CEBP Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Genkinger, J. M.
Right arrow Articles by Smith-Warner, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Genkinger, J. M.
Right arrow Articles by Smith-Warner, S. A.
Cancer Epidemiology Biomarkers & Prevention Vol. 15, 364-372, February 2006
© 2006 American Association for Cancer Research

Dairy Products and Ovarian Cancer: A Pooled Analysis of 12 Cohort Studies

Jeanine M. Genkinger1, David J. Hunter1,2,4, Donna Spiegelman3, Kristin E. Anderson6, Alan Arslan7, W. Lawrence Beeson8, Julie E. Buring2,5, Gary E. Fraser8, Jo L. Freudenheim9, R. Alexandra Goldbohm10, Susan E. Hankinson2,4, David R. Jacobs, Jr.6,11, Anita Koushik1, James V. Lacey, Jr.12, Susanna C. Larsson13, Michael Leitzmann12, Marji L. McCullough14, Anthony B. Miller15, Carmen Rodriguez14, Thomas E. Rohan16, Leo J. Schouten17, Roy Shore7, Ellen Smit9, Alicja Wolk13, Shumin M. Zhang2,5 and Stephanie A. Smith-Warner1,2

Departments of 1 Nutrition, 2 Epidemiology, and 3 Biostatistics, Harvard School of Public Health; 4 Channing Laboratory and Department of Medicine, and 5 Division of Preventive Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts; 6 Division of Epidemiology, School of Public Health, University of Minnesota, Minneapolis, Minnesota; 7 Division of Epidemiology, Department of Environmental Medicine, New York University, New York, New York; 8 The Center for Health Research, Loma Linda University School of Medicine, Loma Linda, California; 9 Department of Social and Preventive Medicine, University at Buffalo, State University of New York, Buffalo, New York; 10 Department of Food and Chemical Risk Analysis, the Netherlands Organization for Applied Scientific Research Quality of Life, Zeist, the Netherlands; 11 Department of Nutrition, University of Oslo, Oslo, Norway; 12 Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Department of Health and Human Services, Bethesda, Maryland; 13 Division of Nutritional Epidemiology, National Institute of Environmental Medicine, Karolinska Institute, Stockholm, Sweden; 14 Epidemiology and Surveillance Research, American Cancer Society, Atlanta, Georgia; 15 Department of Public Health Sciences, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada; 16 Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, New York; and 17 Department of Epidemiology, Nutrition and Toxicology Research Institute Maastricht, Maastricht University, Maastricht, the Netherlands

Requests for reprints: Jeanine Genkinger, Department of Nutrition, Harvard School of Public Health, Room 339, Building 2, 665 Huntington Avenue, Boston, MA 02115. Phone: 617-432-4976; Fax: 617-432-2435. E-mail: pooling{at}hsphsun2.harvard.edu


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results
 Discussion
 References
 
Background: Dairy foods and their constituents (lactose and calcium) have been hypothesized to promote ovarian carcinogenesis. Although case-control studies have reported conflicting results for dairy foods and lactose, several cohort studies have shown positive associations between skim milk, lactose, and ovarian cancer.

Methods: A pooled analysis of the primary data from 12 prospective cohort studies was conducted. The study population consisted of 553,217 women among whom 2,132 epithelial ovarian cases were identified. Study-specific relative risks and 95% confidence intervals were calculated by Cox proportional hazards models and then pooled by a random-effects model.

Results: No statistically significant associations were observed between intakes of milk, cheese, yogurt, ice cream, and dietary and total calcium intake and risk of ovarian cancer. Higher lactose intakes comparing ≥30 versus <10 g/d were associated with a statistically significant higher risk of ovarian cancer, although the trend was not statistically significant (pooled multivariate relative risk, 1.19; 95% confidence interval, 1.01-1.40; Ptrend = 0.19). Associations for endometrioid, mucinous, and serous ovarian cancer were similar to the overall findings.

Discussion: Overall, no associations were observed for intakes of specific dairy foods or calcium and ovarian cancer risk. A modest elevation in the risk of ovarian cancer was seen for lactose intake at the level that was equivalent to three or more servings of milk per day. Because a new dietary guideline recommends two to three servings of dairy products per day, the relation between dairy product consumption and ovarian cancer risk at these consumption levels deserves further examination. (Cancer Epidemiol Biomarkers Prev 2006;15(2):364–72)


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results
 Discussion
 References
 
Ovarian cancer is the sixth leading cause of cancer and seventh most common cause of cancer death among women worldwide (1), but rates vary substantially by country. Incidence and mortality rates in more developed regions (10.2 per 100,000 and 5.7 per 100,000, respectively) are approximately double those in less developed regions (5.0 per 100,000 and 2.9 per 100,000, respectively; ref. 1). Furthermore, the majority of cases are diagnosed with ovarian cancer at later stages (2-5). Due to the current lack of availability of good screening methods for ovarian cancer and low survival rates among women diagnosed with disease at an advanced stage (6), a better understanding of the etiology of cancer may lead to important reductions in ovarian cancer incidence.

Partly as a result of the large international variation in incidence rates of ovarian cancer, diet has been suggested as a possible risk factor. Dairy foods, such as milk, vary in consumption across the world, where highest consumption is found in developed countries compared with developing countries (7). Dairy foods and some of their constituents, such as lactose and calcium, have been hypothesized to promote the development of ovarian cancer. Higher levels of lactose may affect the ovary and ovarian-pituitary axis through its metabolites (e.g., galactose; refs. 8-11). Galactose, whose main food source is lactose, stimulates gonadotropin secretion that may result in toxicity to oocytes and thus may lead to ovarian failure and cancer (9). High intakes of calcium may increase or decrease ovarian cancer risk. High intakes of calcium may depress 1,25-OH vitamin D, which may result in an increase in cellular proliferation and thus tumorigenesis (12, 13). In contrast, high calcium intakes may protect against carcinogenesis by down-regulating the production of parathyroid hormone, which may reduce mitosis and increase apoptosis (14).

