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Anastrozole is an aromatase inhibitor and is used after the menopause for hormone-sensitive breast cancer, usually for five years. It lowers the amount of oestrogen in the body almost completely — this slows the tumour but also affects the joints and bones. Joint pain and a loss of bone density are the two side effects on which treatment most often stumbles. Both can be recognised, treated and often brought under good control.
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| Property | Details |
|---|---|
| Active ingredient | Anastrozole |
| ATC code | L02BG03 |
| Drug class | Non-steroidal aromatase inhibitor; endocrine (anti-hormonal) cancer therapy |
| Dosage forms | Film-coated tablets of 1 mg |
| Half-life | About 40 to 50 hours according to the SmPC; a steady level is reached after around one week |
| Maximum daily dose | 1 mg once a day — a dose increase is not intended |
| Onset of effect | The oestrogen level falls markedly within a few days; the actual benefit, fewer relapses, shows over years |
| Prescription status | Prescription-only medicine |
| Notable feature | Only effective after the menopause; lowers bone density, joint pain is very common. Do not use together with tamoxifen or oestrogens |
In most breast cancers, the tumour cells carry docking sites for oestrogen — the tumour is hormone receptor-positive, and oestrogen acts on it like a growth signal. Anti-hormonal therapy is meant to switch off this signal. There are two ways of doing this: tamoxifen blocks the docking sites, while aromatase inhibitors such as anastrozole ensure that hardly any oestrogen is produced any more. What defines tamoxifen and why it works differently is explained in our article on tamoxifen; here the focus is on the particular features of the aromatase inhibitor.
After the menopause, the ovaries produce hardly any oestrogen. Even so, it does not disappear completely: in fatty tissue, muscles and other tissues, the enzyme aromatase converts male hormone precursors into oestrogen. Anastrozole blocks precisely this enzyme. According to the SmPC, 1 mg a day lowers the oestradiol level in postmenopausal women by more than 80 per cent.¹
Both the benefit and the side effects follow from this:
The following information reflects the SmPC and the guideline. It is not a dosing instruction — which anti-hormonal therapy, in which order and for how long is decided by the treatment team.¹,²
A symptom diary shows at your follow-up appointment when and how badly it hurts — the basis for any solution.
The SmPC names headache, hot flushes, nausea, skin rash, joint pain and stiffness, joint inflammation (arthritis) and weakness as the most frequently reported side effects.¹ Many of them resemble menopausal symptoms and are strongest in the first few months.
If you complain on anastrozole of aching hands, stiff fingers in the morning and knees that protest when you stand up, you are in good company. In the ATAC study, 35.6 per cent of women on anastrozole reported joint pain or stiffness — compared with 29.4 per cent on tamoxifen.¹ These figures include complaints that are common with age anyway. But the difference shows that the aromatase inhibitor noticeably increases them.
There is no miracle cure. But various approaches help many women, and a combination often works best.²,³
Acupuncture and supplements are also often tried. For acupuncture, there are study findings suggesting moderate relief; for supplements, the evidence is thin. Be careful with herbal products with an oestrogen-like effect — they can run counter to the way anastrozole works (section 8).
Oestrogen is one of the most important protective factors for the bones. Because anastrozole sharply lowers the oestrogen level, according to the SmPC it can reduce bone density and increase the risk of fractures.¹ In the ATAC study, 10.2 per cent of women on anastrozole had a fracture during the observation period, compared with 6.8 per cent on tamoxifen; osteoporosis was found in 10.5 versus 7.3 per cent. The SmPC puts this in context: the fracture rate on anastrozole roughly matched that of women of the same age — tamoxifen tends to protect the bones, which partly explains the difference.¹
The good news: the bone loss is known, measurable and treatable. The German osteoporosis guideline explicitly lists aromatase inhibitors as a risk factor and recommends offering a baseline bone assessment when treatment starts — also for women under 70.⁴ After the end of treatment, analyses no longer observed an increased risk of fractures.⁴
For background on the condition itself, read our article on osteoporosis. There you will also find out how a bone density scan works and what the T-score means.
