Skip to main content

Bhumsuk Keam

Seoul National University · Medicine

About the Lab

Professor Bhumsuk Keam's research lab focuses on translational oncology, with a strong emphasis on molecularly targeted therapies and immunotherapy in aggressive and treatment-resistant cancers. The lab investigates biomarkers for predicting response to chemotherapy and targeted agents, particularly in triple-negative breast cancer, anaplastic thyroid cancer, and head and neck squamous cell carcinoma. A key research direction involves understanding the interplay between immune checkpoint expression (e.g., PD-L1) and tumor microenvironment features such as epithelial-mesenchymal transition and natural killer cell-mediated ADCC. The lab also explores end-of-life care patterns in cancer patients, highlighting gaps in palliative care delivery in clinical practice.

targeted therapyimmunotherapybiomarkerstriple-negative breast cancerPD-L1

Research Overview

Papers
437
Total Citations
17,163
Papers (5y)
133
Primary Field
Medicine

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
133total
2021
2022
2023
2024
2025
Citations per year (5y)
2,019total
20212022202320242025

Selected Papers

15
1
Article|860 citations·2017
Dabrafenib and Trametinib Treatment in Patients With Locally Advanced or Metastatic <i>BRAF</i> V600–Mutant Anaplastic Thyroid Cancer
Vivek Subbiah, Robert J. Kreitman, Zev A. Wainberg, Y. Choi, Jan H.M. Schellens, Jean Charles Soria, Patrick Y. Wen, Christoph Zielinski, Maria E. Cabanillas, Gladys Urbanowitz, Bijoyesh Mookerjee, Dazhe Wang
SJR Q1FWCI 42.5Journal of Clinical OncologyOA

Purpose We report the efficacy and safety of dabrafenib (BRAF inhibitor) and trametinib (MEK inhibitor) combination therapy in BRAF V600E-mutated anaplastic thyroid cancer, a rare, aggressive, and highly lethal malignancy with poor patient outcomes and no systemic therapies with clinical benefit. Methods In this phase II, open-label trial, patients with predefined BRAF V600E-mutated malignancies received dabrafenib 150 mg twice daily and trametinib 2 mg once daily until unacceptable toxicity, di

Endocrinology, Diabetes and MetabolismMedicine
2
Article|325 citations·2022
Dabrafenib plus trametinib in patients with BRAF V600E-mutant anaplastic thyroid cancer: updated analysis from the phase II ROAR basket study
Vivek Subbiah, Robert J. Kreitman, Zev A. Wainberg, Y. Choi, Jan H.M. Schellens, Jean‐Charles Soria, Patrick Y. Wen, C. C. Zielinski, Maria E. Cabanillas, Aislyn Boran, Palanichamy Ilankumaran, P. Burgess
SJR Q1FWCI 25.6Annals of OncologyOA
Molecular BiologyBiochemistry, Genetics and Molecular Biology
3
Article|233 citations·2011
Ki-67 can be used for further classification of triple negative breast cancer into two subtypes with different response and prognosis
Bhumsuk Keam, Seock‐Ah Im, Kyung-Hun Lee, Sae‐Won Han, Do‐Youn Oh, Jee Hyun Kim, Se‐Hoon Lee, Wonshik Han, Dong-Wan Kim, Tae‐You Kim, In Ae Park, Dong‐Young Noh
SJR Q1FWCI 6.7Breast Cancer ResearchOA

TNBC with high Ki-67 was associated with a more aggressive clinical feature despite a higher pCR rate. High proliferation index Ki-67 can be used for further classification of TNBC into two subtypes with different responses and prognosis.

Cancer ResearchBiochemistry, Genetics and Molecular Biology
4
Article|151 citations·2007
Prognostic impact of clinicopathologic parameters in stage II/III breast cancer treated with neoadjuvant docetaxel and doxorubicin chemotherapy: paradoxical features of the triple negative breast cancer
Bhumsuk Keam, Seock‐Ah Im, Hee‐Jun Kim, Do‐Youn Oh, Jee Hyun Kim, Se‐Hoon Lee, Eui Kyu Chie, Wonshik Han, Dong-Wan Kim, Woo Kyung Moon, Tae‐You Kim, In Ae Park
SJR Q2FWCI 3.5BMC CancerOA

Several molecular markers provided useful predictive and prognostic information in stage II and III breast cancer patients treated with neoadjuvant docetaxel/doxorubicin chemotherapy. Triple negative phenotype was associated with shorter survival, even though it was associated with a higher response rate to neoadjuvant chemotherapy.

Cancer ResearchBiochemistry, Genetics and Molecular Biology
5
Article|147 citations·2016
PD-L1 expression is associated with epithelial-mesenchymal transition in head and neck squamous cell carcinoma
Chan-Young Ock, Sehui Kim, Bhumsuk Keam, Miso Kim, Tae Min Kim, Jin-Ho Kim, Yoon Kyung Jeon, Ju‐Seog Lee, Seong Keun Kwon, J. Hun Hah, Tack‐Kyun Kwon, Dong‐Wan Kim
SJR Q2FWCI 9.9OncotargetOA

Virus-associated malignancies and sarcomatoid cancers correlate with high PD-L1 expression, however, underlying mechanisms remain controversial. We evaluated the correlation between PD-L1 expression and epithelial-mesenchymal transition (EMT) in head and neck squamous cell carcinomas (HNSCC).Tumor tissues from 50 patients with HNSCC were evaluated for PD-L1 by immunohistochemistry, which showed 32 (64.0%) were PD-L1 positive (PD-L1+). Interestingly, PD-L1 expression was significantly associated

OncologyMedicine
6
Article|121 citations·2013
Erlotinib Versus Gefitinib for Control of Leptomeningeal Carcinomatosis in Non–Small-Cell Lung Cancer
Eunyoung Lee, Bhumsuk Keam, Dong‐Wan Kim, Tae Min Kim, Se‐Hoon Lee, Doo Hyun Chung, Dae Seog Heo
SJR Q1FWCI 10.7Journal of Thoracic OncologyOA
Pulmonary and Respiratory MedicineMedicine
7
Article|117 citations·2008
Aggressiveness of Cancer-Care near the End-of-Life in Korea
Bhumsuk Keam, Djin‐Ye Oh, Se‐Hoon Lee, Dongwook Kim, Mee‐Ran Kim, S. Im, Tae‐Yop Kim, Yung‐Jue Bang, D. S. Heo
SJR Q2FWCI 7.3Japanese Journal of Clinical OncologyOA

Among patients who died of cancer, significant proportions were found to have received chemotherapy up to the end-of-life and to have visited ERs. Hospice referrals and discussions about DNR were not conducted well during the end-of-life period in Korea.

Public Health, Environmental and Occupational HealthMedicine
8
Article|111 citations·2013
Rare and complex mutations of epidermal growth factor receptor, and efficacy of tyrosine kinase inhibitor in patients with non-small cell lung cancer
Bhumsuk Keam, Dong‐Wan Kim, Jin Hyun Park, Jeong‐Ok Lee, Tae Min Kim, Se‐Hoon Lee, Doo Hyun Chung, Dae Seog Heo
SJR Q1FWCI 6.6International Journal of Clinical Oncology
Pulmonary and Respiratory MedicineMedicine
9
Article|86 citations·2017
Changes in programmed death-ligand 1 expression during cisplatin treatment in patients with head and neck squamous cell carcinoma
Chan-Young Ock, Sehui Kim, Bhumsuk Keam, Soyeon Kim, Yong‐Oon Ahn, Eun‐Jae Chung, Jin-Ho Kim, Tae Min Kim, Seong Keun Kwon, Yoon Kyung Jeon, Kyeong Chun Jung, Dong‐Wan Kim
SJR Q2FWCI 3.9OncotargetOA

Programmed death-ligand 1 (PD-L1) expression is regarded as a predictive marker for anti-PD-1/PD-L1 therapy. The purpose of study was to explore the changes in PD-L1 expression in head and neck squamous cell carcinoma (HNSCC) during treatment. Paired HNSCC tissues prior to and after cisplatin-based treatment were evaluated to determine PD-L1 protein expression by immunohistochemistry. Among the 35 HNSCC patient samples, PD-L1 expression status changed after treatment in 37.1% (13/35) of samples.

OncologyMedicine
10
Article|79 citations·2011
Early metabolic response using FDG PET/CT and molecular phenotypes of breast cancer treated with neoadjuvant chemotherapy
Bhumsuk Keam, Seock‐Ah Im, Youngil Koh, Sae‐Won Han, Do‐Youn Oh, Nariya Cho, Jee Hyun Kim, Wonshik Han, Keon Wook Kang, Woo Kyung Moon, Tae‐You Kim, In Ae Park
SJR Q2FWCI 7.1BMC CancerOA

The early metabolic response using FDG PET/CT could have a predictive value for the assessment of histopathologic non-response of stage II/III breast cancer treated with neoadjuvant chemotherapy. Our findings suggest that the initial SUV and the decline in SUV differed based on the molecular phenotype.

