insertion method IC/IS BT plan (short for Optimized-Plan). Dose volume histogram was adopted to evaluate the dose distribution in high-risk clinical target areas and exposure dose to organ at risk (OAR). The plan execution efficiency between two plans was also assessed. \u0000 \u0000 \u0000Results \u0000Comparing these two plans, the differences in conformity and uniformity of dose distribution of the target area were statistically significant (P=0.000, 0.008). The differences of D0.01 cm3, D1 cm3, D2 cm3 and D5 cm3 in bladder, rectum, sigmoid and small bowel were all statistically significant (all P<0.05). Optimized-Plan could reduce the D2 cm3 of bladder, rectum, sigmoid and small bowel by 60.41, 36.43, 27.53 and 12.43 cGy, respectively. The execution time for the Treatment-Plan and Optimized-Plan were (857.92±243.39) s and (804.53±239.13) s with statistical significance (P<0.001). \u0000 \u0000 \u0000Conclusions \u0000Compared with the free-hand method, virtually optimized method yields more conformable coverage of the target area and more uniform dose distribution. At the same time, the doses of each OAR are reduced to different degrees and the execution time of the plan is also shortened. \u0000 \u0000 \u0000Key words: \u0000Cervical neoplasm/brachytherapy; Interstitial implant; Intracavitary irradiation","PeriodicalId":10288,"journal":{"name":"Chinese Journal of Radiation Oncology","volume":"29 1","pages":"215-219"},"PeriodicalIF":0.0,"publicationDate":"2020-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"43008388","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
Daily quality control data analysis and process evaluation of linear accelerator 直线加速器日常质量控制数据分析及工艺评价
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.014
Xiaoli Jin, Ying Lu, Qinying Shi, Lin Hao, Xiaofen Xing
Objective To analyze the quality control data of linear accelerator detected by Daily QA3 and to evaluate this quality control process using statistical process control. Methods After the calibrations of the accelerator and Daily QA3, Daily QA3 device was used to perform daily quality control by technicians and physicists and 100 groups and 30 groups of daily quality control data were collected. After the accelerator and Daily QA3 were re-calibrated, Daily QA3 device was utilized to perform daily quality control by technicians and 100 groups of the daily quality control data were repeatedly collected. The variations of normalized signal-to-noise ratio of quality control data collected after two calibrations were analyzed. The first 30 groups of daily quality control data measured by technicians and physicists were adopted to calculate the I-MR control chartsand compare the location of CL and the range of UCL and LCL. The process capability indices were calculated for three different quality control processes bytechnicians and physicists, respectively. Results For twice calibrations, normalized signal-to-noise ratio of quality control data significantly changed before 6 weeks, became stable between 6 and 8 weeks, and the changes became smaller after 8 weeks. For dose output measured by physicists, the rang of UCL and LCL was more narrow. In terms of flatness and symmetry, the location of CL was closer to zero. Regarding dose output and flatness, the process capability indices of three different quality control process were all satisfied ≥1, whereas unsatisfied for transverse symmetry. Conclusions The first 30-40 data points should be adopted to delineate I-MR control chart of the linear accelerator in daily quality control process. The quality control process should be completed by a fixed and small group of personnel and an optimal tolerance level should be customized. Key words: Linear accelerator; Quality control; Statistical process control; Control chart; Process capability index
目的分析Daily QA3检测直线加速器的质量控制数据,并应用统计过程控制方法对直线加速器的质量控制过程进行评价。方法在对加速器和Daily QA3进行标定后,由技术人员和物理学家利用Daily QA3装置进行日常质控,收集100组和30组日常质控数据。加速器和Daily QA3重新校准后,由技术人员利用Daily QA3装置进行日常质控,重复采集100组日常质控数据。分析了两次标定后质控数据归一化信噪比的变化规律。采用技术人员和物理学家测量的前30组日常质量控制数据计算I-MR控制图,并比较CL的位置以及UCL和LCL的范围。分别由技术人员和物理人员计算了三种不同质量控制过程的过程能力指标。结果两次校准后,质控数据的归一化信噪比在6周前有显著变化,在6 ~ 8周间趋于稳定,8周后变化变小。对于物理学家测量的剂量输出,UCL和LCL的范围较窄。在平整度和对称性方面,CL的位置更接近于零。在剂量输出和平整度方面,3种不同质量控制工艺的工艺能力指标均满足≥1,而横向对称性不满足。结论在日常质量控制过程中,应采用前30-40个数据点划定直线加速器的I-MR控制图。质量控制过程应由固定的小团队人员完成,并应定制最佳公差水平。关键词:直线加速器;质量控制;统计过程控制;控制图;过程能力指数
