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The Intensity Modulated Radiotherapy vs . the 3D-Conformal Radiotherapy Regarding Acute Radiation Skin Toxicity and TreatmentRelated Lymphopenia in Early-Stage Breast Cancer Patients 调强放疗vs。早期乳腺癌患者急性放射皮肤毒性及治疗相关淋巴细胞减少的3d适形放疗
Pub Date : 2019-04-16 DOI: 10.4172/2155-9619.1000401
Osama H Elzaafarany, E. Ali, S. Fadel, A. Kandil
Adjuvant radiotherapy is an integral part of breast cancer treatment, and there was a great evolution of radiotherapy techniques over the past few years. Intensity-modulated radiation therapy (IMRT) was developed in the 1990s as a modern technique aiming to spare normal tissues from toxic effects of radiotherapy. This study aimed at comparing the IMRT technique to the 3D-coformal radiotherapy technique (3D-CRT) in early breast cancer patients regarding the occurrence of acute skin toxicities and treatment-related lymphopenia (TRL). It is a prospective study conducted on 100 eligible patients who were divided equally between two groups; the first, are patients received adjuvant radiotherapy using IMRT technique and the second group were those who received 3D-CRT. Results showed that sever acute skin toxicity or moist desquamation in IMRT group was 6% vs. 18% in 3DCRT group (p<0.05). And, the sever TRL with IMRT technique was 9% compared 21% among those of the 3D-CRT group (p<0.05). The IMRT technique resulted in statistically significant lower incidence of sever acute skin toxicities as well as less sever TRL when compared with 3D-CRT technique.
辅助放疗是乳腺癌治疗中不可缺少的一部分,在过去的几年里,放疗技术有了很大的发展。调强放射治疗(IMRT)是20世纪90年代发展起来的一种现代技术,旨在使正常组织免受放射治疗的毒性影响。本研究旨在比较IMRT技术与3D-CRT技术在早期乳腺癌患者急性皮肤毒性和治疗相关性淋巴细胞减少症(TRL)发生方面的差异。这是一项对100名符合条件的患者进行的前瞻性研究,这些患者平均分为两组;第一组为接受IMRT辅助放疗的患者,第二组为接受3D-CRT的患者。结果IMRT组严重急性皮肤毒性或湿性脱屑率为6%,3DCRT组为18% (p<0.05)。IMRT组严重TRL发生率为9%,3D-CRT组为21% (p<0.05)。与3D-CRT技术相比,IMRT技术导致严重急性皮肤毒性发生率降低,严重TRL发生率降低,具有统计学意义。
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引用次数: 0
Stereotactic Ablative Body Radiotherapy in Non-small Cell Carcinoma Lung in Elderly: Initial Experience from a Rural Tertiary Cancer Centre 立体定向消融体放疗治疗老年人非小细胞肺癌:来自农村三级肿瘤中心的初步经验
Pub Date : 2019-03-26 DOI: 10.4172/2155-9619.1000398
N. Vinin, Joneetha Jones, M. Geetha, N. Yahiya, Shoaib Nawaz Pn, A. Narendran, Greeshma Ke, D. NidhinRa, R. Bharathan
Aim: The aim of this study was to evaluate the efficacy and outcome of early stage non-small cell lung carcinoma in elderly patients treated with SABR in a tertiary care cancer centre in rural India. Materials and methods: This was a retrospective study. All cases of histopathologically proven, stage 1 lung cancer patients in whom surgical management was not feasible due to various reasons were included. It included patients treated from 2013 to 2018 at our centre. Case records and radiation treatment plans were reviewed and data was collected. All were T1/T2N0 cases. Dose schedules employed were 48 Gy in 4 fractions, 60 Gy in 5 fractions and 60 Gy in 3 fractions. The primary end point was the tolerance and toxicity profile. Results: A total of 5 patients were treated at our center from 2013 to 2017. All were males. Mean age was 72 years. One had squamous cell and four had adenocarcinoma histology. The dose fractionation schedules employed where 48 Gy in 4 fractions, 60 Gy in 5 fractions and 60 Gy in 3 fractions. All tolerated treatment well. No grade 3 or 4 toxicities were observed. Conclusion: SABR is a feasible alternative curative treatment modality in stage 1 NSCLC. It is feasible and was tolerated well even in the elderly age group. This can be offered to medically inoperable patients as a curative treatment and is possible in a resource constrained setting also. This modality is a promise to future for operable stage 1 NSCLC also. But more randomized studies need to be carried out before applying it to operable lung cancer patients.
