1.Simultaneous Viability Assessment and Invasive Coronary Angiography Using a Therapeutic CT System in Chronic Myocardial Infarction Patients
Seongmin HA ; Yeonggul JANG ; Byoung Kwon LEE ; Youngtaek HONG ; Byeong-Keuk KIM ; Seil PARK ; Sun Kook YOO ; Hyuk-Jae CHANG
Yonsei Medical Journal 2024;65(5):257-264
		                        		
		                        			 Purpose:
		                        			In a preclinical study using a swine myocardial infarction (MI) model, a delayed enhancement (DE)-multi-detector computed tomography (MDCT) scan was performed using a hybrid system alongside diagnostic invasive coronary angiography (ICA) without the additional use of a contrast agent, and demonstrated an excellent correlation in the infarct area compared with histopathologic specimens. In the present investigation, we evaluated the feasibility and diagnostic accuracy of a myocardial viability assessment by DE-MDCT using a hybrid system comprising ICA and MDCT alongside diagnostic ICA without the additional use of a contrast agent. 
		                        		
		                        			Materials and Methods:
		                        			We prospectively enrolled 13 patients (median age: 67 years) with a previous MI (>6 months) scheduled to undergo ICA. All patients underwent cardiac magnetic resonance (CMR) imaging before diagnostic ICA. MDCT viability scans were performed concurrently with diagnostic ICA without the use of additional contrast. The total myocardial scar volume per patient and average transmurality per myocardial segment measured by DE-MDCT were compared with those from DE-CMR. 
		                        		
		                        			Results:
		                        			The DE volume measured by MDCT showed an excellent correlation with the volume measured by CMR (r=0.986, p<0.0001). The transmurality per segment by MDCT was well-correlated with CMR (r=0.900, p<0.0001); the diagnostic performance of MDCT in differentiating non-viable from viable myocardium using a 50% transmurality criterion was good with a sensitivity, specificity, positive predictive value, negative predictive value, and accuracy of 87.5%, 99.5%, 87.5%, 99.5%, and 99.1%, respectively. 
		                        		
		                        			Conclusion
		                        			The feasibility of the DE-MDCT viability assessment acquired simultaneously with conventional ICA was proven in patients with chronic MI using DE-CMR as the reference standard. 
		                        		
		                        		
		                        		
		                        	
2.Epidemiologic and Clinical Outcomes of Pediatric Renal Tumors in Korea: A Retrospective Analysis of The Korean Pediatric Hematology and Oncology Group (KPHOG) Data
Kyung-Nam KOH ; Jung Woo HAN ; Hyoung Soo CHOI ; Hyoung Jin KANG ; Ji Won LEE ; Keon Hee YOO ; Ki Woong SUNG ; Hong Hoe KOO ; Kyung Taek HONG ; Jung Yoon CHOI ; Sung Han KANG ; Hyery KIM ; Ho Joon IM ; Seung Min HAHN ; Chuhl Joo LYU ; Hee-Jo BAEK ; Hoon KOOK ; Kyung Mi PARK ; Eu Jeen YANG ; Young Tak LIM ; Seongkoo KIM ; Jae Wook LEE ; Nack-Gyun CHUNG ; Bin CHO ; Meerim PARK ; Hyeon Jin PARK ; Byung-Kiu PARK ; Jun Ah LEE ; Jun Eun PARK ; Soon Ki KIM ; Ji Yoon KIM ; Hyo Sun KIM ; Youngeun MA ; Kyung Duk PARK ; Sang Kyu PARK ; Eun Sil PARK ; Ye Jee SHIM ; Eun Sun YOO ; Kyung Ha RYU ; Jae Won YOO ; Yeon Jung LIM ; Hoi Soo YOON ; Mee Jeong LEE ; Jae Min LEE ; In-Sang JEON ; Hye Lim JUNG ; Hee Won CHUEH ; Seunghyun WON ;
Cancer Research and Treatment 2023;55(1):279-290
		                        		
		                        			 Purpose:
		                        			Renal tumors account for approximately 7% of all childhood cancers. These include Wilms tumor (WT), clear cell sarcoma of the kidney (CCSK), malignant rhabdoid tumor of the kidney (MRTK), renal cell carcinoma (RCC), congenital mesoblastic nephroma (CMN) and other rare tumors. We investigated the epidemiology of pediatric renal tumors in Korea. 
		                        		