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引用次数: 0
Prospective phase II study of postoperative concurrent chemoradiotherapy for patients with high-risk malignant salivary gland tumors 高危涎腺恶性肿瘤患者术后同期放化疗的前瞻性II期研究
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.002
Xin Wang, S. Dou, Rongrong Li, Si-cheng Wu, Gang Chen, Lin Zhang, Wenjun Yang, G. Zhu
Objective To assess the efficacy and safety of post operative adjuvant concurrent chemoradiotherapy for patients with high-risk salivary gland tumors (SGT). Methods Fifty-two patients with moderate or high malignant pathological stage complicated with locally advanced stage Ⅲ/ⅣA±positive margin/close margin admitted to Shanghai Ninth People′s Hospital from 2016 to 2018 were enrolled in this study. Among them, 35 patients were male and 17 female with a median age of 55.5 years old (range: 21-73 years old). All 52 patients were treated with intensity-modulated radiotherapy and concurrent chemotherapy. Patients with adeno carcinoma of the salivary gland receives concurrent chemotherapy with TP regimen. Patients with lympho epithelial cancer and squamous cell carcinoma were treated with cisplatin regimen. Results Forty-seven patients (90%) completed two cycles of concurrent chemotherapy, and five patients (10%) completed one cycle of concurrent chemotherapy. The median follow-up time was 15.7 months (3.2-34.8 months). The 2-year disease-free survival (DFS) and overall survival (OS) rates were 74% and 98%. Three patients experienced regional lymph recurrence and 6 cases had distant metastasis. Grade Ⅲ oral mucositis was observed in 30 patients. Grade Ⅲ dermatitis occurred in 5 cases. Only one patient experienced Grade IV neutropenia, and 2 patients developed Grade Ⅲ neutropenia. DFS was positively correlated with the cycle of postoperative adjuvant concurrent chemotherapy (P=0.006). Conclusions Patients with high-risk SGT can obtain higher 2-year DFS and OS rates and tolerable adverse events after postoperative concurrent chemoradiotherapy. Nevertheless, the long-term outcomes remain to be validated by randomized controlled clinical trials. Key words: High-risk salivary gland tumor; Postoperative adjuvant; Concurrent chemoradiotherapy; Prospective study
目的评价高危涎腺肿瘤(SGT)患者术后辅助同步放化疗的疗效和安全性。方法选取2016 - 2018年上海市第九人民医院收治的中高恶性病理分期合并局部晚期Ⅲ/ⅣA±阳性切缘/闭合切缘患者52例。其中男性35例,女性17例,中位年龄55.5岁(范围21 ~ 73岁)。52例患者均行调强放疗和同期化疗。涎腺腺癌患者同时接受TP方案化疗。淋巴上皮癌和鳞状细胞癌患者采用顺铂方案治疗。结果47例患者(90%)完成2个周期的同步化疗,5例患者(10%)完成1个周期的同步化疗。中位随访时间15.7个月(3.2 ~ 34.8个月)。2年无病生存率(DFS)和总生存率(OS)分别为74%和98%。局部淋巴复发3例,远处转移6例。30例患者发生Ⅲ级口腔黏膜炎。5例发生Ⅲ级皮炎。只有1例患者出现了IV级中性粒细胞减少,2例患者出现了Ⅲ级中性粒细胞减少。DFS与术后辅助同步化疗周期呈正相关(P=0.006)。结论高危SGT患者术后同步放化疗可获得较高的2年DFS和OS率及可耐受的不良事件。然而,长期结果仍有待随机对照临床试验的验证。关键词:高危唾液腺肿瘤;术后辅助;同步放化疗;前瞻性研究
{"title":"Prospective phase II study of postoperative concurrent chemoradiotherapy for patients with high-risk malignant salivary gland tumors","authors":"Xin Wang, S. Dou, Rongrong Li, Si-cheng Wu, Gang Chen, Lin Zhang, Wenjun Yang, G. Zhu","doi":"10.3760/CMA.J.ISSN.1004-4221.2020.03.002","DOIUrl":"https://doi.org/10.3760/CMA.J.ISSN.1004-4221.2020.03.002","url":null,"abstract":"Objective \u0000To assess the efficacy and safety of post operative adjuvant concurrent chemoradiotherapy for patients with high-risk salivary gland tumors (SGT). \u0000 \u0000 \u0000Methods \u0000Fifty-two patients with moderate or high malignant pathological stage complicated with locally advanced stage Ⅲ/ⅣA±positive margin/close margin admitted to Shanghai Ninth People′s Hospital from 2016 to 2018 were enrolled in this study. Among them, 35 patients were male and 17 female with a median age of 55.5 years old (range: 21-73 years old). All 52 patients were treated with intensity-modulated radiotherapy and concurrent chemotherapy. Patients with adeno carcinoma of the salivary gland receives concurrent chemotherapy with TP regimen. Patients with lympho epithelial cancer and squamous cell carcinoma were treated with cisplatin regimen. \u0000 \u0000 \u0000Results \u0000Forty-seven patients (90%) completed two cycles of concurrent chemotherapy, and five patients (10%) completed one cycle of concurrent chemotherapy. The median follow-up time was 15.7 months (3.2-34.8 months). The 2-year disease-free survival (DFS) and overall survival (OS) rates were 74% and 98%. Three patients experienced