Although case-control studies have reported conflicting results for dairy foods (8, 15-28) and lactose (3, 8, 20-22, 25, 29-32) in relation to risk of ovarian cancer, the prospective Iowa Women's Health Study (33), Nurses' Health Study (34), and Swedish Mammography Cohort (35) have each shown positive associations between skim milk and lactose intake and risk of ovarian cancer. Furthermore, the Nurses' Health Study and Swedish Mammography Cohort found a stronger positive association between higher lactose intake and specifically risk of serous ovarian cancer (34, 35). Although only occasionally reported, a lower ovarian cancer risk has been observed with higher intakes of vitamin D (21, 32, 36) and calcium (16, 21, 32, 36). Although dietary factors and ovarian cancer risk have been evaluated in case-control settings, few prospective studies have examined diet and ovarian cancer risk, primarily due to the small number of cases of ovarian cancer that have occurred in the individual studies. Due to temporal ambiguity of the diet and cancer association in case-control studies, further prospective assessment of these associations is needed.

We investigated the association between intakes of dairy foods and nutrients with risk of ovarian cancer in a pooled analysis of 12 cohort studies (33-35, 37-45). Given that the effect of dairy foods and nutrients may vary by risk factors for ovarian cancer, we also considered whether these associations differed by menopausal status, parity, oral contraceptive use, and postmenopausal hormone use. Additionally, because particular histologic subtypes of ovarian cancer resemble different gynecologic tissue (46), behave different clinically (47), and may have genetic differences (47), individual histologic subtypes may be associated with different etiologies. Thus, we examined associations between intakes of dairy foods and nutrients separately with endometrioid, mucinous, and serous ovarian cancers.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results
 Discussion
 References
 
Population
A pooled analysis of the primary data from 12 prospective cohort studies (33-35, 37-45) based in North America and Western Europe was conducted in The Pooling Project of Prospective Studies of Diet and Cancer. Two of these studies, Canadian National Breast Screening Study and the Netherlands Cohort Study, were analyzed as case-cohorts because the investigators of these two studies have processed questionnaires for only a sample of noncases. The methods have been described in detail elsewhere.18 To be included in the ovarian cancer analyses, each study needed a minimum of 50 incident ovarian cancer cases, an assessment of usual food and nutrient intake and validation of the dietary assessment tool or a closely related instrument. The studies that met these criteria were the Adventist Health Study, Breast Cancer Detection Demonstration Project Follow-up Study, Canadian National Breast Screening Study, Cancer Prevention Study II Nutrition Cohort, Iowa Women's Health Study, the Netherlands Cohort Study, New York State Cohort, New York University Women's Health Study, Nurses' Health Study (part a—NHSa and part b—NHSb), Nurses' Health Study II, Swedish Mammography Cohort, and Women's Health Study as shown in Table 1. The follow-up of the Nurses' Health Study was divided into two sections, where part (a), NHSa, followed individuals from the completion of the 1980 food frequency questionnaire to 1986, and part (b), NHSb, followed individuals from the completion of the 1986 food frequency questionnaire to 2002. The follow-up time for the Nurses' Health Study was divided into two separate time periods to take advantage of the expanded food frequency questionnaire administered in 1986. The standard theory of survival data has established that blocks of person-time in different time periods are asymptotically uncorrelated regardless of the extent to which they are derived from the same people (48). Thus, pooling estimates from these two time periods, and the cases that arise within them, produces estimates and estimated SEs that are as valid as those from a single combined period. The total study population consisted of 553,217 women among whom 2,132 developed invasive epithelial ovarian cancer.


View this table:
[in this window]
[in a new window]
  		Table 1. Daily mean intakes of dairy nutrients and foods by cohort study in the ovarian cancer analyses in the Pooling Project of Prospective Studies of Diet and Cancer

 
Exclusions
In addition to applying the exclusions that each study had predefined for their cohort, we excluded individuals if they had a prior cancer diagnosis other than nonmelanoma skin cancer at baseline, had a bilateral oophorectomy before baseline, or if they had loge-transformed energy intakes beyond three SDs from the study-specific loge-transformed mean energy intake of their respective population. The Adventist Health Study (37) and New York State Cohort (42) did not obtain information on oophorectomy at baseline, and thus we were not able to exclude individuals who had a bilateral oophorectomy before baseline in these studies.

Exposure Assessment
Usual frequency of consumption of dairy foods (total milk, whole milk, low-fat milk, hard cheese, cottage cheese, yogurt, and ice cream) was estimated at baseline from study-specific food frequency questionnaires. All dairy foods were analyzed in gram units to take into account differences in portion sizes across studies. Whole milk, low-fat milk, skim milk, buttermilk, and evaporated milk contributed to the total milk summary measure. Hard cheese included cheese (type unspecified), hard cheese, high-fat cheese, and low-fat cheese, whereas yogurt comprised yogurt and low-fat yogurt. Three studies, which have assessed correlations between measurement of dairy products, cheese, and milk from a food frequency questionnaire and 24-hour recalls or food records, have shown reasonable correlations that were >0.63 (49), 0.47 (50, 51), and 0.60 (50, 51), respectively.

Most studies estimated nutrient intakes using the food composition method (52), but the New York State Cohort used the "regression weight" method to estimate nutrient values (42). The regression-residual method (52) was used to adjust nutrient intakes to an energy intake of 1,600 kcal/d. Intake of calcium from diet was estimated from their food frequency questionnaires in all studies, whereas vitamin D from diet was estimated from their food frequency questionnaires in most studies. Because only half of the studies included in our analyses had calculated lactose intake, we calculated lactose intake in the remaining studies. Specifically, the values of lactose from dairy products and foods containing dairy products (e.g., pizza) were based on the Nutrition Data System created by the University of Minnesota Nutrition Coordinating Center (53). A summary score was generated for lactose for each study in which the lactose content (per 100 g) for a given food item (e.g., milk, cheese, and pizza) was multiplied by the grams consumed of that item and then summed over all food items containing lactose. Among those studies that had previously calculated lactose intake [Canadian National Breast Screening Study, Iowa Women's Health Study, the Netherlands Cohort Study, New York State Cohort, Nurses' Health Study (NHSa and NHSb), Nurses' Health Study II, Swedish Mammography Cohort, and Women's Health Study], our calculated lactose intake from the Nutrition Data System was highly correlated with the lactose intake data provided by the original study investigators (median Pearson's correlation across studies = 0.99, minimum correlation across studies = 0.80). When analyzing lactose data, study-specific estimates were used, if available.

