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Cancer Health Library : Oncology


Clinical Trials Overview

Clinical trials for breast cancer research

There are many breast cancer clinical trials and studies underway across the United States and in other countries. They are sponsored by government agencies, health care organizations, private industry, and nonprofit foundations, working together in an unprecedented spirit of collegial and collaborative cooperation.

In this country, trials and studies are overseen by the government, under the auspices of the Department of Health and Human Services, National Institutes of Health, FDA, and others. Most breast cancer trials are managed under the guidance of the National Surgical Adjuvant Breast and Bowel Project.

What are clinical trials?

Clinical trials are studies, managed by government agencies, educational institutions, private not-for-profit organizations, or commercial businesses, to develop, produce, and evaluate the effectiveness of new treatments and therapies for diseases.

What are some types of clinical trials?

According to the National Cancer Institute, there are different types of cancer clinical trials, including:

  • Prevention trials. These are designed to keep cancer from developing in people who have not previously had cancer.
  • Prevention trials. These are designed to prevent a new type of cancer from developing in people who have had cancer.
  • Early detection trials. These are done to find cancer, especially in its early stages.
  • Treatment trials. Such trials test new therapies in people who have cancer.
  • Quality of life studies. These are done to improve comfort and quality of life for people who have cancer.
  • Behavioral studies. Such studies are done to evaluate ways of modifying cancer-causing behaviors, such as tobacco use.
  • Genetic studies. These studies address how genetic makeup affects detection, diagnosis, and treatment of cancer.

What are the phases of a clinical trial?

Most clinical research progresses in an orderly series of steps or phases.

  • Phase 0 trials. These are the earliest steps in testing new treatments in humans. A small number of people are studied and the focus is on learning how the agent is processed by the body and how the agent affects the body. No information is gathered on safety or effectiveness in treating cancer.
  • Phase I trials. These are the first studies to evaluate how a new therapy should be administered--how it should be given, how often, and in what dosage. The focus is to determine safety (drug dose, device safety, or other therapy's safety) for the next phase of testing.
  • Phase II trials. These provide preliminary information about how well the new therapy works, and generates more information about its safety and benefits. A Phase II study usually focuses on a particular type of cancer.
  • Phase III trials. These compare a promising new therapy, combination of treatments, or procedure with a current standard of treatment. These trials often enroll large numbers of people and may be done at may doctors' offices, clinics, and cancer centers nationwide, or even worldwide.
  • Phase IV trials. These include the continuing evaluation that takes place after FDA approval, when the therapy is already available for general use.

What is a clinical trial protocol?

Clinical trial protocols are the action plans or guidelines that must be followed during the course of any study. Guidelines may cover:

  • The design of the study--what will be studied and how
  • Who may participate--criteria for patients who enter the study
  • What treatments and medical tests will be used to follow the participants
  • Specific research questions
  • What information will be collected

Several research centers may be involved in the study, and each uses the same protocols to ensure that information from all centers can be combined and compared.

Where are trials conducted?

Large cancer centers, university hospitals, local medical centers, or doctor offices; all may be included in managing clinical trials. Informed consent is a process designed to protect potential participants through detailed description of important facts about a specific clinical trial. There may be only one or two locations involved in a particular study, or hundreds around the country, or even around the world.

Who can participate in a trial?

Each protocol in a trial defines specific characteristics, called eligibility criteria, that participants should have in order to participate in the study. Characteristics may include type of disease and its stage, as well as the participant's age and general health.

Eligibility criteria help assure that the study results answer the research question and identify who will benefit in the future from the approach being studied.

How are trial participants protected?

There are several procedures in place, as part of the protocols, to protect the safety of the participants. Informed consent is a process designed to protect potential participants through detailed description of important facts about a specific clinical trial. Two groups that oversee the safety procedures are the:

  • Organization that sponsors the study, for example, the National Cancer Institute
  • Institutional Review Board (IRB) that oversees clinical research in the health care institution. The IRB includes doctors, other health care providers, consumers, and sometimes members of the clergy, who do not have any personal interest in the results of the study. As neutral reviewers, they ensure that the study is conducted fairly and that there is not a high probability of harm to the participants.

Some clinical trials, especially Phase III trials, also have a special group called a Data Safety and Monitoring Committee that looks at the test results, monitors the safety of the participants, and decides whether the study should go forward as originally planned.

For information on how to participate in a clinical trial, please talk with your doctor.

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