JNCI Journal of the National Cancer Institute Advance Access published November 11, 2008 EDITORIALS Breast Cancer Prevention Using Calcium and Vitamin D: A Bright Future?
Despite aggressive treatment and screening efforts, breast cancer the risk of breast cancer among postmenopausal women. Breast remains the second leading cause of cancer-related deaths among cancer incidence was a prospectively planned secondary endpoint women in the United States ( 1 ). Because of the large number of in the WHI study. This trial had a large number of racially diverse women dying from this disease and the toxicity of breast cancer women who maintained relatively good adherence to the study treatments, recent efforts have focused on identifying effective can-
protocol. Despite the meticulous design, careful control, and ade-
cer preventive agents. These efforts have led to the development of
quate adherence, Chlebowski et al. report that calcium and vitamin
antiestrogen agents, such as tamoxifen and raloxifene, which pre-
D supplementation did not reduce the incidence of breast cancer.
vent approximately 50% of invasive breast cancers in women who
Previous groups ( 17 , 18 ) have reported the results of the other
are at high risk for breast cancer. However, the use of these agents
components of the WHI study. In these studies, there was a small
for breast cancer prevention has been limited by their toxicity.
but statistically signifi cant increase in hip bone density, suggesting
A large amount of evidence exists to indicate that vitamin D the possibility of a clinically relevant effect of CaD supplementa-
may be a particularly promising cancer preventive agent. Vitamin
tion. Analysis of this WHI data also demonstrated that there was
D is a fat-soluble vitamin that is essential for bone formation and no decrease in hip bone fractures or colorectal cancer incidence, calcium homeostasis. The potential link between vitamin D levels
which were the other primary and secondary endpoints of the trial
and reduced cancer incidence was suggested by results from epide-
( 17 , 18 ). These results, along with the results presented in this issue
miological studies by Garland et al., Giovannucci, and others ( 2 – 5 )
( 16 ), suggest that women who received the CaD in this trial did not
and by recent data suggesting a strong association between low experience the predicted benefi ts of calcium and vitamin D supple-vitamin D levels and increased colon cancer risk ( 6 ). Several case –
mentation — a reduction in bone fractures, colon cancer, and breast
control and cohort studies support an inverse relationship between
vitamin D intake and breast cancer incidence ( 7 – 11 ); however,
Should these negative results discourage the use of calcium and
other studies show either no association or an association with vitamin D in future breast cancer prevention studies? Not neces-increased breast cancer risk ( 10 , 12 – 14 ). In addition, recent studies
sarily. Although Chlebowski et al. ( 16 ) did not fi nd a statistically
found that vitamin D defi ciency was linked to poor outcomes in signifi cant association between calcium and vitamin D supplemen-patients with early breast cancer ( 15 ).
tation and reduced incidence of breast cancer, there could be sev-
It is against this backdrop that Chlebowski et al. ( 16 ) report the
eral important confounders at play. The fi rst confounder is that of
results of a randomized controlled clinical trial evaluating the variable baseline vitamin D levels. The authors measured the base-breast cancer preventive effect of vitamin D and calcium supple-
line level of plasma 25-hydroxyvitamin D and compared this level
mentation. This study, which was compiled from the calcium plus
with self-reported vitamin D intake. There was a large overlap of
vitamin D (CaD) arm of the Women’s Health Initiative (WHI), baseline self-reported vitamin D intake across the plasma 25-randomly assigned 36 282 postmenopausal women to receive daily
hydroxyvitamin D quintiles, suggesting that factors besides intake
doses of either 1000 mg calcium with 400 IU vitamin D3 supple-
(such as sunlight exposure, body mass index, metabolism, physical
mentation or placebo and were followed up for an average of 7 activity, and genetic factors) have a stronger infl uence on plasma years. To maximize participation and size, the WHI trial had over-
25-hydroxyvitamin D than just intake quantity alone.
lapping groups, including a dietary modifi cation (DM) group, a
A second potential confounder is the high level of calcium and
vitamin D self-supplementation (up to 1000 mg of calcium and
hormone therapy (HT) group, and a CaD group, which was added
1000 IU of vitamin D) that was allowed during the study. This
in the second year of the study. As a result, 69% of women in the
“outside of study” supplementation led to 15% of placebo patients
calcium with vitamin D trial were also part of the DM group, 54%
“dropping in” to the active treatment component of the study.
were part of the HT group, and 14% had participated in both the DM and the HT trials ( 17 ). Furthermore, in this trial, personal use of calcium and vitamin D was permitted in both the supplementa-
Affiliations of authors: Department of Molecular and Cellular Biology (CS),
Lester and Sue Smith Breast Center and Department of Medicine (PB), Baylor
Chlebowski et al. should be congratulated for successfully com-
pleting such a large and sophisticated trial. The well-designed and
Correspondence to: Powel H. Brown, MD, PhD, Lester and Sue Smith Breast Center, Baylor College of Medicine, One Baylor Plaza, BCM 600, Houston, TX
well-executed randomized, double-blinded, placebo-controlled 77030 (e-mail: [email protected] ). trial with a nested case – control study is unrivaled in its scope and DOI: 10.1093/jnci/djn390 complexity. This current study tested the hypothesis that 1000 mg/
The Author 2008. Published by Oxford University Press. All rights reserved.
day calcium plus 400 IU vitamin D3 supplementation would reduce
For Permissions, please e-mail: [email protected].
1562 Editorials | JNCI
Such “outside of study” supplementation, sometimes at levels more addition, future trials may need to be carefully controlled for diet, than twice the trial dose, may have diminished the observed differ-
sunlight exposure, HT, and physical activity. Finally, such trials
ence in breast cancer incidence between the placebo and CaD arms.
may require earlier initiation and longer duration. Given the long
Another very important issue is the dose of vitamin D given in
latency of breast cancer, longer follow-up times may be needed to
this trial. Recent reports suggest that higher doses of vitamin D evaluate the effect of vitamin D on breast cancer incidence. (1000 – 2000 IU/day) may be required to prevent cancer ( 19 ). It is
Because preclinical, epidemiological, and clinical trial results of
possible that doses suffi cient to prevent osteoporosis are not suffi -
vitamin D supplementation are confl icting, additional studies will
cient to prevent cancer. The results of this trial suggest that a dose
be needed to determine whether vitamin D plus calcium will pre-
of 400 IU of vitamin D could be insuffi cient to prevent breast vent breast cancer. However, this article by Chlebowski et al. cancer ( 16 ) or colon cancer ( 17 ).
offers an important fi rst step in addressing this issue. Future clini-
Another important aspect of this trial is the age of the study cal trials should address the above questions to help determine
population. The women in the WHI trial were postmenopausal whether higher doses of vitamin D supplements will be cancer and aged 50
– 79 years. Previous epidemiological studies preventive. The potential health benefi ts of vitamin D and calcium
( 8 , 10 , 14 , 20 ) have not shown a clear association between vitamin may yet still have a bright future. D intake and breast cancer in postmenopausal women (relative risks [RRs] = 0.55 to 1.3); however, results from epidemiological
References
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JNCI | Editorials 1563
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1564 Editorials | JNCI
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