What are Clinical Trials?
A clinical trial is a study that helps doctors and researchers find better ways to prevent, treat or diagnose diseases such as cancer. There are several types of cancer clinical trials — some test new ways to treat cancer; others test new methods of prevention, detection or diagnosis.
When laboratory research shows that a new treatment method has promise, cancer patients can receive the treatment in carefully controlled trials. These trials can help the researcher evaluate the effectiveness of new drugs and interventions, and are essential for studying treatments and possible cures. Often, clinical trials compare a new treatment with a standard approach so that doctors can learn which is more effective. Researchers also look for ways to reduce the side effects of treatment and improve the quality of patients’ lives.
Through Hunterdon Regional Cancer Center’s partnership with Philadelphia’s Fox Chase Cancer Center, physicians have access to many clinical research trials, which are administered by specially trained staff. The availability of clinical research at Hunterdon Regional Cancer Center allows our patients the ability to receive their treatment in their own community and lessen the burden of travel to distant academic institutions.
What are the benefits of joining a Clinical Trial?
Taking part in a clinical trial allows you to play an active role in your healthcare and receive excellent medical care. Because a clinical trial must follow a strict protocol, or plan, people in clinical trials are very closely observed. They may have access to new cancer treatments and techniques before they are widely available. Doctors perform clinical trials because they believe the drugs or techniques they’re testing could be more effective or safer than the standard treatments they are using now. Doctors hope the information learned from trials will help future patients.
Am I eligible for a Clinical Trial?
When planning a clinical trial, researchers decide on eligibility criteria — characteristics about the people they would like to study. These characteristics generally include how young or old a person must be to join; what type and stage of cancer that person has; what previous treatments the patient has undergone; and other medical problems the person may have. If you think you would like to take part in a clinical trial, one good place to start is by asking your doctor or nurse about the trials available for your cancer.
The Hunterdon Regional Cancer Center is committed to providing our patients with the most advanced treatment options. Our center has two specially trained Research Coordinators who are available to answer questions about current clinical research trials and prevention trials.
To learn more about available clinical research trials contact:
Hunterdon Regional Cancer Center
2100 Wescott Drive
Flemington, NJ 08822
If you are considering participation in a clinical trial, here are some questions to ask your doctor:
- What is the purpose of the clinical trial?
- What are the pros and cons of participating in a clinical trial?
- What are my other treatment options?
- Will there be extra costs because of the trial?
- How long will the trial last?
How are Clinical Trials conducted?
Clinical Trials are conducted in phases. The trials at each phase have a different purpose and help scientists answer different questions.
- Phase I trials – researchers test a new drug or treatment in a small group of people for the first time. These studies evaluate how a new drug should be given, how often it should be administered, and the most effective dose with the fewest and least serious side effects.
- Phase II trials – these studies continue to test the safety of the drug and how well it works in a selected tumor type.
- Phase III trials – these studies will confirm the new drug effectiveness, observe side effects, compare the new treatment with currently used standard treatments, and collect information that will allow the new drug to be used safely.
- Phase IV trials – these studies test the drug or treatment after FDA approval to find out additional information about the treatment’s risks and benefits and the best way to use it. These studies help doctors understand the long-term safety.
Depending on what is being studied, a particular clinical study may involve patients with cancer or people who do not have cancer but are at higher risk than most people for developing it. By participating in a clinical trial, patients may benefit from a new drug, procedure, or symptom-control method while helping scientists evaluate its effectiveness. Participation may also contribute directly to finding better ways to prevent, detect, or treat the disease. Many of today’s most effective interventions are the direct result of knowledge gained through clinical research.
Clinical trials are reviewed at a national and local level. The Institutional Review Board (IRB) at Hunterdon Medical Center is a committee that has reviewed the clinical research studies to help ensure that the rights and welfare of each research participant are protected and that the study will be carried out in an ethical manner. The IRB has many different members, including doctors, nurses, patient advocates, and people from the community.
Current trials offered at Hunterdon Regional Cancer Center include new treatment protocols conducted by pharmaceutical companies and The National Institute of Health (Cooperative Group Trials).
Current trials may include treatment options for breast, colon, prostate or lung cancers, as well as treatment options for leukemia, lymphomas, melanoma and hematologic conditions.
To learn more about the current Clinical Trials that Hunterdon Regional Cancer Center is participating in, please call Ronda Cichielo, Clinical Research Coordinator, at 908-237-2330 ext. 2.
Jae Y. Lee, MDRadiation Oncologist
Brian H. Chon, MDRadiation Oncologist
Robert M. Cardinale, MDRadiation Oncologist
Myron E. Bednar, MDMedical Oncologist
Kenneth B. Blankstein, MDMedical Oncologist
Waqas Rehman, MDMedical Oncologist
Swee Jian Ngeow, MDMedical Oncologist
Megha Shah, MDMedical Oncologist
John C. Baumann, MDRadiation Oncologist
Andrew S. Greenberg, MDRadiation Oncologist
Todd W. Flannery, MDRadiation Oncologist
Edward M. Soffen, MDRadiation Oncologist
Catherine Gleason, MDBreast Surgery
Jennifer A. Montes, MDBreast Surgery
Henry K. Tsai, MDRadiation Oncologist
Neesha A. Rodrigues, MDRadiation Oncologist
Joseph M. Pepek, MDRadiation Oncologist
Hiral Patel Fontanilla, MDRadiation Oncologist
Additional Staff & Specialists
Barbara Tofani, RN, MSN, NEA-BC
Samantha Geiger, RN
Nancy Satnowski, RN
Jessica Danik, RN, BSN, CBCN
Barbara Surhoff, PT
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