Patients Who Refractory Cancer Conqueror for Bio New Drug Development Translational Research Establishment

August 27, 2013 updated by: Do-hyun Nam, Samsung Medical Center

Patients Who Refractory Cancer Conqueror for Bio New Drug Development Translational Research Establishment - Establishment of Personalized Cell Library

■ Unmet medical needs for Refractory cancer Conquest

- Many advanced cancers are still detected Despite remarkable technological advances for the early diagnosis of cancer in the field last 20 years.

In the type of progressive carcinoma is very high malignancy despite a variety of therapeutic target treatment for refractory cancer.

The refractory cancer patients who main focus of this research defined as the adult solid tumor patients who have failed standard therapy according to the criteria

NCCN / ASCO (American Society of imsangam) / KCSG (Study Group for chemotherapy).

The survival rate of refractory cancer patients are estimated to be 30-40% of the total patients with metastatic solid tumors and these refractory cancers are

difficult to deal with or control to conventional treatment so shows almost close to 100% mortality.

Therefore the new development of therapies for conquer of refractory cancer are urgently required.

■ Preclinical translational research Unmet Needs of Bio-new drug development for conquer of refractory cancer

- The stage of preclinical translational research (Translational Research) connects between the early stages of development and clinical trials in the stage drug development.

The establishment of foundation based on the translational research is very necessary and this must have proven ability to treat refractory cancer.

The most anti-cancer drugs developed by existing preclinical testing method actually does not show a remarkable effect in many cases in the clinical trials,

even if showed a remarkable inhibitory cancer effect in animal testing.

The exact molecular diagnosis to treat targets and paradigm for the development of new drugs at the same time requires for target treatment.

The tailored cell lines by patients and the proven technology by animal models and unmet need for preclinical translational research is increasing

Study Overview

Status

Unknown

Conditions

Detailed Description

■ The specimen obtainer in surgery room contact with the manager of Institute Refractory Cancer Research team by calling to Medi-call system(Phone No.system T.9825).

The specimen obtainer gives the information of speciman to the manager .

The manager contact to the speciman deleverer and The speciman deleverer transported the specimens safely to the laboratory space.

The written informed consent form should obtained from the subject prior to the surgery.

In the case of blood samples, The total 15 ~ 20 ㎖ blood (only once) extracted from the subject and about 10 ~ 15 ㎖ blood is used for the genomic DNA extraction.

Study Type

Observational

Enrollment (Anticipated)

1523

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Gyunggido
      • Seoul, Gyunggido, Korea, Republic of, 135-710
        • Samsung Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

The subject diagnosed with cancer(GBM, Colon Cancer, Ovarian Cancer, Lung Cancer, Breast Cancer, Brain metastases, Bone Metastatic Cancer, Lymphoma, Gastric Cancer, Pancreatic Cancer, Gall bladder Cancer, Prostate Cancer, Kidney Cancer, Bladder cancer, Osteosarcoma, Soft tissue sarcoma, Head and neck cancer),and other Brain tumor

Description

Inclusion Criteria:

  1. The patients who agreed and written consent to participate in this research
  2. The patients who are scheduled for collection such as the patient tissue, pleural fluid, cerebro spinal fluid, blood samples for the purpose of surgery and diagnostics
  3. The patients who diagnosed with cancer as below - GBM, Colon Cancer, Ovarian Cancer, Lung Cancer, Breast Cancer, Brain metastases, Lymphoma, Bone Metastatic Cancer , Gastric Cancer, Pancreatic Cancer, Gall bladder Cancer, Prostate Cancer, Kidney Cancer, Bladder cancer, Osteosarcoma, Soft tissue sarcoma, Head and neck cancer, 기타 Brain tumor

Exclusion Criteria:

  • 1) Those who do not agree in writing to participate in research

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The amount of sample size
Time Frame: 10years

■ Target number of subjects (years) GBM : 120 case Colon Cancer : 200 case Gastric Cancer : 345 case Ovarian Cancer : 40 case Lung Cancer : 30 case Breast Cancer : 100 case Brain metastases : 120 case Bone metastases : 50 case Lymphoma : 10 case Pancreatic Cancer : 100 case Gall Bladder cancer : 20 case Prostate Cancer : 50 case Kidney Cancer : 100 case Bladder Cancer : 200 case Osteosarcoma : 15 case Soft tissue sarcoma : 50 case Head & neck cancer : 30 case Other Brain tumor : 100case

- Total case : 1680 case

10years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The size of real tumor portion on obtained tumor specimen
Time Frame: 10 years
  1. In the samples of frozen tissue stored at -80 ° C are processed by the method Frozen Hematoxylin & Eosin Stain.
  2. The criteria of evaluation : tumor size, Tumor Area, Tumor Cell Density, Tumor Nucleus Amount, Necrosis.
  3. The Results are distincted by Accept, Intermediate, Fail.
10 years

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Genomic DNA Extraction from blood specimen
Time Frame: 10 years
  1. Using QIAGEN kit: QIAmp DNA mini kit (Cat. No. 51306)
  2. The Volume measurement: Using Spectrophotometer (Nanodrop, ND-1000)
10 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Jueun Kim, Coordinator, Institutional Refractory Cancer Research

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2010

Primary Completion (Actual)

August 1, 2013

Study Completion (Anticipated)

April 1, 2015

Study Registration Dates

First Submitted

August 27, 2013

First Submitted That Met QC Criteria

August 27, 2013

First Posted (Estimate)

August 30, 2013

Study Record Updates

Last Update Posted (Estimate)

August 30, 2013

Last Update Submitted That Met QC Criteria

August 27, 2013

Last Verified

August 1, 2013

More Information

Terms related to this study

Other Study ID Numbers

  • 2010-04-004

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Refractory Cancer

Subscribe