Skip to content

What is Evista for? A Guide to Raloxifene Uses and Effects

5 min read

According to the National Cancer Institute, Evista (raloxifene) is a selective estrogen receptor modulator (SERM) that blocks the effects of estrogen in breast tissue to reduce the risk of invasive breast cancer in postmenopausal women at high risk. It also mimics estrogen's beneficial effects on bone density, making it effective for treating and preventing postmenopausal osteoporosis.

Quick Summary

Evista is a selective estrogen receptor modulator for postmenopausal women to treat and prevent osteoporosis and reduce the risk of invasive breast cancer.

Key Points

  • Dual Purpose: Evista is a SERM used in postmenopausal women to both treat and prevent osteoporosis and reduce the risk of invasive breast cancer.

  • Selective Action: It acts like estrogen on bones to increase density but blocks estrogen in breast tissue to reduce cancer risk.

  • Osteoporosis Benefits: Clinical trials have shown Evista reduces the risk of vertebral (spine) fractures but not hip fractures.

  • Serious Risks: Evista carries an FDA boxed warning for an increased risk of venous thromboembolism (VTE) and death due to stroke in women at risk.

  • Contraindications: It is contraindicated in women with a history of VTE, stroke, severe liver disease, or who are pregnant or may become pregnant.

  • Daily Oral Dosage: The standard dose is a 60 mg oral tablet taken once daily, with or without food.

  • Not a Cure-All: Evista does not prevent all types of breast cancer, nor does it treat hot flashes; regular screenings are still necessary.

In This Article

Evista, the brand name for the drug raloxifene, belongs to a class of medications called selective estrogen receptor modulators (SERMs). Its primary applications are focused on addressing health concerns in women following menopause. By acting differently on estrogen receptors in various tissues, Evista provides targeted benefits while mitigating some risks associated with traditional hormone replacement therapy.

What is Evista and how does it work?

Evista's mechanism of action as a SERM means it can have both estrogen-like (agonist) and anti-estrogen (antagonist) effects depending on the tissue. This selective behavior is key to its therapeutic profile.

  • Estrogen Agonist: In bone tissue, raloxifene mimics estrogen to inhibit bone resorption (breakdown), helping to increase or maintain bone mineral density (BMD). This effect is crucial for combating osteoporosis, where a loss of BMD can lead to a higher risk of fractures.
  • Estrogen Antagonist: In breast and uterine tissues, raloxifene blocks the effects of estrogen. This antagonist action helps reduce the risk of invasive breast cancer, as many breast cancers rely on estrogen for growth. Unlike some estrogen therapies, Evista does not stimulate the uterine lining, thereby avoiding an increased risk of uterine cancer.

Key Uses of Evista (Raloxifene)

Treatment and prevention of postmenopausal osteoporosis

Osteoporosis is a common condition after menopause where bone density decreases, leading to an increased risk of fractures. Evista is a standard treatment for postmenopausal women to combat this bone loss. Clinical studies have shown that it can effectively reduce the risk of vertebral fractures, though it has not been shown to reduce the risk of hip fractures. Taking calcium and vitamin D supplements alongside Evista is often recommended to maximize bone health benefits.

Reduction of invasive breast cancer risk

For postmenopausal women at high risk of invasive breast cancer or those who have osteoporosis, Evista is an approved medication for risk reduction. Its ability to block estrogen's effect on breast tissue helps prevent the growth of estrogen receptor-positive breast cancers. It is important to note that Evista is not used to treat active breast cancer and does not prevent all types of breast cancer. Regular breast examinations and mammograms are still necessary while on this medication.

Dosage and Administration

Evista is prescribed as a 60 mg oral tablet, taken once daily, with or without food. It is intended for long-term use, and patients should follow their doctor's instructions precisely to achieve the maximum benefit. Consistent daily intake is important, and patients should not double their dose if one is missed.

Evista (Raloxifene) Side Effects and Risks

While generally well-tolerated, Evista does have a range of potential side effects and carries some serious risks, which are important to discuss with a healthcare provider.

Common side effects include:

  • Hot flashes, especially during the first six months of treatment
  • Leg cramps and muscle spasms
  • Swelling of the hands, ankles, or feet (peripheral edema)
  • Flu-like symptoms
  • Joint pain
  • Increased sweating

Serious risks and precautions: Evista carries a boxed warning from the FDA regarding an increased risk of venous thromboembolism (VTE), which includes deep vein thrombosis (DVT), pulmonary embolism (PE), and retinal vein thrombosis. The risk is highest in the first few months of treatment and is increased by prolonged periods of inactivity, such as during long trips or after surgery.

