Joon Oh Park

ORCID: 0000-0001-6502-2612
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About
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Research Areas
  • Colorectal Cancer Treatments and Studies
  • Pancreatic and Hepatic Oncology Research
  • Gastric Cancer Management and Outcomes
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Cancer Genomics and Diagnostics
  • Lung Cancer Treatments and Mutations
  • Gastrointestinal Tumor Research and Treatment
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Genetic factors in colorectal cancer
  • Colorectal and Anal Carcinomas
  • Metastasis and carcinoma case studies
  • Cancer Treatment and Pharmacology
  • Gallbladder and Bile Duct Disorders
  • Neuroendocrine Tumor Research Advances
  • Colorectal Cancer Surgical Treatments
  • Fibroblast Growth Factor Research
  • Cancer Immunotherapy and Biomarkers
  • Lung Cancer Research Studies
  • Cancer Cells and Metastasis
  • PARP inhibition in cancer therapy
  • HER2/EGFR in Cancer Research
  • Peptidase Inhibition and Analysis
  • Cancer, Lipids, and Metabolism
  • Cancer Mechanisms and Therapy
  • Renal cell carcinoma treatment

Samsung Medical Center
2016-2025

Sungkyunkwan University
2016-2025

University of Ulsan
2007-2025

Ulsan College
2025

Seoul Medical Center
2025

Seoul National University Hospital
2006-2024

Samsung (South Korea)
2018-2024

ABL Bio (South Korea)
2023

Merck Serono (Switzerland)
2023

AstraZeneca (Brazil)
2023

The epidermal growth factor receptor (EGFR) kinase inhibitors gefitinib and erlotinib are effective treatments for lung cancers with EGFR activating mutations, but these tumors invariably develop drug resistance. Here, we describe a gefitinib-sensitive cancer cell line that developed resistance to as result of focal amplification the MET proto-oncogene. inhibition signaling in cells restored their sensitivity gefitinib. was detected 4 18 (22%) specimens had or erlotinib. We find causes by...

10.1126/science.1141478 article EN Science 2007-04-27

10.1016/s0140-6736(15)00986-1 article EN The Lancet 2015-11-29

Purpose The ARTIST (Adjuvant Chemoradiation Therapy in Stomach Cancer) trial was the first study to our knowledge investigate role of postoperative chemoradiotherapy therapy patients with curatively resected gastric cancer D2 lymph node dissection. This designed compare treatment capecitabine plus cisplatin (XP) versus XP radiotherapy (XP/XRT/XP). Patients and Methods arm received six cycles (capecitabine 2,000 mg/m 2 per day on days 1 14 60 1, repeated every 3 weeks) chemotherapy. XP/XRT/XP...

10.1200/jco.2011.39.1953 article EN Journal of Clinical Oncology 2011-12-20

When designing this trial, there was no evidence that salvage chemotherapy (SLC) in advanced gastric cancer (AGC) resulted substantial prolongation of survival when compared with best supportive care (BSC). However, SLC is often offered to pretreated patients AGC for anecdotal reasons.Patients one or two prior regimens involving both fluoropyrimidines and platinum an Eastern Cooperative Oncology Group performance status (PS) 0 1 were randomly assigned a ratio 2:1 plus BSC alone. Choice...

10.1200/jco.2011.39.4585 article EN Journal of Clinical Oncology 2012-03-13

To evaluate the efficacy of adding lapatinib to capecitabine and oxaliplatin (CapeOx) in patients with previously untreated human epidermal growth factor receptor 2 (HER2) -amplified advanced gastroesophageal adenocarcinoma.Patients HER2-positive adenocarcinoma were randomly assigned at a one-to-one ratio CapeOx plus 1,250 mg or placebo daily. Primary end point was overall survival (OS) centrally confirmed HER2 amplification primary population.A total 545 assigned, 487 comprised population....

10.1200/jco.2015.62.6598 article EN Journal of Clinical Oncology 2015-12-02

Objective: This study was performed to determine whether neoadjuvant treatment increases survival in patients with BRPC. Summary Background Data: Despite many promising retrospective data on the effect of for borderline resectable pancreatic cancer (BRPC), no high-level evidence exists support role such treatment. Methods: phase 2/3 multicenter randomized controlled trial designed enroll 110 BRPC who were randomly assigned gemcitabine-based chemoradiation (54 Gray external beam radiation)...

10.1097/sla.0000000000002705 article EN Annals of Surgery 2018-02-18
Robin Kate Kelley Makoto Ueno Changhoon Yoo Richard S. Finn Junji Furuse and 95 more Zhenggang Ren Thomas Yau Heinz‐Josef Klümpen Stephen L. Chan Masato Ozaka Chris Verslype Mohamed Bouattour Joon Oh Park Olga Barajas Uwe Pelzer Juan W. Valle Li Yu Usha Malhotra Abby B. Siegel Julien Edeline Arndt Vogel Mehmet Akce Inmaculada Alés Díaz Gustavo R. Alves Sumitra Anand Çağatay Arslan Jamil Asselah Éric Assenat F. Aubin Li‐Yuan Bai Yuxian Bai Olga Barajas Susan E. Bates Stephen Begbie Irit Ben‐Aharon Nina Beri Marie‐Luise Berres Jean‐Frédéric Blanc Ivan Borbath Robert Bordonaro Mohamed Bouattour Giovanni Brandi Adam M. Burgoyne Kritiya Butthongkomvong Marcos Pedro Guedes Camandaroba Ke Cao Marcela Carballido Stephen L. Chan Jen‐Shi Chen Ming‐Huang Chen Xiaohong Chen Ashley Cheng Tai‐Jan Chiu Hye Jin Choi Hong Jae Chon Joëlle Collignon Antonio Cubillo Gracián S. Lindsey Davis Ricardo Saraiva de Carvalho D.J.A. de Groot Anne Demols Judith De Vos Maria Diab Jacob C. Easaw Martin Eatock Julien Edeline Rawad Elias Fredericus Eskens Alfredo Falcone Plinio Fernández Richard S. Finn Fábio Franke Masayuki Furukawa Junji Furuse Olumide B. Gbolahan Karen Geboes Keri-Lee Geneser Zhimin Geng Ravit Geva Roopinder Gillmore Thorsten Oliver Goetze Hongfeng Gou Julieta Grasselli Shanzhi Gu Mahmut Gümüş Nadia Haj Mohammad Chunyi Hao Hakan Harputluoğlu Hassan Hatoum Volker Heinemann Wang Kwong Ho Chiun Hsu Ayala Hubert Jun‐Eul Hwang Mevlüde İnanç Soledad Iseas Vaishnavi Jeyasingam Paula Jiménez Fonseca Warren Joubert Jitlada Juengsamarn

