1.Time to Disease Recurrence Is a Predictor of Metastasis and Mortality in Patients with High-risk Prostate Cancer Who Achieved Undetectable Prostate-specific Antigen Following Robot-assisted Radical Prostatectomy.
Do Kyung KIM ; Kyo Chul KOO ; Kwang Suk LEE ; Yoon Soo HAH ; Koon Ho RHA ; Sung Joon HONG ; Byung Ha CHUNG
Journal of Korean Medical Science 2018;33(45):e285-
BACKGROUND: Robot-assisted radical prostatectomy (RARP) is a feasible treatment option for high-risk prostate cancer (PCa). While patients may achieve undetectable prostate-specific antigen (PSA) levels after RARP, the risk of disease progression is relatively high. We investigated metastasis-free survival, cancer-specific survival (CSS), and overall survival (OS) outcomes and prognosticators in such patients. METHODS: In a single-center cohort of 342 patients with high-risk PCa (clinical stage ≥ T3, biopsy Gleason score ≥ 8, and/or PSA levels ≥ 20 ng/mL) treated with RARP and pelvic lymph node dissection between August 2005 and June 2011, we identified 251 (73.4%) patients (median age, 66.5 years; interquartile range [IQR], 63.0–71.0 years) who achieved undetectable PSA levels (< 0.01 ng/mL) postoperatively. Survival outcomes were evaluated for the entire study sample and in groups stratified according to the time to biochemical recurrence dichotomized at 60 months. RESULTS: During the median follow-up of 75.9 months (IQR, 59.4–85.8 months), metastasis occurred in 38 (15.1%) patients, most often to the bones, followed by the lymph nodes, lungs, and liver. The 5-year metastasis-free, cancer-specific, and OS rates were 87.1%, 94.8%, and 94.3%, respectively. Multivariate Cox-regression analysis revealed time to recurrence as an independent predictor of metastasis (P < 0.001). Time to metastasis was an independent predictor of OS (P = 0.003). Metastasis-free and CSS rates were significantly lower among patients with recurrence within 60 months of RARP (log-rank P < 0.001). CONCLUSION: RARP confers acceptable oncological outcomes for high-risk PCa. Close monitoring beyond 5 years is warranted for early detection of disease progression and for timely adjuvant therapy.
Biopsy
;
Cohort Studies
;
Disease Progression
;
Early Diagnosis
;
Follow-Up Studies
;
Humans
;
Liver
;
Lung
;
Lymph Node Excision
;
Lymph Nodes
;
Mortality*
;
Neoplasm Grading
;
Neoplasm Metastasis*
;
Passive Cutaneous Anaphylaxis
;
Prostate*
;
Prostate-Specific Antigen*
;
Prostatectomy*
;
Prostatic Neoplasms*
;
Recurrence*
2.Reproductive ability of a cloned male detector dog and behavioral traits of its offspring.
Ji Hyun LEE ; Geon A KIM ; Rak Seung KIM ; Jong Su LEE ; Hyun Ju OH ; Min Jung KIM ; Do Kyo HONG ; Byeong Chun LEE
Journal of Veterinary Science 2016;17(3):407-411
In 2007, seven detector dogs were produced by somatic cell nuclear transfer using one nuclear donor dog, then trained and certified as excellent detector dogs, similar to their donor. In 2011, we crossed a cloned male and normal female by natural breeding and produced ten offspring. In this study, we investigated the puppies' temperaments, which we later compared with those of the cloned parent male. The results show that the cloned male had normal reproductive abilities and produced healthy offspring. All puppies completed narcotic detector dog training with a success rate for selection of 60%. Although the litter of cloned males was small in this study, a cloned male dog bred by natural mating produced puppies that later successfully completed the training course for drug detection. In conclusion, cloning an elite dog with superior genetic factors and breeding of the cloned dog was found to be a useful method to efficiently procure detector dogs.