Use of multivitamins and single supplements, including calcium and vitamin D, was also ascertained in several studies. If available, total (supplemental and dietary) vitamin D and calcium intakes were calculated by summing the contributions of that nutrient from dietary, multivitamin, and single supplement sources. Because the Adventist Health Study and the New York State Cohort had not estimated the amount of calcium in multivitamins, we estimated the contribution of calcium for multivitamin users as 130 mg/d (the calcium value for generic multivitamins that was used in the Nurses' Health Study) to derive total calcium intake from foods and supplements. Studies have observed good correlations of calcium intake measured from a food frequency questionnaires and 24-hour recall or diet record, ranging from 0.46 to 0.72 (49, 50, 54-58).19

Information on nondietary factors was collected on the baseline self-administered questionnaires within each individual study. The majority of studies obtained information on other known and suspected risk factors for ovarian cancer, including several reproductive factors, body mass index (BMI), smoking status, and physical activity.

Outcome Assessment
Participants were followed from the date of the baseline questionnaire until date of diagnosis of ovarian cancer, date of death, date the participant moved out of the study area (if applicable), or end of follow-up, whichever came first. Invasive epithelial ovarian cancer was ascertained by self-report with subsequent medical record review (34, 44, 45), cancer registry linkage (33, 35, 39, 41, 42), or both (37, 38, 40, 59). Some studies also obtained incident outcome and mortality information from death registries (33, 34, 38, 40, 42, 44, 59, 60). Invasive epithelial ovarian cancer was defined by International Classification of Diseases-9 code 183.0 or International Classification of Diseases-10 code C56. Borderline and nonepithelial ovarian cancer cases were not included as cases. Histologic information was ascertained from the International Classification of Diseases for Oncology morphology codes (61) or the histologic information supplied by individual studies.

Statistical Analysis
Studies were excluded from the analysis of a particular dietary factor if they did not measure intake of that specific dietary exposure or if that item was not consumed in that population. Intakes of dietary antioxidant nutrients were analyzed using two different estimates, one crude nutrient estimate and one adjusted for energy intake by residual analysis. Dietary exposures were modeled continuously and categorically according to absolute cut points based on serving sizes and quantiles defined within each individual study. Relative risks (RR) and 95% confidence intervals (95% CI) were calculated by Cox proportional hazards models for each individual study, and the study-specific RRs were then pooled using a random-effects model (62). The model included stratification by age at baseline (in years) and the year the baseline questionnaire was returned and treated the follow-up time (in years) as the time scale, resulting in a time metric that simultaneously accounts for age, calendar time, and time since entry into the study. Multivariate RRs were adjusted for age at menarche (<13, 13, >13 years), menopausal status at baseline (premenopausal, postmenopausal, dubious), oral contraceptive use (ever, never), menopausal hormone therapy use among postmenopausal women (never, past, current), parity (0, 1, 2, >2), BMI (<23, 23 to <25, 25 to <30, ≥30 kg/m2), smoking status (never, past, current), physical activity (low, medium, high), and energy intake (continuously), with covariates defined identically across studies. A missing indicator variable was also generated within a study for each covariate, if needed. In general, data on age, education, BMI, smoking status, physical activity, multivitamin use, age at menarche, parity, menopausal status, oral contraceptive use, and postmenopausal hormone use was missing for <10% of each study population.

For each study, we corrected the RR for calcium and lactose for measurement error using the regression coefficients between dairy nutrient intake estimated by the food frequency questionnaires and by the reference methods that were either multiple diet records or 24-hour recalls (63, 64). We did not calculate measurement error-corrected RRs for vitamin D because intake of this nutrient was not calculated for the reference method in several studies.

SAS software (65) was used for the cohort analyses, and Epicure software (66) was used for case-cohort analyses of the Canadian National Breast Screening Study (39) and the Netherlands Cohort Study (41). Between-study heterogeneity was investigated using the Q test statistic (62). To test whether there was a linear trend in the risk of disease with increasing intake, a continuous variable with values corresponding to the median value for each exposure category was included in the model, and the coefficient for that variable was evaluated using the Wald test. If heterogeneity was present between studies, mixed-effects meta-regression analyses (67) were conducted to evaluate whether there was heterogeneity by follow-up time, number of questions for that particular food item, and age at diagnosis.

Stratified analyses were conducted by menopausal status at baseline (premenopausal, postmenopausal), parity (<1 live births, 1+ live births), oral contraceptive use (ever, never), hormone replacement therapy (ever, never), and study-specific median fat intake (high, low). For each factor of interest, a cross-product term of the ordinal score for the level of each factor and intake of a specific dairy food or nutrient expressed as a continuous variable was included in the model. Participants with missing values of the factor of interest were excluded from these analyses. Separate analyses were conducted for endometrioid, mucinous, and serous subtypes among those studies having >10 cases of the specific histologic subtype. We tested whether results differed across the subtypes using a contrast test (68).


   Results
Top
 Abstract
 Introduction
 Materials and Methods
 Results
Discussion
 References
 
Table 1 presents the study-specific characteristics and daily mean intakes of dairy foods and nutrients. Studies had a maximum follow-up time ranging from 7 years in the New York State Cohort to 22 years in the Nurses' Health Study. The Nurses Health Study II contributed the smallest number of invasive epithelial ovarian cancer cases with 52, whereas the Nurses' Health Study contributed the largest number with 435 cases. Daily mean dietary intakes for dairy foods and nutrients differed across studies, particularly for total calcium, lactose, hard cheese, and yogurt.

