1.Oncologic and obstetric outcomes of conservative surgery for borderline ovarian tumors in women of reproductive age.
Se Yun LEE ; Min Chul CHOI ; Bo Ram KWON ; Sang Geun JUNG ; Hyun PARK ; Won Duk JOO ; Chan LEE ; Je Ho LEE ; Joon Mo LEE
Obstetrics & Gynecology Science 2017;60(3):289-295
OBJECTIVE: To compare the oncologic and obstetric outcomes in reproductive-age females with borderline ovarian tumors (BOTs) treated with cyst enucleation (CE) or unilateral salpingo-oophorectomy (USO). METHODS: The medical records of patients with BOTs treated between 1998 and 2014 were retrospectively reviewed. The recurrence rates in the USO and CE groups were compared, and the postoperative obstetric outcomes were assessed via telephone survey. RESULTS: Eighty-nine patients with BOTs underwent USO, and 19 underwent CE. Of these, six patients had recurrent BOTs. The recurrence rate was significantly lower in the USO group (3/89, 3.4%) than in the CE group (3/19, 15.8%) (P=0.032). All patients with recurrent disease were successfully treated with further surgery. Of the 76 patients interviewed by telephone, 71 (93.4%) resumed regular menstruation after surgery. Twenty-six of the 32 patients (81.3%) who attempted to conceive had successful pregnancies. USO (19/24, 79.2%), like CE (7/8, 87.5%), resulted in favorable pregnancy rates for patients with BOTs. CONCLUSION: USO is a suitable fertility-preserving surgery for women with BOTs. CE is also an acceptable option for select patients.
Female
;
Fertility Preservation
;
Humans
;
Medical Records
;
Menstruation
;
Pregnancy
;
Pregnancy Rate
;
Recurrence
;
Retrospective Studies
;
Telephone
2.Erratum to: Prognosis of Patients with Behavioral Variant Frontotemporal Dementia Who have Focal Versus Diffuse Frontal Atrophy.
Jin San LEE ; Na Yeon JUNG ; Young Kyoung JANG ; Hee Jin KIM ; Sang Won SEO ; Juyoun LEE ; Yeo Jin KIM ; Jae Hong LEE ; Byeong C KIM ; Kyung Won PARK ; Soo Jin YOON ; Jee H JEONG ; Sang Yun KIM ; Seung Hyun KIM ; Eun Joo KIM ; Key Chung PARK ; David S KNOPMAN ; Duk L NA
Journal of Clinical Neurology 2017;13(4):447-447
The original version of this article contained wrong information of an author which should be changed.
3.Patient-Derived Xenograft Models of Epithelial Ovarian Cancer for Preclinical Studies.
Eun Jin HEO ; Young Jae CHO ; William Chi CHO ; Ji Eun HONG ; Hye Kyung JEON ; Doo Yi OH ; Yoon La CHOI ; Sang Yong SONG ; Jung Joo CHOI ; Duk Soo BAE ; Yoo Young LEE ; Chel Hun CHOI ; Tae Joong KIM ; Woong Yang PARK ; Byoung Gie KIM ; Jeong Won LEE
Cancer Research and Treatment 2017;49(4):915-926
PURPOSE: Patient-derived tumor xenografts (PDXs) can provide more reliable information about tumor biology than cell line models. We developed PDXs for epithelial ovarian cancer (EOC) that have histopathologic and genetic similarities to the primary patient tissues and evaluated their potential for use as a platform for translational EOC research. MATERIALS AND METHODS: We successfully established PDXs by subrenal capsule implantation of primary EOC tissues into female BALB/C-nude mice. The rate of successful PDX engraftment was 48.8% (22/45 cases). Hematoxylin and eosin staining and short tandem repeat analysis showed histopathological and genetic similarity between the PDX and primary patient tissues. RESULTS: Patients whose tumors were successfully engrafted in mice had significantly inferior overall survival when compared with those whose tumors failed to engraft (p=0.040). In preclinical tests of this model, we found that paclitaxel-carboplatin combination chemotherapy significantly deceased tumor weight in PDXs compared with the control treatment (p=0.013). Moreover, erlotinib treatment significantly decreased tumor weight in epidermal growth factor receptor–overexpressing PDX with clear cell histology (p=0.023). CONCLUSION: PDXs for EOC with histopathological and genetic stability can be efficiently developed by subrenal capsule implantation and have the potential to provide a promising platform for future translational research and precision medicine for EOC.
