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OpenTrials
Completed

NCT Number: NCT00280761

Biomarkers in Patients With Rectal Cancer Undergoing Chemotherapy and Radiation Therapy

RATIONALE: Studying samples of tumor tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors understand how patients respond to treatment.

PURPOSE: This clinical trial is studying biomarkers in patients with rectal cancer undergoing chemotherapy and radiation therapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill

Chapel Hill, North Carolina, 27599-7295, United States

About this study

OBJECTIVES:

Primary

  • Observe whether NF-kappa B is activated in response to treatment with external beam radiotherapy.
  • Correlate NF-kappa B pathway activation (presumed to be anti-apoptotic in nature) with therapeutic outcomes (as measured by rate of pathologic complete response or downstaging by endoscopic ultrasound [EUS]).

Secondary

  • Study downstream events induced by NF-kappa B activation.
  • Determine global gene expression profiles at baseline and during chemoradiotherapy.
  • Correlate changes in gene expression (compared with the baseline gene expression pattern) induced by a single dose of external beam radiotherapy with patient outcomes (as measured by pathologic response rate or downstaging by EUS).
  • Study downstream events related to activation of p53 in response to treatment with radiotherapy.
  • Correlate p53 pathway-mediated events with clinical outcomes.

OUTLINE: Patients receive fluorouracil or capecitabine and undergo radiotherapy and surgery per standard care.

Patients undergo tumor pinch biopsies at baseline and on days 1 and 2 of chemoradiotherapy. At the time of final surgical resection, a portion of the remaining rectal tumor will be liquid nitrogen banked. Patients not deemed surgical candidates are evaluated by transrectal ultrasound 6-8 weeks after completion of chemoradiotherapy to assess ultrasound response (downstaging versus no downstaging).

Tumor tissue samples are analyzed for NF-kappa B pathway activation; downstream events induced by NF-kappa B activation; changes in global gene expression; p53 function; apoptosis; and mRNA expression. Laboratory techniques used include tissue microarray, ELISA, RNase protection assay, fluorescence semi-quantitative PCR, TUNEL, IHC, and cDNA microarray analysis.

If normal tissue from biopsies is not available, whole blood may be collected at any point while patient remains on study for correlative analysis or research related to rectal cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

DISEASE CHARACTERISTICS:

  • Must have rectal or sigmoid-rectal junction adenocarcinoma confirmed by sigmoidoscopy and pathologic diagnosis of biopsy sample
  • Inferior margin of the tumor less than 15 cm from anal verge by rigid sigmoidoscopy or below the level of S1-2 at surgery
  • Candidate for chemotherapy and radiotherapy, as defined by any of the following:
  • Tumor staged as T3 or N1-2 by rectal sonography
  • Tumor occupying > 40% of circumference of rectum
  • Tumor fixed to extra colonic structures as determined by digital rectal examination
  • Tumor < 5 cm from sphincter mechanism
  • Patient has inoperable disease and is being treated for palliation
  • Pelvic or anastomotic recurrences of previously resected rectal cancer
  • Planning to undergo chemotherapy and radiotherapy
  • No sigmoid carcinoma (carcinoma proximal to the pelvic peritoneal reflection)

PATIENT CHARACTERISTICS:

  • Not pregnant

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics

Treatment and study plan

Capecitabine

Drug

Capecitabine administration (where deemed appropriate by the treating medical oncologist) will commence on the second day of radiotherapy after the 24-hour biopsy has been performed. Dosing will be per current standard of care at the discretion of the treating Medical, Radiation and Surgical Oncologist

Other names: Xeloda

5-fluorouracil

Drug

Administration of 5-fluorouracil (where deemed appropriate by the treating medical oncologist) will commence on the second day of radiotherapy after the 24-hour biopsy has been performed. Dosing and dose modification will be per current standard of care at the discretion of the treating Medical, Radiation and Surgical Oncologist.

Other names: 5-FU

Surgical resection

Procedure

Surgery will occur approximately 2-6 weeks after chemoradiation depending on clinical factors (i.e. resectability, presence or absence of metastatic disease).

radiation therapy

Radiation

Dosing and dose modification will be per current standard of care at the discretion of the treating Radiation Oncologist.

Other names: EBRT - External Beam Radiation Therapy

Primary outcomes

  1. Activation of NF-kappa B in response to treatment with external beam radiotherapy

    Time frame: 6-8 weeks after chemoradiation

  2. Correlation of NF-kappa B pathway activation with therapeutic outcomes

    Time frame: 6-8 weeks after chemoradiation

Secondary outcomes

  1. Downstream events induced by NF-kappa B activation

    Time frame: 12 months

  2. Global gene expression profiles at baseline and during chemoradiotherapy

    Time frame: prior to chemoradiation and 72 days post chemoradiation

  3. Correlation of changes in gene expression with patient outcomes

    Time frame: 72 days post chemoradiation

  4. Downstream events related to activation of p53 in response to treatment with radiotherapy

    Time frame: 72 post radiotherapy

  5. Correlation of p53 pathway-mediated events with clinical outcomes

    Time frame: 72 days post chemoradiation

Sponsors and collaborators

Lead sponsor

UNC Lineberger Comprehensive Cancer Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

A Biologic Study of Global Gene Expression, NF-Kappa B and p53 in Adenocarcinoma of the Rectum.

Important dates

Study start
2003
Primary completion
2021
Study completion
2021
First posted
Jan 23, 2006
Registry last updated
Aug 11, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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