Hoon Jai Chun

Hoon Jai Chun


Research Focus & Metrics

Academic Career Length

27Years (2000-Present)

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

Representative Publications

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30 March 2020 in Clinical Endoscopy
Verified
Journal Article
Open access
PDF file
CPChan Hyuk Park
Chan Hyuk Park
DYDong-Hoon Yang
Dong-Hoon Yang
JKJong Wook Kim
Jong Wook Kim
JKJie-Hyun Kim
Jie-Hyun Kim
YMYang Won Min
Yang Won Min
HCHoon Jai Chun
Hoon Jai Chun
Although surgery was the standard treatment for early gastrointestinal cancers, endoscopic resection is now a standard treatment for early gastrointestinal cancers without regional lymph node metastasis. High-definition white light endoscopy, chromoendoscopy, and image-enhanced endoscopy such as narrow band imaging are performed to assess the edge and depth of early gastrointestinal cancers for delineation of resection boundaries and prediction of the possibility of lymph node metastasis before the decision of endoscopic resection. Endoscopic mucosal resection and/or endoscopic submucosal dissection can be performed to remove early gastrointestinal cancers completely by en bloc fashion. Histopathological evaluation should be carefully made to investigate the presence of risk factors for lymph node metastasis such as depth of cancer invasion and lymphovascular invasion. Additional treatment such as radical surgery with regional lymphadenectomy should be considered if the endoscopically resected specimen shows risk factors for lymph node metastasis. This is the first Korean clinical practice guideline for endoscopic resection of early gastrointestinal cancer. This guideline was developed by using mainly de novo methods and encompasses endoscopic management of superficial esophageal squamous cell carcinoma, early gastric cancer, and early colorectal cancer. This guideline will be revised as new data on early gastrointestinal cancer are collected.

6 July 2022 in Gut and Liver
Verified
Journal Article
Open access
PDF file
YCYoon Jin Choi
Yoon Jin Choi
YLYong Chan Lee
Yong Chan Lee
Jung Mogg KimJung Mogg Kim
Jung Mogg Kim
JKJie-Hyun Kim
Jie-Hyun Kim
JMJeong Seop Moon
Jeong Seop Moon
JJJae Young Jang
Jae Young Jang
Yoon Jin Choi, Yong Chan Lee, Jung Mogg Kim, Jin Il Kim, Jeong Seop Moon, Yun Jeong Lim, Gwang Ho Baik, Byoung Kwan Son, Hang Lak Lee, Kyoung Oh Kim, Nayoung Kim, Kwang Hyun Ko, Hye-Kyung Jung, Ki-Nam Shim, Hoon Jai Chun, Byung-Wook Kim, Hyuk Lee, Jie-Hyun Kim, Hyunsoo Chung, Sang Gyun Kim, and Jae Young Jang. Gut and Liver 2022;16:535-46. https://doi.org/10.5009/gnl220055

1 February 2012 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
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HPHee-Jung Park
Hee-Jung Park
CLChang Su Lim
Chang Su Lim
EKEun-Sun Kim
Eun-Sun Kim
JHJi Hee Han
Ji Hee Han
TLTae Hee LEE
Tae Hee LEE
BCBong Rae Cho
Bong Rae Cho

6 July 2021 in Alimentary Pharmacology & Therapeutics
Verified
Journal Article
Open access
PDF file
SKSeung Han Kim
Seung Han Kim
KCKwang Bum Cho
Kwang Bum Cho
HCHoon Jai Chun
Hoon Jai Chun
SLSang Woo Lee
Sang Woo Lee
JKJoong Goo Kwon
Joong Goo Kwon
GSGeun Seog Song
Geun Seog Song
Summary: Background: Tegoprazan is a novel, fast‐ and long‐acting potassium‐competitive acid blocker that suppresses gastric acid secretion, which could benefit patients with non‐erosive reflux disease (NERD), a type of gastroesophageal reflux disease.Aim: To evaluate the efficacy and safety profiles of tegoprazan compared with those of a placebo in Korean patients with NERD.Methods: In this phase 3, double‐blind, placebo‐controlled, multicentre study, 324 Korean patients with NERD were randomised into three treatment groups: tegoprazan 50 mg, tegoprazan 100 mg and placebo. These drugs were provided once daily for 4 weeks. The primary endpoint was the proportion of patients with complete resolution of major symptoms (both heartburn and regurgitation) for the last 7 days of the 4‐week treatment period. Other outcomes related to efficacy, safety and tolerability were also evaluated.Results: Among all, 42.5% (45/106), 48.5% (48/99) and 24.2% (24/99) of patients showed complete resolution of major symptoms at week 4 after receiving tegoprazan 50 mg, tegoprazan 100 mg, and placebo, respectively. Both doses of tegoprazan showed superior efficacy than the placebo (P = 0.0058 and P = 0.0004, respectively). The complete resolution rates of heartburn and proportions of heartburn‐free days (as other efficacy outcomes) were significantly higher in both tegoprazan groups than in the placebo group (P < 0.05 for all). No significant difference in the incidence of treatment‐emergent adverse events were noted.Conclusions: Tegoprazan 50 and 100 mg showed superior therapeutic efficacy compared with the placebo, as well as a favourable safety profile in patients with NERD.Registration number: ClinicalTrials.gov identifier NCT02556021.

27 July 2000 in Organic Letters
Verified
Journal Article
Closed access
KOKyung Seok Oh
Kyung Seok Oh
CLChi-Wan Lee
Chi-Wan Lee
HCHoon Jai Chun
Hoon Jai Chun
SLSeok Jong Lee
Seok Jong Lee
KKKwang S. Kim
Kwang S. Kim

1 January 2011 in World Journal of Gastroenterology
Verified
Journal Article
Open access
SPSung Chul Park
Sung Chul Park
HCHoon Jai Chun
Hoon Jai Chun
CKChang Don Kang
Chang Don Kang
DSDonggeun Sul
Donggeun Sul
Non-steroidal anti-inflammatory drug (NSAID)-induced small bowel injury is a topic that deserves attention since the advent of capsule endoscopy and balloon enteroscopy. NSAID enteropathy is common and is mostly asymptomatic. However, massive bleeding, stricture, or perforation may occur. The pathogenesis of small intestine injury by NSAIDs is complex and different from that of the upper gastrointestinal tract. No drug has yet been developed that can completely prevent or treat NSAID enteropathy. Therefore, a long-term randomized study in chronic NSAID users is needed.