GOG-0263

Terminated

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Protocol Information

Tab containing protocol details, study design, and eligibility criteria
Tab containing study documents, informed consent forms, and study materials
Tab containing information for potential study participants

Randomized Phase III Clinical Trial of Adjuvant Radiation Versus Chemoradiation in Intermediate Risk, Stage I/IIA Cervical Cancer Treated with Initial Radical Hysterectomy and Pelvic Lymphadenectomy (NCT #01101451)

Principal Investigator

Sang-Young Ryu

Status

Terminated

Open to Accrual

April 12, 2010

Closed to Accrual

April 11, 2022

Closed to Accrual & Treatment

April 19, 2022

Terminated

October 27, 2025


Disease Site

Gynecologic [GY] Cervix

Phase

III

Developmental Therapeutics

No

Primary Objective

To determine if post-operative adjuvant chemo-radiation therapy (CRT) can significantly improve recurrence-free survival (RFS) when compared to radiation therapy (RT) alone in Stage I-IIA cervical cancer patients with intermediate risk factors after treatment with radical hysterectomy.

Patient Population

Post-operative adjuvant chemo-radiation therapy (CRT) or radiation therapy (RT) alone in Stage I-IIA cervical cancer patients with intermediate risk factors after treatment with radical hysterectomy.

Target Accrual

360

Protocol Documents

Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.


Patient Study Webpage

There is no available patient study webpage available for this trial at this time.