		                        			Materials and Methods:
		                        			From January 2001 to December 2015, data of pediatric patients (0–18 years) newly-diagnosed with renal tumors at 26 hospitals were retrospectively analyzed. 
		                        		
		                        			Results:
		                        			Among 439 patients (male, 240), the most common tumor was WT (n=342, 77.9%), followed by RCC (n=36, 8.2%), CCSK (n=24, 5.5%), MRTK (n=16, 3.6%), CMN (n=12, 2.7%), and others (n=9, 2.1%). Median age at diagnosis was 27.1 months (range 0-225.5) and median follow-up duration was 88.5 months (range 0-211.6). Overall, 32 patients died, of whom 17, 11, 1, and 3 died of relapse, progressive disease, second malignant neoplasm, and treatment-related mortality. Five-year overall survival and event free survival were 97.2% and 84.8% in WT, 90.6% and 82.1% in RCC, 81.1% and 63.6% in CCSK, 60.3% and 56.2% in MRTK, and 100% and 91.7% in CMN, respectively (p < 0.001). 
		                        		
		                        			Conclusion
		                        			The pediatric renal tumor types in Korea are similar to those previously reported in other countries. WT accounted for a large proportion and survival was excellent. Non-Wilms renal tumors included a variety of tumors and showed inferior outcome, especially MRTK. Further efforts are necessary to optimize the treatment and analyze the genetic characteristics of pediatric renal tumors in Korea. 
		                        		
		                        		
		                        		
		                        	
3.Distalization with a modified C-palatal plate for severe upper crowding and a missing lower incisor
Jae Hyun PARK ; Traci SAITO ; Sun Kyong YOO ; Mohammed ALFAIFI ; Yoon Ah KOOK
The Korean Journal of Orthodontics 2020;50(1):52-62
		                        		
		                        			
		                        			 This case report presents the orthodontic treatment of a 25-year-old patient with skeletal Class II and severe maxillary arch crowding, moderate mandibular arch crowding, anterior crossbite, and a missing lower incisor. He was treated with molar distalization using a modified C-palatal plate and temporary anchorage devices to create sufficient space for retraction. The total treatment duration was 21 months. After treatment, his occlusion and smile esthetics showed significant improvement. The modified C-palatal plate represents a treatment modality that enhances the prospects of non-extraction treatment and reduces the need for extraction. 
		                        		
		                        		
		                        		
		                        	
4.Concurrent Chemoradiotherapy with Temozolomide Followed by Adjuvant Temozolomide for Newly Diagnosed Glioblastoma Patients: A Retrospective Multicenter Observation Study in Korea.
Byung Sup KIM ; Ho Jun SEOL ; Do Hyun NAM ; Chul Kee PARK ; Il Han KIM ; Tae Min KIM ; Jeong Hoon KIM ; Young Hyun CHO ; Sang Min YOON ; Jong Hee CHANG ; Seok Gu KANG ; Eui Hyun KIM ; Chang Ok SUH ; Tae Young JUNG ; Kyung Hwa LEE ; Chae Yong KIM ; In Ah KIM ; Chang Ki HONG ; Heon YOO ; Jin Hee KIM ; Shin Hyuk KANG ; Min Kyu KANG ; Eun Young KIM ; Sun Hwan KIM ; Dong Sup CHUNG ; Sun Chul HWANG ; Joon Ho SONG ; Sung Jin CHO ; Sun Il LEE ; Youn Soo LEE ; Kook Jin AHN ; Se Hoon KIM ; Do Hun LIM ; Ho Shin GWAK ; Se Hoon LEE ; Yong Kil HONG
Cancer Research and Treatment 2017;49(1):193-203
		                        		
