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Byoung Chul Cho

Researcher at Yonsei University

Publications -  570
Citations -  23868

Byoung Chul Cho is an academic researcher from Yonsei University. The author has contributed to research in topics: Medicine & Lung cancer. The author has an hindex of 57, co-authored 429 publications receiving 15603 citations. Previous affiliations of Byoung Chul Cho include University Health System & AstraZeneca.

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A randomized, phase II study of gefitinib alone versus nimotuzumab plus gefitinib after platinum-based chemotherapy in advanced non-small cell lung cancer (KCSG LU12-01).

TL;DR: The dual inhibition of EGFR with nimotuzumab plus gefitinib was not associated with better outcomes than gefithinib alone as a second-line treatment of advanced NSCLC and combined treatment did not increase EGFR inhibition-related adverse events with manageable toxicities.
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Identification of Local Clusters of Mutation Hotspots in Cancer-Related Genes and Their Biological Relevance

TL;DR: A Smith-Waterman algorithm-based mutation hotspot discovery method, MutClustSW, is developed to identify mutation hotspots of either single or clustered amino acid residues and shows that hotspot mutations have higher mutation allele frequency than non-hotspots, and the hotspot information can be used to prioritize the cancer drivers.
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A randomized phase II trial of ERCC1 and RRM1 mRNA expression-based chemotherapy versus docetaxel/carboplatin in advanced non-small cell lung cancer

TL;DR: ERCC1 and RRM1 mRNA expression-based chemotherapy did not improve clinical outcomes in advanced NSCLC and was prematurely terminated after the futility analysis of 43 progression-free survival (PFS) events.
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SKYSCRAPER-07: A phase III, randomized, double-blind, placebo-controlled study of atezolizumab with or without tiragolumab in patients with unresectable ESCC who have not progressed following definitive concurrent chemoradiotherapy.

TL;DR: It is hypothesize that combination therapy will prolong PFS and OS compared with placebo in this setting, and concomitant blockade of PD-L1/PD-1 and TIGIT pathways demonstrated prolonged survival over the respective single-agents.