What are the main uses of Arimidex for breast cancer treatment. How does Arimidex work to inhibit estrogen production. What are the most common side effects of taking Arimidex. How effective is Arimidex at improving breast cancer survival rates. What are some alternatives to Arimidex for treating hormone-receptor positive breast cancer.

Understanding Arimidex and Its Role in Breast Cancer Treatment

Arimidex (anastrozole) is a prescription medication primarily used to treat certain types of breast cancer in postmenopausal women. As an aromatase inhibitor, Arimidex works by lowering estrogen levels in the body, which can help slow or stop the growth of hormone-receptor positive breast cancers.

The main approved uses for Arimidex include:

• Adjuvant treatment of early stage hormone-receptor positive breast cancer
• First-line treatment of locally advanced or metastatic hormone-receptor positive breast cancer
• Treatment of advanced breast cancer that has progressed after taking tamoxifen

Arimidex is not approved for use in children, men, or premenopausal women. However, doctors may sometimes prescribe it off-label for men in certain situations.

How Arimidex Works to Inhibit Estrogen Production

As an aromatase inhibitor, Arimidex blocks the action of the enzyme aromatase in the body. Aromatase is responsible for converting androgens into estrogen. By inhibiting this enzyme, Arimidex dramatically reduces estrogen levels in postmenopausal women.

Lower estrogen levels can help slow or stop the growth of hormone-receptor positive breast cancers, which rely on estrogen to grow and spread. This makes Arimidex an effective targeted therapy for many breast cancer patients.

How quickly does Arimidex work to lower estrogen?

Arimidex begins lowering estrogen levels soon after the first dose. Studies have shown that it can suppress estrogen production by up to 80% within 24 hours of taking the medication. Maximum estrogen suppression is typically achieved within 3-4 days of starting treatment.

Common Side Effects of Taking Arimidex

As with any medication, Arimidex can cause side effects. Some of the most commonly reported side effects include:

• Hot flashes
• Joint pain or stiffness
• Weakness
• Mood changes
• Nausea
• Headache
• Back pain
• Osteoporosis (bone thinning)

Side effects can occur at any time during treatment, even after taking Arimidex for several years. Some side effects, like hot flashes, may start soon after beginning treatment. Others, like osteoporosis, may develop more gradually over time.

Are there any serious side effects to be aware of?

While less common, some serious side effects of Arimidex can include:

• Severe allergic reactions
• Blood clots
• Heart problems
• Liver problems
• Bone fractures

Patients should contact their doctor immediately if they experience signs of these more serious side effects. Regular monitoring by a healthcare provider can help detect any developing issues early on.

Arimidex Dosage and Administration

The standard dosage of Arimidex for breast cancer treatment is 1 mg taken orally once daily. The tablet should be swallowed whole with water. It can be taken with or without food.

Arimidex is typically prescribed as a long-term treatment, often for 5-10 years. The exact duration will depend on the individual patient and their specific type of breast cancer.

What if I miss a dose of Arimidex?

If a dose is missed, it should be taken as soon as remembered. However, if it is almost time for the next scheduled dose, the missed dose should be skipped. Patients should not take a double dose to make up for a missed one.

Effectiveness of Arimidex in Improving Breast Cancer Survival Rates

Clinical studies have demonstrated that Arimidex can significantly improve survival rates and reduce the risk of breast cancer recurrence in postmenopausal women with hormone-receptor positive breast cancer.

In one major study comparing Arimidex to tamoxifen as adjuvant therapy for early breast cancer, Arimidex improved disease-free survival by 13% after 5 years of treatment. The absolute difference in recurrence rates was 2.8% in favor of Arimidex.

How does Arimidex compare to other treatments in terms of survival benefit?

Studies have shown Arimidex to be at least as effective as tamoxifen in improving survival, with some research suggesting it may be superior. For example, one study found that switching to Arimidex after 2-3 years of tamoxifen resulted in a 40% reduction in the risk of recurrence compared to continuing tamoxifen.

However, the effectiveness can vary based on individual factors. Your oncologist can provide more personalized information on expected survival benefits based on your specific diagnosis and medical history.

Alternatives to Arimidex for Breast Cancer Treatment

While Arimidex is a widely used and effective treatment, it is not the only option for hormone-receptor positive breast cancer. Some alternatives include:

1. Other aromatase inhibitors: Letrozole (Femara) and exemestane (Aromasin)
2. Selective estrogen receptor modulators (SERMs): Tamoxifen and raloxifene
3. Estrogen receptor downregulators: Fulvestrant (Faslodex)
4. CDK4/6 inhibitors: Palbociclib (Ibrance), ribociclib (Kisqali), abemaciclib (Verzenio)
5. mTOR inhibitors: Everolimus (Afinitor)

The choice of treatment depends on various factors, including the specific type and stage of breast cancer, menopausal status, and individual patient characteristics.

How do these alternatives compare to Arimidex in terms of effectiveness and side effects?

Each alternative has its own profile of benefits and potential side effects. For example, tamoxifen may be preferred in premenopausal women, while aromatase inhibitors like Arimidex are typically more effective in postmenopausal women. CDK4/6 inhibitors have shown promise in improving progression-free survival when combined with hormonal therapies.

Your oncologist can provide detailed information on how these alternatives compare to Arimidex for your specific situation.

Cost Considerations and Insurance Coverage for Arimidex

The cost of Arimidex can vary significantly depending on factors such as insurance coverage, pharmacy pricing, and whether a brand-name or generic version is prescribed. Without insurance, a month’s supply of brand-name Arimidex can cost several hundred dollars.

However, generic anastrozole is typically much less expensive. Many insurance plans cover Arimidex or its generic equivalent, often with a copay or coinsurance requirement.

Are there assistance programs available for patients who can’t afford Arimidex?

Yes, there are several options for patients who need help affording Arimidex:

• Manufacturer patient assistance programs
• Nonprofit organizations offering financial assistance
• State pharmaceutical assistance programs
• Medicare Extra Help program for those who qualify
• Discount cards and coupons from various sources

Patients should discuss cost concerns with their healthcare provider or a hospital social worker, who can provide information on available assistance programs.

