1.Phase II Study of Gemcitabine and Vinorelbine as a Combination Chemotherapy for the Second-Line Treatment of Nonsmall Cell Lung Carcinoma.
EunJoo LEE ; EunSil HA ; SangHoon PARK ; GyuYoung HUR ; KiHwan JUNG ; HyeCheol JEONG ; SungYong LEE ; JeHyeong KIM ; SangYeub LEE ; Chol SIN ; JaeJeong SHIM ; KwangHo IN ; KyungHo KANG ; SeHwa YOO
Tuberculosis and Respiratory Diseases 2005;59(5):510-516
BACKGROUND: Lung cancer is the leading cause of cancer deaths in Korea and the number of lung cancer deaths is increasing. The higher response rates, decreased toxicity and improved performance status of the first-line treatments have resulted in an increased number of patients becoming candidates for second-line therapy. Several new anti??neoplastic agents, including gemcitabine, docetaxel and paclitaxel, have recently demonstrated second-line activity. This phase II study evaluated the efficacy and toxicity of gemcitabine and vinorelbine as combination chemotherapy for Korean patients with NSCLC as a second-line treatment. METHODS: Sixty response-evaluable patients were enrolled from December 2000 to July 2003. We conducted a phase II study of a combination gemcitabine and vinorelbine chemotherapy for patients with histologically confirmed NSCLC that was stage IIIB and IV disease at the time of diagnosis, and the disease had progressed onward or the patients had relapsed after first-line platinum-based chemotherapy. They were treated with intravenous gemcitabine 1000mg/m2 and intravenous vinorelbine 25mg/m2 on days 1 and 8. This chemotherapy regimen was repeated every 3 weeks. RESULTS: A total of 215 cycles of treatment were given and the mean number of cycles was 3.6 cycles. All the patients were evaluable for the toxicity profile. The response rate was 10% according to the WHO criteria.?The median progression free survival was 3.8 months and the median survival time was 10.1 months. The 1-year survival rate was 32.9%. Grade III and IV neutropenia were seen in 20 (33.3%) and 7 (11.7%) patients, respectively. CONCLUSION: The combination of gemcitabine and vinorelbine is active and well tolerated as a second-line therapy for patients with advanced nonsmall cell lung carcinoma.
Carcinoma, Non-Small-Cell Lung
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Diagnosis
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Disease-Free Survival
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Drug Therapy
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Drug Therapy, Combination*
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Humans
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Korea
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Lung Neoplasms
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Lung*
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Neutropenia
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Paclitaxel
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Survival Rate
2.Predictors of Pulmonary Function Response to Treatment with Salmeterol/fluticasone in Patients with Chronic Obstructive Pulmonary Disease.
Jae Seung LEE ; Jin Won HUH ; Eun Jin CHAE ; Joon Beom SEO ; Seung Won RA ; Ji Hyun LEE ; Eun Kyung KIM ; Young Kyung LEE ; Tae Hyung KIM ; Woo Jin KIM ; Jin Hwa LEE ; Sang Min LEE ; Sangyeub LEE ; Seong Yong LIM ; Tae Rim SHIN ; Ho Il YOON ; Seung Soo SHEEN ; Yeon Mok OH ; Sang Do LEE
Journal of Korean Medical Science 2011;26(3):379-385
Chronic obstructive pulmonary disease (COPD) is a heterogeneous disease and responses to therapies are highly variable. The aim of this study was to identify the predictors of pulmonary function response to 3 months of treatment with salmeterol/fluticasone in patients with COPD. A total of 127 patients with stable COPD from the Korean Obstructive Lung Disease (KOLD) Cohort, which were prospectively recruited from June 2005 to September 2009, were analyzed retrospectively. The prediction models for the FEV1, FVC and IC/TLC changes after 3 months of treatment with salmeterol/fluticasone were constructed by using multiple, stepwise, linear regression analysis. The prediction model for the FEV1 change after 3 months of treatment included wheezing history, pre-bronchodilator FEV1, post-bronchodilator FEV1 change and emphysema extent on CT (R = 0.578). The prediction models for the FVC change after 3 months of treatment included pre-bronchodilator FVC, post-bronchodilator FVC change (R = 0.533), and those of IC/ TLC change after 3 months of treatment did pre-bronchodilator IC/TLC and post-bronchodilator FEV1 change (R = 0.401). Wheezing history, pre-bronchodilator pulmonary function, bronchodilator responsiveness, and emphysema extent may be used for predicting the pulmonary function response to 3 months of treatment with salmeterol/fluticasone in patients with COPD.
Aged
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Albuterol/*analogs & derivatives/therapeutic use
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Androstadienes/*therapeutic use
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Bronchodilator Agents/*therapeutic use
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Emphysema
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Female
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Humans
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Linear Models
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Lung/physiopathology
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Male
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Middle Aged
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Prognosis
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Pulmonary Disease, Chronic Obstructive/*drug therapy
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Republic of Korea
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Respiratory Function Tests
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Retrospective Studies
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Tomography Scanners, X-Ray Computed
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Treatment Outcome
3.Contributors of the Severity of Airflow Limitation in COPD Patients.