		                        			
		                        			PURPOSE: The purpose of this study was to investigate the feasibility and survival benefits of combined treatment with radiotherapy and adjuvant temozolomide (TMZ) in a Korean sample. MATERIALS AND METHODS: A total of 750 Korean patients with histologically confirmed glioblastoma multiforme, who received concurrent chemoradiotherapy with TMZ (CCRT) and adjuvant TMZ from January 2006 until June 2011, were analyzed retrospectively. RESULTS: After the first operation, a gross total resection (GTR), subtotal resection (STR), partial resection (PR), biopsy alone were achieved in 388 (51.7%), 159 (21.2%), 96 (12.8%), and 107 (14.3%) patients, respectively. The methylation status of O6-methylguanine-DNA methyltransferase (MGMT) was reviewed retrospectively in 217 patients. The median follow-up period was 16.3 months and the median overall survival (OS) was 17.5 months. The actuarial survival rates at the 1-, 3-, and 5-year OS were 72.1%, 21.0%, and 9.0%, respectively. The median progression-free survival (PFS) was 10.1 months, and the actuarial PFS at 1-, 3-, and 5-year PFS were 42.2%, 13.0%, and 7.8%, respectively. The patients who received GTR showed a significantly longer OS and PFS than those who received STR, PR, or biopsy alone, regardless of the methylation status of the MGMT promoter. Patients with a methylated MGMT promoter also showed a significantly longer OS and PFS than those with an unmethylated MGMT promoter. Patients who received more than six cycles of adjuvant TMZ had a longer OS and PFS than those who received six or fewer cycles. Hematologic toxicity of grade 3 or 4 was observed in 8.4% of patients during the CCRT period and in 10.2% during the adjuvant TMZ period. CONCLUSION: Patients treated with CCRT followed by adjuvant TMZ had more favorable survival rates and tolerable toxicity than those who did not undergo this treatment.
		                        		
		                        		
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Chemoradiotherapy*
		                        			;
		                        		
		                        			Disease-Free Survival
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Glioblastoma*
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Korea*
		                        			;
		                        		
		                        			Methylation
		                        			;
		                        		
		                        			Radiotherapy
		                        			;
		                        		
		                        			Retrospective Studies*
		                        			;
		                        		
		                        			Survival Rate
		                        			
		                        		
		                        	
5.Texture Analysis of Supraspinatus Ultrasound Image for Computer Aided Diagnostic System.
Byung Eun PARK ; Won Seuk JANG ; Sun Kook YOO
Healthcare Informatics Research 2016;22(4):299-304
		                        		
		                        			
		                        			OBJECTIVES: In this paper, we proposed an algorithm for recognizing a rotator cuff supraspinatus tendon tear using a texture analysis based on a histogram, gray level co-occurrence matrix (GLCM), and gray level run length matrix (GLRLM). METHODS: First, we applied a total of 57 features (5 first order descriptors, 40 GLCM features, and 12 GLRLM features) to each rotator cuff region of interest. Our results show that first order statistics (mean, skewness, entropy, energy, smoothness), GLCM (correlation, contrast, energy, entropy, difference entropy, homogeneity, maximum probability, sum average, sum entropy), and GLRLM features are helpful to distinguish a normal supraspinatus tendon and an abnormal supraspinatus tendon. The statistical significance of these features is verified using a t-test. The support vector machine classification showed accuracy using feature combinations. Support Vector Machine offers good performance with a small amount of training data. Sensitivity, specificity, and accuracy are used to evaluate performance of a classification test. RESULTS: From the results, first order statics features and GLCM and GLRLM features afford 95%, 85%, and 100% accuracy, respectively. First order statistics and GLCM and GLRLM features in combination provided 100% accuracy. Combinations that include GLRLM features had high accuracy. GLRLM features were confirmed as highly accurate features for classified normal and abnormal. CONCLUSIONS: This algorithm will be helpful to diagnose supraspinatus tendon tear on ultrasound images.
		                        		