Long-Term Effects and Considerations of Arimidex Treatment

While Arimidex can be an effective long-term treatment for breast cancer, it’s important to be aware of potential long-term effects. Some issues that may develop or worsen with prolonged use include:

• Osteoporosis and increased risk of fractures
• Joint pain and stiffness
• Cardiovascular risks
• Cognitive changes
• Sexual side effects

Regular monitoring and follow-up with your healthcare team is crucial to manage these potential long-term effects. Your doctor may recommend bone density scans, cardiovascular check-ups, and other preventive measures.

Can the side effects of Arimidex be reversed after stopping treatment?

Some side effects may improve or resolve after discontinuing Arimidex. For example, joint pain often improves within a few months of stopping the medication. However, bone density loss may not fully reverse, emphasizing the importance of bone health management during and after treatment.

It’s important to note that suddenly stopping Arimidex can lead to a temporary increase in estrogen levels. Always consult with your doctor before making any changes to your treatment regimen.

Side Effects, Alternatives, Dosage, Cost, and More

If you have breast cancer, your doctor may recommend Arimidex as a treatment option for you.

Arimidex is a prescription medication used in females* who’ve gone through menopause. It’s used to treat certain forms of:

• hormone-receptor positive (HR+) early stage breast cancer, as an adjuvant (post-surgery) treatment
• HR+ or HR-unknown breast cancer that’s locally advanced or metastatic (has spread to other areas of the body), as the first treatment
• advanced breast cancer that has worsened after taking tamoxifen (Nolvadex, Soltamox)

Arimidex is not approved for use in children, males,* or females who haven’t gone through menopause.

To learn more about the forms of breast cancer that Arimidex treats, see the “What is Arimidex used for?” section below.

* In this article, we use the terms “female” and “male” to refer to someone’s sex assigned at birth. For information about the difference between sex and gender, see this article.

Arimidex basics

Arimidex contains the active drug anastrozole. This drug is also available as a generic.

Arimidex comes as a tablet that you’ll swallow once per day. It belongs to a group of drugs called aromatase inhibitors.

Read on to learn about Arimidex’s side effects, uses, and more.

Find answers below to some commonly asked questions about Arimidex.

Is Arimidex used for bodybuilding?

Arimidex is not currently approved for bodybuilding purposes. It’s only approved to treat certain forms of breast cancer.

Arimidex is sometimes taken to lower estrogen levels that are high due to anabolic steroid use. High estrogen levels can cause side effects such as gynecomastia (unusual breast gland enlargement). Some people use Arimidex to help reduce such side effects.

Using Arimidex this way is not recommended, and may not be safe. You should not take Arimidex or other drugs unless they’re prescribed for you. In fact, the World Anti-Doping Agency lists aromatase inhibitor drugs as banned substances. Arimidex is a type of aromatase inhibitor.

It’s not known what side effects Arimidex may cause if taken for bodybuilding or whether the drug could lead to more serious problems if used this way. Its dosage for this use also isn’t known, such as the dosage if taken during steroid cycles.

See this article for details about Arimidex and bodybuilding. You might also have questions such as how much Arimidex would be taken with 200 mg of testosterone, or the differences between Arimidex versus Aromasin. Your doctor can help answer such questions and determine whether Arimidex is safe for you.

Do doctors prescribe Arimidex for use in men?

It’s possible. Arimidex is only approved for use in certain females* who’ve gone through menopause. This is because it’s only been studied in females.

But doctors might prescribe Arimidex for off-label use in males* to treat breast cancer that’s fueled by estrogen. Off-label means using a drug for a purpose other than what it’s been approved for.

Arimidex may also be prescribed off-label for certain males who are taking testosterone replacement therapy (TRT). TRT can cause increased estrogen levels in the body, and your doctor might prescribe Arimidex to lower estrogen levels.

Side effects in females may differ from those in males. Recommended dosages may differ as well.

If you’re a male and you’re interested in taking Arimidex, talk with your doctor. They can help determine if Arimidex is a safe option for you.

* In this article, we use the terms “male” and “female” to refer to someone’s sex assigned at birth. For information about the difference between sex and gender, see this article.

How soon will side effects of Arimidex start? Are there side effects after using the drug for 5 years?

Side effects from Arimidex vary, but can start right after your first dose. Some may occur sooner than others. For example, you can experience headaches, nausea, or vomiting after only one dose of Arimidex.

Other side effects of Arimidex may take longer to happen. For example, side effects such as osteoporosis (weakened bones) or liver problems may not occur for months or years after taking the drug. Your doctor will monitor you for these side effects.

It’s possible to have any of the side effects from Arimidex even after taking the drug for a long time, such as 5 years.

If you have questions about specific side effects or side effects that may occur after taking Arimidex for years, talk with your doctor.

How much does Arimidex increase survival? What’s the percentage of breast cancer recurrence during Arimidex treatment?

Arimidex has been shown to increase breast cancer survival rates. Your type of breast cancer and how advanced it is (how much it has spread) affects how likely it is to recur (worsen or return).

In a study of females taking Arimidex as a first treatment for advanced breast cancer, it took an average of 11.1 months for the cancer to worsen. In comparison, in females who took tamoxifen (Nolvadex, Soltamox), it took an average of 5.6 months before their cancer worsened.

In this study, Arimidex wasn’t compared with a placebo (a treatment with no active drug). So it’s not known how much the drug might improve survival or recurrence compared with no treatment.

If you’d like to learn more about Arimidex’s effectiveness for your type of cancer, talk with your doctor. They can help determine the best treatment option for your condition and what to expect from your treatment.

Is Arimidex a steroid, chemotherapy drug, or estrogen blocker? How much does it lower estrogen levels?

Arimidex is considered an estrogen blocker because it decreases the amount of the hormone estrogen in your body. It isn’t a steroid drug or a type of chemotherapy (traditional drugs used to treat cancer).

Arimidex belongs to a class of drugs called aromatase inhibitors. It works by blocking an enzyme (a type of protein) called aromatase. This enzyme works to change hormones into estrogen.

By blocking this change, Arimidex decreases the amount of estrogen in your body. This decreases the growth of breast cancer.

In studies, Arimidex lowered levels of estradiol (a form of estrogen) by about 70% within 24 hours. After 14 days of treatment, estradiol levels were lowered by about 80%. And estradiol levels continued to be reduced for 6 days after stopping treatment.

Is Arimidex similar to Nolvadex or Clomid?

