Sheau‑Fang Yang

Dr. Sheau‑Fang Yang

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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1 January 2015 in American Journal of Surgical Pathology
Verified
Journal Article
Closed access
KTKatsuyoshi Takata
Katsuyoshi Takata
MHMin-Eui Hong
Min-Eui Hong
PSPanitta Sitthinamsuwan
Panitta Sitthinamsuwan
FLFlorence Loong
Florence Loong
STSoo-Yong Tan
Soo-Yong Tan
SCShih-Sung Chuang
Shih-Sung Chuang
Primary cutaneous, extranodal natural killer/T-cell lymphoma, nasal type (PC-ENKTL), is a rare Epstein-Barr virus (EBV)-associated neoplasm with poorly defined clinicopathologic features. We performed a multinational retrospective study of PC-ENKTL and CD56-positive EBV-negative peripheral T-cell lymphoma (PC-CD56+PTCL) in Asia in an attempt to elucidate their clinicopathologic features. Using immunohistochemistry for T-cell receptors (TCRs), in situ hybridization for EBV, and TCR gene rearrangement, we classified 60 tumors into 51 with PC-ENKTL (20 of NK-cell, 17 T-cell, and 14 indeterminate lineages) and 9 with PC-CD56+PTCL. Tumors of T-cell origin accounted for 46% of PC-ENKTLs with half of these cases being TCR-silent. As compared with T-lineage tumors, PC-ENKTLs of NK-cell lineage had more frequent involvement of regional lymph nodes and more frequently CD8-negative and CD56-positive. Cases of PC-ENKTL showed more frequent tumor necrosis, younger age, and a higher frequency of CD16 and CD30 expression than cases of PC-CD56+PTCL. CD56-positive T-lineage PC-ENKTL tumors (n=8) had more localized disease in the TNM (tumor-node-metastasis) staging and were more often of γδ T-cell origin compared with cases of PC-CD56+PTCL (n=9). PC-ENKTLs and PC-CD56+PTCLs were equally aggressive, with a 5-year overall survival rate of 25%. Tumor necrosis and CD16 expression may serve as useful surrogates for differentiating PC-ENKTL from PC-CD56+PTCL. A single lesion, an elevated lactate dehydrogenase level, and the presence of B symptoms were independent poor prognostic factors for PC-ENKTL in multivariate analysis. Further studies with more cases are warranted to delineate the clinicopathologic features and significance of EBV in these rare lymphomas.

28 April 2014 in BioMed Research International
Verified
Journal Article
Open access
PDF file
SYSheau‑Fang Yang
Sheau‑Fang Yang
CCChien-Wei Chang
Chien-Wei Chang
RWRen-Jie Wei
Ren-Jie Wei
YSYow-Ling Shiue
Yow-Ling Shiue
SWShen-Nien Wang
Shen-Nien Wang
YYYao-Tsung Yeh
Yao-Tsung Yeh
Hepatocellular carcinoma (HCC) has been known as one of the most lethal human malignancies, due to the difficulty of early detection, chemoresistance, and radioresistance, and is characterized by active angiogenesis and metastasis, which account for rapid recurrence and poor survival. Its development has been closely associated with multiple risk factors, including hepatitis B and C virus infection, alcohol consumption, obesity, and diet contamination. Genetic alterations and genomic instability, probably resulted from unrepaired DNA lesions, are increasingly recognized as a common feature of human HCC. Dysregulation of DNA damage repair and signaling to cell cycle checkpoints, known as the DNA damage response (DDR), is associated with a predisposition to cancer and affects responses to DNA-damaging anticancer therapy. It has been demonstrated that various HCC-associated risk factors are able to promote DNA damages, formation of DNA adducts, and chromosomal aberrations. Hence, alterations in the DDR pathways may accumulate these lesions to trigger hepatocarcinogenesis and also to facilitate advanced HCC progression. This review collects some of the most known information about the link between HCC-associated risk factors and DDR pathways in HCC. Hopefully, the review will remind the researchers and clinicians of further characterizing and validating the roles of these DDR pathways in HCC.