		                        		
		                        		
		                        			Classification
		                        			;
		                        		
		                        			Data Interpretation, Statistical
		                        			;
		                        		
		                        			Entropy
		                        			;
		                        		
		                        			Image Processing, Computer-Assisted
		                        			;
		                        		
		                        			Rotator Cuff
		                        			;
		                        		
		                        			Sensitivity and Specificity
		                        			;
		                        		
		                        			Subject Headings
		                        			;
		                        		
		                        			Support Vector Machine
		                        			;
		                        		
		                        			Tears
		                        			;
		                        		
		                        			Tendons
		                        			;
		                        		
		                        			Ultrasonography*
		                        			
		                        		
		                        	
6.Characteristics and Outcomes of Second Malignant Neoplasms after Childhood Cancer Treatment: Multi-Center Retrospective Survey.
Kyung Nam KOH ; Keon Hee YOO ; Ho Joon IM ; Ki Woong SUNG ; Hong Hoe KOO ; Hyo Sun KIM ; Jung Woo HAN ; Jong Hyung YOON ; Hyeon Jin PARK ; Byung Kiu PARK ; Hee Jo BAEK ; Hoon KOOK ; Jun Ah LEE ; Jae Min LEE ; Kwang Chul LEE ; Soon Ki KIM ; Meerim PARK ; Young Ho LEE ; Chuhl Joo LYU ; Jong Jin SEO
Journal of Korean Medical Science 2016;31(8):1254-1261
		                        		
		                        			
		                        			This retrospective study investigated the clinical characteristics and outcomes of second malignant neoplasms (SMNs) in survivors of childhood cancer from multiple institutions in Korea. A total of 102 patients from 11 institutions who developed SMN after childhood cancer treatment between 1998 and 2011 were retrospectively enrolled. The most common primary malignant neoplasms (PMNs) were central nervous system (CNS) tumors (n = 17), followed by acute lymphoblastic leukemia (n = 16), non-Hodgkin lymphoma (n = 13), and osteosarcoma (n = 12). The most common SMNs were therapy-related myeloid neoplasms (t-MNs; acute myeloid leukemia [AML], 29 cases; myelodysplastic syndrome [MDS], 12 cases), followed by thyroid carcinomas (n = 15) and CNS tumors (n = 10). The median latency period was 4.9 years (range, 0.5-18.5 years). Among 45 patients with solid tumors defined as an SMN, 15 (33%) developed the lesion in a field previously subjected to radiation. The 5-year overall survival (OS) rate of patients with an SMN was 45% with a median follow-up time of 8.6 years. Patients with AML, MDS, and CNS tumors exhibited the poorest outcomes with 5-year OS rates of 18%, 33%, and 32%, respectively, whereas those with second osteosarcoma showed comparable outcomes (64%) to patients with primary counterpart and those with second thyroid carcinoma had a 100% OS rate. Further therapeutic efforts are recommended to improve the survival outcomes in patients with SMNs, especially in cases with t-MNs and CNS tumors.
		                        		
		                        		
		                        		
		                        			Adolescent
		                        			;
		                        		
		                        			Antineoplastic Agents/therapeutic use
		                        			;
		                        		
		                        			Central Nervous System Neoplasms/diagnosis/drug therapy/radiotherapy
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Child, Preschool
		                        			;
		                        		
		                        			Disease-Free Survival
		                        			;
		                        		
		                        			Hospitals
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Infant
		                        			;
		                        		
		                        			Leukemia, Myeloid, Acute/diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Myelodysplastic Syndromes/diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Neoplasms, Second Primary/*diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Osteosarcoma/diagnosis/epidemiology
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Stem Cell Transplantation
		                        			;
		                        		
		                        			Survival Rate
		                        			;
		                        		
		                        			Transplantation, Autologous
		                        			;
		                        		
		                        			Young Adult
		                        			
		                        		
		                        	
7.Characteristics and Outcomes of Second Malignant Neoplasms after Childhood Cancer Treatment: Multi-Center Retrospective Survey.
Kyung Nam KOH ; Keon Hee YOO ; Ho Joon IM ; Ki Woong SUNG ; Hong Hoe KOO ; Hyo Sun KIM ; Jung Woo HAN ; Jong Hyung YOON ; Hyeon Jin PARK ; Byung Kiu PARK ; Hee Jo BAEK ; Hoon KOOK ; Jun Ah LEE ; Jae Min LEE ; Kwang Chul LEE ; Soon Ki KIM ; Meerim PARK ; Young Ho LEE ; Chuhl Joo LYU ; Jong Jin SEO
Journal of Korean Medical Science 2016;31(8):1254-1261
		                        		
