S
Sang-We Kim
Researcher at Sungkyunkwan University
Publications - 6
Citations - 295
Sang-We Kim is an academic researcher from Sungkyunkwan University. The author has contributed to research in topics: Cancer & Point mutation. The author has an hindex of 3, co-authored 6 publications receiving 279 citations.
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Journal ArticleDOI
Phase III trial of two versus four additional cycles in patients who are nonprogressive after two cycles of platinum-based chemotherapy in non small-cell lung cancer
Joon Oh Park,Sang-We Kim,Jin Seok Ahn,Cheolwon Suh,Jung Shin Lee,Joung Soon Jang,Eun Kyung Cho,Sung Hyun Yang,Jin-Hyuk Choi,Dae Seog Heo,Suk Young Park,Sang Won Shin,Myung-Ju Ahn,Jong Seok Lee,Young Ho Yun,Jae-Won Lee,Keunchil Park +16 more
TL;DR: In this paper, the optimal duration of chemotherapy for advanced non-small-cell lung cancer (NSCLC) patients with stages IIIB to IV was determined in a randomized trial, where patients who had not progressed after two cycles of chemotherapy were randomly assigned to receive either four (arm A) or two (arm B) more cycles of platinum doublet treatment.
Journal ArticleDOI
A randomized phase III trial of stereotactic radiosurgery (SRS) versus observation for patients with asymptomatic cerebral oligo-metastases in non-small-cell lung cancer
Sung Hee Lim,J.Y. Lee,Min-Young Lee,Hyera Kim,J.W. Lee,Jong-Mu Sun,Jin-Seok Ahn,Sang-Won Um,Hongsik Kim,Byung Sup Kim,Sang-We Kim,D. L. Na,J-M. Sun,Sin-Ho Jung,Sin-Ho Jung,Kwan Park,O. J. Kwon,Jeeyun Lee,Myung-Ju Ahn +18 more
TL;DR: SRS followed by chemotherapy did not improve OS in oligo-brain metastases NSCLC patients compared with upfront chemotherapy, and further study with large number of patients should be needed to confirm the use of upfront chemotherapy alone in this subgroup of patients.
Clinicopathologic Significance of the K-ras Gene Codon 12 Point Mutation in Stomach Cancer
Kyoo-Hyung Lee,Jung-Shin Lee,Cheolwon Suh,Sang-We Kim,Sung-Bae Kim,Je-Hwan Lee,Moo-Song Lee,Hee-Sik Sun,Sanghee Kim +8 more
TL;DR: In this article, the frequency of K-ras codon 12 point mutations in stomach cancer was investigated using a sensitive polymerase chain reaction (PCR)-based method in 140 samples and correlated the findings with various clinicopathologic characteristics of the patients.
Gefi tinib plus chemotherapy versus placebo plus chemotherapy in EGFR-mutation-positive non-small-cell lung cancer after progression on fi rst-line gefi tinib (IMPRESS): a phase 3 randomised trial
Jean-Charles Soria,Yi Long Wu,Kazuhiko Nakagawa,Sang-We Kim,Jin-Ji Yang,Myung Ju Ahn,Jie Wang,James Chih-Hsin Yang,You Lu,Shinji Atagi,Santiago Ponce,Ho Lee,Yunpeng Liu,Kiyotaka Yoh,Jianying Zhou,Xiaojin Shi,Alan Webster,Haiyi Jiang,Tony Sk Mok +18 more
TL;DR: In this article, the effi cacy and safety of continuing gefi tinib combined with chemotherapy versus chemotherapy alone in patients with EGFR-mutation-positive advanced non-small-cell lung cancer (NSCLC) with acquired resistance to fi rst-line gefifi tinib was evaluated.
Journal ArticleDOI
BIW-8962, an Anti GM2 Ganglioside Monoclonal Antibody, in Previously Treated Advanced/Recurrent Lung Cancer: a Phase I/II Study
Vincent Strout,Keunchil Park,Jong Seok Lee,Sang-We Kim,Jin-Hyoung Kang,D.H. Lee,Byoung Chul Cho,Norihiko Shiraishi,Joo-Hang Kim +8 more
TL;DR: Given the complete lack of response in the study population, further development of BIW- 8962 has been discontinued and it is hoped that the negative findings of this study will contribute to other investigations of GM2 as a therapeutic target, possibly by combination therapy, and of alternative tumor markers in patients with SCLC.