Stereotactic Body Radiotherapy Boost for Pelvic Nodes in Cervical Cancer
Official title: Stereotactic Body Radiotherapy Boost Versus Simultaneous Integrated Boost to Pelvic Nodes Among Patients Receiving Radical Chemoradiation in Carcinoma Cervix
Run by All India Institute of Medical Sciences · NCT07585929 · Data updated 2026-11-12
Doctors are testing whether delivering a precise SBRT boost to involved pelvic lymph nodes is safe for patients with stage IIIC cervical cancer who are receiving standard chemoradiation.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 65 Years |
| Sex | Women only |
| Enrollment | 150 (estimated) |
| Sponsor | All India Institute of Medical Sciences Academic / other |
| Drugs / interventions | radiation, chemotherapy |
| Locations | 3 sites (Delhi, National Capital Territory of Delhi and 2 other locations) |
| Status | Recruiting |
| Started | November 20, 2024 |
| Main results expected | November 19, 2025 |
| Study ends | November 19, 2026 |
| Registry record updated | May 29, 2026 |
| Trial ID | NCT07585929 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Patients with stage IIIC cervical cancer, no prior pelvic radiation or surgery, and ECOG 0-2.
✕Probably not a fit
Patients with different cancer stages, prior pelvic treatments, or significant uncontrolled health issues may not benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational comparison of two radiotherapy approaches for cervical cancer: a SBRT boost to involved pelvic nodes versus a conventional Simultaneous Integrated Boost to the pelvic nodes, in patients with stage IIIC disease. The study focuses on safety by tracking acute gastrointestinal and genitourinary toxicity greater than grade 3 within 30 days after completing treatment. Eligible participants have no prior pelvic radiation or surgery and an ECOG performance status of 0-2, while those with non-Stage IIIC disease, prior malignancies, uncontrolled comorbidities, or autoimmune conditions are excluded. The lead institution is AIIMS, Delhi, with collaboration across participating centers in India.
Why it matters
Potential benefit: If successful, the approach could reduce damage to surrounding tissues while maintaining effective nodal control during chemoradiation.
How similar studies have gone: Similar radiotherapy approaches have shown promise in improving precision and sparing healthy tissue, but direct comparisons like this are relatively novel in this specific setup.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Patients with stage IIIC cervical cancer 2. No previous pelvic radiation therapy or surgery 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 Exclusion Criteria: 1. Patients with stage I or stage II or stage IV disease. 2. Patients with prior malignancies or active autoimmune diseases 3. Uncontrolled medical comorbidity
Where it's running
-
All India Institute of Medical Sciences
Delhi, National Capital Territory of Delhi, India Recruiting -
Karun Kamboj
Delhi, National Capital Territory of Delhi, India Recruiting -
National Cancer Institute, All India Institute of Medical Sciences, New Delhi, India
New Delhi, New Delhi, India Recruiting
Study contacts
- Study coordinator: Karun Kamboj, Md
- Email: karunkamboj04@aiims.edu
- Phone: 9416613389
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.