		                        			
		                        			This retrospective study investigated the clinical characteristics and outcomes of second malignant neoplasms (SMNs) in survivors of childhood cancer from multiple institutions in Korea. A total of 102 patients from 11 institutions who developed SMN after childhood cancer treatment between 1998 and 2011 were retrospectively enrolled. The most common primary malignant neoplasms (PMNs) were central nervous system (CNS) tumors (n = 17), followed by acute lymphoblastic leukemia (n = 16), non-Hodgkin lymphoma (n = 13), and osteosarcoma (n = 12). The most common SMNs were therapy-related myeloid neoplasms (t-MNs; acute myeloid leukemia [AML], 29 cases; myelodysplastic syndrome [MDS], 12 cases), followed by thyroid carcinomas (n = 15) and CNS tumors (n = 10). The median latency period was 4.9 years (range, 0.5-18.5 years). Among 45 patients with solid tumors defined as an SMN, 15 (33%) developed the lesion in a field previously subjected to radiation. The 5-year overall survival (OS) rate of patients with an SMN was 45% with a median follow-up time of 8.6 years. Patients with AML, MDS, and CNS tumors exhibited the poorest outcomes with 5-year OS rates of 18%, 33%, and 32%, respectively, whereas those with second osteosarcoma showed comparable outcomes (64%) to patients with primary counterpart and those with second thyroid carcinoma had a 100% OS rate. Further therapeutic efforts are recommended to improve the survival outcomes in patients with SMNs, especially in cases with t-MNs and CNS tumors.
		                        		
		                        		
		                        		
		                        			Adolescent
		                        			;
		                        		
		                        			Antineoplastic Agents/therapeutic use
		                        			;
		                        		
		                        			Central Nervous System Neoplasms/diagnosis/drug therapy/radiotherapy
		                        			;
		                        		
		                        			Child
		                        			;
		                        		
		                        			Child, Preschool
		                        			;
		                        		
		                        			Disease-Free Survival
		                        			;
		                        		
		                        			Hospitals
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Infant
		                        			;
		                        		
		                        			Leukemia, Myeloid, Acute/diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Myelodysplastic Syndromes/diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Neoplasms, Second Primary/*diagnosis/epidemiology/mortality/therapy
		                        			;
		                        		
		                        			Osteosarcoma/diagnosis/epidemiology
		                        			;
		                        		
		                        			Retrospective Studies
		                        			;
		                        		
		                        			Stem Cell Transplantation
		                        			;
		                        		
		                        			Survival Rate
		                        			;
		                        		
		                        			Transplantation, Autologous
		                        			;
		                        		
		                        			Young Adult
		                        			
		                        		
		                        	
8.Three-month Treatment Response and Exacerbation in Chronic Obstructive Pulmonary Disease.
Jung Su LEE ; Chin Kook RHEE ; Kwang Ha YOO ; Ji Hyun LEE ; Ho Il YOON ; Tae Hyung KIM ; Woo Jin KIM ; JinHwa LEE ; Seong Yong LIM ; Tai Sun PARK ; Jae Seung LEE ; Sei Won LEE ; Sang Do LEE ; Yeon Mok OH
Journal of Korean Medical Science 2015;30(1):54-59
		                        		
		                        			
		                        			The aim of this study was to investigate relationships between acute exacerbation and Forced Expiratory Volume 1 second (FEV1) improvement after treatment with combined long-acting beta-agonist (LABA) and inhaled corticosteroid (ICS) in patients with chronic obstructive pulmonary disease (COPD). A total of 137 COPD patients were classified as responders or nonresponders according to FEV1 improvement after 3 months of LABA/ICS treatment in fourteen referral hospitals in Korea. Exacerbation occurrence in these two subgroups was compared over a period of 1 yr. Eighty of the 137 COPD patients (58.4%) were classified as responders and 57 (41.6%) as nonresponders. Acute exacerbations occurred in 25 patients (31.3%) in the responder group and in 26 patients (45.6%) in the nonresponder group (P=0.086). FEV1 improvement after LABA/ICS treatment was a significant prognostic factor for fewer acute exacerbations in a multivariate Cox proportional hazard model adjusted for age, sex, FEV1, smoking history, 6 min walk distance, body mass index, exacerbation history in the previous year, and dyspnea scale.Three-month treatment response to LABA/ICS might be a prognostic factor for the occurrence of acute exacerbation in COPD patients.
		                        		