It’s possible that your doctor may recommend Arimidex, tamoxifen (Nolvadex, Soltamox) or clomiphene (Clomid) for similar uses. But these medications belong to different groups of drugs and work in different ways.

Arimidex and Nolvadex are both used to treat certain forms of breast cancer. They both work by lowering estrogen levels, but in different ways. They have different side effects and dosages, as well.

Clomid is not approved to treat breast cancer. But the drug does lower estrogen levels. It’s used to stimulate (activate) ovulation in females who are trying to become pregnant. It can also be prescribed off-label for other uses. Off-label means using a drug for a purpose other than what it’s been approved for.

Talk with your doctor about the best treatment plan for your condition. They can help you determine if Arimidex, Nolvadex, or Clomid is the best treatment option for you.

What happens when you stop taking Arimidex? Can you stop it ‘cold turkey’?

If you’re thinking about stopping Arimidex, talk with your doctor about the best way to do this. Sometimes, they may recommend stopping Arimidex even after 5 years of treatment or more.

Your doctor may recommend that you stop taking Arimidex “cold turkey,” meaning all at once. Its dosage doesn’t usually need to be decreased slowly over time. If you’re continuing treatment for breast cancer, your doctor may recommend switching to a different drug when you stop Arimidex.

You may want to talk with your doctor about how long side effects last after stopping Arimidex. How long they last may depend on which side effects you experience.

For example, if you have nausea, it may go away right after you stop taking Arimidex. Other side effects such as liver problems or osteoporosis (weakened bones) may remain even after you stop treatment.

You should not stop taking Arimidex without first discussing it with your doctor.

Like most drugs, Arimidex may cause mild or serious side effects. The lists below describe some of the more common side effects it may cause. These lists don’t include all possible side effects.

Keep in mind that side effects of a drug can depend on:

• your age
• other health conditions you have
• other medications you take

Your doctor or pharmacist can tell you more about the potential side effects of Arimidex. They can also suggest ways to help reduce side effects.

Mild side effects

Here’s a list of some of the mild side effects Arimidex can cause. To learn about other mild side effects, talk with your doctor or pharmacist, or read Arimidex’s prescribing information.

Mild side effects of Arimidex that have been reported include:

• hot flashes
• weakness
• pain, such as bone pain, joint pain, or back pain
• sore throat
• nausea or vomiting
• rash
• high blood pressure
• insomnia (trouble falling asleep or staying asleep)
• headache
• water retention (excess fluid in your body)*
• cough
• hair loss*

Mild side effects of many drugs may go away within a few days to a couple of weeks. But if they become bothersome, talk with your doctor or pharmacist.

Serious side effects

Serious side effects from Arimidex can occur, but they aren’t common. If you have serious side effects from Arimidex, call your doctor right away. But if you think you’re having a medical emergency, you should call 911 or your local emergency number.

Serious side effects of Arimidex that have been reported include:

• osteoporosis (weakened bones)
• broken bones
• heart disease
• skin reactions, such as ulcers (open sores), blisters, or lesions (areas of unusual-looking skin)
• high cholesterol levels
• liver problems
• blood clots*
• allergic reaction*

* For more information about this side effect, see the “Side effect focus” section below.

Side effect focus

Learn more about some of the side effects Arimidex may cause.

Water retention

You may experience water retention (excess fluid in your body) from taking Arimidex. This can cause swelling, which tends to occur most often in the ankles, feet, or legs. This was a common side effect reported in people taking Arimidex in studies.

What might help

If you have swelling or water retention from taking Arimidex, talk with your doctor about how to treat this. They may recommend that you take a medication along with Arimidex to reduce swelling.

Hair loss

It’s possible to have hair loss or hair thinning with Arimidex. This side effect was only reported in people taking the drug for advanced breast cancer. Hair loss was not a common side effect in studies.

What might help

If you notice hair loss or hair thinning during your treatment with Arimidex, talk with your doctor. They may recommend ways to reduce this side effect or keep it from getting worse.

Blood clots

Very rarely, it’s possible to develop blood clots from taking Arimidex. In studies, blood clots were reported in the lungs, eyes, and legs.

Symptoms of a blood clot may include:

• swelling, redness, or warmth in one leg
• chest pain
• trouble breathing
• pain in your eyes or loss of vision

What might help

If you develop symptoms of a blood clot, it’s important to see a doctor right away. Blood clots can be life threatening, and should be treated as soon as possible.

Also talk with your doctor about your risk of blood clots. If you’re taking certain medications or have other medical conditions, your risk may be higher.

Throughout your treatment with Arimidex, your doctor will monitor you for symptoms of blood clots. If you develop a clot, your doctor will treat it and may recommend a different treatment for your breast cancer.

Allergic reaction

Although uncommon, some people may have an allergic reaction to Arimidex.

Symptoms of a mild allergic reaction can include:

• skin rash
• itchiness
• flushing (temporary warmth, redness, or deepening of skin color)

A more severe allergic reaction is rare but possible. Symptoms of a severe allergic reaction can include swelling under your skin, typically in your eyelids, lips, hands, or feet. They can also include swelling of your tongue, mouth, or throat, which can cause trouble breathing or swallowing.

Call your doctor right away if you have an allergic reaction to Arimidex. But if you think you’re having a medical emergency, call 911 or your local emergency number.

You may wonder how Arimidex compares with Aromasin and other alternatives. Read on to learn more about how this drug is similar and different from others.

Arimidex vs. Aromasin

To see how Arimidex compares with Aromasin, check out this detailed breakdown. Talk with your doctor if you’d like to know more about these drugs.

Arimidex vs. tamoxifen

If you’d like, ask your doctor whether Arimidex or tamoxifen is better for your condition. And see this comparison for more information about the drugs.

Arimidex vs. letrozole

Read this article to find out how Arimidex and letrozole are alike and different. Check with your doctor about which drug is right for you.

Your doctor will recommend the dosage of Arimidex that’s right for you. Below are commonly used dosages, but always take the dosage your doctor prescribes.

Form and strength

Arimidex comes as a tablet that you take by mouth. It’s available in a strength of 1 milligram (mg).

Recommended dosage

The recommended dosage of Arimidex is one tablet, once daily.

