Therapeutic Effect of Surgical Debulking of Metastatic Lymph Nodes in Cervical Cancer Stage IIICr
1 other identifier
interventional
240
5 countries
26
Brief Summary
This study is a prospective, multicenter and randomized clinical trial (DEBULK trial) to determine the therapeutic effect of surgical debulking of bulky or multiple lymph nodes before concurrent chemoradiation therapy (CCRT) in cervical cancer stage IIICr.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2022
Longer than P75 for not_applicable
26 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 13, 2022
CompletedFirst Posted
Study publicly available on registry
June 16, 2022
CompletedStudy Start
First participant enrolled
August 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2030
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2030
April 9, 2025
April 1, 2025
8.4 years
June 13, 2022
April 5, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
PFS
Progression-free survival
3 years
Secondary Outcomes (3)
OS
3 years
Treatment-related complications
3 years
False positive rate & positive predictive value of bulky or multiple LN imaging
6 months
Study Arms (2)
Control group
ACTIVE COMPARATORConcurrent chemoradiation therapy (CCRT)
Experimental group
EXPERIMENTALSurgical debulking of bulky or multiple lymph node + CCRT
Interventions
Surgical debulking of lymph nodes + CCRT
Eligibility Criteria
You may qualify if:
- (1) Women aged ≥ 20 years and ≤ 70 years (2) Patients newly diagnosed with squamous cell carcinoma (SCC), adenocarcinoma, or adenosquamous carcinoma (3) Patients with a short-axis diameter of the pelvic LN or para-aortic LN under the renal vein of ≥ 1.5 cm or ≥ 2 LNs with a short-axis diameter ≥ 1 cm in CT or MRI (PET-CT can be used as an auxiliary tool) (4) Patients with CCRT planned as a treatment for cervical cancer (5) Patients whose competency is Eastern Cooperative Oncology Group performance score 0-1 (6) Patients who have signed the approved informed consent form for study participants (7) Patients in whom surgical debulking for LN metastasis was possible, as confirmed by radiological examination.
You may not qualify if:
- (1) Patients who have been diagnosed with cancer of any organ other than thyroid cancer (excluding stage 0 cancer) within the previous 5 years (2) Patients who are pregnant or plans to conceive during the clinical study period (3) Patients with any active infectious disease or incurable severe inflammation (4) Patients who cannot undergo surgery due to internal or surgical disease (5) Patients who cannot receive chemotherapy due to internal or surgical disease (6) Patients with a history of pelvic RT (7) Patients with a history of subtotal hysterectomy (8) Patients with remote metastasis other than a pelvic or para-aortic LN (e.g., lung, subclavian, and inguinal LNs)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- CHA Universitylead
- Korean Gynecologic Oncology Groupcollaborator
Study Sites (26)
Aster CMI Hospital
Bengaluru, India
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Rome, 00168, Italy
First Obstetrics and Gynecology Clinic, "G. E. Palade" University of Medicine, Pharmacy, Science and Technology
TĂ¢rgu MureÅŸ, 540136, Romania
Soon Chun Hyang University Hospital Cheonan
Cheonan, Chungcheongnam-do, 31151, South Korea
Korea University Ansan Hospital
Ansan-si, Gyeonggi-do, 15355, South Korea
Dongguk University Medical Center
Goyang-si, Gyeonggi-do, 10326, South Korea
National Cancer Center
Goyang-si, Gyeonggi-do, 10408, South Korea
CHA Bundang Medical Center, CHA University
Seongnam-si, Gyeonggi-do, 13496, South Korea
Pusan National University Yangsan Hospital
Yangsan, Gyeongsangbuk-do, 50612, South Korea
Samsung Changwon Medical Center
Changwon, Gyeongsangnam-do, 51353, South Korea
Chonnam National University Hwasun Hospital
Hwasun, Jeollanam-do, 58128, South Korea
Dongnam Institute of Radiological & Medical Sciences
Busan, 46033, South Korea
Inje University Busan Paik Hospital
Busan, 47392, South Korea
Kyungpook National University Chilgok Hospital
Daegu, 41404, South Korea
Keimyung University Dongsan Hospital
Daegu, 42601, South Korea
Gachon University Gil Medical Center
Incheon, 21565, South Korea
Korea University Anam Hospital
Seoul, 02841, South Korea
Seoul National University Hospital
Seoul, 03080, South Korea
Severance Hospital
Seoul, 03722, South Korea
Hanyang University Medical Center
Seoul, 04763, South Korea
Konkuk University Medical Center
Seoul, 05030, South Korea
Asan Medical Center
Seoul, 05505, South Korea
Gangnam Severance Hospital
Seoul, 06273, South Korea
Samsung Medical Center
Seoul, 06351, South Korea
Seoul ST. Mary's Hospital
Seoul, 06591, South Korea
Ho Chi Minh City Oncology Hospital
Ho Chi Minh City, Vietnam
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PMID: 38330380DERIVED
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ju-Won Roh
CHA University Ilsan Medical Center
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 13, 2022
First Posted
June 16, 2022
Study Start
August 1, 2022
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
December 31, 2030
Last Updated
April 9, 2025
Record last verified: 2025-04
Data Sharing
- IPD Sharing
- Will not share