Animals
;
Breeding
;
Clone Cells*
;
Cloning, Organism
;
Dogs*
;
Female
;
Humans
;
Male*
;
Methods
;
Parents
;
Temperament
;
Tissue Donors
3.A Comparative Study on the Efficacy of Covered Metal Stent and Plastic Stent in Unresectable Malignant Biliary Obstruction.
Jae Myoung CHOI ; Jin Hong KIM ; Soon Sun KIM ; Jun Hwan YU ; Jae Chul HWANG ; Byung Moo YOO ; Sang Heum PARK ; Ho Gak KIM ; Dong Ki LEE ; Kang Hyun KO ; Kyo Sang YOO ; Do Hyun PARK
Clinical Endoscopy 2012;45(1):78-83
BACKGROUND/AIMS: The placement of self expandable metal stent (SEMS) is one of the palliative therapeutic options for patients with unresectable malignant biliary obstruction. The aim of this study was to compare the effectiveness of a covered SEMS versus the conventional plastic stent. METHODS: We retrospectively evaluated 44 patients with unresectable malignant biliary obstruction who were treated with a covered SEMS (21 patients) or a plastic stent (10 Fr, 23 patients). We analyzed the technical success rate, functional success rate, early complications, late complications, stent patency and survival rate. RESULTS: There was one case in the covered SEMS group that had failed technically, but was corrected successfully using lasso. Functional success rates were 90.5% in the covered SEMS group and 91.3% in the plastic stent group. There was no difference in early complications between the two groups. Median patency of the stent was significantly prolonged in patients who had a covered SEMS (233.6 days) compared with those who had a plastic stent (94.6 days) (p=0.006). During the follow-up period, stent occlusion occurred in 11 patients of the covered SEMS group. Mean survival showed no significant difference between the two groups (covered SEMS group, 236.9 days; plastic stent group, 222.3 days; p=0.182). CONCLUSIONS: The patency of the covered SEMS was longer than that of the plastic stent and the lasso of the covered SEMS was available for repositioning of the stent.
Acetamides
;
Follow-Up Studies
;
Humans
;
Plastics
;
Retrospective Studies
;
Stents
4.Randomized, Multicenter, Phase III Trial of Heptaplatin 1-hour Infusion and 5-Fluorouracil Combination Chemotherapy Comparing with Cisplatin and 5-Fluorouracil Combination Chemotherapy in Patients with Advanced Gastric Cancer.
Kyung Hee LEE ; Myung Soo HYUN ; Hoon Kyo KIM ; Hyung Min JIN ; Jinmo YANG ; Hong Suk SONG ; Young Rok DO ; Hun Mo RYOO ; Joo Seop CHUNG ; Dae Young ZANG ; Ho Yeong LIM ; Jong Youl JIN ; Chang Yeol YIM ; Hee Sook PARK ; Jun Suk KIM ; Chang Hak SOHN ; Soon Nam LEE
Cancer Research and Treatment 2009;41(1):12-18
PURPOSE: Heptaplatin (Sunpla) is a cisplatin derivative. A phase IIb trial using heptaplatin resulted in a 34% response rate with mild nephrotoxicity. We conducted a randomized phase III trial of heptaplatin plus 5-FU compared with cisplatin plus 5-FU in patients with advanced gastric cancer. MATERIALS AND METHODS: One hundred seventy-four patients (heptaplatin, n=88; cisplatin, n=86) from 13 centers were enrolled. The eligibility criteria were as follows: patients with pathologically-proven adenocarcinoma, chemonaive patients, or patients who had received only single adjuvant chemotherapy, and who had a measurable or evaluable lesion. On day 1, heptaplatin (400 mg/m2) or cisplatin (60 mg/m2) was given over 1 hour with 5-FU (1 gm/m2) on days 1~5 every 4 weeks. RESULTS: At the time of survival analysis, the median overall survival was 7.3 months in the 5-FU + heptaplatin (FH) arm and 7.9 months in the 5-FU + cisplatin (FP) arm (p=0.24). Of the FH patients, 34.2% (complete response [CR], 1.3%; partial response [PR], 32.9%) experienced a confirmed objective response compared with 35.9% (CR 0%, PR 35.9%) of FP patients (p=0.78). The median-time-to-progression was 2.5 months in the FH arm and 2.3 months in the FP arm. The incidence of neutropenia was higher with FP (28%) than with FH (16%; p=0.06); grade 3~4 nausea and vomiting were more frequent in the FP than in the FH arm (p=0.01 and p=0.05, respectively). The incidence of increased proteinuria and creatininemia was higher with FH than with FP; however, there was no statistical difference. There were no treatment-related deaths. CONCLUSION: Heptaplatin showed similar effects to cisplatin when combined with 5-FU in advanced gastric cancer patients with tolerable toxicities.
