The cuttable C-related genotype and allele for the E-cadherin 3 '-UTR Pml I polymorphism are associated with higher susceptibility to endometriosis

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Title:	The cuttable C-related genotype and allele for the E-cadherin 3 '-UTR Pml I polymorphism are associated with higher susceptibility to endometriosis
Authors:	Hsieh, YY;Chang, CC;Tsai, FJ;Hsu, CM;Lin, CC;Tsai, CH
Contributors:	附設醫院兒科部;China Med Univ Hosp, Dept Pediat & Med Genet, Taichung, Taiwan;China Med Univ Hosp, Dept Obstet & Gynecol, Taichung, Taiwan;China Med Univ Hosp, Dept Family Med, Taichung, Taiwan;Natl Chiao Tung Univ, Dept Biol Sci & Technol, Hsinchu, Taiwan;Taichung Hlth Care & Management Univ, Taichung, Taiwan
Date:	2005
Issue Date:	2010-09-24 14:28:10 (UTC+8)
Publisher:	SOC BRASIL GENETICA
Abstract:	This study compared the target volume coverage and normal tissues sparing of simultaneous integrated boost (SIB-IMRT, 1-phase) and sequential-IMRT (2-phase) for nasopharyngeal carcinoma (NPC). Fourteen consecutive patients with newly diagnosed primary NPC were enrolled in this study. The CT images were transferred to a commercial planning system for structural delineation. The gross tumor volume (GTV) included gross nasopharyngeal tumor and involved lymph nodes of more than 1-cm diameter. The clinical target volume (CTV) modeled two regions considered to represent different risks. CTV1 encompassed the GTV with 5-10-mm margin of adjacent tissues. CTV2 encompassed ipsilateral or contralateral elective nodal regions at risk of harboring microscopic tumor. A commercial IMRT treatment planning system (Eclipse Version 7.1) was used to provide treatment planning. Seven fixed-gantry (0 degrees, 50 degrees, 100 degrees, 150 degrees, 210 degrees, 260 degrees, 310 degrees) angles were designated. The 14 patients were treated with sequential-IMRT, and treatment was then replanned with an SIB strategy to compare the dosimetric difference. For the sequential strategy, the dose delivered to CTV1/CTV2 in the first course was 54 Gy (1.8 Gy X 30 Fr); while CTV1 was boosted by an additional 16.2 Gy (1.8 Gy X 9 Fr) in the second course. For SIB-IMRT, the dose prescribed to CTV1 was 69.7 Gy (2.05 Gy X 34 Fr); 56.1 Gy was given to CTV2 (1.65 Gy X 34 Fr). A statistical analysis of the dose-volume-histogram of target volumes and critical organs was performed. Paired Student's t-test was used to compare the dosimetric differences between the two techniques. The mean dose to CTV1 was 101.7 +/- 2.4% and 102.3 +/- 3.1% of the prescribed dose for SIB-IMRT and sequential-IMRT, respectively. The mean CTV2 dose was 109.8 +/- 4.7% of the prescribed dose for SIB-IMRT and 112.6 +/- 6.0% of the prescribed dose for sequential-IMRT. The maximal dose to the spinal cord was 4489 +/- 495 cGy and 3547 +/- 767 cGy for SIB and sequential-IMRT (p = 0.0001), respectively. The maximal dose to brain stem was significantly higher using SIB technique (5284 +/- 551 cGy) than sequential-IMRT (4834 +/- 388 cGy) (p = 0.0001). The mean dose to the parotid gland and ear apparatus was significantly lower using SIB-IMRT. The mean dose to the right/left parotids was 2865 +/- 320 cGy/2903 +/- 429 cGy and 3567 +/- 534 cGy/3476 +/- 489 cGy for SIB and sequential-IMRT, respectively (p = 0.0001). Target coverage was the same for both techniques; the dose distribution in the elective nodal area with SIB was superior to that with sequential-IMRT. SIB-IMRT provides better sparing of parotid gland and inner ear structures. Extra caution should be taken when applying SIB-IMRT since critical organs close to the boost volume may receive higher doses. (c) 2005 American Association of Medical Dosimetrists.
Relation:	GENETICS AND MOLECULAR BIOLOGY 28(4):661-664
Appears in Collections:	[China Medical University Hospital] Jurnal articles

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