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A Randomised Trial of Preoperative Radiotherapy for Stage T3 Adenocarcinoma of Rectum - Article


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Clinical Trial: A Randomised Trial of Preoperative Radiotherapy for Stage T3 Adenocarcinoma of Rectum

This study is currently recruiting patients.
Verified by Trans-Tasman Radiation Oncology Group (TROG) September 2005

Sponsors and Collaborators: Trans-Tasman Radiation Oncology Group (TROG)
Australasian Gastro-Intestinal Trials Group
Colorectal Surgical Society of Australasia (CSSA)
Royal Australasian College of Surgeons (RACS)
Information provided by: Trans-Tasman Radiation Oncology Group (TROG)
ClinicalTrials.gov Identifier: NCT00145769

Purpose

This is a multi-centre randomised trial comparing long course (LC) preoperative chemoradiation with short course (SC) preoperative radiotherapy for patients with localised T3 rectal cancer.
Condition Intervention Phase
Adenocarcinoma of rectum
 Drug: 5-fluorouracil
 Drug: folinic acid
 Procedure: radiotherapy
 Procedure: surgery
Phase III

MedlinePlus related topics:  Cancer;   Colorectal Cancer

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study

Further Study Details: 
Primary Outcomes: - Local recurrence
Secondary Outcomes: - Survival; - Toxicity; - Abdominoperineal resection rate; - Quality of life
Expected Total Enrollment:  325

Study start: July 2001;  Expected completion: April 2010
Last follow-up: September 2009;  Data entry closure: December 2009

Objective:

Eligibility Criteria:

Endpoints:

  • Primary endpoint is local recurrence.
  • Secondary endpoints are overall survival, toxicity, abdminoperineal resection rate, quality of life.

Treatment arms:

  • SC arm: Radiotherapy (RT) 25 Gy in 5 fr in 1 week to be followed by surgery within 1 week and 6 cycles of postoperative chemotherapy 5FU/Folinic acid.
  • LC arm: RT 50.4 Gy in 28 fr in 5½weeks with 5FU 225 mg/m2/day throughout the course of RT, to be followed by surgery 4-6 weeks after completion of RT. 4 cycles of adjuvant 5FU/Folinic acid will be given.

Eligibility

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

All of the following must apply:

  • 1. Pathologically documented and clinically resectable adenocarcinoma of the rectum.
  • 2. The patient must be considered by the surgeon to be suitable for a curative resection.
  • 3. The patient must be considered by the radiation oncologist to have no contraindication to pre-operative radiotherapy.
  • 4. Clinical T3 stage tumour on endorectal ultrasound or MRI. When endorectal ultrasound cannot be performed satisfactorily due to a technical reason, such as stenosis or proximity of the tumour, and MRI is not available, infiltration of perirectal fat on CT scan is also acceptable.
  • 5. Tumour with lower border within 12 cm from anal verge on rigid sigmoidoscopy.
  • 6. ECOG performance status 0, 1 or 2.
  • 7. Adequate bone marrow function with neutrophil count at least 1.5 x 109/L and platelet count at least 100 x 109/L.
  • 8. Adequate liver function with bilirubin and alanine aminotransferase (ALT) £ 1.5 times the upper limit of normal.
  • 9. Adequate renal function with serum creatinine £1.5 times the upper limit of normal.
  • 10. Accessibility for treatment and follow-up.
  • 11. Written informed consent.

Exclusion Criteria:

  • None of the following must apply:
  • 12. Evidence of distant metastases.
  • 13. Recurrent rectal cancer.
  • 14. Unstable cardiac disease or clinically significant active infection.
  • 15. Other cancer in the last 5 years except treated non-melanoma skin cancer or carcinoma in situ of the cervix.
  • 16. Pregnant or lactating females or female patients of childbearing potential who have not been surgically sterilized or are without adequate contraceptive measures.
  • 17. Contraindication to insertion of a suitable indwelling venous catheter e.g. implantable central venous device (infuse-a-port), Hickman catheter or peripherally inserted central catheter.
  • 18. Prior pelvic or abdominal radiotherapy.

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00145769

Sam Ngan, FRANZCR      +61 3 96561111    Sam.Ngan@petermac.org

Australia, Victoria
      Peter MacCallum Cancer Centre, Melbourne,  Victoria,  3002,  Australia; Recruiting
Sam Ngan, FRANZCR  +61 3 96561111    Sam.Ngan@petermac.org 

Study chairs or principal investigators

Sam Ngan, FRANZCR,  Study Chair,  Peter MacCallum Cancer Centre, Australia   

More Information

TROG website access via the Royal Australian and New Zealand College of Radiologists (RANZCR) website.

Publications

Kapiteijn E, Marijnen CA, Nagtegaal ID, Putter H, Steup WH, Wiggers T, Rutten HJ, Pahlman L, Glimelius B, van Krieken JH, Leer JW, van de Velde CJ; Dutch Colorectal Cancer Group. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer. N Engl J Med. 2001 Aug 30;345(9):638-46. Summary for patients in: Can J Surg. 2003 Feb;46(1):54-6. Med J Aust. 2002 Nov 18;177(10):563-4.

Folkesson J, Birgisson H, Pahlman L, Cedermark B, Glimelius B, Gunnarsson U. Swedish Rectal Cancer Trial: long lasting benefits from radiotherapy on survival and local recurrence rate. J Clin Oncol. 2005 Aug 20;23(24):5644-50.

Ngan SY, Fisher R, Burmeister BH, Mackay J, Goldstein D, Kneebone A, Schache D, Joseph D, McKendrick J, Leong T, McClure B, Rischin D. Promising results of a cooperative group phase II trial of preoperative chemoradiation for locally advanced rectal cancer (TROG 9801). Dis Colon Rectum. 2005 Jul;48(7):1389-96.

Study ID Numbers:  TROG 01.04
Last Updated:  September 2, 2005
Record first received:  September 2, 2005
ClinicalTrials.gov Identifier:  NCT00145769
Health Authority: Australia: Department of Health and Ageing Therapeutic Goods Administration
ClinicalTrials.gov processed this record on 2005-09-06

Resources

  • T3 (Lab Tests Online)


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Page Updated: June 1, 2005
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