目的利用Compass三维验证系统对乳腺癌保乳术后调强放射治疗计划进行剂量验证,研究其影响因素并进行分类分析。方法选择乳腺癌保乳放射治疗女性患者20例,年龄45~74岁,中位年龄59岁;侧别,左侧10例,右侧10例。用Compass系统进行计划剂量验...目的利用Compass三维验证系统对乳腺癌保乳术后调强放射治疗计划进行剂量验证,研究其影响因素并进行分类分析。方法选择乳腺癌保乳放射治疗女性患者20例,年龄45~74岁,中位年龄59岁;侧别,左侧10例,右侧10例。用Compass系统进行计划剂量验证,包括独立核算验证和实测重建剂量验证;将Monaco计划系统蒙卡算法计算的剂量(MCD)、Compass卷积/超分割算法独立核算剂量(CCD)和Compass实测重建剂量(CRD)三者之间两两剂量验证结果进行两两比较(CCD-MCD、CRD-CCD、CRD-MCD),比较参数包括靶区剂量最大限值10%生成区域的γ结果及剂量体积直方图(DVH)结果。结果CRD-MCD与CRD-CCD的γ通过率和平均γ值差异均有统计学意义[(95.23±2.38)%vs(96.33±2.72)%、(94.78±2.56)%vs(95.97±2.95)%、0.41±0.04 vs 0.37±0.04、0.42±0.04 vs 0.38±0.04。P<0.05],CRD-MCD与CCD-MCD的γ通过率和平均γ值差异也均有统计学意义[(95.23±2.38)%vs(99.29±0.46)%、(94.78±2.56)%vs(99.26±0.46)%、0.41±0.04 vs 0.26±0.03、0.42±0.04 vs 0.27±0.03。P<0.05],CRD-CCD与CCD-MCD的γ通过率和平均γ值差异也均有统计学意义[(96.33±2.72)%vs(99.29±0.46)%、(95.97±2.95)%vs(99.26±0.46)%、0.37±0.04 vs 0.26±0.03、0.38±0.04 vs 0.27±0.03。P<0.05]。计划肿瘤靶区(PGTV)的D_(98%)和计划靶区(PTV)的D_(mean)、健侧乳腺的D_(mean)、V5和患侧肺的V20、V30的剂量体积相对偏差在CRD-MCD与CRD-CCD比较,差异有统计学意义[(2.01±1.27)%vs(2.60±1.05)%、(2.84±0.55)%vs(2.55±0.71)%、(-11.15±7.87)%vs(-18.29±7.91)%、(-1.45±5.45)%vs(-2.76±3.83)%、(-0.85±0.36)%vs(-0.65±0.23)%、(-0.56±0.37)%vs(-0.38±0.27)%。P<0.05]。PGTV的D98%、D_(2%)、D_(mean),PTV的D_(98%)、D_(2%)、D_(mean),心脏的D_(mean)、健侧乳腺的D_(mean)、V_(5),健侧肺的V_(5)和患侧肺的V_(5)、V_(20)、V_(30)的剂量体积相对偏差在CRD-MCD与CCD-MCD比较,差异均有统计学意义[(2.01±1.27)%vs(-0.51±0.54)%、(2.86±1.22)%vs(-0.002±0.92)%、(2.63±0.75)%vs(-0.19±0.40)%、(2.17±0.82)%vs(0.38±1.01)%、(2.81±0.95)%vs(-0.17±0.70)%、(2.84±0.55)%vs(0.29±0.43)%、(-17.39±7.79)%vs(0.87±3.30)%、(-11.15±7.87)%vs(9.27±4.87)%、(-1.45±5.45)%vs(2.01±1.30)%、(-0.24±0.80)%vs(0.01±0.04)%、(-4.60±0.87)%vs(0.27±0.59)%、(-0.85±0.36)%vs(-0.21±0.21)%、(-0.56±0.37)%vs(-0.22±1.34)%。P<0.05]。PGTV的D_(98%)、D_(2%)、D_(mean),PTV的D_(98%)、D_(2%)、D_(mean),心脏的D_(mean)、健侧乳腺的D_(mean)、V_(5),健侧肺的V_(5)和患侧肺的V5、V20、V30的剂量体积相对偏差在CRD-CCD与CCD-MCD比较,差异均有统计学意义[(2.60±1.05)%vs(-0.51±0.54)%、(2.88±1.12)%vs(-0.002±0.92)%、(2.83±0.68)%vs(-0.19±0.40)%、(1.81±0.90)%vs(0.38±1.01)%、(2.87±0.82)%vs(-0.17±0.70)%、(2.55±0.71)%vs(0.29±0.43)%、(-18.10±7.40)%vs(0.87±3.30)%、(-18.29±7.91)%vs(9.27±4.81)%、(-2.76±3.83)%vs(2.01±1.30)%、(-0.25±0.81)%vs(0.01±0.04)%、(-4.90±1.03)%vs(0.27±0.59)%、(-0.65±0.23)%vs(-0.21±0.21)%、(0.38±0.27)%vs(-0.22±1.34)%。P<0.05]。结论不同算法在高剂量区、低剂量区和肺等组织密度比较大或者含空腔的组织中计算精度偏差更加显著;机器的稳定性状态对剂量差异亦有影响。展开更多
OBJECTIVE It has been supposed that mast cells have important participation in the physiopathology of RA,however,the role of mast cells in the pathogenesis of RA remains unclear.In this study,we observed the antiapopt...OBJECTIVE It has been supposed that mast cells have important participation in the physiopathology of RA,however,the role of mast cells in the pathogenesis of RA remains unclear.In this study,we observed the antiapoptotic effects of tryptase released by mast cell on RA synovial fibroblasts.METHODS Mast cells and fibroblasts synovial were obtained from mouse.Chemical mediator release was assessed by measuringβ-hexosa-minidase release.TSCS and bone marrow-derived