Adenocarcinoma
;
Arm
;
Chemotherapy, Adjuvant
;
Cisplatin
;
Drug Therapy, Combination
;
Fluorouracil
;
Humans
;
Incidence
;
Malonates
;
Nausea
;
Neutropenia
;
Organoplatinum Compounds
;
Proteinuria
;
Stomach Neoplasms
;
Vomiting
5.Protein Expression and Gene Amplification of Epidermal Growth Factor Receptor in Non-Small Cell Lung Cancer: Correlation with the Response to Gefitinib Therapy.
Jinyoung YOO ; Kyungji LEE ; Ji Han JUNG ; Byoung Yong SHIM ; Sung Hwan KIM ; Deog Gon CHO ; Myeong Im AHN ; Chi Hong KIM ; Kyu Do CHO ; Hoon Kyo KIM ; Seok Jin KANG
Korean Journal of Pathology 2008;42(1):1-8
BACKGROUND: Gefitinib is an EGFR tyrosine kinase inhibitor that has shown dramatic effectiveness in a subset of non-small cell lung cancer (NSCLC) patients. We evaluated the response rate to gefitinib, and the significance of the EGFR and HER2/neu status as predictive markers of the tumor response. METHODS: The EGFR and HER2/neu protein expressions, as determined by immunohistochemistry (IHC) and gene amplification via chromogenic in situ hybridization (CISH), were analyzed in biopsy specimens from 46 patients with advanced NSCLC. After their failure with the first-line treatment, all the patients had received gefitinib treatment. RESULTS: A partial response (PR) was achieved in 8 patients (17.4%). An EGFR overexpression was detected in 80.4% (37/46) of the tumors, and this was observed exclusively in patients with a PR (100% vs 75.3%, respectively; p=0.076). EGFR gene amplification was present in 47.8% of the tumors (22/46). HER2/neu was overexpressed in 13%(6/46) and it was amplified in 17% (7/46). The overall survival was prolonged in the female patients (p=0.007), and in patients with T1 and T2 disease (p=0.039), adenocarcinoma (p=0.010), a PR (p=0.022), an EGFR IHC+ status (p=0.033), an EGFR IHC+/CISH+ status (p=0.010), or an EGFR+/HER2/neu+ status (p=0.030). On multivariate analysis, gender, T disease and EGFR IHC/CISH remained the significant predictors of survival. CONCLUSIONS: Gefitinib showed a modest effect for the patients with chemotherapy-refractory advanced NSCLC. A combination of EGFR IHC and CISH might be important for identifying those patients who are most likely to benefit from gefitinib therapy.
Female
;
Humans
;
Adenocarcinoma
;
Biopsy
;
Lung Neoplasms
6.The Caspase-3 and c-myc Expressions in Completely Resected Non-small Cell Lung Cancer and Its Prognostic Significance.