1 February 2014 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
CKChao-Hung Kuo
Chao-Hung Kuo
BWBi-Chuang Weng
Bi-Chuang Weng
CWChun-Chieh Wu
Chun-Chieh Wu
SYSheau‑Fang Yang
Sheau‑Fang Yang
DWDeng-Chyang Wu
Deng-Chyang Wu
YWYuan-Chuen Wang
Yuan-Chuen Wang

8 March 2015 in International Wound Journal
Verified
Journal Article
Closed access
PDF file
Chia-Chi WangChia-Chi Wang
Chia-Chi Wang
PYPo‐Wei Yang
Po‐Wei Yang
SYSheau‑Fang Yang
Sheau‑Fang Yang
KHKun-Pin Hsieh
Kun-Pin Hsieh
Sung-Pin TsengSung-Pin Tseng
Sung-Pin Tseng
YLYing-Chi Lin
Ying-Chi Lin

11 June 2021 in Biomedicines
Verified
Journal Article
Open access
PDF file
YSYung-Chun Su
Yung-Chun Su
SWSheng-Chen Wen
Sheng-Chen Wen
CLChing-Chia Li
Ching-Chia Li
HSHsiao-Chun Su
Hsiao-Chun Su
HKHung-Lung Ke
Hung-Lung Ke
HYHsin-Chih Yeh
Hsin-Chih Yeh
The importance of blood cell markers in patients with malignant tumors has been studied, but there are few studies on the prognostic value of hemoglobin-to-red cell distribution width ratio (HRR) in cancer. This is the first study to investigate the effect of preoperative HRR on patients with upper tract urothelial carcinoma (UTUC). Our retrospective cohort study included 730 UTUC patients who underwent nephroureterectomy from 2000 to 2019. Clinicopathological parameters were compared according to HRR levels, and the relationship between blood cell markers (HRR, white blood cell [WBC] count, platelet count) and prognosis was evaluated using Kaplan–Meier method and Cox regression model. We found that patients with HRR ≤ 1.05 tended to have worse renal function, higher pathological stages, and more high-grade tumors. In univariate analysis, HRR ≤ 1.05, WBC > 8.65 × 103 cells/μL and platelets >309 × 103 cells/μL were associated with poor progression-free survival (PFS), cancer-specific survival (CSS), and overall survival (OS). Multivariate analysis demonstrated that HRR ≤ 1.05 and WBC > 8.65 × 103 cells/μL were independent prognostic factors for predicting deterioration of PFS, CSS, and OS. In conclusion, HRR and WBC are easy to obtain in clinical practice and are useful indicators to provide prognostic information before surgery for UTUC.

21 April 2012 in The Kaohsiung Journal of Medical Sciences
Verified
Journal Article
Open access
HCHung‐Sheng Chi
Hung‐Sheng Chi
KLKa‐Wo Lee
Ka‐Wo Lee
FCFeng‐Yu Chiang
Feng‐Yu Chiang
CTChih‐Feng Tai
Chih‐Feng Tai
LWLing‐Feng Wang
Ling‐Feng Wang
WKWen‐Rei Kuo
Wen‐Rei Kuo
The study's purposes are to identify patient characteristics, treatment response and survival rate, and to describe the important prognostic factors for our patients with extranodal head and neck lymphoma. Furthermore, no study has systemically discussed the overall figure of this disease in Taiwan and we analyzed our data on this topic. A retrospective review was performed for 86 patients with extranodal head and neck lymphoma, diagnosed in Kaohsiung Medical University Hospital, between 1990 and 2007. We evaluated the medical records and analyzed the possible factors affecting treatment outcomes, survival rate, and free‐from‐disease (FFD) survival rate. Forty‐nine male and 37 female patients were included with a male:female ratio of 1.32:1. The most frequent histologic type was diffuse large B cell lymphoma, accounting for 41.9% of the total. The most common primary site involved with extranodal head and neck non‐Hodgkin's lymphoma was a tonsil with 27 cases (31.4%). Stage, international prognostic index (IPI) score, B symptoms, lactate dehydrogenase (LDH) level, and lymph node status significantly affected treatment response. The overall 5‐ and 10‐year survival rates were 68.0% and 57.8%, respectively. The FFD survival rate was 53.6% and 49.3% at 5 and 10 years, respectively. Factors including stage, lymph node status, LDH level, and IPI score produced significant differences in both overall survival and FFD survival. Our analyzed information is similar to other previously presented studies. Stage, IPI score, B symptoms, LDH level, and neck nodal status can be used to evaluate the treatment outcomes. Neck nodal status and stage are the two significant prognostic factors for overall survival.