The median Pearson correlations for dairy foods and nutrients are shown in Table 2. Lactose intake was highly correlated with total milk (all study-specific correlations exceeded 0.59, median correlation = 0.83), dietary calcium (all correlations >0.69, median = 0.90), and, except for the Swedish Mammography Cohort (r = 0.36), dietary vitamin D (all other correlations >0.73, median = 0.83). Milk intake was also highly correlated with dietary calcium (median = 0.77) and dietary vitamin D (median = 0.71) intake. Weaker correlations were observed between lactose and cheese and yogurt intake.


View this table:
[in this window]
[in a new window]
  		Table 2. Median Pearson correlations for dairy products and nutrients across all studies included in the ovarian cancer analyses in the Pooling Project of Prospective Studies of Diet and Cancer

 
No statistically significant associations with ovarian cancer risk were present by categories of hard cheese, cottage cheese, yogurt, ice cream, and calcium intake (Table 3). No association between higher intake of milk and ovarian cancer risk (pooled multivariate RR, 1.11; 95% CI, 0.87-1.41 comparing 500 to 0 g/d) was observed. When we examined a larger contrast in intake, >750 g/d of milk, a nonstatistically significant higher risk of ovarian cancer was observed (pooled multivariate RR, 1.23; 95% CI, 0.79-1.92), although the number of cases within most studies was <10 (total case N = 58). Results from the multivariate-adjusted models were similar to those from age-adjusted models. A positive association was present for intakes >400 IU/d of dietary vitamin D and risk of ovarian cancer (pooled multivariate RR for 400 to <500 IU/d, 1.56; 95% CI, 1.17-2.08 and pooled multivariate RR for ≥500 IU/d, 1.37; 95% CI, 0.78-2.40) comparing with <100 IU/d. However, the association was not present for total (dietary and supplemental) vitamin D intake and ovarian cancer risk. A statistically significant higher risk of ovarian cancer was observed with higher intakes of lactose (pooled multivariate RR, 1.19; 95% CI, 1.01-1.40, Ptrend = 0.19) comparing ≥30 g/d (equivalent to ≥3 servings or 750 g milk/d) versus <10 g/d (equivalent to <1 serving or 250 g milk/d). Although the study-specific risk estimates for the ≥30 g/d category compared with the <10 g/d were all nonsignificant (Fig. 1), 8 of the 13 studies included in this analysis reported a higher risk of ovarian cancer with higher lactose intake (Pheterogeneity = 0.58).


View this table:
[in this window]
[in a new window]
  		Table 3. Pooled age and multivariate adjusted RRs and 95% CIs for ovarian cancer according to intake of dairy foods and nutrients

 

Figure 1
View larger version (14K):
[in this window]
[in a new window]
  		Figure 1. Multivariate adjusted RRs and 95% CI for ovarian cancer according to lactose intake (>30 compared with <10 g/d) by study. Multivariate RRs were adjusted for age at menarche (<13, 13, >13 years), menopausal status at baseline (premenopausal, postmenopausal, dubious), oral contraceptive use (ever, never), hormone replacement therapy use among postmenopausal women (never, past, current), parity (0, 1, 2, >2), BMI (<23, 23 to <25, 25 to <30, ≥30 kg/m2), smoking status (never, past, current), physical activity (low, medium, high), and energy intake (continuously), modeled identically across studies. Black squares and horizontal lines, study-specific RRs and 95% CIs for ≥30 g/d lactose intake compared with <10 g/d. The area of the black squares is proportional to the inverse of the sum of the between-study variance and the study-specific variance, which is related to the sample size, the total number of cases, and the range of variation in intake. Diamond, pooled multivariate RR and the 95% CI. Vertical dashed line, pooled multivariate RR.

 
In multivariate-adjusted continuous models, no association with dietary calcium and total calcium (includes intake from supplements) intake was observed with risk of ovarian cancer (Table 4). Higher intakes of lactose were associated with a nonstatistically significant higher risk of ovarian cancer (pooled multivariate RR for 10 g/d increment of lactose, 1.04; 95% CI, 0.99-1.08). Higher intake of dietary vitamin D was also associated with a higher risk of ovarian cancer (pooled multivariate RR for 100 IU/d increment of vitamin D, 1.06; 95% CI, 1.00-1.12), although, again, the association was not present for dietary and supplement vitamin D intake (Table 4). When conducting calcium and lactose continuous multivariate analyses with measurement error correction, we found that the associations between calcium (pooled multivariate RR for 350 mg/d increment of calcium, 1.09; 95% CI, 0.91-1.29) and lactose (pooled multivariate RR for 10 g/d increment of lactose, 1.09; 95% CI, 0.96-1.25) and ovarian cancer risk were similar to the results presented. Of the cases with histology information collected (94% of cases), ~13% were endometrioid, 7% were mucinous, and 48% of cases were serous. Only 5% of cases with histologic information were clear cell, whereas similar or even smaller percentages represented Brenner or transitional tumors, poorly differentiated tumors, carcinosarcomas, and mixed histology, so we were unable to analyze these groups. Generally, when examining serous, mucinous, endometrioid ovarian cancers separately, the results were similar to the overall findings (Table 4). A slightly higher risk of serous ovarian cancer was observed for higher intakes of low-fat milk and ice cream, whereas a positive association between total (dietary and supplemental) vitamin D intake and endometrioid ovarian cancer was seen. There was no statistically significant difference in the common effect between endometrioid, mucinous, and serous ovarian cancers for dairy nutrients and foods.


View this table:
[in this window]
[in a new window]
  		Table 4. Pooled multivariate adjusted RRs and 95% CIs for histologic subtypes of ovarian cancer according to dairy food and nutrient intake, continuous model

 
Similar estimates to the overall findings were observed when participants were stratified by age at diagnosis, parity, oral contraceptive use, hormone replacement therapy use, baseline menopausal status, and median fat intake (data not shown). Results were similar when using the crude nutrient estimate of dietary calcium, lactose, and vitamin D compared with the energy-adjusted nutrient models presented (data not shown). In addition, cases that occurred close in time to the completion of the food frequency questionnaires may represent individuals who altered their diet due to factors, such as prediagnostic disease symptoms. To assess this, sensitivity analyses, excluding cases diagnosed during the first year and second year of follow-up, were conducted to determine if the estimates were affected by including cases with an early diagnosis. Estimates from both models were comparable with the overall estimates (data not shown). Additionally, results were similar when we limited analyses to the first 6 years of follow-up compared with ≥6 years of follow-up (data not shown).


   Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
References
 
Higher intakes of milk and lactose are hypothesized to increase the risk of ovarian cancer. However, in this pooled analysis of 12 cohort studies that prospectively assessed the association between diet and ovarian cancer risk, no statistically significant associations were observed for milk or calcium intake. A weak, marginally significant positive association was observed for lactose and ovarian cancer risk, although lactose was highly correlated with milk and calcium intake within this pooled analysis (median r across studies >0.83 and 0.90, respectively). For the lactose analysis, we were able to analyze the amount of lactose found in the equivalent of three or more servings of milk (750 g) per day due to the contribution of lactose from other food sources. If lactose is truly a causal factor, the accurate assessment of lactose intake per se would reduce measurement error compared with the use of milk consumption as a surrogate of lactose intake because the latter ignores other dietary sources. Also, we cannot exclude the possibility that other correlated factors in dairy products, such as hormones, could be causal factors for ovarian cancer. For example, high milk consumption increases blood levels of insulin-like growth factor-I (69, 70), which has been associated with ovarian cancer (71, 72).

Similar to our results, some (17, 20, 25, 28), but not all (15, 21, 22, 24, 27), case-control studies of milk intake have reported no association with ovarian cancer risk. In contrast to our results showing a positive association between lactose intake and risk of ovarian cancer, many case-control studies examining lactose intake and ovarian cancer risk have found no association (8, 20, 22, 25, 29, 31, 32) or an inverse association (21, 27, 30). However, two case-control studies have found higher risk of ovarian cancer with lactose absorption (22) and metabolism (18).

Some (32, 36), although not all (21), case-control studies have shown a lower risk of ovarian cancer with higher intakes of dietary vitamin D. In our analysis, a nonsignificant higher risk of ovarian cancer was associated with higher intakes of dietary vitamin D, but not with higher total (dietary and supplemental) vitamin D intake. To better understand this inconsistency, we also examined other nondairy sources of dietary vitamin D (73-75), such as fish and cereal, and saw no association between intakes of these foods and ovarian cancer risk (data not shown). Because neither of these other food sources of vitamin D nor supplemental vitamin D was related to ovarian cancer, vitamin D is unlikely to be a causal factor.

Our analyses were conducted using baseline food frequency questionnaires that generally covered intakes during the year before the beginning of the follow-up period of each study. Thus, a limitation of our analyses is that we could not assess whether there was a change in intake during follow-up. Additionally, because we only measured intake during adulthood, we may not have captured the relevant exposure time for ovarian cancer risk. It may be that dietary factors during a different life period (i.e., adolescence) may be the biologically relevant exposure period (76).

Because diet was measured before diagnosis of ovarian cancer, reporting of dairy foods would not be expected to be systematically biased by disease status in these prospective studies, but general misclassification of dairy food intake was likely nondifferential misclassification, and such misclassification would have attenuated the RR estimates for the relation between intakes of dairy foods and nutrients and risk of ovarian cancer. When conducting calcium and lactose continuous multivariate analyses with measurement error correction, we found that the associations between calcium and lactose and ovarian cancer risk were similar to results presented.

In this study, not all cohorts were included in each dairy food and nutrient analysis because some items were not ascertained on the study food frequency questionnaire. The dietary assessment methods used differed across studies by number of questions and type of questions. For all analyses conducted, there was no between-study heterogeneity present. Thus, even with different questionnaires and populations, the individual studies estimated similar risks of ovarian cancer for each exposure.

Similarly, not all covariates were measured in each study. Within our models, we adjusted for most of the important ovarian cancer risk factors (e.g., age at menarche, oral contraceptive use, and parity) if they were measured in a study; results from age-adjusted and multivariate models were similar, suggesting that residual or unmeasured confounding would be small. A major advantage of pooling compared with a literature-based meta-analysis is the ability to characterize and control for covariates uniformly and classify the main exposures similarly. Furthermore, this prospective analysis was less susceptible to recall and selection biases and minimized the possibility of differential misclassification compared with case-control studies. Due to the inclusion of 12 cohort studies in North America and Europe, we had far greater statistical power than any of the individual cohort studies to examine specific histologic subtypes. Because the studies were conducted in a variety of populations with different dietary habits, we could examine associations over a wide range of dietary intakes.

In summary, we found no association between intakes of several specific dairy foods, dietary calcium, total calcium, and dietary and supplemental vitamin D and risk of ovarian cancer in this pooled analysis of 553,217 women. Our analysis suggests that high intakes of lactose, equivalent to three or more glasses (750 g) of milk per day, may weakly raise the risk of ovarian cancer. As this intake is similar to current U.S. dietary recommendations (77), the relation between dairy product consumption and ovarian cancer deserves further examination.


   Footnotes
 
Grant support: NIH grants CA098566 and CA55075.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Note: This study was done at Harvard School of Public Health, Boston, Massachusetts.

18 Smith-Warner SA, Spiegelman D, Ritz J, et al. Methods for retrospective pooling of results of studies: the Pooling Project of prospective studies of diet and cancer. Am J Epidemiol, in press. Back

19 A. Wolk, personal communication. Back

Received 8/ 3/05; revised 10/26/05; accepted 12/ 1/05.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results
 Discussion
 References
 