目的:本研究的目的是评估在印度农村三级保健癌症中心接受SABR治疗的早期非小细胞肺癌老年患者的疗效和结果。材料与方法:本研究为回顾性研究。所有经组织病理学证实的1期肺癌患者由于各种原因无法进行手术治疗。它包括2013年至2018年在我们中心接受治疗的患者。回顾病例记录和放射治疗计划并收集数据。均为T1/T2N0病例。剂量表为48 Gy / 4次,60 Gy / 5次,60 Gy / 3次。主要终点是耐受性和毒性。结果:2013 - 2017年我中心共收治5例患者。所有人都是男性。平均年龄72岁。1例为鳞状细胞癌,4例为腺癌。所采用的剂量分级方案是48 Gy分为4份,60 Gy分为5份,60 Gy分为3份。所有人都能很好地耐受治疗。未见3级或4级毒性反应。结论:SABR是1期非小细胞肺癌的一种可行的替代治疗方式。它是可行的,即使在老年人中也能很好地耐受。这可以作为一种治愈性治疗提供给医学上不能手术的病人,也可以在资源有限的情况下使用。这种方式对可手术的1期非小细胞肺癌也是一种承诺。但在将其应用于可手术的肺癌患者之前,还需要进行更多的随机研究。
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引用次数: 0
Portal Dosimetry for Pre-treatment Verification of Imrt/Vmat Plan: A Comparison with 2D Array Detector for Quality Assurance 入口剂量法用于Imrt/Vmat计划的前处理验证:与2D阵列检测器质量保证的比较
Pub Date : 2018-03-16 DOI: 10.4172/2155-9619.1000359
Ayman G Mohamed, Ismail E. Mohamed, H. M. Zidan
Purpose: The present study is to investigate the measured and calculated doses for different malignant tumours utilizing various gamma criteria and QA for confirmation of IMRT/VMAT with portal dosimetry and 2D array. Methods: Different malignant tumors are treated by IMRT/VMAT techniques on Varian IX linear accelerator with 6 MV photon beams. Treatment planning system (TPS) is used to plan Patient’s charts. Gamma Index (GI) variation is compared to the procedure of pre-treatment verification in IMRT/VMAT plans. Results: The gamma criteria (DD/ DTA) of IMRT for (3%/3 mm), mean ± SD are γ≤ 1%=99.41% ± 0.67%, γmax=2.11 ± 0.56 and γavg=0.23 ± 0.03 by EPID, and γ% ≤ 1=98.55% ± 0.79%, γmax=1.65 ± 0.45 and γavg=0.27 ± 0.04 by using 2D array. For VMAT mean ± SD are γ% ≤ 1= 99.42% ± 0.67%, γmax=2.11 ± 0.56 and γavg= 0.19 ± 0.05 using portal dosimetry, and γ% ≤ 1=99.36% ± 0.53%, γmax=1.65 ± 0.45 and γavg=0.22 ± 0.05 using 2D array. Conclusions: Specific QA of IMRT/VMAT patient using (portal dosimetry or 2D array) to verify IMRT/VMAT fields. 3%/3 mm is the most appropriate of gamma criteria (DD/DTA) for IMRT/VMAT plans quality assurance. The control chart is an effective tool to detect uncontrolled variation.