Questions about Arimidex’s dosage

• What if I miss a dose of Arimidex? If you miss your dose of Arimidex, take it as soon as you remember, unless it’s almost time for your next dose. In that case, skip the dose you missed and continue with your normal schedule. Never take two doses of Arimidex to make up for a missed dose. If you miss a dose and you’re not sure when to take your next dose, talk with your doctor or pharmacist.
• Will I need to use Arimidex long term? If Arimidex works for you, your doctor will likely recommend that you take it long term.
• How long does Arimidex take to work? Arimidex begins working to treat your breast cancer after you take your first dose. You may not notice any changes from taking Arimidex. But your doctor will monitor your condition during your treatment to see how well the drug is working.

Costs of prescription drugs can vary depending on many factors. These factors include what your insurance plan covers and which pharmacy you use.

Arimidex is available as the generic drug anastrozole. Generics usually cost less than brand-name drugs. Talk with your doctor if you’d like to know about taking generic anastrozole.

If you have questions about how to pay for your prescription, talk with your doctor or pharmacist. You can also visit the Arimidex manufacturer’s website to see if they have support options.

You can also check out this article to learn more about saving money on prescriptions.

Arimidex is used to treat certain forms of breast cancer in females* who’ve gone through menopause.

Breast cancer causes cells in your breast to grow quickly and out of control. This fast growth can cause a tumor to form in your breast. The cancer cells may also spread to other parts of the body.

Your doctor may test your breast cancer to determine if it’s hormone-receptor positive (HR+). This means the cancer is affected by hormones such as estrogen. Arimidex works by lowering estrogen levels in your body, which can decrease cancer growth.

Specifically, Arimidex is used to treat:

• Early stage HR+ cancer. Early stage cancer is cancer that has not yet spread to lymph nodes or other parts of your body. For this use, Arimidex is used as an adjuvant treatment. This is treatment to prevent cancer from coming back or worsening after it’s been surgically removed.
• Locally advanced or metastatic breast cancer that’s HR+ or HR-unknown. Locally advanced means the cancer has spread to your armpit lymph nodes or areas that are close to your breast. Metastatic means the cancer has spread to other areas of your body. And HR-unknown means that the cancer might or might not be affected by hormones.
• Advanced breast cancer that has worsened after taking tamoxifen. Tamoxifen (Nolvadex, Soltamox) is another drug used for breast cancer treatment. For this use, Arimidex can be taken for cancer that’s HR+, HR negative (HR-), or HR-unknown. It’s important to note that Arimidex is rarely effective for cancer that:
  • hasn’t improved with past tamoxifen treatment, or
  • is estrogen-receptor negative

Arimidex is not approved for use in children, males,* or females who haven’t gone through menopause.

* In this article, we use the terms “female” and “male” to refer to someone’s sex assigned at birth. For information about the difference between sex and gender, see this article.

Before you start taking Arimidex, talk with your doctor about any other medical conditions you have and other medications you take. In some cases, Arimidex may not be the best treatment option for you. Below are some medications and medical conditions that you should discuss with your doctor before starting Arimidex.

Interactions

Taking a medication with certain vaccines, foods, and other things can affect how the medication works. These effects are called interactions.

Before taking Arimidex, be sure to tell your doctor about all medications you take, including prescription and over-the-counter types. Also describe any vitamins, herbs, or supplements you use. Your doctor or pharmacist can tell you about any interactions these items may cause with Arimidex.

Interactions with drugs or supplements

Arimidex can interact with several types of drugs. These drugs include:

• Drugs that contain the hormone estrogen. Arimidex works by lowering estrogen levels in your body. Taking drugs that increase your estrogen levels may decrease the effectiveness of Arimidex. Due to this risk, your doctor will likely recommend that you avoid taking drugs that contain estrogen while you’re taking Arimidex. Examples include hormone replacement therapy and estrogen creams.
• Tamoxifen. In studies, taking Arimidex with tamoxifen was not a more effective treatment option than taking tamoxifen alone. And taking both drugs increased the risk of side effects from treatment. Your doctor will likely not recommend taking these medications together.

This list does not contain all types of drugs that may interact with Arimidex. Your doctor or pharmacist can tell you more about these interactions and any others that may occur with use of Arimidex.

Warnings

Arimidex may not be right for you if you have certain medical conditions or other factors that affect your health. Talk with your doctor about your health history before you take Arimidex. Factors to consider include those in the list below.

• High cholesterol levels. Arimidex may increase your cholesterol levels. If you have high cholesterol, this medication may make it worse. Your doctor may recommend medication to lower your cholesterol levels while you’re taking Arimidex.
• Allergic reaction. If you’ve had an allergic reaction to Arimidex or any of its ingredients, your doctor will likely recommend that you don’t take Arimidex. Ask your doctor what other medications are better options for you.
• Osteoporosis (weakened bones). If you have osteoporosis, tell your doctor before starting Arimidex. This medication may increase your risk of osteoporosis or broken bones, and can make existing osteoporosis worse. Your doctor may monitor your bone strength while you’re taking Arimidex, or may recommend a different treatment option for you.
• Ischemic heart disease (a heart condition that affects blood flow to your heart). Tell your doctor about any heart problems you have, especially ischemic heart disease (also called coronary artery disease). Arimidex may increase the risk of serious heart or blood vessel problems in females* with ischemic heart disease. These problems can include a heart attack or stroke. Your doctor may recommend more frequent monitoring of your heart health during Arimidex treatment, or a different treatment option.
• Liver problems. Arimidex may cause increased liver enzyme levels, which may be a sign of liver damage. If you already have liver problems, Arimidex can make your liver problems even worse. Your doctor may monitor your liver function more often than usual if you take Arimidex. Or they may recommend a different medication for your condition.
• Females who have not gone through menopause. Arimidex is only approved for use in females who’ve gone through menopause. It’s not known if the drug is effective when used in females who haven’t gone through menopause. Your doctor will likely recommend a different medication for you.

* In this article, we use the terms “female” and “male” to refer to someone’s sex assigned at birth. For information about the difference between sex and gender, see this article.

Arimidex and alcohol

There are no known interactions between Arimidex and alcohol. But they may cause similar side effects, such as nausea, vomiting, or headache. So alcohol may worsen certain side effects of Arimidex.

Also, Arimidex and alcohol can each cause liver damage. So the two together may increase your risk of developing a liver condition, such as liver failure.