  1. Ferlay J, Bray F, Pisani P, Parkin DM. GLOBOCAN 2002: cancer incidence, mortality and prevalence worldwide. IARC CancerBase No. 5 version 2.0, IARC Press, Lyon, France, 2004.
  2. Goff BA, Mandel L, Muntz HG, Melancon CH. Ovarian carcinoma diagnosis. Cancer 2000;89:2068–75.[CrossRef][Medline]
  3. Cancer Facts & Figures 2004. Atlanta (Georgia): American Cancer Society; 2004.
  4. Vine MF, Ness RB, Calingaert B, Schildkraut JM, Berchuck A. Types and duration of symptoms prior to diagnosis of invasive or borderline ovarian tumor. Gynecol Oncol 2001;83:466–71.[Medline]
  5. Webb PM, Purdie DM, Grover S, Jordan S, Dick ML, Green AC. Symptoms and diagnosis of borderline, early and advanced epithelial ovarian cancer. Gynecol Oncol 2004;92:232–9.[CrossRef][Medline]
  6. Holschneider CH, Berek JS. Ovarian cancer: epidemiology, biology, and prognostic factors. Semin Surg Oncol 2000;19:3–10.[CrossRef][Medline]
  7. Delgado CL. Rising consumption of meat and milk in developing countries has created a new food revolution. J Nutr 2003;133:3907–10S.
  8. Cramer DW, Greenberg ER, Titus-Ernstoff L, et al. A case-control study of galactose consumption and metabolism in relation to ovarian cancer. Cancer Epidemiol Biomarkers Prev 2000;9:95–101.[Abstract/Free Full Text]
  9. Cramer DW, Welch WR. Determinants of ovarian cancer risk. II. Inferences regarding pathogenesis. J Natl Cancer Inst 1983;71:717–21.
  10. Swartz WJ, Mattison DR. Galactose inhibition of ovulation in mice. Fertil Steril 1988;49:522–6.[Medline]
  11. Kaufman F, Kogut M, Donnell G, Goebelsmann U, March C, Koch R. Hypergonadotropic hypogonadism in female patients with galactosemia. N Engl J Med 1981;304:994–8.[Abstract]
  12. Jiang F, Bao J, Li P, Nicosia SV, Bai W. Induction of ovarian cancer cell apoptosis by 1,25-dihydroxyvitamin D3 through the down-regulation of telomerase. J Biol Chem 2004;279:53213–21.[Abstract/Free Full Text]
  13. Guzey M, DeLuca HF. A group of deltanoids (vitamin D analogs) regulate cell growth and proliferation in small cell carcinoma cell lines. Res Commun Mol Pathol Pharmacol 1997;98:3–18.[Medline]
  14. McCarty MF. Parathyroid hormone may be a cancer promoter—an explanation for the decrease in cancer risk associated with ultraviolet light, calcium, and vitamin D. Med Hypotheses 2000;54:475–82.[CrossRef][Medline]
  15. Bertone ER, Hankinson SE, Newcomb PA, et al. A population-based case-control study of carotenoid and vitamin A intake and ovarian cancer (United States). Cancer Causes Control 2001;12:83–90.[CrossRef][Medline]
  16. Pan SY, Ugnat AM, Mao Y, Wen SW, Johnson KC. A case-control study of diet and the risk of ovarian cancer. Cancer Epidemiol Biomarkers Prev 2004;13:1521–7.[Abstract/Free Full Text]
  17. Bosetti C, Negri E, Franceschi S, et al. Diet and ovarian cancer risk: a case-control study in Italy. Int J Cancer 2001;93:911–5.[CrossRef][Medline]
  18. Cramer DW, Harlow BL, Willett WC, et al. Galactose consumption and metabolism in relation to the risk of ovarian cancer. Lancet 1989;2:66–71.[CrossRef][Medline]
  19. Cramer DW, Welch WR, Hutchison GB, Willett W, Scully RE. Dietary animal fat in relation to ovarian cancer risk. Obstet Gynecol 1984;63:833–8.[Abstract/Free Full Text]
  20. Engle A, Muscat JE, Harris RE. Nutritional risk factors and ovarian cancer. Nutr Cancer 1991;15:239–47.[Medline]
  21. Goodman MT, Wu AH, Tung KH, et al. Association of dairy products, lactose, and calcium with the risk of ovarian cancer. Am J Epidemiol 2002;156:148–57.[Abstract/Free Full Text]
  22. Meloni GF, Colombo C, La Vecchia C, et al. Lactose absorption in patients with ovarian cancer. Am J Epidemiol 1999;150:183–6.[Abstract/Free Full Text]
  23. Mettlin CJ, Piver MS. A case-control study of milk-drinking and ovarian cancer risk. Am J Epidemiol 1990;132:871–6.[Abstract/Free Full Text]
  24. Mori M, Harabuchi I, Miyake H, Casagrande JT, Henderson BE, Ross RK. Reproductive, genetic, and dietary risk factors for ovarian cancer. Am J Epidemiol 1988;128:771–7.[Abstract/Free Full Text]
  25. Risch HA, Jain M, Marrett LD, Howe GR. Dietary lactose intake, lactose intolerance, and the risk of epithelial ovarian cancer in southern Ontario (Canada). Cancer Causes Control 1994;5:540–8.[CrossRef][Medline]
  26. Webb PM, Bain CJ, Purdie DM, Harvey PW, Green A. Milk consumption, galactose metabolism and ovarian cancer (Australia). Cancer Causes Control 1998;9:637–44.[CrossRef][Medline]
  27. Yen ML, Yen BL, Bai CH, Lin RS. Risk factors for ovarian cancer in Taiwan: a case-control study in a low-incidence population. Gynecol Oncol 2003;89:318–24.[CrossRef][Medline]
  28. Zhang M, Yang ZY, Binns CW, Lee AH. Diet and ovarian cancer risk: a case-control study in China. Br J Cancer 2002;86:712–7.[Medline]
  29. Cramer DW. Lactase persistence and milk consumption as determinants of ovarian cancer risk. Am J Epidemiol 1989;130:904–10.[Abstract/Free Full Text]
  30. Harlow BL, Cramer DW, Geller J, Willett WC, Bell DA, Welch WR. The influence of lactose consumption on the association of oral contraceptive use and ovarian cancer risk. Am J Epidemiol 1991;134:445–53.[Abstract/Free Full Text]
  31. Herrinton LJ, Weiss NS, Beresford SA, et al. Lactose and galactose intake and metabolism in relation to the risk of epithelial ovarian cancer. Am J Epidemiol 1995;141:407–16.[Abstract/Free Full Text]
  32. Salazar-Martinez E, Lazcano-Ponce EC, Gonzalez Lira-Lira G, Escudero-De los Rios P, Hernandez-Avila M. Nutritional determinants of epithelial ovarian cancer risk: a case-control study in Mexico. Oncology 2002;63:151–7.[CrossRef][Medline]
  33. Kushi LH, Mink PJ, Folsom AR, et al. Prospective study of diet and ovarian cancer. Am J Epidemiol 1999;149:21–31.[Abstract/Free Full Text]
  34. Fairfield KM, Hunter DJ, Colditz GA, et al. A prospective study of dietary lactose and ovarian cancer. Int J Cancer 2004;110:271–7.[CrossRef][Medline]
  35. Larsson SC, Bergkvist L, Wolk A. Milk and lactose intakes and ovarian cancer risk in the Swedish Mammography Cohort. Am J Clin Nutr 2004;80:1353–7.[Abstract/Free Full Text]
  36. Bidoli E, La Vecchia C, Talamini R, et al. Micronutrients and ovarian cancer: a case-control study in Italy. Ann Oncol 2001;12:1589–93.[Abstract/Free Full Text]
  37. Beeson WL, Mills PK, Phillips RL, Andress M, Fraser GE. Chronic disease among Seventh-Day Adventists, a low-risk group. Rationale, methodology, and description of the population. Cancer 1989;64:570–81.[CrossRef][Medline]
  38. Lacey JV, Jr., Mink PJ, Lubin JH, et al. Menopausal hormone replacement therapy and risk of ovarian cancer. JAMA 2002;288:334–41.[Abstract/Free Full Text]
  39. Terry PD, Miller AB, Jones JG, Rohan TE. Cigarette smoking and the risk of invasive epithelial ovarian cancer in a prospective cohort study. Eur J Cancer 2003;39:1157–64.
