Investigator

Sangjoon Park

Resident · Severance Hospital, Radiation Oncology

SPSangjoon Park
Papers(1)
Postoperative convent…
Collaborators(10)
Won Kyung ChoWon ParkYeon Joo KimYeon‐Sil KimYoung Seok KimDong-Yun KimEuncheol ChoiHyun-Cheol KangJong Hoon LeeKeun-Yong Eom
Institutions(9)
Yonsei Cancer HospitalBrown UniversityAsan Medical CenterCatholic University O…Chung Ang UniversityKeimyung University D…Seoul National Univer…The Catholic Universi…Seoul National Univer…

Papers

Postoperative conventional versus hypofractionated intensity-modulated radiation therapy with concurrent chemotherapy in cervical cancer: a prospective multicenter randomized phase III trial (POHIM_P3 trial)

For patients with high-risk factors such as pelvic lymph node metastasis, positive surgical margins, or parametrial involvement, concurrent chemoradiotherapy (CCRT) with whole-pelvic radiotherapy significantly improves survival outcomes. Hypofractionated radiation therapy, which delivers higher radiation doses over fewer sessions, enhances tumor control but raises concerns about increased normal tissue toxicity. A recent Korean phase II study (POHIM-CCRT) evaluated the safety of hypofractionated intensity-modulated radiation therapy (IMRT), delivering 40 Gy in 16 fractions with weekly cisplatin following radical surgery. The results showed minimal acute toxicity. Based on these findings, the present study was designed to assess the oncologic efficacy of hypofractionated CCRT compared to conventional treatment strategies in high-risk cervical cancer patients after radical surgery. The POHIM-P3 trial is a phase 3, randomized, multicenter study designed for women with cervical cancer requiring adjuvant CCRT after radical hysterectomy. Participants in the experimental arm receive hypofractionated IMRT to whole pelvis, delivering a total dose of 40 Gy in 16 fractions, and the control arm receive conventional radiotherapy with a total dose of 45-50.4 Gy in 25-28 fractions in combination with weekly cisplatin. The primary endpoint of the study is the 3-year disease-free survival and the secondary endpoints included acute and late side-effects, local control rates, and overall survival rates. ClinicalTrials.gov Identifier: NCT06509724.

25Works
1Papers
11Collaborators
1Trials
Carcinoma, HepatocellularLiver NeoplasmsBreast NeoplasmsDiagnosis, Computer-AssistedBone NeoplasmsPrognosisBiomarkers, Tumor

Positions

2015–

Resident

Severance Hospital · Radiation Oncology

2014–

Intern

Severance Hospital

Education

2019

Ph.D. (Doctor's degree)

Korea Advanced Institute of Science and Technology · Bio and Brain Engineering

2019

M.S. (Master's degree)

Yonsei University College of Medicine

2014

M.D.

Yonsei University College of Medicine