Talk with your doctor about how much alcohol, if any, is safe for you to drink during your Arimidex treatment.

Pregnancy and breastfeeding

Arimidex may cause harm to a fetus if taken during pregnancy or within 3 weeks of becoming pregnant. Due to this risk, your doctor will likely recommend that you do not take Arimidex if you’re pregnant or planning to become pregnant. They’ll also likely recommend that you do not breastfeed while taking Arimidex and for at least 2 weeks after your last dose.

If you’re able to become pregnant, your doctor will likely recommend that you take a pregnancy test before starting Arimidex. You’ll also be advised to use an effective form of birth control throughout treatment and for at least 3 weeks after your last dose.

Your doctor will explain how you should take Arimidex. They’ll also explain how much to take and how often. Be sure to follow your doctor’s instructions.

Taking Arimidex

Arimidex comes as a tablet you’ll take by mouth.

Questions about taking Arimidex

• Can Arimidex be chewed, crushed, or split? No, Arimidex tablets should not be chewed, crushed, or split. You should swallow your Arimidex tablet whole. If you have trouble with this, see this article for tips on how to swallow pills.
• Should I take Arimidex with food? You can take Arimidex with or without food.

Questions for your doctor

You may have questions about Arimidex and your treatment plan. It’s important to discuss all your concerns with your doctor.

Here are a few tips that might help guide your discussion:

• Before your appointment, write down questions such as:
  • How will Arimidex affect my body, mood, or lifestyle?
• Bring someone with you to your appointment if doing so will help you feel more comfortable.
• If you don’t understand something related to your condition or treatment, ask your doctor to explain it to you.

Remember, your doctor and other healthcare professionals are available to help you. And they want you to get the best care possible. So, don’t be afraid to ask questions or offer feedback on your treatment.

Do not take more Arimidex than your doctor prescribes. Using more than this can lead to serious side effects.

What to do in case you take too much Arimidex

Call your doctor if you think you’ve taken too much Arimidex. You can also call 800-222-1222 to reach the American Association of Poison Control Centers or use its online resource. However, if you have severe symptoms, immediately call 911 or your local emergency number. Or, go to the nearest emergency room.

Before you start taking Arimidex, talk to your doctor about any questions you may have. Here are some questions you may wish to discuss with your doctor:

• Will Arimidex cause memory loss?
• What other treatment options are available if I can’t take Arimidex?
• Is there an Arimidex dosage for gynecomastia?
• How can I prevent Arimidex side effects from occurring?

If you would like to learn more about breast cancer treatment options, see this article. You may also wish to learn about complementary and alternative medicine for breast cancer.

For updates on breast cancer treatment, sign up for the Healthline newsletter.

Q:

Can my doctor lower my dosage of Arimidex if I’m having side effects from the medication?

Anonymous

A:

This isn’t likely. Arimidex’s recommended dosage is one tablet per day. Doses lower than this may not be effective. There aren’t any studies showing that lowering the dosage can help reduce side effects.

Depending on how severe your side effects are, your doctor may suggest treatments to manage the side effect. Or they may have you stop Arimidex treatment. Make sure you do not change your treatment without first talking with your doctor.

If you’d like to learn more about how to manage side effects from this medication, talk with your doctor or pharmacist. They can help determine the best treatment for your condition.

Tanya Kertsman, PharmDAnswers represent the opinions of our medical experts. All content is strictly informational and should not be considered medical advice.

Was this helpful?

Disclaimer: Healthline has made every effort to make certain that all information is factually correct, comprehensive, and up to date. However, this article should not be used as a substitute for the knowledge and expertise of a licensed healthcare professional. You should always consult your doctor or another healthcare professional before taking any medication. The drug information contained herein is subject to change and is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. The absence of warnings or other information for a given drug does not indicate that the drug or drug combination is safe, effective, or appropriate for all patients or all specific uses.

Arimidex and bodybuilding. What to know

Some bodybuilders take Arimidex to reduce the side effects of anabolic steroids. The drug is a breast cancer treatment that lowers estrogen levels and should not be used for other means.

Bodybuilders who take anabolic steroids to try to increase muscle mass and improve athletic performance can experience a range of symptoms. In some cases, males might start to grow breasts due to an increase in estrogen levels.

Arimidex lowers estrogen levels and can prevent breast growth in males. However, the drug also has side effects of its own.

In this article, we discuss what Arimidex does, why bodybuilders might use it, and the possible side effects.

Share on PinterestArimidex may cause side effects such as joint pain, nausea, and hot flashes.

Arimidex is the brand name for anastrozole. Doctors may prescribe the drug to postmenopausal women with certain types of breast cancer.

Arimidex stops aromatase from working in the body. Aromatase is an enzyme that makes estrogen from steroid hormones, including testosterone. By doing this, it lowers the amount of estrogen in the body.

People who use anabolic steroids for bodybuilding can experience a range of side effects.

These drugs disrupt hormone production in the body and may increase estrogen. Higher levels of estrogen can cause males to develop gynecomastia, which is the enlargement of the breast glands.

By reducing estrogen levels, Arimidex could prevent gynecomastia in males taking anabolic steroids.

Arimidex can cause several side effects by disrupting hormone production in the body. For example, lower estrogen levels can lead to the thinning and weakening of bones.

Some other common side effects include:

• joint pain
• nausea and vomiting
• hot flashes
• weakness
• tiredness

It is possible to have an allergic reaction to Arimidex, which can cause:

• swelling around the body
• chest pain
• blurred vision
• rapid heart rate
• rashes
• breast pain

Arimidex comes as a small tablet for oral use only. The tablets are usually 1 milligram in size.

The Food and Drug Administration (FDA) have only approved Arimidex for use in cancer treatment. There are no formal guidelines for its use in bodybuilding.

The FDA guidelines for breast cancer suggest a typical dosage of one tablet per day, but a doctor may prescribe a different dosage, depending on the case.

Taking Arimidex for bodybuilding is not recommended. Many of the side effects of anabolic steroids usually go away after a person stops using them. Estrogen levels should return to normal, and gynecomastia should reduce.