Anastrozole has comparatively few interactions. According to the SmPC, clinically relevant interactions mediated by liver enzymes are unlikely; no clinically significant interactions have been observed with bisphosphonates either.¹ Unlike with tamoxifen, the enzyme CYP2D6 plays no role here — antidepressants such as paroxetine or fluoxetine do not slow anastrozole down. The most important points concern anything that runs counter to the way it works.
| Combination | Consequence | What to do |
|---|---|---|
| Tamoxifen (at the same time) | Can reduce the effect of anastrozole; in the ATAC study the combination brought no advantage | One after the other rather than at the same time, as planned by the team |
| Medicines containing oestrogen, e.g. estradiol for hormone replacement therapy | Cancels out the way it works — anastrozole is meant precisely to remove oestrogen | Avoid according to the SmPC; vaginal products too only after consulting the treatment team |
| Herbal remedies with an oestrogen-like effect (red clover, high-dose soy isoflavones) | Safety in hormone-sensitive breast cancer is unclear | Not without checking first; see herbal medicines |
| Bisphosphonates, denosumab | No clinically relevant interaction; protect the bones | Are often deliberately combined |
| Anti-inflammatory painkillers (for joint pain) | No direct interaction, but their own risks with long-term use | Use for a limited time and as agreed |
| Alcohol | No known direct interaction, but an independent risk factor for breast cancer and osteoporosis | Drink as little as possible |
In everyday life, the risk lies less in a single combination than in the course of the years: someone recommends a “natural” product for hot flushes, a hormone cream is prescribed for vaginal dryness, and a long-term painkiller is added for the joint pain. An up-to-date medication plan and an interaction check before every new medicine keep track of everything — supplements included. More on hormonal products in the guide hormone replacement therapy.
Both active ingredients lower the risk of relapse in hormone-sensitive breast cancer, and both are taken for years — but their side effect profiles differ considerably. The ATAC study compared the two directly; the anastrozole SmPC lists the predefined adverse events.¹
| Event (ATAC study) | Anastrozole | Tamoxifen |
|---|---|---|
| Joint pain/stiffness | 35.6% | 29.4% |
| Fractures | 10.2% | 6.8% |
| Hot flushes | 35.7% | 40.9% |
| Vaginal bleeding | 5.4% | 10.2% |
| Vaginal discharge | 3.5% | 13.2% |
| Venous thromboembolism | 2.8% | 4.5% |
| Cancer of the lining of the womb (endometrial cancer) | 0.2% | 0.6% |
Put simply: tamoxifen tends to burden the veins and womb, anastrozole the joints and bones. Which therapy fits depends on the tumour's characteristics, menopausal status, other conditions and personal risks — someone who has already had a thrombosis, for example, has different priorities from someone with osteoporosis. The decision is made by the treatment team together with you.²
For many women, the joint complaints become more bearable after the first few months; for some, they remain. What is worth doing: regular exercise, even if it takes an effort at first, a gentle start to the morning and an honest conversation if the pain dominates everyday life. Switching to another aromatase inhibitor or to tamoxifen is a real option. After the end of treatment, the complaints usually improve. Helpful for the conversation: two weeks of notes on which joints hurt, when and how badly.
Usually yes, but not without bone protection. Precisely in this case, the SmPC recommends a scan at the start and during treatment and, if needed, osteoporosis treatment. With bisphosphonates or denosumab, the additional bone loss can be offset in many cases. Whether another medicine would suit you better than anastrozole is weighed up by the treatment team — protection against relapse and bone health both belong in the calculation.
Many women say that, and it is a legitimate issue. Hormone-free moisturising gels and lubricants are the first step and are no problem with anastrozole. Hormone-containing vaginal products, on the other hand, are not a given, because even small amounts of oestrogen can run counter to the way it works — whether a product is an option, and which one, is decided by the treatment team. Raise it; staying silent is no sign of strength here.
Because the choice depends on several factors: above all on whether the menopause is complete, and also on the tumour's characteristics, the risk of relapse, and the risk of thrombosis and bone problems. After the menopause, aromatase inhibitors were somewhat more effective than tamoxifen for disease-free survival in studies; before the menopause, tamoxifen is the basis. Two women with the “same” breast cancer can therefore receive different tablets for good reasons.
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