		                        		
		                        		
		                        			Adrenal Cortex Hormones/*therapeutic use
		                        			;
		                        		
		                        			Adrenergic beta-2 Receptor Agonists/*therapeutic use
		                        			;
		                        		
		                        			Bronchodilator Agents/*therapeutic use
		                        			;
		                        		
		                        			Budesonide/therapeutic use
		                        			;
		                        		
		                        			Drug Therapy, Combination
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Fluticasone/therapeutic use
		                        			;
		                        		
		                        			Forced Expiratory Volume/drug effects/*physiology
		                        			;
		                        		
		                        			Formoterol Fumarate/therapeutic use
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Pulmonary Disease, Chronic Obstructive/*drug therapy/physiopathology
		                        			;
		                        		
		                        			Recurrence
		                        			;
		                        		
		                        			Republic of Korea
		                        			;
		                        		
		                        			Salmeterol Xinafoate/therapeutic use
		                        			;
		                        		
		                        			Smoking
		                        			;
		                        		
		                        			Spirometry
		                        			;
		                        		
		                        			Treatment Outcome
		                        			
		                        		
		                        	
9.Analysis of Mutations in Epidermal Growth Factor Receptor Gene in Korean Patients with Non-small Cell Lung Cancer: Summary of a Nationwide Survey.
Sang Hwa LEE ; Wan Seop KIM ; Yoo Duk CHOI ; Jeong Wook SEO ; Joung Ho HAN ; Mi Jin KIM ; Lucia KIM ; Geon Kook LEE ; Chang Hun LEE ; Mee Hye OH ; Gou Young KIM ; Sun Hee SUNG ; Kyo Young LEE ; Sun Hee CHANG ; Mee Sook RHO ; Han Kyeom KIM ; Soon Hee JUNG ; Se Jin JANG
Journal of Pathology and Translational Medicine 2015;49(6):481-488
		                        		
		                        			
		                        			BACKGROUND: Analysis of mutations in the epidermal growth factor receptor gene (EGFR) is important for predicting response to EGFR tyrosine kinase inhibitors. The overall rate of EGFR mutations in Korean patients is variable. To obtain comprehensive data on the status of EGFR mutations in Korean patients with lung cancer, the Cardiopulmonary Pathology Study Group of the Korean Society of Pathologists initiated a nationwide survey. METHODS: We obtained 1,753 reports on EGFR mutations in patients with lung cancer from 15 hospitals between January and December 2009. We compared EGFR mutations with patient age, sex, history of smoking, histologic diagnosis, specimen type, procurement site, tumor cell dissection, and laboratory status. RESULTS: The overall EGFR mutation rate was 34.3% in patients with non-small cell lung cancer (NSCLC) and 43.3% in patients with adenocarcinoma. EGFR mutation rate was significantly higher in women, never smokers, patients with adenocarcinoma, and patients who had undergone excisional biopsy. EGFR mutation rates did not differ with respect to patient age or procurement site among patients with NSCLC. CONCLUSIONS: EGFR mutation rates and statuses were similar to those in published data from other East Asian countries.
		                        		
		                        		
		                        		
		                        			Adenocarcinoma
		                        			;
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Biopsy
		                        			;
		                        		
		                        			Carcinoma, Non-Small-Cell Lung*
		                        			;
		                        		
		                        			Diagnosis
		                        			;
		                        		
		                        			Epidermal Growth Factor*
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lung Neoplasms
		                        			;
		                        		
		                        			Mutation Rate
		                        			;
		                        		
		                        			Pathology
		                        			;
		                        		
		                        			Protein-Tyrosine Kinases
		                        			;
		                        		
		                        			Receptor, Epidermal Growth Factor*
		                        			;
		                        		
		                        			Smoke
		                        			;
		                        		
		                        			Smoking
		                        			
		                        		
		                        	
