Chih-Cheng Chen

Prof. Dr. Chih-Cheng Chen


Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 2006 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
MCMiao-Fen Chen
Miao-Fen Chen
CLChing-Tai Lin
Ching-Tai Lin
WCWen-Cheng Chen
Wen-Cheng Chen
CYCheng-Ta Yang
Cheng-Ta Yang
CCChih-Cheng Chen
Chih-Cheng Chen
KLKuan-Der Lee
Kuan-Der Lee

1 April 2004 in Annals of Oncology
Verified
Journal Article
Open access
PDF file
JYJ.-Y. You
J.-Y. You
KCK.-H. Chi
K.-H. Chi
MYM.-H. Yang
M.-H. Yang
CCChih-Cheng Chen
Chih-Cheng Chen
CHC.-H. Ho
C.-H. Ho
TCTzeon-Jye Chiou
Tzeon-Jye Chiou
Background: To clarify the role of intention to treat for patients with localized nasal natural killer (NK)/T-cell lymphoma, and to determine the prognostic factors for these patients. Patients and methods: We conducted a retrospective review of 46 patients with localized nasal NK/T-cell lymphomas treated at a single institute between January 1988 and July 2002. Results: The type of intended treatment was a significant factor for overall survival (OS) (5-year OS: RT versus CT = 83.3% versus 28.6%, P = 0.0269) or failure-free survival (FFS) (5-year FFS: RT versus CT = 83.3% versus 27.1%, P = 0.0247). In the intended chemotherapy group, salvage with radiotherapy was superior to chemotherapy alone for OS (5-year OS: 42.2% versus 20.0%, P = 0.0252) or FFS (5-year FFS: 41.0% versus 20.0%, P = 0.0352). On multivariate analysis, both N stage and serum lactate hehydrogenase level were independent factors for OS and FFS. No radiotherapy was an independent adverse factor for OS; advanced T stage and more than one extranodal involvement were independent adverse factors for FFS. Conclusions: Patients with localized nasal NK/T-cell lymphomas were better managed with radiotherapy as front-line therapy. The advantage of radiotherapy persisted even as palliative therapy after chemotherapy.

1 October 2008 in Cancer Epidemiology, Biomarkers & Prevention
Verified
Journal Article
Open access
PDF file
KLKuan-Der Lee
Kuan-Der Lee
SCShin-Cheh Chen
Shin-Cheh Chen
CCChunghuang Hubert Chan
Chunghuang Hubert Chan
CLChang-Hsien Lu
Chang-Hsien Lu
CCChih-Cheng Chen
Chih-Cheng Chen
MCMin-Chi Chen
Min-Chi Chen
Studies conducted in Western countries have reported excess risks for second primary malignancies after breast cancer. However, there is little documentation of ethnic differences in these excess risks. Asian women are characterized by younger age at diagnosis of breast cancer, but very few reports are available on the incidences and risks for second primary cancers in this region. Using population-based data from the Taiwan National Cancer Registry (TNCR) for the period 1979 to 2003, we quantified standardized incidence ratios and cumulative incidence of second cancers among 53,783 women with initial diagnoses of breast cancer. Age-specific incidences showed peaks among women in their 40s, and 1,085 cases (2.02%) developed nonbreast second primary cancers. The risk for second cancers differs significantly according to age at diagnosis of breast cancer. In comparison with women diagnosed when ≥50 years (standardized incidence ratio, 0.96; 95% confidence interval; 0.89-1.04), there were significantly greater risks for bone, corpus uterine, ovarian, thyroid, esophageal, kidney and lung cancers, nonmelanoma skin cancer, and leukemia or lymphoma in women diagnosed when <50 years (standardized incidence ratio, 1.43; 95% confidence interval, 1.29-1.58). The survival probabilities differed between breast cancer patients with and without second cancers (P < 0.001). After diagnosis of the second cancer, the median survival time was only 2.87 years. In conclusion, we confirmed that young age at diagnosis of breast cancer predicted a subsequently increased risk for second malignancies, and the second cancers indeed worsen survivorship in patients who survived breast cancer. (Cancer Epidemiol Biomarkers Prev 2008;17(10):2647–55)