目的:本研究利用不同的伽玛标准和QA对不同恶性肿瘤的测量和计算剂量进行研究,以确定门静脉剂量学和二维阵列的IMRT/VMAT。方法:采用IMRT/VMAT技术,在瓦里安IX型直线加速器上以6 MV光子束治疗不同类型恶性肿瘤。治疗计划系统(TPS)用于规划患者的图表。将Gamma指数(GI)变化与IMRT/VMAT计划的治疗前验证程序进行比较。结果:IMRT的γ标准(DD/ DTA)为(3%/3 mm), EPID的平均±SD为γ≤1%=99.41%±0.67%,γmax=2.11±0.56,γavg=0.23±0.03,二维阵列的γ%≤1=98.55%±0.79%,γmax=1.65±0.45,γavg=0.27±0.04。门脉剂量法测量VMAT平均值±SD为γ%≤1= 99.42%±0.67%,γmax=2.11±0.56,γavg= 0.19±0.05;二维阵列测量VMAT平均值±SD为γ%≤1=99.36%±0.53%,γmax=1.65±0.45,γavg=0.22±0.05。结论:IMRT/VMAT患者的特异性QA使用(门脉剂量法或二维阵列)来验证IMRT/VMAT场。3%/ 3mm是最适合IMRT/VMAT计划质量保证的伽马标准(DD/DTA)。控制图是检测非受控变化的有效工具。
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引用次数: 1
Technological Development, Clinical Application, Quality Assurance and Dosimetric Validation of Volumetric Modulated Arc Therapy (VMAT): A Comprehensive Literature Review 容积调节电弧疗法(VMAT)的技术发展、临床应用、质量保证和剂量学验证:综合文献综述
Pub Date : 2018-03-16 DOI: 10.4172/2155-9619.S9-003
C. P. Bhatt, I. Ahmad, M. Semwal, K. Chufal
Volumetric Modulated Arc Therapy (VMAT) is a recently developed technology which, similar to Intensity Modulated Radiotherapy (IMRT), utilizes optimization algorithms to find an acceptable solution. VMAT optimization algorithms are more complex and resource intensive than IMRT algorithms, as the former have to account for many more variables including machine-specific limitations. VMAT is distinguished from traditional fixed-beam IMRT in that radiation is delivered while the gantry rotates around the patient. It is a significant advancement over fixed gantry angle IMRT in terms of the efficiency of delivery of desired complex dose distributions (dose painting) in modern-day radiotherapy. The purpose of this review is to discuss the technological development, clinical applications and quality assurance of VMAT.
体积调制弧线治疗(VMAT)是一项新开发的技术,类似于强度调制放疗(IMRT),利用优化算法找到可接受的解决方案。VMAT优化算法比IMRT算法更复杂,资源更密集,因为前者必须考虑更多变量,包括机器特定的限制。VMAT与传统的固定光束IMRT的区别在于,放射是在龙门架围绕患者旋转时传递的。在现代放射治疗中,就所需复杂剂量分布(剂量涂绘)的递送效率而言,它是固定门门角IMRT的重大进步。本文就VMAT的技术发展、临床应用及质量保证进行综述。
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引用次数: 1
Neoadjuvant Radiotherapy of Early-Stage and Locally Advanced Breast Cancer: Review of the Literature 早期和局部晚期乳腺癌的新辅助放疗:文献综述
Pub Date : 2018-03-08 DOI: 10.4172/2155-9619.1000357
A. Maghous, E. Marnouche, N. Zaghba, K. Andaloussi, M. Elmarjany, K. Hadadi, H. Sifat, R. Moussaoui, H. Mansouri
Breast cancer is the most frequently diagnosed cancer type among women worldwide. The treatment of breast cancer is multimodal and the current standard approach is surgery followed by adjuvant radiotherapy (RT) based on prognostic scores. Neoadjuvant chemotherapy and RT delivered in advance of surgery are used in some early stage and locally advanced cases, may offer an advantage over adjuvant therapy related to the potential benefits in the pathologic response and survival outcomes based the hypothesis of Abscopal effect.
