Actively Recruiting

All Genders
NCT07400809

Cervical Cancer Oligo States (Recurrence, Metastasis) Multicentre Outcomes Study.

Led by Tata Memorial Hospital · Updated on 2026-02-17

350

Participants Needed

1

Research Sites

198 weeks

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

Systemic chemotherapy with or without palliative radiation represents the current standard of care in patients with recurrent or metastatic cervix cancer. In addition, pelvic radiotherapy including brachytherapy is also recommended. There is no consensus on the treatment of metastatic site in patients with oligo-metastatic or oligo-recurrent cervix cancer. Also, it is not clear if addition of local treatment to systemic chemotherapy benefits all patients with metastatic disease or a select few with limited systemic disease burden. It's presently unclear which patients derive maximum benefit with integration of radiation at both primary and metastatic site, who develop infield recurrence if performing salvage surgery, locally directed treatments or re-irradiation in addition to systemic chemotherapy improves overall outcomes. The heterogeneity in clinical practice provides an important opportunity to develop a framework for data collection and future studies within such subgroup of patients. In this retrospective study, we aim to determine overall survival, Infield progression free survival, overall progression free survival, dose response relationship of nodal and visceral progressions, and within setting of re-irradiation (infield progressions), severe adverse events and toxicity, risk groups identification, a nomogram which correlates risk groups with expected outcomes, and framework for tissue collection for translational research Investigators will record the parameters in a predesigned proforma without including personal identifiers.

CONDITIONS

Official Title

Cervical Cancer Oligo States (Recurrence, Metastasis) Multicentre Outcomes Study.

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of 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 presenting with new oligo-progression
  • Patients treated with other local therapies such as surgery or ablation for oligo-metastasis or oligo-recurrence
Not Eligible

You will not qualify if you...

  • Diagnosis of gynecological cancers other than cervical cancer
  • Persistent poly-metastatic disease after systemic treatment
  • Receiving investigational new drugs at relapse as part of other ongoing trials
  • Lack of clinical follow-up after treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Tata Memorial Hospital

Mumbai, Maharashtra, India, 400012

Actively Recruiting

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Research Team

D

Dr. Supriya Chopra, MD

CONTACT

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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