5 August 2015 in Health and Quality of Life Outcomes
Verified
Journal Article
Open access
PDF file
CCChih-Cheng Chen
Chih-Cheng Chen
CTChih-Chien Tsai
Chih-Chien Tsai
CCChia-Ying Chung
Chia-Ying Chung
CCChia-Ling Chen
Chia-Ling Chen
QXQiao-Xuan Xie
Qiao-Xuan Xie
HCHsieh-Ching Chen
Hsieh-Ching Chen
Improving HRQOL is the desired outcome for patients with stroke undergoing inpatient rehabilitation services. This study aimed to comprehensively identify the potential health-related quality of life (HRQOL) predictors in patients with stroke undergoing inpatient rehabilitation within the first year after stroke; thus far, such an investigation has not been conducted. We enrolled 119 patients (88 males, 31 females) with stroke, and examined 12 potential predictors: age, sex, stroke type, stroke side, duration after onset, cognition (Mini-Mental State Examination; MMSE), depression (Beck Depression Inventory-II), stroke severity (National Institutes of Health Stroke Scale; NIHSS), upper- and lower-extremity motor function scores of the Fugl–Meyer Assessment (FMA) scale, balance (Berg Balance Scale; BBS), and functional status (Functional Independence Measure). HRQOL was measured using Stroke Impact Scale (SIS) 3.0. NIHSS score predicted the strength domain and total SIS score (41.5 % and 41.7 % of the variances, respectively). BBS score was a major predictor of mobility and participation/role domains (48.6 % and 10 % of the variances, respectively). MMSE score predicted the memory and communication domains (22.5 % and 36.3 % of the variances, respectively). Upper extremity score of the FMA scale predicted the daily living/instrumental activities of daily life and hand function domains (40.3 % and 20.6 % of the variances, respectively). Stroke side predicted the emotion domain (11.6 % of the variance). NIHSS, MMSE, BBS, FMA, and stroke side predicted most HRQOL domains. These findings suggest that different factors predicted various HRQOL domains in patients with stroke.

30 January 2008 in Annals of Oncology
Verified
Journal Article
Closed access
PDF file
MCM.-C. Chen
M.-C. Chen
IFI.-J. Feng
I.-J. Feng
CLC.-H. Lu
C.-H. Lu
CCChih-Cheng Chen
Chih-Cheng Chen
JLJ.-T. Lin
J.-T. Lin
KLK.-D. Lee
K.-D. Lee
Background: Very few reports are available on the incidence and risk of second primary cancers in nasopharyngeal carcinoma (NPC) cases, and most of these are single-institution reviews with relatively small case numbers and short follow-up. Patients and methods: A population-based study was conducted. We quantified standardized incidence ratios (SIRs) and cumulative incidence of second cancers among 23 639 individuals with initial diagnoses of NPC. Results: We found a 24% increased risk of second cancers in NPC patients compared with the general population [SIR = 1.24, 95% confidence interval 1.15–1.33]. Elevated SIRs were observed in the following second primary cancers: oral/pharyngeal, salivary gland, sarcoma, skin and leukemia/lymphoma. The cumulative incidence >10 years was 3.26%. The risk was higher in younger patients, especially those <40 years old. After diagnosis of second cancers, the median survival time was 1.7 years. Conclusions: This is the largest population-based study to date from a high-incidence area. We found that NPC is associated with an increased risk of second malignancies, which had a negative impact on the survival of patients who survived NPC.

1 October 2013 in Biochemical Pharmacology
Verified
Journal Article
Closed access
CCChih-Cheng Chen
Chih-Cheng Chen
CCChia-Bao Chu
Chia-Bao Chu
KLKo-Jiunn Liu
Ko-Jiunn Liu
Chi-Ying F. HuangChi-Ying F. Huang
Chi-Ying F. Huang
JCJang-Yang Chang
Jang-Yang Chang
LCLi-Tzong Chen
Li-Tzong Chen