AACR 2018: Short-Acting Calcium Channel Blockers Associated With Increased Risk of Pancreatic Cancer in Postmenopausal Women

Key Points

  • A 66% higher risk of incident pancreatic cancer was found among the women who had ever used short-acting calcium channel blockers (CCBs).
  • Postmenopausal women who had used short-acting CCBs for 3 or more years were found to have a 107% higher risk of pancreatic cancer than those who had used other non-CCB antihypertensive drugs.
  • CCBs, in particular short-acting CCBs, were the only antihypertensive medication that was associated with an increase in pancreatic cancer risk. Ever-use of ACEi, beta blockers, diuretics, and long-acting CCBs was not associated with increased risk of pancreatic cancer. 

Calcium channel blockers (CCBs)—specifically the short-acting form of CCBs, which are prescribed to treat high blood pressure—were associated with an increased risk of pancreatic cancer in postmenopausal women, according to a study presented at the American Assocation for Cancer Research (AACR) Annual Meeting 2018 (Abstract 4946).

“Pancreatic cancer is the fourth leading cause of cancer-related mortality in the United States, with an estimated 44,330 deaths in 2018,” said the study’s lead author, Zhensheng Wang, PhD, a postdoctoral associate at the Dan L Duncan Comprehensive Cancer Center at Baylor College of Medicine in Houston.

“Pancreatic cancer typically occurs in elderly individuals who also have chronic comorbid medical conditions, such as hypertension,” Dr. Wang said. “Antihypertensive medication use has increased significantly; therefore, it is of great public health significance to address the potential association between antihypertensive medication use and risk of pancreatic cancer in the general population.”

This study sought to evaluate how antihypertensive drugs and a receptor called soluble receptor for advanced glycation end-product (sRAGE) might influence pancreatic cancer risk. Previous research has suggested that sRAGE has an anti-inflammatory effect on the body, and it has been associated with lower risk of pancreatic cancer. Because antihypertensive medications have been shown to increase the concentration of sRAGE levels, the researchers hypothesized that there would be an inverse association between the use of antihypertensive medications and pancreatic cancer risk.

“We were, however, surprised by the unexpected increased risk of pancreatic cancer observed among users of short-acting CCBs,” Dr. Wang said.

Study Findings

The authors conducted a prospective cohort study of 145,551 postmenopausal women ages 50 to 79 who were enrolled in the Women’s Health Initiative, a long-term national health study, between 1993 and 1998. They collected data on any medications the women were taking, including product and generic name, duration of use, and dosage form. They analyzed four types of antihypertensive drugs: beta blockers, diuretics, angiotensin converting enzyme inhibitors (ACEi), and CCBs, and used Cox proportional hazard regression models to obtain hazard ratios for the association of the four types of medication with risk of pancreatic cancer.

By August 29, 2014, the researchers had ascertained 841 pancreatic cancer cases among the women. In these women, the researchers measured serum levels of sRAGE using immunoassay among a subset of 489 pancreatic cancer patients and 977 noncancer controls.

A 66% higher risk of incident pancreatic cancer was found among the women who had ever used short-acting CCBs. Women who had used short-acting CCBs for 3 or more years were found to have a 107% higher risk of pancreatic cancer than those who had used other non-CCB antihypertensive drugs.

CCBs, in particular short-acting CCBs, were the only antihypertensive medication that was associated with an increase in pancreatic cancer risk. Ever-use of ACEi, beta blockers, diuretics, and long-acting CCBs was not associated with increased risk of pancreatic cancer.

The study also found that women who had ever used short-acting CCBs had significantly lower sRAGE levels than women who used any other antihypertensive medications.

“sRAGE is thought to mitigate the inflammatory response by blocking proinflammatory RAGE signaling,” explained senior author Li Jiao, MD, PhD, Associate Professor at the Center for Innovations in Quality, Effectiveness and Safety, Michael E. DeBakey VA Medical Center at Baylor College of Medicine.

The authors noted that while further research will be necessary to confirm these findings and understand the mechanisms, “the blockage of the calcium channel caused by use of CCBs may potentially reduce sRAGE release and thus further decrease the levels of anti-inflammatory sRAGE. This is important, as chronic inflammation is a well-recognized risk factor for pancreatic as well as many other cancers.”

“Our findings on short-acting CCB use and pancreatic cancer risk are novel and of potential broad medical and public health significance if confirmed. Short-acting CCBs are still prescribed to manage hypertension, which is one of the components of metabolic syndrome, and metabolic syndrome is a possible risk factor for pancreatic cancer,” Dr. Wang said.

Dr. Jiao noted that since this observational study was conducted among postmenopausal women in the United States, the results may not be generalizable to men, to premenopausal women, or to populations outside the United States. Unadjusted confounding factors or residual confounding factors may also contribute to the findings.

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


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