O Kyu Noh

Dr. O Kyu Noh

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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1 January 2019 in Journal of Korean Medical Science
Verified
Journal Article
Open access
JLJang Hoon Lee
Jang Hoon Lee
ONO Kyu Noh
O Kyu Noh
YCYun Sil Chang
Yun Sil Chang
KNKorean Neonatal Network
Korean Neonatal Network
Lee JH, et al. J Korean Med Sci. 2019 Jan;34(5):e40. https://doi.org/10.3346/jkms.2019.34.e40

15 January 2016 in Cancer Research and Treatment
Verified
Journal Article
Open access
PDF file
JHJaesung Heo
Jaesung Heo
MCMison Chun
Mison Chun
ONO Kyu Noh
O Kyu Noh
YOYoung-Taek Oh
Young-Taek Oh
KSKwang Wook Suh
Kwang Wook Suh
OCOyeon Cho
Oyeon Cho
The objective of this study was to explore the relationship between the circulating lymphocyte level during preoperative chemoradiotherapy (CRT) and pathologic complete response (pCR) in locally advanced rectal cancer. From May 2010 to May 2013, 52 patients treated with preoperative CRT followed by surgery, were analysed. Patients received conventional fractionated radiotherapy (50-54 Gy) with fluorouracil-based chemotherapy. Surgical resection was performed at 4 to 8 weeks after the completion of preoperative CRT. Absolute blood lymphocyte counts and their relative percentage in total white blood cell counts were obtained from complete blood count tests performed prior to and after 4, 8, and 12 weeks of CRT. We analysed the association between achieving pCR and change in blood lymphocyte level during CRT, as well as clinical parameters. Among 52 patients, 14 (26.9%) had evidence of pCR. Sustaining the blood lymphocyte count during CRT (lymphocyte count at 4 weeks/baseline lymphocyte count > 0.35; odds ratio, 8.33; p=0.02) and initial carcinoembryonic antigen < 4.4 ng/mL (odds ratio, 6.71; p=0.03) were significantly associated with pCR in multivariate analyses. Sustaining blood lymphocyte count during preoperative CRT was predictive for pCR in rectal cancer. Further studies are warranted to investigate the association between pathologic responses and circulating lymphocyte count with its subpopulation during preoperative CRT.

1 July 2016
Verified
Journal Article
Closed access
OCOyeon Cho
Oyeon Cho
MCMison Chun
Mison Chun
SCSuk-Joon Chang
Suk-Joon Chang
YOYoung-Taek Oh
Young-Taek Oh
ONO Kyu Noh
O Kyu Noh

1 January 2018 in Technology in Cancer Research & Treatment
Verified
Journal Article
Open access
SOSeung Yeop Oh
Seung Yeop Oh
JHJaesung Heo
Jaesung Heo
ONO Kyu Noh
O Kyu Noh
MCMison Chun
Mison Chun
OCOyeon Cho
Oyeon Cho
YOYoung-Taek Oh
Young-Taek Oh
We analyzed the changes in absolute lymphocyte count and its changes over time in 139 patients treated with preoperative chemoradiotherapy for locally advanced rectal cancer. The baseline absolute lymphocyte count was defined as the median of absolute lymphocyte count levels measured during 30 days before preoperative chemoradiotherapy. Absolute lymphocyte count at 1 month, 0.5 to 1 year, 1 to 2 years, and 2 to 3 years were determined by the median values of the absolute lymphocyte counts during the respective periods. Absolute lymphocyte count decreased after delivering preoperative chemoradiotherapy, reached minimum level at 1 month, and then gradually increased after the completion of chemoradiotherapy. Baseline absolute lymphocyte count had significant correlations with the absolute lymphocyte count of every period (range of coefficient, 0.41-0.64, P < .001). The overall survival of the group with high baseline absolute lymphocyte count was significantly higher than that of the group with low baseline absolute lymphocyte count (5-year overall survival: 82.4% vs 62.9%, P = .012). In multivariable analyses, the baseline absolute lymphocyte count remained as a significant prognostic factor for overall survival, favoring the group with a high baseline absolute lymphocyte count (hazard ratio = 0.405, P = .017). This study showed that the level of baseline absolute lymphocyte count was an independent prognostic factor, and it correlated with the absolute lymphocyte counts across varying periods of treatments and follow-up in patients treated with preoperative chemoradiotherapy for rectal adenocarcinoma.

18 November 2015 in International Journal of Radiation Oncology, Biology, Physics
Verified
Journal Article
Closed access
PDF file
HLHyun Woo Lee
Hyun Woo Lee
ONO Kyu Noh
O Kyu Noh
YOYoung-Taek Oh
Young-Taek Oh
JCJin-Hyuk Choi
Jin-Hyuk Choi
MCMison Chun
Mison Chun
DYDukyong Yoon
Dukyong Yoon

6 November 2018 in BMC Nephrology
Verified
Journal Article
Open access
PDF file
JHJaesung Heo
Jaesung Heo
ONO Kyu Noh
O Kyu Noh
YOYoung-Taek Oh
Young-Taek Oh
MCMison Chun
Mison Chun
LKLogyoung Kim
Logyoung Kim
This study aimed to evaluate patterns of posttransplant malignancies among renal transplant recipients (RTRs) in South Korea using nationwide data. The nationwide cohort assessed in this study included RTRs from January 1, 2010, to December 31, 2014. We analyzed cancer incidence during the time course after renal transplantation. Additionally, we calculated standardized incidence ratios (SIRs) to evaluate the risk of malignancies in RTRs. A total of 1343 RTRs (871 males and 472 females, mean age 48.5 ± 11.6 years) were assessed. Among them, 104 (7.7%) developed malignancies after transplantation, most commonly in the thyroid cancer (23.1%). The SIR for all cancers was 3.54; particularly, the SIRs for renal cancer, myeloma, and non-Hodgkin lymphoma were 16.31, 24.02, and 28.64, respectively. Females showed a higher risk of malignancy than males (SIRs: 4.04 for women and 3.26 for men). The median interval between transplantation and malignancy diagnosis was 27.2 months (range 12.3–54.8 months). RTRs in South Korea demonstrated a high risk of malignancy after transplantation compared with the general population. This indicates that close surveillance and routine screening for cancer in RTRs are needed.