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Induction Chemotherapy Followed By Chemoradiotherapy in Treating Patients With Locally Advanced Adenocarcinoma of the Rectum

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: Southwest Oncology Group
National Cancer Institute (NCI)
Information provided by: National Cancer Institute (NCI)
ClinicalTrials.gov Identifier: NCT00070434
  Purpose

RATIONALE: Drugs used in chemotherapy, such as irinotecan, leucovorin, fluorouracil, and oxaliplatin, use different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combining radiation therapy with chemotherapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well different regimens of induction chemotherapy followed by chemoradiotherapy work in treating patients with locally advanced adenocarcinoma of the rectum.


Condition Intervention Phase
Colorectal Cancer
Drug: capecitabine
Drug: fluorouracil
Drug: irinotecan hydrochloride
Drug: leucovorin calcium
Drug: oxaliplatin
Procedure: radiation therapy
Phase II

MedlinePlus related topics:   Cancer    Colorectal Cancer   

Drug Information available for:   Leucovorin Calcium    Citrovorum factor    Folinic acid calcium salt pentahydrate    Leucovorin    Irinotecan    Irinotecan hydrochloride    Capecitabine    Fluorouracil    Oxaliplatin    Calcium gluconate   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Open Label
Official Title:   A Phase II Feasibility Translational Research Trial of Induction Chemotherapy Followed by Concomitant Chemoradiation in Patients With Clinical T4 Rectal Cancer

Further study details as provided by National Cancer Institute (NCI):

Primary Outcome Measures:
  • Response (confirmed and unconfirmed response, complete response, partial response) [ Designated as safety issue: No ]

Study Start Date:   August 2004

Detailed Description:

OBJECTIVES:

  • Determine the feasibility of obtaining a pre-treatment determination of intratumoral molecular markers (TS, DPD, and ERCC-1) for use in selection of the appropriate regimen for induction cytotoxic combination chemotherapy in patients with cT3-4 rectal adenocarcinoma.
  • Determine the response probability (unconfirmed, complete and partial) in patients treated with targeted induction cytotoxic chemotherapy.
  • Determine the toxicity of targeted induction cytotoxic chemotherapy and chemoradiotherapy in these patients.
  • Determine the response probability in these patients treated with chemoradiotherapy.

OUTLINE: This is a multicenter study.

  • Induction chemotherapy: Patients are assigned to 1 of 3 treatment groups based on molecular analysis of the pretreatment tumor specimen.

    • Group I (lower likelihood of resistance to a fluorouracil-based regimen): Patients receive irinotecan IV over 90 minutes and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV over 46 hours beginning on day 1.
    • Group II (higher likelihood of resistance to a fluorouracil-based regimen): Patients receive oxaliplatin IV over 2 hours and irinotecan IV over 90 minutes on day 1.
    • Group III (high likelihood of sensitivity to oxaliplatin and fluorouracil therapy): Patients receive oxaliplatin IV over 90 minutes and leucovorin calcium IV over 2 hours on day 1 and fluorouracil IV over 46 hours beginning on day 1.

Treatment in all groups repeats every 2 weeks for 4 courses in the absence of disease progression or unacceptable toxicity.

Patients are evaluated for response approximately 2 weeks after the completion of induction chemotherapy. Patients with stable disease or better receive chemoradiotherapy.

  • Chemoradiotherapy: Beginning approximately 3 weeks after the completion of induction chemotherapy, patients receive oral capecitabine twice daily continuously for 5 weeks and concurrent radiotherapy once daily 5 days a week for 5 weeks.

After chemoradiotherapy, patients may undergo attempted surgical resection at the discretion of the treating physician.

Patients are followed every 3 months for 1 year and then every 6 months for 2 years.

PROJECTED ACCRUAL: A total of 10-65 patients will be accrued for this study.