  • Discontinuation for immobility: Evista should be stopped at least 72 hours before and during any extended period of immobilization.
  • Stroke Risk: For postmenopausal women with a history of stroke or significant stroke risk factors, Evista may increase the risk of fatal stroke.

How Evista Compares to Other Treatments

For postmenopausal women, Evista is one of several treatment options for osteoporosis. Below is a comparison with other common alternatives.

Feature Evista (Raloxifene) Bisphosphonates (e.g., Fosamax) Hormone Replacement Therapy (HRT)
Drug Class Selective Estrogen Receptor Modulator (SERM) Slows bone breakdown Replaces estrogen
Mechanism Estrogen agonist on bone; antagonist on breast/uterus Directly inhibits bone resorption Systemic estrogen replacement
Effect on Bone Increases BMD, prevents vertebral fractures Increases BMD, prevents vertebral, hip, and non-vertebral fractures Increases BMD, prevents fractures
Effect on Breast Tissue Blocks estrogen; reduces invasive breast cancer risk No effect on breast tissue Stimulates breast tissue; may increase breast cancer risk
Effect on Uterine Tissue Anti-estrogen effect; no increase in uterine cancer risk No effect Stimulates uterine lining; may increase uterine cancer risk
Key Side Effects Hot flashes, leg cramps, VTE, stroke risk Gastrointestinal issues, rare but serious jaw problems VTE, breast cancer, uterine cancer, stroke risk
Administration Daily oral tablet Daily or weekly oral tablet Oral pills or patches

Who Should Not Take Evista?

Evista is not suitable for everyone. Patients should not take Evista if they have:

  • A history of or currently active venous thromboembolic events (DVT, PE, retinal vein thrombosis).
  • A history of a stroke or transient ischemic attack (mini-stroke).
  • A history of significant stroke risk factors, such as atrial fibrillation or high blood pressure.
  • Severe hepatic impairment.
  • Unexplained uterine bleeding.
  • Pregnancy, potential for pregnancy, or breastfeeding.

Evista and Tamoxifen: What's the Difference?

Both Evista (raloxifene) and tamoxifen are SERMs used for breast cancer risk reduction, but they have key differences. Tamoxifen can be used in both pre- and postmenopausal women, while raloxifene is for postmenopausal women only. Tamoxifen has a broader range of uses for treating active breast cancer. The risk profile also differs; raloxifene may have a lower risk of uterine cancer and potentially fewer venous thromboembolic events compared to tamoxifen, making it a preferred option for some postmenopausal women. A comprehensive discussion with a healthcare provider is essential for selecting the appropriate medication. More details on the differences are available from reputable sources like the National Cancer Institute's website: The Study of Tamoxifen and Raloxifene (STAR) Trial.

Conclusion

In summary, Evista (raloxifene) is a valuable medication for postmenopausal women, offering a dual benefit of treating and preventing osteoporosis and reducing the risk of invasive breast cancer. As a SERM, it provides a unique therapeutic profile, protecting bone health while blocking estrogen in breast tissue. However, its use is associated with serious risks, including VTE and stroke, and it is not suitable for all women. The decision to use Evista, or any osteoporosis or breast cancer risk-reducing medication, must be made in consultation with a healthcare provider who can evaluate individual health history and risk factors to determine if the potential benefits outweigh the risks.

Frequently Asked Questions

Evista should not be taken by women who are pregnant, may become pregnant, or are nursing. It is also contraindicated in women with a history of venous thromboembolic events (like deep vein thrombosis or pulmonary embolism) or a history of stroke.

No, Evista is used to reduce the risk of invasive breast cancer, primarily estrogen receptor-positive types, in high-risk postmenopausal women. It is not a treatment for active breast cancer and does not protect against all types.

No, Evista is only indicated for use in postmenopausal women. It is not approved for premenopausal women.

You should inform your doctor and discontinue Evista at least 72 hours before any planned surgery or prolonged period of immobility to reduce the risk of blood clots. You can typically restart it once you are mobile again.

The recommended dose of Evista is one 60 mg tablet taken by mouth once a day, and it can be taken with or without food.

Evista does not treat hot flashes and may actually cause them in some women, particularly during the first six months of treatment. Other common side effects include leg cramps and swelling.

Both are SERMs used for breast cancer risk reduction, but Tamoxifen is used for both pre- and postmenopausal women and can treat active breast cancer. Raloxifene (Evista) is for postmenopausal women only and has a different side effect profile, with a lower risk of uterine cancer compared to Tamoxifen.

The most serious risks include an increased risk of venous thromboembolism (blood clots in legs, lungs, or eyes) and a potential increase in fatal strokes in women with specific risk factors.

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.