乳腺癌是全世界女性中最常见的癌症类型。乳腺癌的治疗是多模式的,目前的标准方法是手术后辅助放疗(RT)基于预后评分。在一些早期和局部晚期病例中,手术前给予新辅助化疗和放疗可能比辅助治疗在病理反应和生存结果方面具有潜在的优势,基于Abscopal效应的假设。
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引用次数: 3
Comparison of Unblocked, Directionally Blocked and Full Blocked Plans in Helical Tomotherapy for Breast Cancer Radiotherapy 非阻断、定向阻断和完全阻断方案在乳腺癌放疗螺旋层析治疗中的比较
Pub Date : 2018-03-08 DOI: 10.4172/2155-9619.1000358
E. Kucuktulu, A. F. Yurekli, Eray Bilcan, Mahmut Serdar Sisecioglu, M. Topbaş, U. Kucuktulu
Introduction: The doses received by the contralateral breast, lung and heart either directionally or full blocked techniques in Hi-Art Tomotherapy systems in partial or whole breast radiotherapy has been studied. Method: In 20 breast cancer patients 3 plans with non-blocked, directionally blocked and full blocked methods were designed in Hi-Art planning system. In all planning method the dose received by the contralateral breast, the heart volume percentages V5 and V30 and the lung volume percentages V5 and V20 were compared. Results: The mean doses received by contralateral breast were 6.24 Gy (4.50-8.74 Gy) in unblocked group 3.85 Gy (2.08-5.81 Gy) in directionally blocked group and 0.99 Gy (0.69-1.39 Gy) in full blocked group. The mean Lung V5 values were 98% (79-100%) in unblocked group and it was 98% (91-100%) in directionally blocked group while it was 93% (89-97%) in full blocked group. The mean V20 values were 16% (7-23%), 20% (17-24%) and 22% (18-28%) in unblocked, directionally blocked and full blocked groups respectively. The mean Heart V5 value 100% (99-100%) in unblocked group, and it was 99% (85-100%) in directionally blocked group while it was 92% (73- 100%) in full blocked group. The mean V30 values were 11% (2-25%), 6% (0-12%) and 9% (1-22%) in unblocked, directionally blocked and full blocked groups respectively. The mean beam-on time was 261.6 s (237.6-318.2) for unblocked, 277.9 s (237.6-338.5) for directionally blocked and 314.2 s (272.6-429.1) full blocked group. The mean numbers of MUs were 3712 (3353-4536) for unblocked, 3951 (3357-4834) for directionally blocked and 4506 (3866- 6168) for full blocked group. In full blocked group both beam on time and MU values were higher. Conclusion: We propose that further efforts needed to reduce low dose volumes to normal tissues, meanwhile when using directionally and full blocked plans all parameters should be considered together.