The primary use of Arimidex is to treat breast cancer. It may be part of treatment for postmenopausal women with:

• Early hormone receptor-positive (HR+) breast cancer. Arimidex can lower the risk of cancer returning or spreading following surgery.
• Advanced or metastatic HR+ or HR-unknown breast cancer. It is not usually possible to treat these cancers using surgery, so doctors may prescribe Arimidex as a first-line treatment.
• Advanced or metastatic breast cancer that returns following initial treatment with tamoxifen (Nolvadex). Arimidex is a second-line treatment in these cases.

Sometimes, treatments for other types of cancer, such as ovarian cancer, might include Arimidex. However, the FDA only recommend its use for breast cancer.

Several other drugs — typically, those for the treatment of breast cancer — lower estrogen levels in the body.

For example, other aromatase inhibitors, such as exemestane (Aromasin), and a class of drugs called selective estrogen receptor modulators (SERMs) that act on estrogen receptors. Doctors may use SERMs to treat breast cancer, female infertility, and dyspareunia.

Although these drugs may lower estrogen levels, the FDA do not recommend that people take them for bodybuilding purposes.

Several natural products may also play a role in lowering estrogen levels, although there is limited scientific evidence to confirm their effectiveness. These include:

• wild nettle root
• grape seed extract
• chrysin
• maca

Arimidex is primarily for breast cancer treatment, and most of the research relates to postmenopausal women.

Estrogen plays a more significant role in the bodily function of females than males. Lowering estrogen levels can, therefore, have a more serious effect on females.

For this reason, female bodybuilders should avoid taking Arimidex or any other drug that lowers estrogen levels.

It is best to consult a doctor before taking any drug that disrupts normal hormone production.

Some people may be taking other medications or have medical conditions that affect hormone levels. Taking Arimidex could cause more serious issues in these cases.

It is essential to stop taking the drug and see a doctor right away if there are signs of an allergic reaction, such as swelling or rashes.

Some bodybuilders use Arimidex to control gynecomastia, which is a side effect of taking anabolic steroids. It causes males to grow breasts.

Arimidex can have several side effects and is usually a treatment for breast cancer. It is not advisable for people to take Arimidex for bodybuilding.

It is best to speak to a doctor before taking any drugs that may affect hormone levels.

Read this article in Spanish.

MATERIALS OF CONGRESSES AND CONFERENCES: VIII RUSSIAN ONCOLOGICAL CONGRESS

ENDOCRINOTHERAPY OF DISSEMINATED

BREAST CANCER IN MENOPAUSE:

DISCUSSION I-II LINES

V.F. Semiglazov
Federal State Budgetary Institution National Medical Research Center of Oncology named after N.N. N.N. Petrov” of the Ministry of Health of Russia, St. Petersburg

Progress in endocrine therapy over the past 100 years has almost not expanded the efficiency framework of 30% (in terms of all treated patients). The discovery of estrogen receptors (ER) and progesterone receptors (RP) made it possible to more reliably identify candidates for endocrine therapy. It is known that at high concentrations of RE and RP (above 20 fmol/mg of protein), up to 70% of patients with breast cancer (BC) “respond” to hormone therapy. However, in the entire population of patients with breast cancer, including those with no receptors in the tumor, it turns out that only 30% of patients respond positively to hormone therapy (1-3).

And yet, it cannot be said that the rapid progress of the pharmaceutical industry, which offers more and more new hormonal drugs, has not affected the improvement of the results of breast cancer treatment. Firstly, the appearance of the first antiestrogen tamoxifen a quarter of a century ago, which became the “gold” standard in breast cancer patients with ER+/RP+ tumors, significantly increased the life expectancy of patients. The use of an LH-releasing hormone agonist (zoladex) in combination with tamoxifen in menstruating breast cancer patients instead of surgical oophorectomy also increased the duration and quality of life of patients. The appointment of new generation aromatase inhibitors (Arimidex, Femara, Aromasin) in the event of a relapse of the disease against the background of previous adjuvant therapy with tamoxifen leads to an objective remission in another 25% of patients who have lost sensitivity to antiestrogen. The same scheme of sequential use of antiestrogens (tamoxifen) for 2-3 years first, followed by aromatase inhibitors (Femara, Arimidex, Aromasin) is now being tested in clinical trials of adjuvant hormone therapy (4-11).

After the development of the immunohistochemical technique, information on the content of receptors can be obtained from archival paraffin blocks containing the primary tumor. It has been proven that tumors containing more than 10% of cells stained for estrogen or progesterone receptors are sensitive to hormone therapy. Patients with ER-/RP- tumors are characterized by only 5-10% probability of response to endocrine therapy. These patients are better treated with cytotoxic or other therapy.

In hormone-dependent metastatic breast cancer, regardless of the age of the patients, tamoxifen is most often used as the first line of therapy. Treatment with tamoxifen allows you to control the disease for 9-12 months. In patients with early stages of breast cancer (I-II) and EC+ tumors, adjuvant therapy with tamoxifen reduces the risk of recurrence by 45-50%. It has recently been shown that the use of tamoxifen for 5 years in healthy high-risk women also reduces the risk of breast cancer by 50%.

Despite the significant beneficial effect of tamoxifen in changing the natural history of breast cancer, more than half of patients develop a relapse of the disease after tamoxifen therapy. The question naturally arises as to how to treat these patients.

It is important to establish a morphological diagnosis of recurrence, the degree and nature of the spread of the process, and re-evaluate the receptor status of a recurrent tumor. Patients with significant organ dysfunction due to involvement in the tumor process (eg, metastatic lymphangitis in the lungs, multiple or massive liver metastases), even with a high level of steroid hormone receptors, respond better to palliative treatment with cytotoxic therapy. Patients who relapse after discontinuing tamoxifen therapy more than 1 year ago retain a chance of responding to re-treatment with tamoxifen. Patients who relapse during tamoxifen treatment or less than 1 year after tamoxifen treatment have antiestrogen-resistant tumors and should be treated with some other alternative approach (Piccart M.J., 2003). For patients with RE-/RP- endocrine therapy is not indicated, it is advisable to prescribe chemotherapy. In patients with receptor-positive tumors, the second and subsequent lines of hormone therapy also depend on the menopausal status.

