A follow-up study of women who stopped taking the hormone therapy of estrogen plus progestin after this intervention was discontinued as part of a clinical trial indicates that these women may have an increased risk of cancer, compared to women in the placebo group, according to a study in the March 5 issue of JAMA.

Cardiovascular disease and fracture risks were similar between the two groups, but women who took hormone therapy had an overall higher global risk index reflecting the balance of risks and benefits from a number of endpoints combined, including deaths.

The Women’s Health Initiative (WHI) trial of estrogen plus progestin, which included 16,608 postmenopausal women, assessed whether conjugated equine estrogens (CEE) plus medroxyprogesterone acetate (MPA) prevents heart disease and hip fractures and increases the risk of breast cancer.

Further analysis showed that women who stopped taking hormones had higher risks of cardiovascular disease (CVD), coronary heart disease (CHD), stroke and venous thromboembolism and lower risks of fracture and colorectal cancer.

Gerardo Heiss, M.D., of the University of North Carolina, Chapel Hill, N.C., and colleagues examined the risks and benefits experienced by 15,730 trial participants who had follow-up, from July 2002 to March 2005, after they stopped hormone therapy.

The researchers found that the annualized event rates for the outcome “all cancer” was higher during the postintervention follow-up for the CEE plus MPA group (1.56 percent per year [n = 281]) than the placebo group (1.26 percent per year [n = 218]).

The rates of colorectal cancer did not differ significantly between the two groups; rates of endometrial cancer were lower in the CEE plus MPA group.

Though risk of breast cancer remained elevated during the follow-up, the risk was less than that experienced towards the end of the trial period.

The risk of cardiovascular events after the intervention were comparable, with an annualized rate of 1.97 percent, meaning that the increased risks found during the trial period weakened after study drugs were stopped.

The risk of fractures during the postintervention follow-up was similar among women in both groups for each type of fracture considered: hip, vertebral and other osteoporotic fractures.

“This reflects a greater increase in the annualized risk of fractures after the intervention in the women who had been assigned to CEE plus MPA compared with women assigned to placebo, particularly for hip and vertebral fractures. Thus, the protective effects of CEE plus MPA previously evident during the trial were not observed to carry over into the postintervention phase …,” the researchers write. 

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