简介:研究了Hi-Art断层治疗系统中对侧乳腺、肺和心脏定向或全阻断技术在部分或全乳房放疗中的剂量。方法:对20例乳腺癌患者在Hi-Art计划系统中设计无阻断、定向阻断和全阻断3种方案。在所有计划方法中,比较对侧乳房接受的剂量、心脏容积百分比V5和V30以及肺容积百分比V5和V20。结果:未阻断组对侧乳腺接受的平均剂量为6.24 Gy (4.50 ~ 8.74 Gy),定向阻断组为3.85 Gy (2.08 ~ 5.81 Gy),完全阻断组为0.99 Gy (0.69 ~ 1.39 Gy)。无阻断组肺V5平均值为98%(79 ~ 100%),定向阻断组肺V5平均值为98%(91 ~ 100%),完全阻断组肺V5平均值为93%(89 ~ 97%)。未阻断组、定向阻断组和完全阻断组的平均V20值分别为16%(7-23%)、20%(17-24%)和22%(18-28%)。无阻断组心脏V5平均值为100%(99 ~ 100%),定向阻断组为99%(85 ~ 100%),完全阻断组为92%(73 ~ 100%)。未阻断组、定向阻断组和完全阻断组的平均V30值分别为11%(2 ~ 25%)、6%(0 ~ 12%)和9%(1 ~ 22%)。未阻断组平均光照时间261.6 s(237.6 ~ 318.2),定向阻断组平均光照时间277.9 s(237.6 ~ 338.5),完全阻断组平均光照时间314.2 s(272.6 ~ 429.1)。未阻断组平均有3712个(3353 ~ 4536个),定向阻断组平均有3951个(3357 ~ 4834个),完全阻断组平均有4506个(3866 ~ 6168个)。完全阻断组的波束时间和MU值均较高。结论:我们建议进一步减少正常组织的低剂量体积,同时在使用定向和全阻断方案时应综合考虑各项参数。
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引用次数: 0
Dosimetric Comparison of a-Si 1200 and a-Si 1000 Electronic Portal Imager for Intensity Modulated Radiation Therapy (IMRT) 调强放射治疗(IMRT)中a- si1200和a- si1000电子门脉成像仪剂量学比较
Pub Date : 2018-02-20 DOI: 10.4172/2155-9619.1000354
V. Mhatre, S. Pilakkal, P. Chadha, Kaustav Talpatra
Aim: This study investigates the dosimetric impact of a-Si 1200 over a-Si 1000 portal imager for 6 MV photon beam of a Varian Amorphous Silicon Electronic Portal Imaging Device (a-Si EPID) installed on Edge and Novalis TxLinac. Materials and Methods: The performance of an a-Si EPID 1200 was assessed and compared to its performance with a-Si EPID 1000 and dose measurements using an ionization chamber. This study was conducted for 6MV photon energy and the EPID performance was assessed as function of the delivered dose, dose rate, field size, SDD effect, Ghosting effect, Backscatter arm shielding impact and intensity-modulated radiation therapy fields. Results: The dose response for a-Si 1200 was within 0.5% for low MU (2-10) as compared to 1.4% for a-Si 1000 portal imager and less than 1% for both the imager above 10 MU. The output factor variation for 25 × 25 cm2 was 1.3% for a-Si 1200 and 3.8% for a-Si 1000 when compared with ionisation chamber. The ghosting was measured to be 0.2% for a-Si 1200 as compared to 0.8% for a-Si 1000 portal imager. There is a significant improvement in a-Si 1200 portal image due to backscatter shielding material attached to the back of the panel of a-Si 1200 portal imager. Conclusion: The new aS1200 detector showed a significant dosimetric improvement when compared with previous aS1000 hence providing more accurate measurements for pre-treatment patient specific Quality Assurance (QA).
目的:研究安装在Edge和Novalis TxLinac上的瓦里安非晶硅电子传送门成像装置(a- si EPID)的6 MV光子束中,a- si 1200对a- si 1000传送门成像仪的剂量学影响。材料和方法:评估了a-Si epid1200的性能,并将其与a-Si epid1000的性能和使用电离室的剂量测量进行了比较。本研究以6MV光子能量为研究对象,通过传递剂量、剂量率、场大小、SDD效应、重影效应、后向散射臂屏蔽冲击和调强放疗场的函数来评估EPID的性能。结果:低MU(2-10)时,a-Si 1200的剂量反应在0.5%以内,而a-Si 1000门静脉成像仪的剂量反应为1.4%,10 MU以上的剂量反应均小于1%。与电离室相比,25 × 25 cm2的a-Si 1200输出因子变化为1.3%,a-Si 1000输出因子变化为3.8%。经测量,a-Si 1200的重影率为0.2%,而a-Si 1000的重影率为0.8%。由于在a- si 1200传送门成像仪面板背面附加了后向散射屏蔽材料,使得a- si 1200传送门成像有了明显的改善。结论:与以前的aS1000相比,新的aS1200检测仪显示出显著的剂量学改进,因此为治疗前患者特异性质量保证(QA)提供了更准确的测量。