10.Preventive Efficacy and Safety of Rebamipide in Nonsteroidal Anti-Inflammatory Drug-Induced Mucosal Toxicity.
Jeong Ho KIM ; Soo Heon PARK ; Chul Soo CHO ; Soo Teik LEE ; Wan Hee YOO ; Sung Kook KIM ; Young Mo KANG ; Jong Sun REW ; Yong Wook PARK ; Soo Kon LEE ; Yong Chan LEE ; Won PARK ; Don Haeng LEE
Gut and Liver 2014;8(4):371-379
		                        		
		                        			
		                        			BACKGROUND/AIMS: The use of proton pump inhibitors or misoprostol is known to prevent the gastrointestinal complications of nonsteroidal anti-inflammatory drugs (NSAIDs). Rebamipide is known to increase the mucosal generation of prostaglandins and to eliminate free oxygen radicals, thus enhancing the protective function of the gastric mucosa. However, it is unknown whether rebamipide plays a role in preventing NSAID-induced gastropathy. The aim of this study was to determine the effectiveness of rebamipide compared to misoprostol in preventing NSAID-induced gastrointestinal complications in patients requiring continuous NSAID treatment. METHODS: We studied 479 patients who required continuous NSAID treatment. The patients were randomly assigned to groups that received 100 mg of rebamipide three times per day or 200 microg of misoprostol three times per day for 12 weeks. The primary endpoint of the analysis was the occurrence rate of gastric ulcers, as determined by endoscopy after 12 weeks of therapy. RESULTS: Of the 479 patients in the study, 242 received rebamipide, and 237 received misoprostol. Ultimately, 44 patients (18.6%) withdrew from the misoprostol group and 25 patients (10.3%) withdrew from the rebamipide group. There was a significant difference in withdrawal rate between the two groups (p=0.0103). The per protocol analysis set was not valid because of the dropout rate of the misoprostol group; thus, the intention to treat (ITT) analysis set is the main set for the efficacy analysis in this study. After 12 weeks, the occurrence rate of gastric ulcers was similar in the rebamipide and misoprostol groups (20.3% vs 21.9%, p=0.6497) according to ITT analysis. In addition, the therapeutic failure rate was similar in the rebamipide and misoprostol groups (13.6% vs 13.1%, p=0.8580). The total severity score of the gastrointestinal symptoms was significantly lower in the rebamipide group than in the misoprostol group (p=0.0002). The amount of antacid used was significantly lower in the rebamipide group than in the misoprostol group (p=0.0258). CONCLUSIONS: Rebamipide can prevent gastric ulcers when used with NSAIDs and can decrease the gastrointestinal symptoms associated with NSAID administration. When the possibility of poor compliance and the potential adverse effects of misoprostol are considered, rebamipide appears to be a clinically effective and safe alternative.
		                        		
		                        		
		                        		
		                        			Adult
		                        			;
		                        		
		                        			Aged
		                        			;
		                        		
		                        			Alanine/administration & dosage/adverse effects/*analogs & derivatives
		                        			;
		                        		
		                        			Anti-Inflammatory Agents, Non-Steroidal/*adverse effects
		                        			;
		                        		
		                        			Anti-Ulcer Agents/*administration & dosage/adverse effects
		                        			;
		                        		
		                        			Arthritis/drug therapy
		                        			;
		                        		
		                        			Butanones/adverse effects
		                        			;
		                        		
		                        			Diclofenac/adverse effects/analogs & derivatives
		                        			;
		                        		
		                        			Double-Blind Method
		                        			;
		                        		
		                        			Drug Administration Schedule
		                        			;
		                        		
		                        			Gastric Mucosa
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Middle Aged
		                        			;
		                        		
		                        			Misoprostol/*administration & dosage/adverse effects
		                        			;
		                        		
		                        			Quinolones/*administration & dosage/adverse effects
		                        			;
		                        		
		                        			Stomach Ulcer/chemically induced/*prevention & control
		                        			;
		                        		
		                        			Thiazines/adverse effects
		                        			;
		                        		
		                        			Thiazoles/adverse effects
		                        			;
		                        		
		                        			Treatment Outcome
		                        			
		                        		
		                        	
            
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