You have a lot to process when you receive a cancer diagnosis. Part of that discussion can include a decision about off-label treatment options.
You’re probably familiar with the U.S. Food and Drug Administration (FDA). Their research determines a drug therapy’s safety and its designated use.
But a particular drug’s effectiveness doesn’t stop there
What is “off-label?”
Simply put, an off-label treatment would involve use of a specific (FDA approved) drug for a purpose other than the FDA designation. A drug’s secondary use is therefore not listed on its “label”.
For example, you’ll notice a few things when examining a drug’s label.
- How it’s designed to work
- Relevant research data that supports its approval
- Side effects
The FDA takes seriously their responsibility for assuring a medication is safe and effective for its specific use. That said, their control does not extend to your doctor’s decision about what drugs to prescribe you.
FDA approval is valid and essential. But your doctor has the latitude to prescribe it for a purpose that’s in your best interest following additional tests.
Off-label use can vary greatly from one doctor to another, depending on doctors preferences, knowledge, and past patient experiences. A 2008 study found that 8 out of 10 cancer doctors surveyed had prescribed drugs off-label. 1
Off-label isn’t off-the-grid
An FDA approved drug therapy can be used off-label for a specific health condition such as
- A cancer that’s different than one the drug is specifically designed to treat
- A different prescribed dosage or use frequency
- Treating a child instead of an adult
Keep in mind that off-label treatments still require approval from the FDA at the manufacturing company’s request. Additional approvals also require research that shows the treatment to be safe and effective for new or innovative uses. This research requires time and money from the manufacturer.
What about off-label treatment for cancer?
Off-label use of drugs is common for treating cancer. The stages and types of cancer can be treated with off-label use of one or more drug therapies.
A cancer drug can be effective against more than one type of cancer. For example, combination chemotherapy uses more than one drug to effectively treat different types of cancer.
Research is trusted to discover new uses for approved drugs. These studies are accessible by your doctor and will be used to evaluate a drug’s effectiveness for treating your type of cancer.
At the same time an off-label use of a drug might not be safe. Circumstances can include:
- No proof of effectiveness for a certain type of cancer or reason to believe it would be
- The potential risks of usage are greater than the possible benefits
Again, your doctor will prescribe an off-label use of a particular drug based on their knowledge and experience with it and the drug’s effectiveness as revealed by research.
Ask these questions before you proceed with off-label cancer treatment
We’re prepared to help you understand the reason off-label treatment could be a viable solution for treating your type of cancer. We encourage you to ask and discuss these questions with us:
Why will my specific cancer respond to the off-label use of this drug?
What difference in results will I experience between the off-label drug and the one specifically approved for treatment?
What risks and benefits can I expect from the off-label use of this drug?
Does my health insurance cover my treatment with this drug?
Will my health insurance cover combination chemotherapy and the use an off-label drug?
These questions and more are common and important to ask prior to beginning cancer treatment with off-label drug therapies. Our goal is to give you the best opportunity for eliminating cancer and restoring your health.
Contact us about cancer treatment solutions. Schedule a consultation and ask us about off-label drug therapies for treating and eliminating cancer.