Animals
;
Biology
;
Cell Line
;
Drug Therapy, Combination
;
Eosine Yellowish-(YS)
;
Epidermal Growth Factor
;
Erlotinib Hydrochloride
;
Female
;
Hematoxylin
;
Heterografts*
;
Humans
;
Mice
;
Microsatellite Repeats
;
Molecular Targeted Therapy
;
Ovarian Neoplasms*
;
Precision Medicine
;
Translational Medical Research
;
Tumor Burden
4.Proton Pump Inhibition Enhances the Cytotoxicity of Paclitaxel in Cervical Cancer.
Taejong SONG ; Hye Kyung JEON ; Ji Eun HONG ; Jung Joo CHOI ; Tae Joong KIM ; Chel Hun CHOI ; Duk Soo BAE ; Byoung Gie KIM ; Jeong Won LEE
Cancer Research and Treatment 2017;49(3):595-606
PURPOSE: This study was conducted to investigate whether a proton pump inhibitor (PPI) could enhance chemosensitivity via the inhibition of vacuolar-type H⁺ ATPase (V-ATPase) in cervical cancer. MATERIALS AND METHODS: The expression of V-ATPase was evaluated in 351 formalin-fixed, paraffin-embedded human cervical cancer tissues using immunohistochemistry and compared with clinicopathologic risk factors for disease prognosis. The influence of cell proliferation and apoptosis following V-ATPase siRNA transfection or esomeprazole pretreatment was assessed in cervical cancer cell lines using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide and enzyme-linked immunosorbent assay, respectively. RESULTS: Immunohistochemical analysis revealed that V-ATPase was expressed in about 60% of cervical cancer tissue samples (211/351), and the expression was predominantly found in adenocarcinoma histology (p=0.016). Among patients with initially bulky cervical cancer (n=89), those with V-ATPase expression had shorter disease-free survival (p=0.005) and overall survival (p=0.023). Co-treatment with V-ATPase siRNA or esomeprazole with paclitaxel significantly decreased the cell proliferation of cervical cancer cell lines, including HeLa and INT407, compared to cell lines treated with paclitaxel alone (p < 0.01). Moreover, V-ATPase siRNA or esomeprazole followed by paclitaxel significantly increased the expression of active caspase-3 in these cells compared to cells treated with paclitaxel alone (both, p < 0.05). CONCLUSION: V-ATPase was predominantly expressed in cervical adenocarcinoma, and the expression of V-ATPases was associated with poor prognosis. The inhibition of V-ATPase via siRNA or PPI (esomeprazole) might enhance the chemosensitivity of paclitaxel in cervical cancer cells.
Adenocarcinoma
;
Adenosine Triphosphatases
;
Antineoplastic Agents
;
Apoptosis
;
Caspase 3
;
Cell Line
;
Cell Proliferation
;
Disease-Free Survival
;
Enzyme-Linked Immunosorbent Assay
;
Esomeprazole
;
Humans
;
Immunohistochemistry
;
Paclitaxel*
;
Prognosis
;
Proton Pump Inhibitors
;
Proton Pumps*
;
Protons*
;
Risk Factors
;
RNA, Small Interfering
;
Transfection
;
Uterine Cervical Neoplasms*
;
Vacuolar Proton-Translocating ATPases
5.Prediction of Cancer Incidence and Mortality in Korea, 2017.
Kyu Won JUNG ; Young Joo WON ; Chang Mo OH ; Hyun Joo KONG ; Duk Hyoung LEE ; Kang Hyun LEE
Cancer Research and Treatment 2017;49(2):306-312
PURPOSE: This study aimed to report on cancer incidence and mortality for the year 2017 in Korea in order to estimate the nation’s current cancer burden. MATERIALS AND METHODS: Cancer incidence data from 1999 to 2014 were obtained from the Korea National Cancer Incidence Database, and cancer mortality data from 1993 to 2015 were acquired from Statistics Korea. Cancer incidence and mortality were projected by fitting a linear regression model to observe age-specific cancer rates against observed years, and then multiplying the projected age-specific rates by the age-specific population. The Joinpoint regression model was used to determine at which year the linear trend changed significantly; we only used data of the latest trend. RESULTS: A total of 221,143 new cancer cases and 80,268 cancer deaths are expected to occur in Korea in 2017. The most common cancer sites are the colorectum, stomach, lung, thyroid, and breast. These five cancers represent half of the overall burden of cancer in Korea. For mortality, the most common sites are the lung, liver, colorectal, stomach, and pancreas. CONCLUSION: The incidence rate of all cancers in Korea appears to have decreased mainly because of a decrease in thyroid cancer. These up-to-date estimates of the cancer burden in Korea could be an important resource for planning and evaluation of cancer-control programs.