mast cells were co-cultured;the toxic effects of TSCS on mast cell was measured by MTT and CCK-8 method;the releasing amount of tryptase in cell supernatants was measured by Elisa assay;the expression of FLS cell membrane receptor PAR-2 was detected by flow cytometry;the apoptosis of FLS cell was detected through flow cytometry and Western blotting;the level of activated Rho-GTP was detected by the pull-down method and Western blotting.RESULTS In this study,we observed the antiapoptotic effects of tryptase released by mast cell on RA synovial fibroblasts,and found that tryptase significantly increased the expression of PAR-2 on the surface of fibroblast-like synovial cell,significantly activated Rho kinase,significantly inhibited apoptosis of fibroblast-like synovial cell induced by CH11.The release rates ofβ-hexosaminidase and the level of tryptase from bone marrow-derived mast cells after stimulation with different antigen and co-cultured with TSCS significantly decreased compared to the control group.In the co-culture system of mast cells and fibroblast-like synovial cells,TSCS treatment significantly inhibited Rho kinase(P<0.05),significantly promoted apoptosis of fibroblast-like synovial cell induced by CH11(P<0.05).CONCLUSION These results demonstrate that tryptase may play a key role in the physiopathology of RA.TSCS can inhibit mast cells activation and promote FLS cells apoptosis.This provide theoretical and experimental basis for the study of mast cells as targets for new anti-RA drugs.展开更多
文摘目的利用Compass三维验证系统对乳腺癌保乳术后调强放射治疗计划进行剂量验证,研究其影响因素并进行分类分析。方法选择乳腺癌保乳放射治疗女性患者20例,年龄45~74岁,中位年龄59岁;侧别,左侧10例,右侧10例。用Compass系统进行计划剂量验证,包括独立核算验证和实测重建剂量验证;将Monaco计划系统蒙卡算法计算的剂量(MCD)、Compass卷积/超分割算法独立核算剂量(CCD)和Compass实测重建剂量(CRD)三者之间两两剂量验证结果进行两两比较(CCD-MCD、CRD-CCD、CRD-MCD),比较参数包括靶区剂量最大限值10%生成区域的γ结果及剂量体积直方图(DVH)结果。结果CRD-MCD与CRD-CCD的γ通过率和平均γ值差异均有统计学意义[(95.23±2.38)%vs(96.33±2.72)%、(94.78±2.56)%vs(95.97±2.95)%、0.41±0.04 vs 0.37±0.04、0.42±0.04 vs 0.38±0.04。P<0.05],CRD-MCD与CCD-MCD的γ通过率和平均γ值差异也均有统计学意义[(95.23±2.38)%vs(99.29±0.46)%、(94.78±2.56)%vs(99.26±0.46)%、0.41±0.04 vs 0.26±0.03、0.42±0.04 vs 0.27±0.03。P<0.05],CRD-CCD与CCD-MCD的γ通过率和平均γ值差异也均有统计学意义[(96.33±2.72)%vs(99.29±0.46)%、(95.97±2.95)%vs(99.26±0.46)%、0.37±0.04 vs 0.26±0.03、0.38±0.04 vs 0.27±0.03。P<0.05]。计划肿瘤靶区(PGTV)的D_(98%)和计划靶区(PTV)的D_(mean)、健侧乳腺的D_(mean)、V5和患侧肺的V20、V30的剂量体积相对偏差在CRD-MCD与CRD-CCD比较,差异有统计学意义[(2.01±1.27)%vs(2.60±1.05)%、(2.84±0.55)%vs(2.55±0.71)%、(-11.15±7.87)%vs(-18.29±7.91)%、(-1.45±5.45)%vs(-2.76±3.83)%、(-0.85±0.36)%vs(-0.65±0.23)%、(-0.56±0.37)%vs(-0.38±0.27)%。P<0.05]。PGTV的D98%、D_(2%)、D_(mean),PTV的D_(98%)、D_(2%)、D_(mean),心脏的D_(mean)、健侧乳腺的D_(mean)、V_(5),健侧肺的V_(5)和患侧肺的V_(5)、V_(20)、V_(30)的剂量体积相对偏差在CRD-MCD与CCD-MCD比较,差异均有统计学意义[(2.01±1.27)%vs(-0.51±0.54)%、(2.86±1.22)%vs(-0.002±0.92)%、(2.63±0.75)%vs(-0.19±0.40)%、(2.17±0.82)%vs(0.38±1.01)%、(2.81±0.95)%vs(-0.17±0.70)%、(2.84±0.55)%vs(0.29±0.43)%、(-17.39±7.79)%vs(0.87±3.30)%、(-11.15±7.87)%vs(9.27±4.87)%、(-1.45±5.45)%vs(2.01±1.30)%、(-0.24±0.80)%vs(0.01±0.04)%、(-4.60±0.87)%vs(0.27±0.59)%、(-0.85±0.36)%vs(-0.21±0.21)%、(-0.56±0.37)%vs(-0.22±1.34)%。