In postmenopausal age, ovarian steroid production decreases and estrogen production occurs mainly in peripheral tissues such as adipose tissue and adrenal glands, where the corticosteroid androstenedione is converted first to estrone and then to estradiol. This peripheral conversion occurs with the help of aromatase (an enzyme complex consisting of cytochrome P450 and flavoproteins, which catalyze the conversion of androgens to estrogens). In addition to aromatase activity in peripheral tissues, approximately 2/3 of primary tumors also exhibit aromatase activity, which provides a local source of estrogen production within the tumor itself (Moiseenko V.M., 1997). Therefore, the suppression of aromatase should provide a more complete blockade of estrogen production than the removal of the endocrine glands.

A new generation of aromatase inhibitors is rapidly becoming the first-line therapy for postmenopausal women with advanced breast cancer that progresses on tamoxifen therapy.

Until recently, in postmenopausal patients with breast cancer, adrenalectomy or hypophysectomy was performed as a secondary endocrine therapy; a little later, progestins were commonly used as a second line. The use of aromatase inhibitors for advanced breast cancer in postmenopausal women began at 1980 from the introduction of aminoglutethimide. Numerous studies have confirmed the effectiveness of this drug in the first and second line of therapy. Aminoglutethimide, studied in clinical trials as a second-line drug, has shown similar efficacy to surgical adrenalectomy. However, aminoglutethimide is not specific for the aromatase enzyme, simultaneously inhibiting the synthesis of both glucocorticoids and mineralocorticoids. Therefore, the use of the drug requires the simultaneous appointment of hydrocortisone. The study of new generation aromatase inhibitors (anastrozole, letrozole) showed their greater efficiency and lower toxicity compared to progestins and aminoglutethimide.

The two aromatase inhibitors most commonly used as second-line therapy are anastrozole (Arimidex) (1 mg/day daily) and letrozole (Femara) (2.5 mg/day daily). These new aromatase inhibitors are selective (i.e. do not interact with other cytochrome P450 enzymes), so patients do not need additional replacement therapy even in cases of acute infections or surgery. Anastrozole (Arimidex), letrozole (Femara) and exemestane (Aromasin) are safer than all previous hormonal drugs, so these drugs are preferred for first-line hormone therapy.

Two clinical trials comparing anastrozole and tamoxifen have been published (12, 13). A North American study in the US and Canada demonstrated superiority of anastrozole over tamoxifen in terms of time to disease progression, but no superiority in overall objective response rates (9). It should be noted that in the larger TARGET (Tamoxifen or Anastrozole Randomized Group Efficacy and Tolerability) clinical study, which was conducted in Europe, Australia, New Zealand, South America and South Africa, no increase in time to progression was found in patients treated with anastrozole, compared with patients treated with tamoxifen (median 8.2 vs. 8.3 months) (13). The design of these two studies was designed to allow for a pooled data analysis that has recently been published (14). There were no significant differences between the tamoxifen and anastrozole groups in any of the main efficacy parameters (time to progression, overall efficacy, clinical improvement rate, time to discontinuation of therapy were assessed). These retrospective analyzes showed that anastrozole outperformed tamoxifen in a subgroup of patients with receptor-positive tumors.

In a multicentre clinical study comparing letrozole and tamoxifen in postmenopausal women with advanced breast cancer (RE+/PR+ or unknown), the demographic and clinical characteristics of the patients, as previously shown (10-16), were well balanced between the two treatment groups. The end date for data inclusion in the primary analysis was March 2000, by which time the follow-up period was about 18 months. The study involved 916 women. Of these, 458 received letrozole (2.5 mg/day) and 458 received tamoxifen (20 mg/day) before disease progression was recorded. By decision of the attending physician, it was allowed to transfer patients to treatment with an alternative drug. This article provides updated data on efficacy at a median follow-up of 32 months.

Letrozole outperformed tamoxifen in terms of time to disease progression (median 9. 4 vs. 6.0 months, respectively; p<0.0001) (Figure 1.), overall objective response rate (32% vs. 21% respectively; p=0.0002) and the rate of clinical improvement. Median overall survival was slightly longer in the letrozole group (34 vs. 30 months, respectively), although this difference reached statistical significance; in the first 2 years of the study, survival was best in the letrozole group. Approximately half of the patients in each treatment group were switched to an alternative drug. The total duration of endocrine therapy (time to chemotherapy) was significantly longer (p = 0.005) among patients who were initially randomized to the letrozole group (median, 16 months) compared with patients who were initially randomized to the tamoxifen group (median, 9months). The time to deterioration of the functional status according to the Karnofsky scale in the letrozole group compared to the tamoxifen group was significantly (p=0.001) longer.

Data from a phase III head-to-head study investigating the efficacy and safety of exemestane (25 mg/day) and tamoxifen (20 mg/day) in first-line hormonal therapy for advanced breast cancer were presented at ASCO in 2004. In the study 382 patients from 81 research centers in 25 countries participated. All patients were menopausal and had a positive or unknown tumor receptor status. Paridaens (20) showed that exemestane significantly increased the median time to progression (11 months) compared with tamoxifen (7 months). The frequency of complete and partial remission was also higher in the exemestane group, while complete remission was observed in 7% of patients, partial – in 37%, while in the tamoxifen group, the corresponding rates were 3% and 27%. Both drugs were well tolerated. The median follow-up was 23.3 months, which is insufficient to assess overall survival, so data collection is ongoing.

Studies evaluating the use of steroidal anti-aromatase agents (the inactivator exemestane) after desensitization to non-steroidal aromatase inhibitors report objective responses in 4.2-6.6% of patients and clinical improvement (complete response + partial response + 6 months stabilization). and more) in 24-25% of patients. Thus, when the effect of nonsteroidal aromatase inhibitors has been exhausted, there is a possibility of switching to steroidal aromatase inactivators, for example, exemestane, in the next line (21).

The hopes pinned on pure antiestrogen (Fulvestrant – Faslodex) did not quite come true. A large randomized trial that included 587 patients with metastatic primary breast cancer showed similar efficacy of fulvestrant and tamoxifen: the frequency of objective effects was 33.2% and 31.1%, respectively (M.R. Lichinitser, Howell, Robertson, 2004). Two previous studies have shown that fulvestrant is at least as effective as anastrozole in postmenopausal women with advanced breast cancer after prior endocrine therapy. Therefore, it was surprising that fulvestrant did not show any particular advantage over tamoxifen. However, survival analysis revealed some benefit of fulvestrant in a subgroup of patients with EC+/RP+ tumors. Given that both drugs have a different mechanism of action and are not cross-resistant, they can be used in subsequent lines of endocrine therapy before switching to toxic chemotherapy (Fig. 2). However, further randomized trials are needed to better characterize fulvestrant in first-line endocrine therapy and to determine the most appropriate category of patients in whom fulvestrant should be used (22).