Deog Gon CHO ; Kyu Do CHO ; Chul Ung KANG ; Min Seop JO ; Jinyoung YOO ; Myeong Im AHN ; Chi Hong KIM ; Byoung Yong SHIM ; Sung Whan KIM ; Hoon Kyo KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 2008;41(4):447-456
BACKGROUND: Caspase-3 is a cysteine protease that plays a major role in the process of apoptotic cell death. The dysregulated expression of c-myc contributes to the tumorigenesis in a variety of human cancers. The aim of this study was to investigate the expressions of caspase-3 and c-myc and their significances as prognosis markers in patients with completely resected non-small cell lung cancer (NSCLC). MATERIAL AND METHOD: A total 130 consecutive patients who had undergone complete resection without pre-operative radio-therapy or chemotherapy between May 1996 and December 2003 for NSCLC were retrospectively reviewed. The median follow-up period of the patients was 50 months (range: 3~128 months). The expressions of caspase-3 and c-myc were immunohistochemically examined, and these were correlated with the clinico-pathologic data. RESULT: The prevalence of caspase-3 and c-myc expressions in the patients was 68% (88/130) and 59% (77/130), respectively. Significant association was found between the frequency of the expressions of caspase-3 and c-myc (p=0.025). The caspase-3 and c-myc expressions were not significantly associated with the prognosis in all the patients. However, according to stages, a positive caspase-3 expression was significantly correlated with a favorable prognosis for patients with stage IIIa disease (median survival period: 35 months vs. 10 months, p=0.021). Multivariate analysis showed the pathologic stage to be significantly correlated with a good prognosis in all the patients (p=0.024), and with a positive caspase-3 expression, well differentiated tumor and negative neuronal invasion in the patients with stage IIIa disease (p=0.005, p=0.003, p=0.004, respectively). CONCLUSION: Caspase-3 and c-myc were frequently expressed in NSCLC, suggesting its possible involvement in tumor development. The caspase-3 expression, as determined with performing immunohistochemical staining, may be a favorable prognostic indicator in patients with completely resected NSCLC of an advanced stage (IIIa).
Carcinoma, Non-Small-Cell Lung
;
Caspase 3
;
Cell Death
;
Cell Transformation, Neoplastic
;
Cysteine Proteases
;
Follow-Up Studies
;
Humans
;
Multivariate Analysis
;
Neurons
;
Prevalence
;
Prognosis
;
Retrospective Studies
7.Primary Polymorphous Low-Grade Adenocarcinoma of Lung Treated by Sleeve Bronchial Resection: A Case Report.
Kyu Do CHO ; Ji Han JUNG ; Deog Gon CHO ; Min Seop JO ; Jinyoung YOO ; So Hyang SONG ; Byoung Yong SHIM ; Chi Hong KIM ; Hoon Kyo KIM
Journal of Korean Medical Science 2007;22(2):373-376
We report a surgical case of primary polymorphous low-grade adenocarcinoma (PLGA) of the minor salivary gland-type of the lung. A PLGA originating from the right upper lobar bronchial inlet was successfully treated by sleeve right upper lobectomy. PLGAs are thought to be indolent tumors that are preferentially localized to the palate, and they affect the minor salivary glands almost exclusively. Until now, two cases of distant metastases to the lung have been reported in the English literature. To the best of our knowledge, only one case of PLGA of minor salivary glandtype of the lung without evidence of a previous oropharyngeal primary tumor has been reported in the English literature. But the case was not a single lesion; it was bilateral tumors accompanied by tumors of the cervical lymph nodes. We report here the first case of a single primary PLGA of the minor salivary gland-type of the lung, which was successfully treated by sleeve bronchial resection of right upper lobe.
Treatment Outcome
;
Salivary Gland Neoplasms/pathology/*surgery
;
Lung Neoplasms/pathology/*secondary/*surgery
;
Humans
;
Female
;
Bronchi/*surgery
;
Aged
;
Adenocarcinoma/pathology/*secondary/*surgery
8.Two Cases of Fatal Hypoxemia after Talc Pleurodesis for Recurrent Malignant Pleural Effusion.