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引用次数: 6
Both Percent Diameter Stenosis (%DS) and Coronary Flow Reserve (CFR) can be Derived Directly from Myocardial Perfusion Imaging (MPI) using FMTVDM © ℗ and Measurement of Isotope Redistribution 使用FMTVDM可以直接从心肌灌注成像(MPI)中得出百分比直径狭窄(%DS)和冠状动脉血流储备(CFR)©©and Measurement of Isotope Redistribution
Pub Date : 2018-02-13 DOI: 10.4172/2155-9619.1000353
R. M. Fleming, M. Fleming, T. Chaudhuri, A. McKusick, W. Dooley, Charles Glover
Background: Scientifically published studies have demonstrated that all isotopes, including Sestamibi redistribute. Measurement of this redistribution using FMTVDM©℗ provides an accurate method for determining wash-in and washout. Methods: Using FMTVDM©℗ 1040 human coronary arteries were studied to determine their wash-in and washout redistribution measured on a pixel-by-pixel basis. From FMTVDM©℗ the percent diameter stenosis (%DS) for each artery was determined. This %DS was then used to calculate coronary flow reserve (Calculated SFR) using a proprietary quadratic equation (QCFR©, FCFR©) previously derived from quantitative coronary arteriography (QCA) measurements. These calculated CFR values were then compared with the actual measured CFR obtained directly from QCA. Results: The results of the calculated CFR from FMTVDM©℗ with that obtained by direct QCA measurement showed a regression analysis of y= (0.8758•x)+0.4291, where y=the QCFR© and x=the QCA measured CFR. The R2 value (coefficient of determination) for this demonstrated a strong relationship at 0.87582. Conclusions: The use of the FMTVDM©℗ for measurement of isotope redistribution, including Sestamibi, provides an accurate quantitative method for determining both redistribution wash-in and redistribution washout, from which %DS can be calculated on a pixel-by-pixel basis. This %DS can then be used with the proprietary equation (QCFR©, FCFR©) to calculate the CFR directly from the MPI result using FMTVDM©℗. The implementation of this power tool, will provide for additional determination of the physiological effect of CAD without requiring additional QCA equipment and expertise costs, making QCFR© possible in most if not all hospitals with nuclear medicine departments.
背景:科学发表的研究表明,包括Sestamibi在内的所有同位素都存在再分布。使用FMTVDM©©对这种再分配进行测量,提供了一种确定冲洗和冲洗的准确方法。方法:使用FMTVDM©©1040对人类冠状动脉进行研究,以逐像素测量其洗入和洗出再分布。从FMTVDM©©确定各动脉直径狭窄百分比(%DS)。然后使用先前由定量冠状动脉造影(QCA)测量得出的专有二次方程(QCFR©,FCFR©),使用%DS计算冠状动脉血流储备(计算SFR)。然后将计算出的CFR值与直接从QCA获得的实际测量CFR进行比较。结果:FMTVDM©©©计算的CFR与QCA直接测量结果的回归分析结果为y=(0.8758•x)+0.4291,其中y= QCFR©,x= QCA测量的CFR。R2值(决定系数)在0.87582显示了很强的关系。结论:使用FMTVDM©©用于测量同位素再分布,包括Sestamibi,提供了一种精确的定量方法来确定再分布水洗和再分布水洗,从中可以逐像素计算%DS。这个%DS可以与专有方程(QCFR©,FCFR©)一起使用,使用FMTVDM©©直接从MPI结果计算CFR。这一电动工具的实施将提供对CAD生理效应的额外确定,而不需要额外的QCA设备和专业知识成本,使QCFR©在大多数(如果不是全部的话)拥有核医学部门的医院成为可能。
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引用次数: 13
Evaluation of Hepatocellular Carcinomas and Liver Metastases- How Far can we Go with Diffusion Weighted Imaging? 肝细胞癌和肝转移的评估-弥散加权成像能走多远?
