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Colorectal CancerNCT00173472

Association of MSI, TS, DPD, MVD and EGFR With Chemosensitivity in Stage IV in Colorectal Cancer

An observational study of Colorectal Cancer, run by National Taiwan University Hospital at 1 site in Taiwan.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The present project will follow our previous phaseⅡ study of FOLFOX regimens for the treatment of stage Ⅳ colorectal cancer. We will recruit at least 200 patients for this study. The selection of patients will be based on rigorous eligibility criteria. Read more about this study

Who is it for?
Ages 18 to 75 years
Conditions the study is for
Colorectal Cancer
What is being tested?
Chemotherapy
How many people
200 participants
Where
1 siteTaiwan
Study dates
Jul 2002to Jul 2005
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • The patients recruited met the following eligibility criteria: (1) The sporadic primary colorectal cancer could be palliatively resected and pathologically confirmed as adenocarcinoma; (2) The metastatic lesions were measurable but unresectable; (3) Karnofsky performance status was ≧50%; (4) The life expectancy was greater than 12 weeks; (5) WBC count was ≧4,000/μL, platelet count was ≧100,000/μL, serum bilirubin was ≦2.0 mg/dL, and serum glucose and electrolyte were normal.

Who cannot join

  • Patients with evident family history of colorectal cancer suggestive of familial adenomatous polyposis (FAP) or hereditary nonpolyposis colorectal cancer (HNPCC) were excluded from this study. Moreover, patients with evident carcinosis peritonitis were excluded from this study because their bowel function could not be restored through palliative operation and their prognosis was considered as very poor.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Department of Surgery, National Taiwan University Hospital, No.7, Chung-Shan South Road, Taipei, TAIWAN, R.O.C.

    Taipei, 100

Other trials in Taiwan

About this study

The present project will follow our previous phaseⅡ study of FOLFOX regimens for the treatment of stage Ⅳ colorectal cancer. We will recruit at least 200 patients for this study. The selection of patients will be based on rigorous eligibility criteria. The patients will be allocated based on the expression of each molecular marker (MSI, TS, DPD, MVD and EGFR) and the implementation of chemotherapy. For example, in the examination for the clinical implications of EGFR, the patients will be classified into four groups: EGFR(+) chemotherapy(+); EGFR(+) chemotherapy(-); EGFR(-) chemotherapy(+); EGFR(-) chemotherapy(-). Base on the analysis of this 2×2 table, we will clarify the prognostic significance of a specific molecular marker is due to whether the specific molecular marker predicts biological invasiveness and/or chemosensitivity. We believe the present study will have the following significance: (1)To further clarify the mechanisms for the carcinogenesis and progression of CRC; (2)To facilitate the development of novel chemotherapeutic agents; and (3) To gain the experience for the practice of evidence-based medicine.

Read the detailed description

Stage IV disease represented approximately 25% of all colorectal cancer (CRC) cases. The mainstay treatment for stage IV CRC is chemotherapy and surgery is only for palliation of symptoms including colorectal bleeding and obstruction. If patients with stage IV CRC were not treated, the average survival time was 6 months. Recently, with the progress of chemotherapeutic agents, such as oxaliplatin and irinotecan, the stage IV patients' average survival time considerably increased to 18 months. However, the currently utilized chemotherapeutic regimens, including FOLFOX (Folinic acid + 5-Fu +oxaliplatin) and FOLFIRI (Folinic acid + 5-Fu + irinotecan), their response rate was only around 50-60%. Moreover, these agents had several severe side-effects, such as neurotoxicity and diarrhea. Therefore, it is mandatory for us to seek clinicopathogical parameters or novel molecular markers that predicted chemosensitivity, in terms of increase of response rate and avoidance of side-effects. Recently, the carcinogenesis of CRC was better clarified than before. Some molecular markers, such as p53, K-ras, microsatellite instability (MSI), microvessel density(MVD), and epidermal growth factor receptor(EGFR), and their relation to survival of colorectal cancer patients have become the focus of research.

The present project basically follows our previous study that p53 overexpression predict poorer chemosensitivity(Liang et al. Int. J. Cancer 2002; 97: 451-457), and we plan to further explore the association between chemosensitivity with MSI-H, MVD, and EGFR. In fact, in either FOLFOX or FOLFIRI, they all belong to 5-Fu-based therapy. Therefore, the tumor expression of enzymes related to the metabolism of 5-Fu, such as thymidylate synthase(TS)and dipyrimidine dehydrogenase(DPD), have also become the hot issue of research. In this project, we will explore the clinical implications of MSI, TS, DPD, MVD, and EGFR. This is because our previous study has indicated that MSI-H is a marker of mutator phenotype of colorectal cancer, i.e., colorectal cancers with MSI-H tend to have multiple mutations of downstream genes, especially those with repetitive microsatellite sequences within the genes. Our previous study has shown MSI-H predicted better chemosensitivity(Liang et al. Int. J. Cancer 2002; 101: 519-525). Therefore, we are curious to know that if MSI-H is related to the alterations of TS and DPD in the tumor, i.e., if the alterations for the tumor levels of TS and DPD is one of the mechanisms for the better chemosensitivity in tumors with MSI-H. On the other hand, it has been known that EGFR is related to tumor growth, invasion, angiogenesis, and metastasis of colorectal cancers. Therefore, it is mandatory to further dissect the correlation between EGFR and MVD. To the best of our knowledge, this has not been published before.

The present project will follow our previous phaseⅡ study of FOLFOX regimens for the treatment of stage Ⅳ colorectal cancer. We will recruit at least 200 patients for this study. The selection of patients will be based on rigorous eligibility criteria. The patients will be allocated based on the expression of each molecular marker and the implementation of chemotherapy. For example, in the examination for the clinical implications of EGFR, the patients will be classified into four groups: EGFR(+) chemotherapy(+); EGFR(+) chemotherapy(-); EGFR(-) chemotherapy(+); EGFR(-) chemotherapy(-). Base on the analysis of this 2×2 table, we will clarify the prognostic significance of a specific molecular marker is due to whether the specific molecular marker predicts biological invasiveness and/or chemosensitivity. After the analysis of prognostic significance of each molecular marker, we will explore the interrelationship between these molecular markers. Also, all these 5 molecular markers and various clinicopathological factors will be subjected to multivariate analysis. Because the survival of stage Ⅳ CRC patients will generally not exceed 30 months, the patients study will not have to be followed up for a long time before the final study result appears. We believe the present study will have the following significance: (1)To further clarify the mechanisms for the carcinogenesis and progression of CRC; (2)To facilitate the development of novel chemotherapeutic agents; and (3) To gain the experience for the practice of evidence-based medicine.

Being tested
Chemotherapy
Keywords
colorectal cancer, MSI, TS, DPD, EGFR, chemotherapy.
Medical subject headings
Colorectal Neoplasms, Microsatellite Instability

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ChemotherapyDrug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Sep 2005 (estimated)
  2. Study startJul 2002
  3. Study completionJul 2005

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Defined population
Time perspective
Prospective
Enrolment
200 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00173472
Sponsor's protocol ID
9461700674
Status last verified
Jul 2002
First submitted
12 Sep 2005
Last updated
24 Nov 2005
Results posted
No

Questions about this trial

What is this clinical trial studying?

An observational study of Colorectal Cancer, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 24 Nov 2005. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Nov 2005.

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