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Postoperative Hypofractionated Intensity-modulated Radiation Therapy in Cervical Cancer

Postoperative Hypofractionated Intensity-modulated Radiation Therapy in Cervical Cancer: a Prospective Exploratory Trial (POHIM_RT Trial)

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03239626
Enrollment
120
Registered
2017-08-04
Start date
2017-08-31
Completion date
2025-04-28
Last updated
2025-01-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervix Cancer, Hypofractionated Dose, Radiotherapy, Adjuvant, Radiotherapy, Intensity-Modulated

Brief summary

To investigate the acute toxicities, late toxicities, and treatment results when the early cervical cancer patients are treated by hypofractionated intensity-modulated radiotherapy (2.5 Gy X 16 fractions, once a day) after radical hysterectomy.

Interventions

RADIATIONPOHIM-RT

postoperative adjuvant IMRT with hypofractionation (2.5 Gy/fraction, 16 fractions, once a day)

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

One group for hypofractionaed IMRT for adjvuant cervical cancer patients

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* histologically confirmed cervical cancer * radical hysterectomy and pelvic lymph node dissection was done * histologically indicated adjuvant radiotherapy ( more than one as below) 1. tumor size ≥4 cm 2. positive lymphovascular invasion 3. more than half stromal invasion depth * ECOG performance status 0 or 1 * Bone marrow function: granulocyte ≥1.0 x 1000/µl, platelet ≥30 x 1000/µl, hemoglobin ≥10 g/dl

Exclusion criteria

* positive pelvic lymph node metastasis * positive distant metastasis (including retroperitoneal lymph node metastasis) * positive tumor involvement on resection margin * positive parametrial invasion * previous history of pelvic radiotherapy * more than 3 months after radical surgery for cervical cancer * neoadjuvant chemotherapy was done * previous history of other carcinoma except for thyroid cancer, skin cancer, in situ carcinoma on cervix

Design outcomes

Primary

MeasureTime frameDescription
acute toxicities according to CTCAE v4.03 monthsevaluation of acute toxicities within 3months after radiotherapy according to CTCAE v4.0

Secondary

MeasureTime frameDescription
late toxicities according to CTCAE v4.05-yearsevaluation of late toxicities every year after 3months after radiotherapy according to CTCAE v4.0
Progression free survival rate5-yearsprogression free survival rate after the time of surgery

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026