diltiazem/nifedipine: no significant increased cancer risk

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Reactions 749 - 1 May 1999 Diltiazem/nifedipine: no significant increased cancer risk Short-acting diltiazem therapy in post myocardial infarction (MI) patients was not associated with any increased risk of cancer in a Japanese study. The incidence of cancer in post MI patients treated with short-acting nifedipine was slightly higher compared with patients who did not receive calcium antagonist therapy. However, this difference was not statistically significant (odds ratio 1.34; 95% CI 0.63–2.85). The study involved patients who had experienced an MI and were treated with short-acting nifedipine 30 mg/day (425 patients; mean age 61.3 years) short-acting diltiazem 90 mg/day (141; 58.9) or no calcium antagonist therapy (488; 59.3; controls). The mean time period between the onset of MI and study enrolment was 16 months and the mean observation period following enrolment in the study was 26.3 months. During the study period, 31 patients (2.9%) were found to have newly developed cancers. Of these 31 patients, 15 (3.5%) were in the nifedipine group, 3 (2.1%) were in the diltiazem group and 13 (2.7%) were in the control group. The researchers point out that the relatively short follow-up period in their study may limit the ability to detect the potential increased risk of cancer. They point out that, at this time, results from both clinical and basic research regarding the relationship between calcium antagonist therapy and cancer remains inconclusive. Therefore, they emphasize the need for further studies in this area. Kanamasa K, et al. Incidence of cancer in postmyocardial infarction patients treated with short-acting nifedipine and diltiazem. Cancer 85: 1369-1374, 15 Mar 1999 800752369 1 Reactions 1 May 1999 No. 749 0114-9954/10/0749-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

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Reactions 749 - 1 May 1999

Diltiazem/nifedipine: no significantincreased cancer risk

Short-acting diltiazem therapy in post myocardialinfarction (MI) patients was not associated with anyincreased risk of cancer in a Japanese study. Theincidence of cancer in post MI patients treated withshort-acting nifedipine was slightly higher comparedwith patients who did not receive calcium antagonisttherapy. However, this difference was not statisticallysignificant (odds ratio 1.34; 95% CI 0.63–2.85).

The study involved patients who had experienced anMI and were treated with short-acting nifedipine 30mg/day (425 patients; mean age 61.3 years) short-actingdiltiazem 90 mg/day (141; 58.9) or no calciumantagonist therapy (488; 59.3; controls). The mean timeperiod between the onset of MI and study enrolmentwas 16 months and the mean observation periodfollowing enrolment in the study was 26.3 months.

During the study period, 31 patients (2.9%) werefound to have newly developed cancers. Of these 31patients, 15 (3.5%) were in the nifedipine group, 3(2.1%) were in the diltiazem group and 13 (2.7%) werein the control group. The researchers point out that therelatively short follow-up period in their study may limitthe ability to detect the potential increased risk ofcancer. They point out that, at this time, results fromboth clinical and basic research regarding therelationship between calcium antagonist therapy andcancer remains inconclusive. Therefore, they emphasizethe need for further studies in this area.Kanamasa K, et al. Incidence of cancer in postmyocardial infarction patientstreated with short-acting nifedipine and diltiazem. Cancer 85: 1369-1374, 15 Mar1999 800752369

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Reactions 1 May 1999 No. 7490114-9954/10/0749-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved