Yonsei University · 医学
Professor Kyung Hwan Kim's research lab focuses on advancing cancer immunotherapy, particularly immune checkpoint blockade targeting PD-1/PD-L1, with an emphasis on identifying predictive biomarkers, understanding mechanisms of treatment response and resistance, and elucidating the immunological basis of immune-related adverse events. The lab investigates the clinical and immunological implications of radiation exposure to critical cardiac structures like the sinoatrial node, linking radiotherapy planning to long-term outcomes such as atrial fibrillation and mortality. Their work integrates translational immunology with clinical oncology, primarily in solid tumors including non-small cell lung cancer, thymic epithelial tumors, and hepatocellular carcinoma.
Figures are computed from collected data and may differ slightly.
The proliferative response of peripheral blood PD-1<sup>+</sup>CD8<sup>+</sup> T cells, measured as the fold-change in the percentage of Ki-67<sup>+</sup> cells 7 days after treatment (Ki-67<sub>D7/D0</sub>), may be a useful surrogate biomarker for predicting the response and prognosis to anti-PD-1 therapy in solid tumors.
In this cohort study, results suggest that incidental irradiation of the SAN during chemoradiotherapy may be associated with the development of AF and increased mortality. This supports the need to minimize radiation dose exposure to the SAN during radiotherapy planning and to consider close follow-up for the early detection of AF in patients receiving thoracic irradiation.
Although anti-programmed death-1 (PD-1) treatment has shown remarkable anti-tumor efficacy, immune-related adverse events (irAEs) develop with heterogeneous clinical manifestations. However, the immunological understanding of irAEs is currently limited. In the present study, we analyzed peripheral blood T cells obtained from cancer patients who received anti-PD-1 treatment to determine the immunological characteristics of irAEs. This study included 31 patients with refractory thymic epithelial t
Immune checkpoint blockade targeting PD-1 and PD-L1 has resulted in unprecedented clinical benefit for cancer patients. Anti-PD-1/PD-L1 therapy has become the standard treatment for diverse cancer types as monotherapy or in combination with other anti-cancer therapies, and its indications are expanding. However, many patients do not benefit from anti-PD-1/PD-L1 therapy due to primary and/or acquired resistance, which is a major obstacle to broadening the clinical applicability of anti-PD-1/PD-L1
The median follow-up period was 27.8 months (range, 12.9-121.9 months). The median overall survival (OS) was longer in Groups B (15.3 months) and D (12.8 months) than in Groups A (7.5 months) and C (8.2 months; Group B vs. A, Bonferroni corrected P [P(c)] = 0.04; Group B vs. C, P(c) = 0.02; Group D vs. A, P(c) = 0.01; Group D vs. C, Pc = 0.006). Groups B and D also showed superior progression-free survival (PFS) and intrahepatic control than Groups A and C. In multivariate analysis, tumour multi
Recent advances in breast cancer management might make the use of postmastectomy radiotherapy (PMRT) redundant in the treatment of pT1/T2N1 patients. We investigated the impact of PMRT on disease-free survival (DFS) in these patients who have a low risk of locoregional recurrence (LRR) after contemporary multidisciplinary management.Between 1998 and 2011, 1123 patients underwent upfront surgery for pathologically diagnosed pT1/T2N1 breast cancer, at a single institution. A retrospective review w
Human memory-like NK cells are commonly defined by either a lack of FcεRIγ or gain of NKG2C expression. Here, we investigated the heterogeneity of human CD56<sup>dim</sup> NK cell subpopulations according to the expression of FcεRIγ and NKG2C in a large cohort (<i>n</i> = 127). Although the frequency of FcεRIγ<sup>-</sup> and NKG2C<sup>+</sup> NK cells positively correlated, the FcεRIγ<sup>-</sup> and NKG2C<sup>+</sup> NK cell populations did not exactly overlap. The FcεRIγ<sup>+</sup>NKG2C<sup>
Tumors with ATM and BRCA1/2 mutations exhibited superior tumor response and local control after RT compared to tumors without these mutations. The results are hypothesis generating and suggest the need for integrating the tumor mutation profile of DNA repair genes during treatment planning.
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