  Eligibility
Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed primary adenocarcinoma of the rectum
  • Locally advanced disease (clinical T3-4, N0-2, M0) based on at least 1 of the following criteria:

    • Clinically fixed tumors on rectal examination with tumor adherent to the pelvic sidewall and/or sacrum
    • Sciatica attributed to sacral root invasion with CT scan/MRI evidence of the lack of clear tissue plane is considered evidence of fixation
    • Hydronephrosis on CT scan or intravenous pyelogram of ureteric or bladder invasion by cystoscopy and cytology or biopsy
    • Invasion into the prostate, vagina, or uterus
  • Transmural penetration of tumor through the muscularis propria as evidenced by CT scan or MRI and endorectal ultrasound
  • Distal border of the tumor must be at or below the peritoneal reflection (within 12 cm of the anal verge) by proctoscopic examination
  • Measurable disease by x-ray, scans, or physical examination
  • Available tumor tissue to determine molecular profile of the tumor before study treatment
  • No clinical evidence of high-grade (lumen diameter < 1 cm) large bowel obstruction unless a diverting colostomy has been performed

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Performance status

  • Zubrod 0-2

Life expectancy

  • Not specified

Hematopoietic

  • WBC ≥ 3,500/mm^3
  • Absolute neutrophil count ≥ 1,500/mm^3
  • Platelet count ≥100,000/mm^3

Hepatic

  • Bilirubin ≤ 1.5 times upper limit of normal (ULN)
  • SGOT or SGPT ≤ 2.5 times ULN
  • Alkaline phosphatase ≤ 2.5 times ULN

Renal

  • See Disease Characteristics
  • Creatinine ≤ 1.5 times ULN OR
  • Estimated creatinine clearance > 50 mL/min

Cardiovascular

  • No significant cardiac disease
  • No recent myocardial infarction

Gastrointestinal

  • See Disease Characteristics
  • Able to swallow oral medication
  • No active inflammatory bowel disease

Other

  • Not pregnant or nursing
  • Fertile patients must use effective contraception
  • No other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix
  • No prior unanticipated severe reaction to study drugs
  • No known dihydropyrimidine dehydrogenase deficiency
  • No serious uncontrolled infection
  • No other serious medical illness that would preclude study treatment

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • Not specified

Chemotherapy

  • No prior chemotherapy for colon or rectal cancer

Endocrine therapy

  • Not specified

Radiotherapy

  • No prior pelvic radiotherapy
  • No prior intra-operative radiotherapy or brachytherapy
  • No concurrent intra-operative radiotherapy or brachytherapy
  • No concurrent intensity-modulated radiotherapy

Surgery

  • See Disease Characteristics
  • See Radiotherapy
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00070434

Sponsors and Collaborators
Southwest Oncology Group
National Cancer Institute (NCI)

Investigators
Investigator:     Charles R. Thomas, MD     University of Texas    
Investigator:     Heinz-Josef Lenz, MD     Norris Comprehensive Cancer Center    
Investigator:     Robert P. Whitehead, MD     University of Texas    
Investigator:     James L. Abbruzzese, MD     M.D. Anderson Cancer Center    
Investigator:     Stephen R. Smalley, MD     Radiation Oncology Center of Olathe    
Investigator:     Morton S. Kahlenberg, MD     University of Texas    
  More Information


Clinical trial summary from the National Cancer Institute's PDQ® database  This link exits the ClinicalTrials.gov site
 

Study ID Numbers:   CDR0000334469, SWOG-S0304
First Received:   October 3, 2003
Last Updated:   July 23, 2008
ClinicalTrials.gov Identifier:   NCT00070434
Health Authority:   United States: Federal Government

Keywords provided by National Cancer Institute (NCI):
stage II rectal cancer  
stage III rectal cancer  
adenocarcinoma of the rectum  

Study placed in the following topic categories:
Capecitabine
Digestive System Neoplasms
Rectal Neoplasms
Gastrointestinal Diseases
Irinotecan
Colonic Diseases
Leucovorin
Intestinal Diseases
Rectal Diseases
Camptothecin
Intestinal Neoplasms
Rectal neoplasm
Carcinoma
Oxaliplatin
Digestive System Diseases
Fluorouracil
Gastrointestinal Neoplasms
Adenocarcinoma
Rectal cancer
Colorectal Neoplasms
Neoplasms, Glandular and Epithelial

Additional relevant MeSH terms:
Antimetabolites
Neoplasms by Histologic Type
Antimetabolites, Antineoplastic
Vitamin B Complex
Molecular Mechanisms of Pharmacological Action
Immunologic Factors
Antineoplastic Agents
Growth Substances
Physiological Effects of Drugs
Enzyme Inhibitors
Immunosuppressive Agents
Pharmacologic Actions
Neoplasms
Neoplasms by Site
Vitamins
Therapeutic Uses
Micronutrients
Antineoplastic Agents, Phytogenic

ClinicalTrials.gov processed this record on November 30, 2008




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