Pub Date : 2017-12-24 DOI: 10.4172/2155-9619.1000351
Gozde Arslan, E. Inci
Objective: We aimed to determine the usefulness of the apparent diffusion coefficient (ADC) values for the differential diagnosis of hepatocellular carcinomas and most common metastatic liver tumors and we aimed to compare the characteristic properties. We also aimed to detect novel lesions on ADC maps before the lesion is clinically and radiologically detected by conventional methods. Materials and Methods: We evaluated characteristic properties, contrast enhancement patterns of liver metastasis of malignancies like adenocancer, renal cell carcinoma (RCC), gastrointestinal stromal tumor (GIST) and hepatocellular carcinoma (HCC) on magnetic resonance imaging (MRI) and diffusion weighted (DW) imaging. ADCs were measured both from the cystic and solid parts of the tumoral lesions. Solid and cystic parts were grouped seperately and compared individually. Results: 48 cases, (60% male and 40% female) with ages ranging between 48 and 81 were involved. 28 of them had liver metastasis and 20 of them had HCC. MRIs between the years 2009 and 2012 were analyzed. Among mean ADC values measured from solid contrast-enhancing parts, values of the HCC group were significantly higher than the metastasis group (p=0.004). Also, in metastasis group consisting of many distinct primaries, there were differences in ADC values. A retrospective analysis for follow-up cases showed that the ADC values of the parencyhma where a lesion will appear on later follow-up images were lower than the adjacent parenchyma. Conclusion: We believe that this method may be useful to detect early metastasis. Studies with larger patient groups could give more significant results which would enable diffusion imaging method to be used in this area.
目的:我们旨在确定表观扩散系数(ADC)值在肝细胞癌和大多数常见转移性肝肿瘤鉴别诊断中的有效性,并比较其特征特征。我们还旨在在常规方法检测到临床和放射学病变之前,在ADC图上发现新的病变。材料和方法:我们对腺癌、肾细胞癌(RCC)、胃肠道间质瘤(GIST)和肝细胞癌(HCC)等恶性肿瘤的肝转移特征、磁共振成像(MRI)和扩散加权成像(DW)的增强模式进行了评估。adc从肿瘤病变的囊性部分和实性部分测量。实性部分和囊性部分分别分组,单独比较。结果:48例患者,男性60%,女性40%,年龄48 ~ 81岁。其中肝转移28例,HCC 20例。分析了2009年至2012年的核磁共振成像。在实体增强部分测量的平均ADC值中,HCC组显著高于转移组(p=0.004)。此外,在多个不同原发灶组成的转移组中,ADC值存在差异。对随访病例的回顾性分析显示,在随后的随访图像中,出现病变的实质的ADC值低于相邻的实质。结论:该方法可用于肿瘤早期转移的检测。对更大的患者群体进行研究可以得到更有意义的结果,这将使扩散成像方法在该领域得到应用。
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引用次数: 1
The Development of FMTVDM-BEST IMAGING©℗: The Answer for Breast Cancer. Breast Enhanced Scintigraphy Test (BEST©℗): Quantifying the Detection of Breast Cancer and its Treatment. FMTVDM-BEST成像技术的发展©©:乳腺癌的答案。乳腺增强闪烁成像试验(BEST©©):量化乳腺癌的检测及其治疗。
Pub Date : 2017-12-18 DOI: 10.4172/2155-9619.1000350
R. M. Fleming, W. Dooley, T. Chaudhuri
Background: The diagnostic testing for breast cancer has been limited by the absence of a method, which can quantitatively differentiate tissue differences; specifically differentiation between calcium deposits, normal breast tissue, inflammatory changes in breast tissue and breast cancer. Such a quantitative method would remove the issue of sensitivity and specificity errors and allow for diagnostic decision-making including treatment monitoring. Method: A series of investigations were conducted over an 18-year period of time looking