regional lymph recurrence and 6 cases had distant metastasis. Grade Ⅲ oral mucositis was observed in 30 patients. Grade Ⅲ dermatitis occurred in 5 cases. Only one patient experienced Grade IV neutropenia, and 2 patients developed Grade Ⅲ neutropenia. DFS was positively correlated with the cycle of postoperative adjuvant concurrent chemotherapy (P=0.006). \u0000 \u0000 \u0000Conclusions \u0000Patients with high-risk SGT can obtain higher 2-year DFS and OS rates and tolerable adverse events after postoperative concurrent chemoradiotherapy. Nevertheless, the long-term outcomes remain to be validated by randomized controlled clinical trials. \u0000 \u0000 \u0000Key words: \u0000High-risk salivary gland tumor; Postoperative adjuvant; Concurrent chemoradiotherapy; Prospective study","PeriodicalId":10288,"journal":{"name":"Chinese Journal of Radiation Oncology","volume":"29 1","pages":"166-170"},"PeriodicalIF":0.0,"publicationDate":"2020-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41475213","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
Preliminary exploration of 3D printed individualized applicator for 3D-image-guided intracavitary HDR-brachytherapy for nasopharyngeal carcinoma 3D打印个性化应用器在三维图像引导下鼻咽癌腔内HDR近距离治疗中的初步探索
Pub Date : 2020-03-15 DOI: 10.3760/CMA.J.ISSN.1004-4221.2020.03.012
Yi-Qiang Tang, L. Zeng, Fan Ao, Yulu Liao, Min Huang, Shulan Chen, Xiaowei Rao, Jingao Li
Objective To explore the feasibility of 3D printed individualized applicator for the intracavitary HDR-brachytherapy for nasopharyngeal carcinoma. Methods CT scan was performed in 1 case of recurrent rT1 nasopharyngeal carcinoma and 1 case of T2 residual nasopharyngeal carcinoma and the obtained images were transmitted to 3D image processing software. The geometric contour parameters of the nasopharyngeal cavity were obtained and a pipeline was designed to make it close to the recurrent gross tumor volume (rGTV). Individualized cavity applicators were created by using 3D printer. The applicator was inserted into the patient′s nasopharyngeal cavity through oral cavity. The source tube and false source were inserted into the preset pipe of the applicator. CT scan was performed again and the images were transmitted to the 3D brachytherapy planning system. After delineating the target volume and organ at risk, treatment plan was optimized. After completing the first treatment, the applicator was removed. Before second treatment in a few days, CT scan was reviewed to confirm whether the position was correct. Results When the applicator was inserted into the nasopharyngeal cavity, it could be fully aligned with the nasopharyngeal wall and self-fixed without additional fixation measures. Comparing the location of false source in multiple reviews of CT scan, the error was ≤1 mm. No significant discomfort was reported throughout the treatment. In optimized three-dimensional treatment, 100% prescription dose curve included the full rGTV, maximum dose of the brain stem and spinal cord was<30% prescription dose. Recurrent patients were given with a prescription dose of DT 40Gy/8 fractions/4 weeks and patients with residual tumors were given with 12Gy/2 fractions/1 week. No tumor recurrence was observed at postoperative 3 months in two cases. Conclusions The 3D printed individualized nasopharyngeal intracavitary applicator has the advantages of self-fixation, accurate location, good repeatability and good patient tolerance. The short-term outcome is effective, whereas its long-term clinical effect and adverse reactions need to be further observed. Key words: 3D printed; Individualized applicator; Nasopharyngeal neoplasm/intracavitary radiotherapy
目的探讨3D打印个性化治疗器用于鼻咽癌腔内HDR近距离治疗的可行性。方法对1例复发性rT1鼻咽癌和1例T2残留鼻咽癌进行CT扫描,并将获得的图像传输到3D图像处理软件中。获得鼻咽腔的几何轮廓参数,并设计管道使其接近复发总肿瘤体积(rGTV)。使用3D打印机制作了个性化的空腔喷头。涂抹器通过口腔插入患者的鼻咽腔。将源管和假源插入涂抹器的预设管中。再次进行CT扫描,并将图像传输到3D近距离放射治疗计划系统。在划定目标体积和危险器官后,对治疗方案进行了优化。在完成第一次治疗后,移除施用器。在几天后进行第二次治疗之前,复查CT扫描以确认位置是否正确。结果将敷贴器插入鼻咽腔后,可与鼻咽壁完全对齐并自行固定,无需额外的固定措施。在CT扫描的多次复查中比较假源的位置,误差≤1mm。在整个治疗过程中没有明显的不适报告。在优化的三维治疗中,100%处方剂量曲线包括全rGTV,脑干和脊髓的最大剂量<30%处方剂量。复发患者给予DT 40Gy/8组分/4周的处方剂量,残留肿瘤患者给予12Gy/2组分/1周。两例术后3个月未发现肿瘤复发。结论3D打印个性化鼻咽腔内涂抹器具有自固定、定位准确、重复性好、患者耐受性好的优点。短期结果是有效的,但其长期临床效果和不良反应需要进一步观察。关键词:3D打印;个性化涂抹器;鼻咽肿瘤/腔内放射治疗
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中华放射肿瘤学杂志
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