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Search / Trial NCT00002536

Surgery With or Without Chemotherapy in Treating Patients With Stage IB Cervical Cancer

Launched by GYNECOLOGIC ONCOLOGY GROUP · Mar 25, 2004

Trial Information

Current as of March 19, 2025

Completed

Keywords

Stage Ib Cervical Cancer

ClinConnect Summary

OBJECTIVES: I. Compare disease free survival, overall survival, and local control in patients with bulky stage IB carcinoma of the cervix treated with radical hysterectomy and pelvic and para-aortic lymphadenectomy with or without neoadjuvant vincristine and cisplatin. II. Compare adverse effects of radical hysterectomy and pelvic and para-aortic lymphadenectomy with or without neoadjuvant vincristine and cisplatin in these patients.

OUTLINE: This is a randomized study. Patients are randomized to 1 of 2 treatment arms. Arm I: Surgery. All patients undergo intra-abdominal and retroperitonea...

Gender

FEMALE

Eligibility criteria

  • DISEASE CHARACTERISTICS: Previously untreated, histologically proven invasive carcinoma of the cervix Eligible histologies: Squamous Adenocarcinoma Adenosquamous Eligible stages: Bulky stage IB, i.e.: Exophytic lesions 4 cm or greater in diameter OR Cervix expanded to 4 cm or greater and presumed clinically to result from cancer No extension beyond cervix clinically and by IVP or CT with contrast
  • PATIENT CHARACTERISTICS: Age: Not specified Performance status: GOG 0-2 Hematopoietic: WBC at least 3,000/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 times normal AST no greater than 3 times normal Alkaline phosphatase no greater than 3 times normal Renal: Creatinine no greater than 2.0 mg/dL Other: No septicemia or severe infection No other concurrent malignancy within the past 5 years except curatively treated nonmelanomatous skin cancer and prior malignancy therapy does not contraindicate current protocol therapy Suitability for radical hysterectomy and lymphadenectomy required
  • PRIOR CONCURRENT THERAPY: No prior therapy for cervical cancer No prior pelvic irradiation

Trial Officials

Gary L. Eddy, MD

Study Chair

Kaiser Permanente Medical Center - Bellflower

About Gynecologic Oncology Group

The Gynecologic Oncology Group (GOG) is a leading clinical trial sponsor dedicated to advancing the understanding and treatment of gynecologic cancers. Comprising a network of experts in the field, GOG conducts rigorous, multi-institutional research to evaluate innovative therapeutic strategies and improve patient outcomes. Through its commitment to high-quality clinical trials, the organization aims to enhance the standard of care for women diagnosed with gynecologic malignancies, fostering collaborations with academic institutions and industry partners to translate scientific discoveries into effective treatments. GOG's mission emphasizes patient safety, ethical research practices, and the dissemination of findings to benefit the broader medical community.

Locations

Seattle, Washington, United States

Los Angeles, California, United States

Orange, California, United States

Denver, Colorado, United States

Washington, District Of Columbia, United States

Tampa, Florida, United States

Chicago, Illinois, United States

Chicago, Illinois, United States

Indianapolis, Indiana, United States

Lexington, Kentucky, United States

Worcester, Massachusetts, United States

Detroit, Michigan, United States

Minneapolis, Minnesota, United States

Jackson, Mississippi, United States

Saint Louis, Missouri, United States

Camden, New Jersey, United States

Albany, New York, United States

Brooklyn, New York, United States

Stony Brook, New York, United States

Chapel Hill, North Carolina, United States

Durham, North Carolina, United States

Cincinnati, Ohio, United States

Cleveland, Ohio, United States

Columbus, Ohio, United States

Oklahoma City, Oklahoma, United States

Abington, Pennsylvania, United States

Hershey, Pennsylvania, United States

Philadelphia, Pennsylvania, United States

Philadelphia, Pennsylvania, United States

Philadelphia, Pennsylvania, United States

Tacoma, Washington, United States

Birmingham, Alabama, United States

Bellflower, California, United States

Los Gatos, California, United States

Iowa City, Iowa, United States

Boston, Massachusetts, United States

Morristown, New Jersey, United States

Winston Salem, North Carolina, United States

Nashville, Tennessee, United States

Burlington, Vermont, United States

Charlottesville, Virginia, United States

People applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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