P<0.05]。PGTV的D_(98%)、D_(2%)、D_(mean),PTV的D_(98%)、D_(2%)、D_(mean),心脏的D_(mean)、健侧乳腺的D_(mean)、V_(5),健侧肺的V_(5)和患侧肺的V5、V20、V30的剂量体积相对偏差在CRD-CCD与CCD-MCD比较,差异均有统计学意义[(2.60±1.05)%vs(-0.51±0.54)%、(2.88±1.12)%vs(-0.002±0.92)%、(2.83±0.68)%vs(-0.19±0.40)%、(1.81±0.90)%vs(0.38±1.01)%、(2.87±0.82)%vs(-0.17±0.70)%、(2.55±0.71)%vs(0.29±0.43)%、(-18.10±7.40)%vs(0.87±3.30)%、(-18.29±7.91)%vs(9.27±4.81)%、(-2.76±3.83)%vs(2.01±1.30)%、(-0.25±0.81)%vs(0.01±0.04)%、(-4.90±1.03)%vs(0.27±0.59)%、(-0.65±0.23)%vs(-0.21±0.21)%、(0.38±0.27)%vs(-0.22±1.34)%。P<0.05]。结论不同算法在高剂量区、低剂量区和肺等组织密度比较大或者含空腔的组织中计算精度偏差更加显著;机器的稳定性状态对剂量差异亦有影响。
基金The project supported by National Natural Science Foundation of China(81274166,81673665)Project in Hubei Province Department of Education(B20101201)+1 种基金Yichang City Technology Bureau Project(2010A01301-04)China Three Gorges University Research Fund(0620080702)
文摘OBJECTIVE It has been supposed that mast cells have important participation in the physiopathology of RA,however,the role of mast cells in the pathogenesis of RA remains unclear.In this study,we observed the antiapoptotic effects of tryptase released by mast cell on RA synovial fibroblasts.METHODS Mast cells and fibroblasts synovial were obtained from mouse.Chemical mediator release was assessed by measuringβ-hexosa-minidase release.TSCS and bone marrow-derived mast cells were co-cultured;the toxic effects of TSCS on mast cell was measured by MTT and CCK-8 method;the releasing amount of tryptase in cell supernatants was measured by Elisa assay;the expression of FLS cell membrane receptor PAR-2 was detected by flow cytometry;the apoptosis of FLS cell was detected through flow cytometry and Western blotting;the level of activated Rho-GTP was detected by the pull-down method and Western blotting.RESULTS In this study,we observed the antiapoptotic effects of tryptase released by mast cell on RA synovial fibroblasts,and found that tryptase significantly increased the expression of PAR-2 on the surface of fibroblast-like synovial cell,significantly activated Rho kinase,significantly inhibited apoptosis of fibroblast-like synovial cell induced by CH11.The release rates ofβ-hexosaminidase and the level of tryptase from bone marrow-derived mast cells after stimulation with different antigen and co-cultured with TSCS significantly decreased compared to the control group.In the co-culture system of mast cells and fibroblast-like synovial cells,TSCS treatment significantly inhibited Rho kinase(P<0.05),significantly promoted apoptosis of fibroblast-like synovial cell induced by CH11(P<0.05).CONCLUSION These results demonstrate that tryptase may play a key role in the physiopathology of RA.TSCS can inhibit mast cells activation and promote FLS cells apoptosis.This provide theoretical and experimental basis for the study of mast cells as targets for new anti-RA drugs.
