Testing less intensive radiation therapy with immunotherapy to treat selected low-risk patients with HPV-positive oropharyngeal cancer

If you are over the age of 18 with low-risk, Human Papillomavirus (HPV) positive oropharyngeal cancer, you may be able to participate.

This study has two parts called “phase II” and “phase III”. Doctors want to know if a reduced dose of radiation and immunotherapy results in at least similar same length of time without your cancer getting worse and a better quality of life than the usual approach.

We are doing this study to determine if this approach is at least similarly effective than the usual approach for your cancer. The usual approach is defined as the care most people get for low-risk, HPV positive oropharyngeal cancer.

If you decide to participate in this study, you will either get the usual dose of radiation over 6 weeks plus cisplatin chemotherapy or reduced-dose radiation over 5 weeks plus nivolumab immunotherapy.

The usual approach for patients not in a study is treatment with radiation therapy and chemotherapy. For patients who get the usual approach for this cancer, about 88 out of 100 are free of cancer after 5 years.

If you choose to take part in this study, there is a risk that:

• You may lose time at work or home and spend more time in the hospital or doctor’s office than usual. 
• You may be asked sensitive or private questions that you normally do not discuss. 
• The study approach may not be as good as the usual approach at shrinking or stabilizing your cancer and preventing your cancer from spreading. 
• The drugs used on this trial may cause side effects. Your doctor will review all of the potential side effects with you. It is important to tell your doctor about any side effects, you may experience during the study so that they may be treated and so that potential adjustments to the study drugs may be made.

There is evidence that this study approach could be effective in shrinking or stabilizing your type of cancer. It is not possible to know now if the study approach will control your cancer for the same amount of time compared to the usual approach. This study will help the study doctors learn things that will help people in the future.

After you finish your treatment, your doctor and study team will watch you for side effects and continue to evaluate your disease. They will check you every 3 months for 2 years after treatment. Then they will check you every 6 months for 3 years. After that, they will check you every year for your lifetime unless your doctor thinks you need to be seen sooner.

No. Taking part in this study is voluntary. You are free to choose to participate or not to participate. If you choose to participate in this study, you are able to leave the study at any time. If you decide not to take part in this study, your doctor will discuss other treatment options with you.

You and/or your insurance plan will need to pay for the costs of medical care you get as part of the study, just as you would if you were getting the usual care for your cancer.

This includes:

• the costs of tests, exams, procedures, and drugs that you get during the study to monitor your safety, and prevent and treat side effects. If you are receiving nivolumab, the extra blood tests to monitor thyroid function and organ function will be billed to your health care plan/insurance provider. 
• the costs of cisplatin drug and administration. 
• the costs of getting nivolumab ready and giving it to you. 
• your insurance co-pays and deductibles. 

Talk to your insurance provider and make sure that you understand what your insurance pays for and what it does not pay for if you take part in this clinical trial. Also, find out if you need approval from your plan before you can take part in the study. 

You will not be paid for taking part in this study.

Your privacy is very important to us, and the researchers will make every effort to protect it. Your information may be given out if required by law. For example, certain states require doctors to report to health boards if they find a disease like tuberculosis. However, the researchers will do their best to make sure that any information that is released will not identify you. Some of your health information and/or information about your specimens from this study will be kept in a central database for research. Your name or contact information will not be put in the database.

There are organizations that may inspect your records. These organizations are required to make sure your information is kept private, unless required by law to provide information. Some of these organizations are:

• NRG Oncology and any company supporting the study now or in the future. This would include any organization helping the company with the study. 
• The National Cancer Institute (NCI) Central Investigational Review Board (IRB), which is a group of people who review the research with the goal of protecting the people who take part in the study. 
• The Food and Drug Administration (FDA) and the groups it works with to review research. 
• The NCI and the groups it works with to review research. 
• The NCI’s National Clinical Trials Network (NCTN) and the groups it works with to conduct research, including the Imaging and Radiation Oncology Core (IROC).

Doctors and researchers conduct a clinical study, also called a “clinical trial,” to find better ways to prevent, diagnose, or treat an illness. NRG Oncology is supported by the National Cancer Institute (NCI) and runs clinical studies specifically for patients with cancer or to prevent cancer. Most clinical studies test something we know against something we don’t know. In all situations, these studies are strictly evaluated before they are allowed to be offered to any patient. The study is designed to answer the question that we do not know the answer to, so that current and future patients may have better treatments or information than what we currently have. There are different types of clinical studies that might be available for patients. For more information see “Types of Clinical Trials” and “Phases of Clinical Trials”.

Patients who volunteer to take part in a clinical study are followed closely by their health care professionals and members of the research team. For more information see “Research Team Members”.

Yes. They are exactly the same thing.

The care cancer doctors provide to cancer patients today is the direct result of clinical studies (also known as clinical trials) that were done in the past. Clinical studies give doctors and the treatment team information about what types of treatments work and what treatments do not work, in a number of different situations. Some studies focus on treating the cancer, others on preventing the cancer, and others on helping patients feel better or healthier during or after treatments. When you take part in a clinical study, you add to our knowledge about cancer and it may help improve cancer care for future patients. Clinical studies are available to patients with many types of cancer and at all stages of treatment. In some situations, the only way to get these new treatments is by joining a clinical study.

A clinical study may take place in many locations, such as:

physician offices

hospitals

clinics

A study is typically led by a principal investigator who is a doctor or other advanced health care professional. A clinical study is carried out by following a very specific plan known as the “protocol”. The protocol is designed so all patients in the study are treated as well as possible and in the same way. The protocol also provides rules for the doctors and clinical study staff to follow to keep patients safe and make sure the study is run in an ethical manner.

No, not at all. Participation in a clinical study is completely voluntary. For more information see “Deciding to Take Part in a Clinical Trial”. You are free to choose to participate or not to participate. If you choose to participate in a study, you may still decide to leave the study at any time. If you decide not to participate in a study, your doctor will discuss other treatment options with you. For more information see “Questions to Ask Your Doctor about Treatment Clinical Trials".

• You may choose to have the usual treatment approach (known as “standard of care”)
• You may choose to take part or learn more about a different study, if one is available
• You may choose not to be treated for cancer