🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in India / NCT06804135
Recruiting Observational

Systemic and Tumor Immune Response During Pelvic (Chemo)Radiation and/or Brachytherapy for Cervical Cancer

NCT06804135 · tracked via the Priya Life Science India tracker
Sponsor
Tata Memorial Hospital
Phase
Observational
Started
2025-10-25
Last updated
2026-02-04

Condition(s) studied

Cervical Carcinoma

Study summary

Radiotherapy result in tumor cell death by creating an immune potentiation effect, but can also lead to long lasting immune suppression. Thus the investigators hypothesize that pelvic and/or para-aortic radiotherapy for cervical cancer affects local tumor immunity as well as systemic immune response that may be instrumental for long term cancer cure. The goal of this observational study is to understand the effect of various radiotherapy dose per fraction, total dose and field volumes of radiation on systemic and tumor immune response in cervical cancer. The outcome of the study would be useful in improving the quality of radiation treatment and in reducing disease recurrence and improving survival in patients with cervical cancer.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Common Inclusion Criteria: 1. Age 18 years and above. 2. Ability to tolerate full course of pelvic radiotherapy+/- chemotherapy +/- brachytherapy. 3. Ability to understand and willingness to sign an informed consent document. 4. Should be willing to undergo extra biopsies and blood samples collection for translational research study. Cohort A: 1. Patients diagnosed with LACC Stage IB2 - IIIC1, as per FIGO 2018 Classification for Radical Cohort. 2. Stage IIIB-IVA where palliative RT is indicated for palliative cohort. 3. No previous irradiation to the pelvis or chemo therapy. Cohort B: 1. Patients diagnosed with LACC Stage IIIC2, as per FIGO 2018 Classification. 2. No previous irradiation to the pelvis or chemotherapy. Cohort C: 1. Patients diagnosed with gynecological cancer and presenting with need of infield radiation. 2. Planned for reirradiation. Exclusion Criteria: 1. Severe medical condition impairing complete treatment delivery. 2. Patients with immunocompromised states or active infection. 3. Patients on immunosuppressive drugs for other medical conditions. 4. Patients who will receive immune checkpoint inhibition (ICI) therapy.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tata Memorial Centre Mumbai Maharashtra Recruiting

More Tata Memorial Hospital trials in India

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06804135 on ClinicalTrials.gov ↗ ← All trials in India