Thus, until now, the progress of endocrine therapy has been expressed in an increase in the duration and improvement in the quality of life of patients, but not in an increase in the proportion of patients who respond positively to one or another hormone therapy. And only the latest discoveries of the very mechanism of transmission of the hormonal signal of cell proliferation, clarification of the gene and biochemical structure of the receptor apparatus, in particular estrogen receptors? and ?, make it possible to understand the reason for the loss of hormonal dependence and sensitivity of tumor cells. This creates fundamental prerequisites for expanding the spectrum of hormone-sensitive breast tumors.

Rice. 2. Algorithm for endocrine therapy of metastatic breast cancer.

References:

1. Semiglazov V.F., Nurgaziev N.Sh., Arzumanov A.S. Tumors of the mammary gland (treatment and prevention).-Almaty.-2001.-344 p.

2. Moiseenko V.M., Semiglazov V.F., Tyulyandin S.A. Modern drug treatment of locally advanced and metastatic breast cancer. SPb. Griffin.-1997-254 p.

3. Bershtein L.M. Oncoendocrinology: Traditions, Modernity and Prospects. – St. Petersburg: Nauka.-343 p.

4. Rose C, Mouridsen HT: Endocrine therapy of advanced breast cancer. Acta Oncol 27: 721-728, 1988.

5. Santen RJ, Harvey HA: Use of aromatase inhibitors in breast carcinoma. Endocr Relat Cancer 6: 75-92, 1999.

6. Gale KE, Andersen JW, Tormey DC, et al: Hormonal treatment for metastatic breast cancer: An Eastern Cooperative Oncology Group phase III trial comparing aminoglutethimide to tamoxifen. Cancer 73: 354-361, 1994.

7. Thuerlimann B. Beretta K, Bacchi M, et al: First line fadrozole HC1 (CGS 16949A) versus tamoxifen in postmenopausal patients with advanced breast cancer. Ann Oncol 7: 471-479, 1996.

8. Buzdar A, Jonat W, Howell A, et al: Anastrozole, a potent and selective aromatase inhibitor, versus megestrol acetate in postmenopausal women with advanced breast cancer: Results of overview analysis of two phase III trials. J Clin Oncol 14: 2000-2011, 1996.

9. Dombernowsky P, Smith I, Falkson G, et al: Letrozole, a new oral aromatase inhibitor for advanced breast cancer: Double blind randomized trial showing a dose effect and improved efficacy and tolerance compared with megestrol acetate. J Clin Oncol 16: 453-461, 1998.

10. Gershanovich M, Chaudri HA, Campos D, et al: Letrozole, a new aromatase inhibitor: Randomized trial comparing 0.5 mg and 2.5 mg daily and aminoglutethimide in postmenopausal women with advanced breast cancer. Ann Oncol 9: 639-645, 1998.

11. Kaufmann M, Bajetta E, Dirix LY, et al: Exemestane is superior to megestrol acetate after tamoxifen failure in postmenopausal women with advanced breast cancer: Results of a phase III randomized double blind trial. J Clin Oncol 18:1399-1411, 2000.

12. Nabholtz A, Buzdar A, Pollak M, et al: Anastrozole is superior to tamoxifen as first-line therapy for advanced breast cancer in postmenopausal women: Results of a North American multicenter randomized trial. J Clin Oncoi 18: 3758-3767, 2000.

13. Bonneterre J. Thuerlimann B, Robertson J, et al: Anastrozole versus tamoxifen as first-line therapy for advanced breast cancer in 668 postmenopausal women: Results of the Tamoxifen or Arimidex Randomized Group Efficacy and Tolerability Study. J Clin Oncol 18: 3748-3757, 2000.

14. Bonneterre J, Buzdar A, Nahholtz JM. et al: Anastrozole is superior to tamoxifen as first-line therapy in hormone receptor positive advanced breast carcinoma. Cancer 92: 2247-2258, 2001.

15. Dirix J, Piccart MJ, Lohrisch C, et al: Efficacy of and tolerance to exemestane versus tamoxifen in first-line hormonal therapy of postmenopausal metastatic breast cancer patients: A European Organization for the Research and Treatment of Cancer Phase P Trial with Pharmacia and Upjohn. Proc Am Soc Clin Oncol 20:29a, 2001 (abstr 114).

16. Mouridsen H, Gershanovich M, Sun Y, et al: Superior efficacy of letrozole versus tamoxifen as first-line therapy for postmenopausal women with advanced breast cancer: Results of a phase HI study of the International Letrozole Cancer Group. J Clin Oncol 19: 2596-2606, 2001.

17. Schumacher M: Two-sample tests of Cramer-von Mises and Kolmog-orov-Smirnov-type for randomly censored data. Int Stat Rev 52: 261-281, 1984.

18. Geisler J, Haynes B, Anker G, et al: Influence of letrozole (Femara) and anastrozole (Arimidex) on total body dramatization and plasma estrogen levels in postmenopausal breast cancer patients evaluated in a random, cross-over design study. J Clin Oncol 20: 751-757, 2002.

19. Center for Drug Evaluation and Research: Food and Drag Administration application, http://www.fda.gov/cder/foi/nda/2000/20-541 S006_Arimidex.htm.

20. Paridaens R., Piccart M. First line hormonal treatment for metastatic breast cancer with exemestane or tamoxifen in postmenopausal patients – A randomized phase III trial of the EORTC Breast Group.//Proceeding of ASCO 40 Annual Meeting.-New Orleans .-2004.-Vol.-23.-P.6.abs.515.

21. Lonning P. Activity of exemestane in metastatic breast cancer after failure of nonsteroidal aromatase inhibitors: a phase II trial. J.Clin.Oncol.-2000.-Vol.18.-P.2234-2244.

22. Howell A., Robertson J., Lichinitser M. Comparison of fulvestrant versus tamoxifen for the treatment of advanced breast cancer in postmenopausal women previously untreated with endocrine therapy.// J.Clin.Oncol.-2004.-Vol. -22.-P.1605-1613.

No Doping ! AS : Balkan Anastrozole