Male hormones like testosterone and dihydrotestosterone (DHT) fuel prostate cancer cells. Suppressing these hormones can be an effective way to treat prostate cancer alongside other protocols. This particular hormone therapy is known as androgen deprivation therapy or ADT.
We've asked one of our physician assistants, Victoria Webber, to answer common questions about ADT, including when this hormone therapy is discussed with patients, how ADT is administered, and potential side effects.
As with all content on our blog, the following is educational, not medical advice. Always consult your medical provider regarding your unique healthcare needs.
VICTORIA WEBBER: Androgen deprivation therapy (ADT) is a therapy we use to decrease the level of certain hormones known as androgens (testosterone and DHT) circulating in a patient's body. Androgens play a role in stimulating the growth of prostate cancer cells, so by decreasing the androgens circulating in the body, we are helping to slow or stop the growth of the cancer.
VICTORIA WEBBER: ADT is usually used in addition to radiation therapy in patients with high-risk localized disease (meaning the cancer has not spread outside of the prostate). If a patient has a recurrence after initial treatment, ADT may also be offered at that time.
It is also typically used in any patient that has advanced or metastatic disease (meaning the cancer has spread outside of the prostate).
VICTORIA WEBBER: When ADT is used in combination with radiation therapy, the patient may be kept on ADT for six months or two years. The duration of ADT depends on which "risk group" they are assigned. A risk group is assigned based on factors such as the prostate-specific antigen (PSA) at the time of diagnosis, Gleason Grade, and the number and location of positive biopsy cores, to name a few.
When ADT is used to treat metastatic cancer, it is typically used indefinitely as a means to keep the cancer undetectable.
VICTORIA WEBBER: ADT can be achieved in two separate ways:
1. Medication: There are multiple classes of medications we can use to decrease the production of testosterone or block the receptors for testosterone on the cancer cells.
2. Surgery: Though less common, surgery can be performed to remove the testicles which are responsible for testosterone production.
VICTORIA WEBBER: ADT is not a cure for prostate cancer. When combined with radiation for localized disease, ADT effectively increases survival rates and reduces the risk of recurrence. In metastatic disease, it is effective in slowing disease progression, reducing the size of tumors, and prolonging survival.
VICTORIA WEBBER: Side effects of ADT are often comparable to symptoms a woman would feel during menopause. The most common side effect is hot flashes, but patients may also experience fatigue, muscle weakness, decreased libido, and decreased bone density.
Most side effects are minor and do not require medical management.
VICTORIA WEBBER: Depending on the stage of the cancer, patients can be on ADT for six months, 12 months, intermittently, or indefinitely.
The length of treatment is determined by the patient's risk group and the extent of the disease. Tolerability may also change the length of treatment.
VICTORIA WEBBER: Patients may experience decreased energy levels, hot flashes, and mood changes while on ADT. However, most patients experience minimal impact on their quality of life. Exercise can help with mood and energy levels.
VICTORIA WEBBER: Keep the AC on. Be understanding if they have decreased energy.
VICTORIA WEBBER: The risk of recurrence after completing ADT depends on the initial stage or grade of the cancer. After completing ADT, the patient's PSAs are typically closely monitored to ensure early detection of any recurrence.
VICTORIA WEBBER: Androgen deprivation therapy is not chemotherapy or a cure for prostate cancer, but it is a well-tolerated treatment that increases survival rates in patients with specific stages of prostate cancer.
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