Breast
;
Forecasting
;
Incidence*
;
Korea*
;
Linear Models
;
Liver
;
Lung
;
Mortality*
;
Pancreas
;
Stomach
;
Thyroid Gland
;
Thyroid Neoplasms
6.Cancer Statistics in Korea: Incidence, Mortality, Survival, and Prevalence in 2014.
Kyu Won JUNG ; Young Joo WON ; Chang Mo OH ; Hyun Joo KONG ; Duk Hyoung LEE ; Kang Hyun LEE
Cancer Research and Treatment 2017;49(2):292-305
PURPOSE: This study presents the 2014 nationwide cancer statistics in Korea, including cancer incidence, survival, prevalence, and mortality. MATERIALS AND METHODS: Cancer incidence data from 1999 to 2014 was obtained from the Korea National Cancer Incidence Database and followed until December 31, 2015. Mortality data from 1983 to 2014 were obtained from Statistics Korea. The prevalence was defined as the number of cancer patients alive on January 1, 2015, among all cancer patients diagnosed since 1999. Crude and age-standardized rates (ASRs) for incidence, mortality, prevalence, and 5-year relative survivals were also calculated. RESULTS: In 2014, 217,057 and 76,611 Koreans were newly diagnosed and died from cancer respectively. The ASRs for cancer incidence and mortality in 2014 were 270.7 and 85.1 per 100,000, respectively. The all-cancer incidence rate has increased significantly by 3.4% annually from 1999 to 2012, and started to decrease after 2012 (2012-2014; annual percent change, –6.6%). However, overall cancer mortality has decreased 2.7% annually since 2002. The 5-year relative survival rate for patients diagnosed with cancer between 2010 and 2014 was 70.3%, an improvement from the 41.2% for patients diagnosed between 1993 and 1995. CONCLUSION: Age-standardized cancer incidence rates have decreased since 2012 and mortality rates have also declined since 2002, while 5-year survival rates have improved remarkably from 1993-1995 to 2010-2014 in Korea.
Humans
;
Incidence*
;
Korea*
;
Mortality*
;
Prevalence*
;
Survival Rate
7.Proposal Guidelines for Standardized Operating Procedures of Brain Autopsy: Brain Bank in South Korea.
Kyung Hwa LEE ; Sang Won SEO ; Tae Sung LIM ; Eun Joo KIM ; Byeong Chae KIM ; Yeshin KIM ; Ho Won LEE ; Jae Pil JEON ; Sung Mi SHIM ; Duk L NA ; Gi Yeong HUH ; Min Cheol LEE ; Yeon Lim SUH
Yonsei Medical Journal 2017;58(5):1055-1060
To obtain an in-depth understanding of brain diseases, including neurodegenerative diseases, psychiatric illnesses, and neoplasms, scientific approach and verification using postmortem human brain tissue with or without disease are essential. Compared to other countries that have run brain banks for decades, South Korea has limited experience with brain banking; nationwide brain banks started only recently. The goal of this study is to provide provisional guidelines for brain autopsy for hospitals and institutes that have not accumulated sufficient expertise. We hope that these provisional guidelines will serve as a useful reference for pathologists and clinicians who are involved and interested in the brain bank system. Also, we anticipate updating the provisional guidelines in the future based on collected data and further experience with the practice of brain autopsy in South Korea.
Academies and Institutes
;
Autopsy*
;
Brain Diseases
;
Brain*
;
Dementia
;
Hope
;
Humans
;
Korea*
;
Neurodegenerative Diseases
;
Neuropathology
8.Prognosis of Patients with Behavioral Variant Frontotemporal Dementia Who have Focal Versus Diffuse Frontal Atrophy.
