Androgen suppression therapy (AST) for prostate cancer may be a serious risk factor for cardiovascular (CV) disease, according to a Viewpoint published online in Heart. The scope of the problem is widely underappreciated and is rarely considered in clinical practice, write Liam Bourke and colleagues. The subject was also the topic of a 2010 scientific statement from the American Heart Association, the American Cancer Society, and the American Urological Association.
For every 1000 men treated for 5 years with AST the authors estimate there will be an excess 315 incident cases of coronary heart disease, 360 cases of diabetes, 28 MIs, and 42 strokes.
“The current status quo of no action is, in our view, unsatisfactory for the patient and unlikely to be cost effective,” the authors write. “There is a need to investigate integration of AST specific CVD risk augmentation strategies into standard clinical care.” Cancer nurse specialists, they suggest, are a “potentially cost efficient, efficacious resource to manage CVD risk in these men.”
Here is the press release from Heart:
Heart health risk of prostate cancer treatment being ignored, warn specialists
[Cardiovascular risk in androgen suppression: underappreciated, under-researched, and unresolved Online First 2011; doi 10.1136/heartjnl-2011-300893]
Heart disease and stroke are emerging complications of treating prostate cancer with drugs to suppress testosterone production, yet standard management of the disease is ignoring this risk, warn specialists in a viewpoint published online in Heart.
Drugs to suppress production of the male hormone testosterone, known as androgen suppression therapy (AST), are a mainstay of treatment for advanced prostate cancer, write the authors. And there is good evidence to show that they work well.
But mounting evidence suggests that these drugs may also significantly increase the risk of heart disease and stroke, and may be associated with an increased risk of death from these causes, they add, citing various pieces of published research.
And the advent of prostate specific antigen (PSA) testing, means that many more men are being started on AST at an earlier stage, and remain on it for years, say the authors.
Hormone suppression has various other side effects, including bone thinning and increased fracture risk, lowered muscle function, and fatigue.
Although it is as yet unclear if there is a direct causal link between these drugs and cardiovascular disease, there are certainly plausible explanations for the impact that such treatment might have on risk factors for heart disease and stroke, say the authors.
And this has not escaped the attention of the American Heart Association, the American Cancer Society, and the American Urological Association, who have issued a joint statement to this effect.
Estimates from one study suggest that for every 1,000 men treated for five years with these drugs, there will be an extra 315 cases of heart disease, 360 extra cases of diabetes, 28 additional heart attacks, and 42 more strokes.
This equates to £700 million to £2 billion in NHS costs between 2004 and 2009 alone, say the authors.
“The concept of incorporating cardiovascular disease management into AST as standard has not yet percolated into clinical practice,” they write.
As a result, the cancer and heart disease components are managed separately, with little coordination between doctors, they say. Existing guidelines on prostate cancer do not include the management of cardiovascular disease or make it clear who should be taking the lead on it, they add.
“Presently, we are unaware of any current local or national management plans that attempt to address the increased risk of cardiovascular disease associated with androgen suppressant therapy or recognise these men in screening procedures,” they write.
“The current status quo of no action is, in our view, unsatisfactory for the patient and unlikely to be cost effective,” they conclude, adding that cancer nurse specialists might be a highly effective and relatively inexpensive solution to the problem.