Yoonki HONG ; Eun Jin CHAE ; Joon Beom SEO ; Ji Hyun LEE ; Eun Kyung KIM ; Young Kyung LEE ; Tae Hyung KIM ; Woo Jin KIM ; Jin Hwa LEE ; Sang Min LEE ; Sangyeub LEE ; Seong Yong LIM ; Tae Rim SHIN ; Ho Il YOON ; Seung Soo SHEEN ; Seung Won RA ; Jae Seung LEE ; Jin Won HUH ; Sang Do LEE ; Yeon Mok OH
Tuberculosis and Respiratory Diseases 2012;72(1):8-14
BACKGROUND: Although airway obstruction in chronic obstructive pulmonary disease (COPD) is due to pathologic processes in both the airways and the lung parenchyma, the contribution of these processes, as well as other factors, have not yet been evaluated quantitatively. We therefore quantitatively evaluated the factors contributing to airflow limitation in patients with COPD. METHODS: The 213 COPD patients were aged >45 years, had smoked >10 pack-years of cigarettes, and had a post-bronchodilator forced expiratory volume in one second (FEV1)/forced vital capacity (FVC) <0.7. All patients were evaluated by medical interviews, physical examination, spirometry, bronchodilator reversibility tests, lung volume, and 6-minute walk tests. In addition, volumetric computed tomography (CT) was performed to evaluate airway wall thickness, emphysema severity, and mean lung density ratio at full expiration and inspiration. Multiple linear regression analysis was performed to identify the variables independently associated with FEV1 - the index of the severity of airflow limitation. RESULTS: Multiple linear regression analysis showed that CT measurements of mean lung density ratio (standardized coefficient beta=-0.46; p<0.001), emphysema severity (volume fraction of the lung less than -950 HU at full inspiration; beta=-0.24; p<0.001), and airway wall thickness (mean wall area %; beta=-0.19, p=0.001), as well as current smoking status (beta=-0.14; p=0.009) were independent contributors to FEV1. CONCLUSION: Mean lung density ratio, emphysema severity, and airway wall thickness evaluated by volumetric CT and smoking status could independently contribute to the severity of airflow limitation in patients with COPD.
Aged
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Airway Obstruction
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Cone-Beam Computed Tomography
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Emphysema
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Forced Expiratory Volume
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Humans
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Linear Models
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Lung
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Pathologic Processes
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Physical Examination
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Pulmonary Disease, Chronic Obstructive
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Smoke
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Smoking
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Spirometry
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Tobacco Products
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Tomography, X-Ray Computed
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Vital Capacity
4.Comparison of Clinico-Physiologic and CT Imaging Risk Factors for COPD Exacerbation.
Jung Wan YOO ; Yoonki HONG ; Joon Beom SEO ; Eun Jin CHAE ; Seung Won RA ; Ji Hyun LEE ; Eun Kyung KIM ; Seunghee BAEK ; Tae Hyung KIM ; Woo Jin KIM ; Jin Hwa LEE ; Sang Min LEE ; Sangyeub LEE ; Seong Yong LIM ; Tae Rim SHIN ; Ho Il YOON ; Seung Soo SHEEN ; Jae Seung LEE ; Jin Won HUH ; Yeon Mok OH ; Sang Do LEE
Journal of Korean Medical Science 2011;26(12):1606-1612
To date, clinico-physiologic indices have not been compared with quantitative CT imaging indices in determining the risk of chronic obstructive pulmonary disease (COPD) exacerbation. We therefore compared clinico-physiologic and CT imaging indices as risk factors for COPD exacerbation in patients with COPD. We retrospectively analyzed 260 COPD patients from pulmonary clinics at 11 hospitals in Korea from June 2005 to November 2009 and followed-up for at least one year. At the time of enrollment, none of these patients had COPD exacerbations for at least 2 months. All underwent clinico-physiologic and radiological evaluation for risk factors of COPD exacerbation. After 1 yr, 106 of the 260 patients had at least one exacerbation of COPD. Multiple logistic regression analysis showed that old age, high Charlson Index, and low FEV1 were significant in a clinico-physiologic model, with C-statistics of 0.69, and that increased age and emphysema index were significant in a radiologic model, with C-statistics of 0.64. The difference between the two models was statistically significant (P = 0.04 by bootstrap analysis). Combinations of clinico-physiologic risk factors may be better than those of imaging risk factors in predicting COPD exacerbation.
Aged
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Aged, 80 and over
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Disease Progression
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Female
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Humans
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Male
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Middle Aged
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Pulmonary Disease, Chronic Obstructive/*diagnosis/pathology/*physiopathology
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Retrospective Studies
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Risk Factors
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Severity of Illness Index
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*Tomography, X-Ray Computed