Shin Ae PARK ; Han Hee LEE ; Dae Jun KIM ; Byoung Yong SHIM ; So Hyang SONG ; Chi Hong KIM ; Myeong Im AHN ; Deog Gon CHO ; Kyu Do CHO ; Hoon Kyo KIM
Tuberculosis and Respiratory Diseases 2007;62(3):217-222
Talc pleurodesis is a safe and effective treatment for a recurrent malignant pleural effusion. However, acute hypoxemia, pulmonary edema or acute respiratory failure can develop in a small number of patients. We report 2 patients who developed fatal hypoxemia after talc pleurodesis which was necessary the control recurrent pleural effusion. The first case was an 18-year old male diagnosed with Ewing's sarcoma with bilateral lung metastases and pleural effusion. The performance status was ECOG (Eastern Cooperative Foncology Group) grade 3. Fever along with hypoxemia and leukocytosis developed 10 hours after the second talc pleurodesis on the right side for an uncontrolled pleural effusion, The patient died from respiratory failure after 13 days. The second case was a 66-year old female diagnosed with non-small cell lung cancer with a bone metastasis. Two weeks after systemic chemotherapy, she complained of dyspnea, and a pleural effusion was observed on the right side. Her performance status was ECOG grade 3. Talc pleurodesis was performed for recurrent pleural effusion, but hypoxemia developed 6 days after pleurodesis and she died from respiratory failure 10 days after pleurodesis. In conclusion, talc pleurodesis should be performed very carefully in patients with a poor performance status, in cases with repeated pleurodesis, bilateral pleural effusion, recent chemotherapy, radiotherapy and when there are parenchymal metastatic lesions present.
Adolescent
;
Aged
;
Anoxia*
;
Carcinoma, Non-Small-Cell Lung
;
Drug Therapy
;
Dyspnea
;
Female
;
Fever
;
Humans
;
Leukocytosis
;
Lung
;
Male
;
Neoplasm Metastasis
;
Pleural Effusion
;
Pleural Effusion, Malignant*
;
Pleurodesis*
;
Pulmonary Edema
;
Radiotherapy
;
Respiratory Insufficiency
;
Sarcoma, Ewing
;
Talc*
9.Immunohistochemical Analysis of Non-Small Cell Lung Cancer: Correlation with Clinical Parameters and Prognosis.
Jinyoung YOO ; Ji Han JUNG ; Myung A LEE ; Kyung Jin SEO ; Byoung Yong SHIM ; Sung Hwan KIM ; Deog Gon CHO ; Myeong Im AHN ; Chi Hong KIM ; Kyu Do CHO ; Seok Jin KANG ; Hoon Kyo KIM
Journal of Korean Medical Science 2007;22(2):318-325
Non-small cell lung cancers (NSCLC) vary in their biologic behavior. Recurrence and tumor-related mortality may be attributable to molecular abnormalities in primary tumors. This study evaluated such immunophenotypes with regard to cell cycle regulation and proliferation, apoptosis, and angiogenesis, to determine their significance for patient outcome. Core biopsies from 219 patients with NSCLC were assembled on tissue microarrays, and the expressions of p16, p21, p27, cyclin B1, cyclin E, Ki-67, caspase-3, survivin, bcl-2, VEGF, and endostatin were evaluated by immunohistochemistry. Despite previously described prognostic relevance of some of the investigated molecules, many of those markers were not directly associated with recurrence or survival. However, there was a trend for p16 immunoreactivity to be associated with a good prognosis (57% vs. 42% in 5-yr survival) (p=0.071). bcl-2 expression was strongly correlated with a better outcome (65% vs. 45% in 5-yr survival) (p=0.029), and the hazard of death for bcl-2 positive patients was 0.42 times of that for bcl-2 negative patients (p=0.047). A multivariate analysis with Cox proportional hazards model confirmed that the lymph node status (p=0.043) and stage (p=0.003) were other independent prognostic factors. Our results suggest that p16 and bcl-2 provide prognostic information independent of the TNM stage in NSCLC.