Radiology, Nuclear Medicine and ImagingMedicine
11
Article|78 citations·2019
A phase II study of pembrolizumab and paclitaxel in patients with relapsed or refractory small-cell lung cancer
Yu-Jung Kim, Bhumsuk Keam, Chan-Young Ock, Sanghoon Song, Miso Kim, Se Hyun Kim, Ki Hwan Kim, Jin-Soo Kim, Tae Min Kim, Dong‐Wan Kim, Jong Seok Lee, Dae Seog Heo
SJR Q1FWCI 6.1Lung Cancer
OncologyMedicine
12
Article|77 citations·2015
Phase 2 study of dovitinib in patients with metastatic or unresectable adenoid cystic carcinoma
Bhumsuk Keam, Sung‐Bae Kim, Seong Hoon Shin, Byoung Chul Cho, Keun‐Wook Lee, Min Kyoung Kim, Hwan‐Jung Yun, Se‐Hoon Lee, Dok Hyun Yoon, Yung‐Jue Bang
SJR Q1FWCI 6.5CancerOA

Dovitinib shows modest antitumor activity in the treatment of ACC.

SurgeryMedicine
13
Article|76 citations·2021
Pan-Asian adaptation of the EHNS–ESMO–ESTRO Clinical Practice Guidelines for the diagnosis, treatment and follow-up of patients with squamous cell carcinoma of the head and neck
Bhumsuk Keam, Jean-Pascal Machiels, Hye Ryun Kim, Lisa Licitra, Wojciech Golusiński, Vincent Grégoire, Y.G. Lee, Claus Belka, Ye Guo, Senthil Rajappa, Makoto Tahara, M. Azrif
SJR Q1FWCI 7.9ESMO OpenOA

The most recent version of the European Society for Medical Oncology (ESMO) Clinical Practice Guidelines for the diagnosis, treatment and follow-up of squamous cell carcinoma (SCC) of the oral cavity, larynx, oropharynx and hypopharynx was published in 2020. It was therefore decided by both the ESMO and the Korean Society of Medical Oncology (KSMO) to convene a special, virtual guidelines meeting in July 2021 to adapt the ESMO 2020 guidelines to consider the potential ethnic differences associat

OtorhinolaryngologyMedicine
14
Article|76 citations·2008
Modified FOLFOX-6 chemotherapy in advanced gastric cancer: Results of phase II study and comprehensive analysis of polymorphisms as a predictive and prognostic marker
Bhumsuk Keam, Seock‐Ah Im, Sae‐Won Han, Hye Seon Ham, Sunghoon Kim, Do‐Youn Oh, Se‐Hoon Lee, Jee Hyun Kim, Dong‐Wan Kim, Tae‐You Kim, Dae Seog Heo, Woo Ho Kim
SJR Q2FWCI 3.3BMC CancerOA

Modified FOLFOX-6 chemotherapy appears to be active and well tolerated as first line chemotherapy in AGC patients. The 6-bp deletion in TS-3'UTR might be a candidate to select patients who are likely to benefit from 5-FU based modified FOLFOX-6 in future large scale trial.

OncologyMedicine
15
Article|69 citations·2018
Inhibition of MEK with trametinib enhances the efficacy of anti-PD-L1 inhibitor by regulating anti-tumor immunity in head and neck squamous cell carcinoma
Seong-Ho Kang, Bhumsuk Keam, Yong‐Oon Ahn, Ha-Ram Park, Miso Kim, Tae Min Kim, Dong‐Wan Kim, Dae Seog Heo
SJR Q1FWCI 3.1OncoImmunologyOA

Major histocompatibility complex (MHC) class I downregulation is the primary immune evasion mechanism associated with failure in anti-PD-1/PD-L1 blockade therapies for cancer. Here, we examined the role of MEK signaling pathway inhibition in head and neck squamous cell carcinoma (HNSCC) both <i>in vitro</i> and <i>in vivo</i>. We found that trametinib, a small molecule inhibitor of MEK, significantly enhanced MHC class I and PD-L1 expression in human HNSCC cell lines, and this occurred via STAT3

OncologyMedicine

Research Areas

Pulmonary and Respiratory MedicineOncologySurgeryPublic Health, Environmental and Occupational HealthOtorhinolaryngologyMolecular Biology

Dive deeper into Bhumsuk Keam's research on Nubint

Open this lab's papers in the app to read with AI, summarize, and cite in your writing.