  40. Rodriguez C, Calle EE, Fakhrabadi-Shokoohi D, Jacobs EJ, Thun MJ. Body mass index, height, and the risk of ovarian cancer mortality in a prospective cohort of postmenopausal women. Cancer Epidemiol Biomarkers Prev 2002;11:822–8.[Abstract/Free Full Text]
  41. Schouten LJ, Zeegers MP, Goldbohm RA, van den Brandt PA. Alcohol and ovarian cancer risk: results from the Netherlands Cohort Study. Cancer Causes Control 2004;15:201–9.[Medline]
  42. Bandera EV, Freudenheim JL, Marshall JR, et al. Diet and alcohol consumption and lung cancer risk in the New York State Cohort (United States). Cancer Causes Control 1997;8:828–40.[CrossRef][Medline]
  43. Lukanova A, Lundin E, Micheli A, et al. Risk of ovarian cancer in relation to prediagnostic levels of C-peptide, insulin-like growth factor binding proteins-1 and -2 (USA, Sweden, Italy). Cancer Causes Control 2003;14:285–92.[Medline]
  44. Rockhill B, Willett WC, Hunter DJ, et al. Physical activity and breast cancer risk in a cohort of young women. J Natl Cancer Inst 1998;90:1155–60.[Abstract/Free Full Text]
  45. Lin J, Zhang SM, Cook NR, Lee IM, Buring JE. Dietary fat and fatty acids and risk of colorectal cancer in women. Am J Epidemiol 2004;160:1011–22.[Abstract/Free Full Text]
  46. Serov S, Scully R. International Histological Classification of Tumours, no. 9: histological typing of ovarian tumours. Geneva (Switzerland): WHO; 1973.
  47. Kurian AW, Balise RR, McGuire V, Whittemore AS. Histologic types of epithelial ovarian cancer: have they different risk factors? Gynecol Oncol 2005;96:520–30.[CrossRef][Medline]
  48. Rothman K. Modern epidemiology. Boston: Little Brown and Company; 1986.
  49. Flagg EW, Coates RJ, Calle EE, Potischman N, Thun MJ. Validation of the American Cancer Society Cancer Prevention Study II Nutrition Survey Cohort Food Frequency Questionnaire. Epidemiology 2000;11:462–8.[CrossRef][Medline]
  50. Goldbohm RA, van den Brandt PA, Brants HA, et al. Validation of a dietary questionnaire used in a large-scale prospective cohort study on diet and cancer. Eur J Clin Nutr 1994;48:253–65.[Medline]
  51. Salvini S, Hunter DJ, Sampson L, et al. Food-based validation of a dietary questionnaire: the effects of week-to-week variation in food consumption. Int J Epidemiol 1989;18:858–67.[Abstract/Free Full Text]
  52. Willett W. Nutritional epidemiology. New York: Oxford University Press; 1998.
  53. Nutrition Data System-R. Minneapolis (Minnesota): Nutrition Coordinating Center, Division of Epidemiology, University of Minnesota.
  54. Jain MG, Rohan TE, Soskolne CL, Kreiger N. Calibration of the dietary questionnaire for the Canadian Study of Diet, Lifestyle and Health cohort. Public Health Nutr 2003;6:79–86.[CrossRef][Medline]
  55. Feskanich D, Marshall J, Rimm EB, Litin LB, Willett WC. Simulated validation of a brief food frequency questionnaire. Ann Epidemiol 1994;4:181–7.[Medline]
  56. Munger RG, Folsom AR, Kushi LH, Kaye SA, Sellers TA. Dietary assessment of older Iowa women with a food frequency questionnaire: nutrient intake, reproducibility, and comparison with 24-hour dietary recall interviews. Am J Epidemiol 1992;136:192–200.[Abstract/Free Full Text]
  57. Jain M, Howe GR, Rohan T. Dietary assessment in epidemiology: comparison on food frequency and a diet history questionnaire with a 7-day food record. Am J Epidemiol 1996;143:953–60.[Abstract/Free Full Text]
  58. Johansson I, Hallmans G, Wikman A, Biessy C, Riboli E, Kaaks R. Validation and calibration of food-frequency questionnaire measurements in the Northern Sweden Health and Disease cohort. Public Health Nutr 2002;5:487–96.[CrossRef][Medline]
  59. Zeleniuch-Jacquotte A, Gu Y, Shore R, et al. Postmenopausal levels of sex hormones and risk of breast carcinoma in situ: results of a prospective study. Int J Cancer 2005;114:323–7.[Medline]
  60. Lin J, Zhang SM, Cook NR, Rexrode KM, Lee IM, Buring JE. Body mass index and risk of colorectal cancer in women (United States). Cancer Causes Control 2004;15:581–9.[CrossRef][Medline]
  61. Percy C, Van Holten V, Muir C. International Classification of Diseases for Oncology. Geneva (Switzerland): WHO; 1990.
  62. DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials 1986;7:177–88.[CrossRef][Medline]
  63. Rosner B, Spiegelman D, Willett WC. Correction of logistic regression relative risk estimates and confidence intervals for measurement error: the case of multiple covariates measured with error. Am J Epidemiol 1990;132:734–45.[Abstract/Free Full Text]
  64. Rosner B, Willett WC, Spiegelman D. Correction of logistic regression relative risk estimates and confidence intervals for systematic within-person measurement error. Stat Med 1989;8:1051–69.[Medline]
  65. SAS/STAT software: the PHREG procedure. Preliminary documentation. Cary (North Carolina): SAS Institute.
  66. EPICURE user's guide: the PEANUTS program. Seattle (Washington): Hirosoft; 1993.
  67. Stram DO. Meta-analysis of published data using a linear mixed-effects model. Biometrics 1996;52:536–44.[CrossRef][Medline]
  68. Anderson T. Introduction to multivariate statistics. New York: John Wiley Sons; 1984.
  69. Giovannucci E, Pollak M, Liu Y, et al. Nutritional predictors of insulin-like growth factor I and their relationships to cancer in men. Cancer Epidemiol Biomarkers Prev 2003;12:84–9.[Abstract/Free Full Text]
  70. Holmes MD, Pollak MN, Willett WC, Hankinson SE. Dietary correlates of plasma insulin-like growth factor I and insulin-like growth factor binding protein 3 concentrations. Cancer Epidemiol Biomarkers Prev 2002;11:852–61.[Abstract/Free Full Text]
  71. Dal Maso L, Augustin LS, Franceschi S, et al. Association between components of the insulin-like growth factor system and epithelial ovarian cancer risk. Oncology 2004;67:225–30.[CrossRef][Medline]
  72. Lukanova A, Lundin E, Toniolo P, et al. Circulating levels of insulin-like growth factor-I and risk of ovarian cancer. Int J Cancer 2002;101:549–54.[CrossRef][Medline]
  73. Calvo MS, Whiting SJ, Barton CN. Vitamin D fortification in the United States and Canada: current status and data needs. Am J Clin Nutr 2004;80:1710–6S.
  74. Groff JL, Gropper SS. Advanced Nutrition and Human Metabolism. Belmont (California): Wadsworth; 2000.
  75. Holick MF. Sunlight and vitamin D for bone health and prevention of autoimmune diseases, cancers, and cardiovascular disease. Am J Clin Nutr 2004;80:1678–88S.
  76. Persson I. Estrogens in the causation of breast, endometrial and ovarian cancers—evidence and hypotheses from epidemiological findings. J Steroid Biochem Mol Biol 2000;74:357–64.[CrossRef][Medline]
  77. Dietary Guidelines for Americans 2005. Washington (District of Columbia): U.S. Department of Health and Human Services and the Department of Agriculture; 2005.



