Actively Recruiting
Retrospective Multicenter Outcomes Study of Oligo-Metastatic and Oligo-Recurrent Cervical Cancer
Led by Tata Memorial Hospital · Updated on 2026-02-17
350
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
T
Tata Memorial Hospital
Lead Sponsor
E
Erasmus Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are investigating outcomes in patients with oligo-metastatic and oligo-recurrent cervical cancer, focusing on how local treatments like radiation therapy combined with systemic chemotherapy affect survival and disease progression. This multicenter, retrospective registry study aims to fill gaps in knowledge about which patients benefit most from radiation at primary and metastatic sites, how re-irradiation impacts outcomes, and the toxicity associated with these treatments. The study will also develop risk groups and a nomogram to predict patient outcomes, supporting future research. The study collects anonymized data from multiple centers on patients with oligo-metastatic or oligo-recurrent cervical cancer, some treated with radiation, chemotherapy, immunotherapy, or targeted agents, and others with local therapies such as surgery or ablation. Treatments analyzed include high-dose radiation, stereotactic ablative radiation, and re-irradiation. The registry uses standardized electronic forms to gather detailed clinical information, including treatment doses and responses, while ensuring data quality through validation and oversight. Participants' medical records from about 350-400 patients treated between 2007 and 2021 will be reviewed without direct patient contact. The study measures overall survival over four years as the primary outcome, with secondary outcomes including progression-free survival, dose-response relationships, and severe adverse events. Data will be analyzed statistically to identify risk factors and treatment effects, with all procedures performed under strict data protection and ethical approvals.
CONDITIONS
Brief Title
Cervical Cancer Oligo States (Recurrence, Metastasis) Multicentre Outcomes Study.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Cervical cancer with oligo-metastatic and/or oligo-recurrent disease, treated or untreated with radiation
- Patients with poly-metastatic disease responding well to systemic chemotherapy and treated with radiation to recurrence or metastatic sites
- Patients previously treated with radical doses for oligo-metastasis/oligo-recurrence who now have further oligo-progression
- Patients treated with other local therapies such as surgery or ablation for oligo-metastasis or oligo-recurrence
You will not qualify if you...
- Gynaecological cancers other than cervical cancer
- Persistent poly-metastatic disease after systemic treatment
- Receiving investigational new drugs at relapse as part of other trials
- No clinical follow-up after treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Data is collected retrospectively from participant medical records without direct visits.
Duration - Up to 4 years
Participants who have undergone various treatments for oligo-metastatic or oligo-recurrent cervical cancer are observed through retrospective data collection to evaluate survival and treatment outcomes.
No direct participant visits; data is gathered from existing medical records.
Trial Site Locations
Total: 1 location
1
Tata Memorial Hospital
Mumbai, Maharashtra, India, 400012
Actively Recruiting
Research Team
D
Dr. Supriya Chopra, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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