at more than 1000 women and men suspected of having breast tissue abnormalities. The studies compared pathologic tissue results with outcomes using other diagnostic studies and FMTVDM-BEST©℗ Imaging. The studies began with asking the fundamental questions necessary to produce such a quantitative diagnostic test, followed by correcting for errors encountered by other methods. Following the initial work comparing FMTVDM-BEST©℗ Imaging with other tests and tissue pathology results, the investigations turned to monitoring changes in women over time, demonstrating the ability to monitor treatment results from surgery, chemotherapy, radiation therapy, immune therapy, diet and lifestyle changes. Further work was conducted to assure that the time within a woman’s cycle did not affect FMTVDM-BEST©℗ Imaging. The next series of studies looked at the effect that soy protein, smoking and hormone treatment (HRT) had on breast tissue health and the relationship between breast cancer and these influences. The summation of all of these studies included looking at breast density and breast implants as well as male patients. Results: FMTVDM-BEST©℗ Imaging quantitatively differentiates between breast calcium deposits, normal breast tissue, inflammatory changes and breast cancer. It can monitor transitions in tissue showing both the progression and regression of disease allowing clinicians to monitor treatment outcomes independent of the treatment approach used. FMTVDM-BEST©℗ Imaging is not affected by breast density, breast implants, mastectomy or size of breast; including male patients. : FMTVDM-BEST©℗ Imaging provides the first and only quantitative method, which can differentiate tissues based upon changes in measurements obtained from this patented method. As such, it can detect changes in tissue leading to breast cancer allowing for greater treatment opportunities, as well as monitoring outcomes of treatment for breast cancer and other abnormalities (e.g. fibrocystic disease). FMTVDM-BEST©℗ Imaging works independent of whether the patient has dense breast tissue, breast implants, is on HRT, smokes or has undergone previous treatment in both men and women.
背景:由于缺乏一种定量区分组织差异的方法,乳腺癌的诊断测试一直受到限制;特别是区分钙沉积,正常乳腺组织,乳腺组织炎症变化和乳腺癌。这种定量方法将消除敏感性和特异性错误的问题,并允许包括治疗监测在内的诊断决策。方法:在18年的时间里,对1000多名怀疑患有乳腺组织异常的女性和男性进行了一系列调查。研究将病理组织结果与其他诊断研究和FMTVDM-BEST结果进行了比较©©Imaging。这些研究首先提出了产生这种定量诊断测试所必需的基本问题,然后纠正了其他方法遇到的错误。在将FMTVDM-BEST©©©Imaging与其他测试和组织病理学结果进行比较的初步工作之后,调查转向监测妇女随时间的变化,证明有能力监测手术、化疗、放射治疗、免疫治疗、饮食和生活方式改变的治疗结果。进一步的工作是为了确保女性月经周期内的时间不影响FMTVDM-BEST©©Imaging。接下来的一系列研究着眼于大豆蛋白、吸烟和激素治疗(HRT)对乳腺组织健康的影响,以及乳腺癌与这些影响之间的关系。所有这些研究的总和包括观察乳房密度和乳房植入物以及男性患者。结果:FMTVDM-BEST©©Imaging定量区分乳腺钙沉积,正常乳腺组织,炎症变化和乳腺癌。它可以监测组织中的转变,显示疾病的进展和消退,使临床医生能够监测治疗结果,而不依赖于所使用的治疗方法。FMTVDM-BEST©©影像不受乳房密度、乳房植入物、乳房切除术或乳房大小的影响;包括男性患者。: FMTVDM-BEST©©Imaging提供了第一个也是唯一的定量方法,可以根据从该专利方法中获得的测量值的变化来区分组织。因此,它可以检测导致乳腺癌的组织变化,从而提供更多的治疗机会,并监测乳腺癌和其他异常(例如纤维囊性疾病)的治疗结果。FMTVDM-BEST©©成像工作独立于患者是否有致密的乳房组织,乳房植入物,正在接受激素替代疗法,吸烟或之前接受过治疗的男性和女性。
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引用次数: 11
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Journal of Nuclear Medicine and Radiation Therapy
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