10.1016/s0140-6736(23)00727-4 article EN The Lancet 2023-04-16

The Adjuvant Chemoradiotherapy in Stomach Tumors (ARTIST) trial tested whether the addition of radiotherapy to adjuvant chemotherapy improved disease-free survival (DFS) patients with D2-resected gastric cancer (GC).Between November 2004 and April 2008, 458 GC who received gastrectomy D2 lymph node dissection were randomly assigned either six cycles capecitabine cisplatin (XP) or two XP followed by chemoradiotherapy then additional (XPRT). This final update contains first publication overall...

10.1200/jco.2014.58.3930 article EN Journal of Clinical Oncology 2015-01-06

To evaluate the efficacy and safety of pegvorhyaluronidase alfa (PEGPH20) plus nab-paclitaxel/gemcitabine (AG) in patients with hyaluronan-high metastatic pancreatic ductal adenocarcinoma (PDA).HALO 109-301 was a phase III, randomized, double-blind, placebo-controlled study. Patients ≥ 18 years age untreated, metastatic, PDA were randomly assigned 2:1 to PEGPH20 AG or placebo AG. Treatment administered intravenously 4-week cycles (3 weeks on, 1 week off) until progression intolerable adverse...

10.1200/jco.20.00590 article EN cc-by-nc-nd Journal of Clinical Oncology 2020-07-24

Purpose Gastric cancer cell lines, particularly those with low levels of ataxia telangiectasia mutated (ATM), a key activator DNA damage response, are sensitive to the poly (ADP-ribose) polymerase inhibitor olaparib. We compared efficacy olaparib plus paclitaxel (olaparib/paclitaxel) alone in patients recurrent or metastatic gastric and assessed whether ATM expression is predictive improved clinical outcome for olaparib/paclitaxel. Patients Methods In this phase II, double-blind study (Study...

10.1200/jco.2014.60.0320 article EN Journal of Clinical Oncology 2015-08-18

Adjuvant chemotherapy and chemoradiotherapy are some of the standards care for gastric cancer (GC). The chemoRadioTherapy In Stomach Tumors (ARTIST) 2 trial compares two adjuvant regimens in patients with D2-resected, stage II or III, node-positive GC.The ARTIST compared, a 1:1:1 ratio, three regimens: oral S-1 (40-60 mg twice daily 4 weeks on/2 off) 1 year, (2 on/1 week plus oxaliplatin 130 mg/m2 every 3 (SOX) 6 months, SOX 45 Gy (SOXRT). Randomization was stratified according to surgery...

10.1016/j.annonc.2020.11.017 article EN cc-by-nc-nd Annals of Oncology 2020-12-03

Solid tumors such as pancreatic ductal adenocarcinoma (PDAC) comprise not just tumor cells but also a microenvironment with which the constantly interact. Detailed characterization of cellular composition is critical to understanding disease and treatment patient. Single-cell transcriptomics has been used study different solid types including PDAC. However, almost all those studies primary tissues.In this study, we employed single-cell RNA sequencing technology profile transcriptomes...

10.1186/s13073-020-00776-9 article EN cc-by Genome Medicine 2020-09-28

Futibatinib, a highly selective, irreversible FGFR1-4 inhibitor, was evaluated in large multihistology phase I dose-expansion trial that enrolled 197 patients with advanced solid tumors. Futibatinib demonstrated an objective response rate (ORR) of 13.7%, responses broad spectrum tumors (cholangiocarcinoma and gastric, urothelial, central nervous system, head neck, breast cancer) bearing both known previously uncharacterized FGFR1-3 aberrations. The greatest activity observed FGFR2...

10.1158/2159-8290.cd-21-0697 article EN cc-by-nc-nd Cancer Discovery 2021-09-22

Abstract The VIKTORY (targeted agent eValuation In gastric cancer basket KORea) trial was designed to classify patients with metastatic based on clinical sequencing and focused eight different biomarker groups (RAS aberration, TP53 mutation, PIK3CA mutation/amplification, MET amplification, overexpression, all negative, TSC2 deficient, or RICTOR amplification) assign one of the 10 associated trials in second-line (2L) treatment. Capivasertib (AKT inhibitor), savolitinib (MET selumetinib (MEK...

10.1158/2159-8290.cd-19-0442 article EN Cancer Discovery 2019-07-17

The phase III POLO study demonstrated significant progression-free survival (PFS) benefit for active olaparib maintenance therapy versus placebo patients with metastatic pancreatic adenocarcinoma and a germline BRCA mutation. Here, we report the final analysis of overall (OS) other secondary end points.

10.1200/jco.21.01604 article EN Journal of Clinical Oncology 2022-07-14
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