This article has been cited by other articles:


Home page
 Int J EpidemiolHome page
D. Spiegelman
Commentary: Calculations of EPIC proportions
Int. J. Epidemiol., April 1, 2008; 37(2): 379 - 381.
[Full Text] [PDF]

Home page
 Cancer Epidemiol. Biomarkers Prev.Home page
G. Lurie, L. R. Wilkens, P. J. Thompson, K. E. McDuffie, M. E. Carney, K. Y. Terada, and M. T. Goodman
Vitamin D Receptor Gene Polymorphisms and Epithelial Ovarian Cancer Risk
Cancer Epidemiol. Biomarkers Prev., December 1, 2007; 16(12): 2566 - 2571.
[Abstract] [Full Text] [PDF]

Home page
 JPEN J Parenter Enteral NutrHome page
S. Bengmark
Advanced Glycation and Lipoxidation End Products-Amplifiers of Inflammation: The Role of Food
JPEN J Parenter Enteral Nutr, September 1, 2007; 31(5): 430 - 440.
[Abstract] [Full Text] [PDF]

Home page
 Cancer Epidemiol. Biomarkers Prev.Home page
S. S. Tworoger, I-M. Lee, J. E. Buring, B. Rosner, B. W. Hollis, and S. E. Hankinson
Plasma 25-Hydroxyvitamin D and 1,25-Dihydroxyvitamin D and Risk of Incident Ovarian Cancer
Cancer Epidemiol. Biomarkers Prev., April 1, 2007; 16(4): 783 - 788.
[Abstract] [Full Text] [PDF]

Home page
 Am J EpidemiolHome page
E. T. Chang, V. S. Lee, A. J. Canchola, C. A. Clarke, D. M. Purdie, P. Reynolds, H. Anton-Culver, L. Bernstein, D. Deapen, D. Peel, et al.
Diet and Risk of Ovarian Cancer in the California Teachers Study Cohort
Am. J. Epidemiol., April 1, 2007; 165(7): 802 - 813.
[Abstract] [Full Text] [PDF]

Home page
 CA Cancer J ClinHome page
L. H. Kushi, T. Byers, C. Doyle, E. V. Bandera, M. McCullough, T. Gansler, K. S. Andrews, M. J. Thun, and The American Cancer Society 2006 Nutrition and Phy
American Cancer Society Guidelines on Nutrition and Physical Activity for Cancer Prevention: Reducing the Risk of Cancer With Healthy Food Choices and Physical Activity
CA Cancer J Clin, September 1, 2006; 56(5): 254 - 281.
[Abstract] [Full Text] [PDF]

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Genkinger, J. M.
Right arrow Articles by Smith-Warner, S. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Genkinger, J. M.
Right arrow Articles by Smith-Warner, S. A.

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research