In findings with potentially broad implications for the public’s health, new research has found that some women who treat their high blood pressure with a class of drugs that relaxes the blood vessels were more likely to develop pancreatic cancer than those who use other hypertension medications.
In a large and intensively studied group of middle-aged and older women, the risk of developing pancreatic cancer was more than twice as high for those who took a short-acting calcium channel blocker for more than three years.
Examples of short-acting calcium channel blockers (and the commercial names by which they’re marketed) include nifedipine (Adalat and Procardia), nicardipine (Cardene), isradipine (DynaCirc), diltiazem (Cardizem, Cartia and Dilacor) and verapamil (Calan, Covera, Isoptin and Verelan).
Study participants who took extended release formulations of a calcium channel blocker also saw a modest 12 percent increase in their pancreatic cancer risk relative to those who took a beta blocker, diuretic or ACE inhibitor.
Pancreatic cancer is the fourth-leading cause of cancer-related deaths in the United States, and is most often diagnosed once it has reached advanced stages. While immunotherapy and other advances in cancer care promise new treatments for this malignancy, survival rates have scarcely budged since 1975. It is expected to kill 44,330 Americans in 2018, according to the American Cancer Society.
In this study, 145,551 postmenopausal women were followed for close to 14 years, on average. In this group, 841 women were diagnosed with pancreatic cancer. But those diagnoses were far from evenly distributed.
Among the 4,338 women who had taken a short-acting calcium channel blocker for high blood pressure, 45 (or about 1 percent) were diagnosed with pancreatic cancer. In the group of 36,594 women who took a beta blocker, diuretic or angiotensin converting enzyme (ACE) inhibitor, 212 (or 0.57 percent) were diagnosed with pancreatic cancer.
After adjusting for a variety of factors that contribute to pancreatic cancer risk in the two groups, the researchers judged that those taking the short-acting calcium channel blocker increased their risk of developing the malignancy by 107 percent over those who took other hypertension drugs.
How pancreatic cancer is related to a blood pressure medication is not entirely clear.
But the study authors, from Baylor College of Medicine in Houston, explored evidence that these drugs may set in motion a complex chain of action that increases inflammation throughout the body. Inflammatory processes are considered a contributing factor in many kinds of cancers, including those in the pancreas.
The study’s lead author, Baylor cancer researcher Zhensheng Wang, said he does not want the study’s findings to cause panic among patients treating their high blood pressure with a calcium channel blocker.
Short-acting formulations of the medicine have been declining in use, as drug companies offer more convenient extended-release formulations. But these medications are still prescribed, Wang said, and the Food and Drug Administration should consider investigating their safety.
Patients with a family history of pancreatic cancer who have taken a short-acting calcium channel blocker “definitely need to consult with their physician,” he added.
For now, the findings are limited to postmenopausal women, since that is the population in which the association was tested.
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