Jin San LEE ; Na Yeon JUNG ; Young Kyoung JANG ; Hee Jin KIM ; Sang Won SEO ; Juyoun LEE ; Yeo Jin KIM ; Jae Hong LEE ; Byeong C KIM ; Kyung Won PARK ; Soo Jin YOON ; Jee H JEONG ; Sang Yun KIM ; Seung Hyun KIM ; Eun Joo KIM ; Key Chung PARK ; David S KNOPMAN ; Duk L NA
Journal of Clinical Neurology 2017;13(3):234-242
BACKGROUND AND PURPOSE: Only a few studies have investigated the relationship between different subtypes and disease progression or prognosis in patients with behavioral variant frontotemporal dementia (bvFTD). Since a localized injury often produces more focal signs than a diffuse injury, we hypothesized that the clinical characteristics differ between patients with bvFTD who show diffuse frontal lobe atrophy (D-type) on axial magnetic resonance imaging (MRI) scans versus those with focal or circumscribed frontal lobe atrophy (F-type). METHODS: In total, 94 MRI scans (74 scans from bvFTD and 20 scans from age-matched normal controls) were classified into 35 D- and 39 F-type bvFTD cases based on an axial MRI visual rating scale. We compared baseline clinical characteristics, progression in motor and cognitive symptoms, and survival times between D- and F-types. Survival analyses were performed for 62 of the 74 patients. RESULTS: While D-type performed better on neuropsychological tests than F-type at baseline, D-type had higher baseline scores on the Unified Parkinson's Disease Rating Scale (UPDRS) Part III. Evaluations of motor progression showed that the disease duration with motor symptoms was shorter in D-type than F-type. Moreover, the survival time was shorter in D-type (6.9 years) than F-type (9.4 years). Cox regression analyses revealed that a high UPDRS Part III score at baseline contributed to an increased risk of mortality, regardless of the pattern of atrophy. CONCLUSIONS: The prognosis is worse for D-type than for those with F-type. Shorter survival in D-type may be associated with the earlier appearance of motor symptoms.
Atrophy*
;
Disease Progression
;
Frontal Lobe
;
Frontotemporal Dementia*
;
Frontotemporal Lobar Degeneration
;
Humans
;
Magnetic Resonance Imaging
;
Mortality
;
Neurobehavioral Manifestations
;
Neuropsychological Tests
;
Parkinson Disease
;
Prognosis*
9.Bioresorbable Vascular Scaffold Korean Expert Panel Report.
Jung Min AHN ; Duk Woo PARK ; Sung Jin HONG ; Young Keun AHN ; Joo Yong HAHN ; Won Jang KIM ; Soon Jun HONG ; Chang Wook NAM ; Do Yoon KANG ; Seung Yul LEE ; Woo Jung CHUN ; Jung Ho HEO ; Deok Kyu CHO ; Jin Won KIM ; Sung Ho HER ; Sang Wook KIM ; Sang Yong YOO ; Myeong Ki HONG ; Seung Jea TAHK ; Kee Sik KIM ; Moo Hyun KIM ; Yangsoo JANG ; Seung Jung PARK
Korean Circulation Journal 2017;47(6):795-810
Bioresorbable vascular scaffold (BRS) is an innovative device that provides structural support and drug release to prevent early recoil or restenosis, and then degrades into nontoxic compounds to avoid late complications related with metallic drug-eluting stents (DESs). BRS has several putative advantages. However, recent randomized trials and registry studies raised clinical concerns about the safety and efficacy of first generation BRS. In addition, the general guidance for the optimal practice with BRS has not been suggested due to limited long-term clinical data in Korea. To address the safety and efficacy of BRS, we reviewed the clinical evidence of BRS implantation, and suggested the appropriate criteria for patient and lesion selection, scaffold implantation technique, and management.
Coronary Disease
;
Drug Liberation
;
Drug-Eluting Stents
;
Humans
;
Korea
;
Stents
;
Thrombosis
10.Erratum to: The KMDS-NATION Study: Korean Movement Disorders Society Multicenter Assessment of Non-Motor Symptoms and Quality of Life in Parkinson's Disease NATION Study Group.
Do Young KWON ; Seong Beom KOH ; Jae Hyeok LEE ; Hee Kyung PARK ; Han Joon KIM ; Hae Won SHIN ; Jinyoung YOUN ; Kun Woo PARK ; Sun Ah CHOI ; Sang Jin KIM ; Seong Min CHOI ; Ji Yun PARK ; Beom S. JEON ; Ji Young KIM ; Sun Ju CHUNG ; Chong Sik LEE ; Jeong Ho PARK ; Tae Beom AHN ; Won Chan KIM ; Hyun Sook KIM ; Sang Myung CHEON ; Hee Tae KIM ; Jee Young LEE ; Ji Sun KIM ; Eun Joo KIM ; Jong Min KIM ; Kwang Soo LEE ; Joong Seok KIM ; Min Jeong KIM ; Jong Sam BAIK ; Ki Jong PARK ; Hee Jin KIM ; Mee Young PARK ; Ji Hoon KANG ; Sook Kun SONG ; Yong Duk KIM ; Ji Young YUN ; Ho Won LEE ; Hyung Geun OH ; Jinwhan CHO ; In Uk SONG ; Young H. SOHN ; Phil Hyu LEE ; Jae Woo KIM
Journal of Clinical Neurology 2017;13(3):315-315
The original version of this article contained wrong informations of some authors which should be changed.

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