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Radiation Therapy Plus Chemotherapy Before Surgery With or Without Chemotherapy After Surgery in Treating Patients With Rectal Cancer - Article


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Rectal Diseases

 




Clinical Trial: Radiation Therapy Plus Chemotherapy Before Surgery With or Without Chemotherapy After Surgery in Treating Patients With Rectal Cancer

This study is no longer recruiting patients.

Sponsored by: Chemo Prevention Unit
Information provided by: National Cancer Institute (NCI)

Purpose

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug, giving the drugs in different ways, and combining chemotherapy with radiation therapy may kill more tumor cells. PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy plus fluorouracil and leucovorin before surgery given with or without fluorouracil and leucovorin after surgery in patients with locally advanced rectal cancer.

Condition Treatment or Intervention Phase
stage III rectal cancer
adenocarcinoma of the rectum
recurrent rectal cancer
childhood gastrointestinal cancer
mucinous adenocarcinoma of the rectum
stage II rectal cancer
 Drug: fluorouracil
 Drug: leucovorin calcium
Phase III

MedlinePlus related topics:  Cancer;   Cancer Alternative Therapy;   Colorectal Cancer;   Digestive Diseases

Study Type: Interventional
Study Design: Treatment

Official Title: Phase III Randomized Study of Preoperative Radiotherapy plus Fluorouracil/Leucovorin with vs without Postoperative Fluorouracil/Leucovorin in Locally Advanced Adenocarcinoma of the Rectum

Further Study Details: 

Study start: September 1993

OBJECTIVES: I. Assess the local recurrence rate, cost-benefit ratio, and acute and late toxicity associated with concomitant preoperative radiotherapy and fluorouracil/leucovorin (5-FU/CF) in patients with locally advanced adenocarcinoma of the rectum. II. Compare the relapse rate, survival rate, disease-free interval, and cost-benefit ratio associated with 6 courses of postoperative 5-FU/CF vs. no further treatment in these patients.

PROTOCOL OUTLINE: This is a randomized study. Patients are stratified by tumor stage, age, type of surgery, and participating institution. Patients are randomly assigned to one of two groups. The first group receives radiotherapy to the tumor over 5 weeks and concomitant fluorouracil/leucovorin for 5 consecutive days on the first and fifth weeks. Four to six weeks later, patients undergo complete resection, followed upon recovery by fluorouracil/leucovorin every 4 weeks for 6 courses. The second group receives preoperative chemoradiotherapy followed by surgery, as above, with no postoperative treatment. Patients are followed for survival.

PROJECTED ACCRUAL: A total of 774 patients will be entered on this multicenter study.

Eligibility

Ages Eligible for Study:  up to  75 Years

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

--Prior/Concurrent Therapy--

  • Not specified

--Patient Characteristics--

  • Age: 75 and under
  • Performance status: WHO 0 or 1
  • Hematopoietic: WBC greater than 3,000; Platelets greater than 130,000
  • Hepatic: Not specified
  • Renal: Creatinine less than 1.4 mg/dL
  • Cardiovascular: No unstable angina; No cardiac decompensation
  • Other: No prior or concurrent malignancy

Location Information


Italy
      Ospedale St. Santa Chiara, Pisa,  56100,  Italy

Study chairs or principal investigators

Luca Cionini,  Study Chair,  Chemo Prevention Unit   

More Information

Clinical trial summary from the National Cancer Institute's PDQ® database

Study ID Numbers:  CDR0000065222; CNR-9604; EU-96047
Record last reviewed:  May 2004
Last Updated:  October 13, 2004
Record first received:  November 1, 1999
ClinicalTrials.gov Identifier:  NCT00002896
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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November 30, 2009



Page Updated: January 17, 2009
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