Tumor Markers, Biological/*analysis
;
Survival Rate
;
Survival Analysis
;
Statistics
;
Sensitivity and Specificity
;
Reproducibility of Results
;
Prognosis
;
Outcome Assessment (Health Care)/*methods
;
Neoplasm Proteins/*analysis
;
Male
;
Lung Neoplasms/*diagnosis/*metabolism/mortality
;
Korea/epidemiology
;
Humans
;
Female
;
Carcinoma, Non-Small-Cell Lung/*diagnosis/*metabolism/mortality
;
Aged
10.Treatment Outcome of Locally Advanced Non-small Cell Lung Cancer Patients Who Received Concurrent Chemoradiotherapy with Weekly Paclitaxel.
Suzy KIM ; Sung Whan KIM ; Byoung Yong SHIM ; Chi Hong KIM ; So Hyang SONG ; Meyung Im AHN ; Deog Gon CHO ; Kyu Do CHO ; Jinyoung YOO ; Hoon Kyo KIM
The Journal of the Korean Society for Therapeutic Radiology and Oncology 2006;24(4):230-236
PURPOSE: To analyze the response, toxicity, patterns of failure and survival rate of patients with locally advanced non-small cell lung cancer who were treated with concurrent chemoradiotherapy with weekly paclitaxel. MATERIALS AND METHODS: Twenty-three patients with locally advanced non-small cell lung cancer patients who received radical chemoradiotherapy from October 1999 to September 2004 were included in this retrospective study. Patients received total 55.4~64.8 (median 64.8) Gy (daily 1.8 Gy per fraction, 5 days per weeks) over 7~8 weeks. 50 or 60 mg/m2 of paclitaxel was administered on day 1, 8, 15, 22, 29 and 36 of radiotherapy. Four weeks after the concurrent chemoradiotherapy, three cycles of consolidation chemotherapy consisted of paclitaxel 135 mg/m2 and cisplatin 75 mg/m2 was administered every 3 weeks. RESULTS: Of the 23 patients, 3 patients refused to receive the treatment during the concurrent chemoradiotherapy. One patient died of bacterial pneumonia during the concurrent chemoradiotherapy. Grade 2 radiation esophagitis was observed in 4 patients (17%). Sixteen patients received consolidation chemotherapy. During the consolidation chemotherapy, 8 patients (50%) experienced grade 3 or 4 neutropenia and one of those patients died of neutropenic sepsis. Overall response rate for 20 evaluable patients was 90% including 4 complete responses (20%) and 14 partial responses (70%). Among 18 responders, 9 had local failure, 3 had local and distant failure and 2 had distant failure only. Median progression-free survival time was 9.5 months and 2-year progression-free survival rate was 19%. Eleven patients received second-line or third-line chemotherapy after the treatment failure. The median overall survival time was 21 months. 2-year and 5-year survival rate were 43% and 33%, respectively. Age, performance status, tumor size were significant prognostic factors for progression-free survival. CONCLUSION: Concurrent chemoradiotherapy with weekly paclitaxel revealed high response rate and low toxicity rate. But local failure occurred frequently after the remission and large tumor size was a poor prognostic factor. Further investigations are needed to improve the local control.
Carcinoma, Non-Small-Cell Lung*
;
Chemoradiotherapy*
;
Cisplatin
;
Consolidation Chemotherapy
;
Disease-Free Survival
;
Drug Therapy
;
Esophagitis
;
Humans
;
Neutropenia
;
Paclitaxel*
;
Pneumonia, Bacterial
;
Radiotherapy
;
Retrospective Studies
;
Sepsis
;
Survival Rate
;
Treatment Failure
;
Treatment Outcome*

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