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duminică, 11 decembrie 2011

Potential Breast Cancer Prevention Agent Found To Lower Levels Of 'Good' Cholesterol Over Time

Main Category: Breast Cancer
Also Included In: Cholesterol
Article Date: 10 Dec 2011 - 0:00 PST

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Exemestane steadily lowered levels of "good" cholesterol in women taking the agent as part of a breast cancer prevention study, say researchers at Georgetown Lombardi Comprehensive Cancer Center. Exemestane, an aromatase inhibitor used to treat estrogen receptor-positive breast cancer, is being tested to prevent breast cancer in women at an increased risk of developing the disease.

Georgetown researchers say their findings, presented at the 2011 CTRC-AACR San Antonio Breast Cancer Symposium (SABCS), suggest that the effect this agent has on blood lipids may prove to be significant for women at high risk for heart disease due to elevated blood cholesterol, although no such effects have been seen yet in patients studied over two years of treatment.

There are two types of cholesterol transported in our blood - HDL and LDL. HDL cholesterol is known as "good" cholesterol, because high levels of it protect against heart attack. LDL cholesterol is known as "bad" cholesterol because it can buildup in the inner walls of the arteries that feed the heart and brain, and lead to atherosclerosis.

"Lower levels of the HDL, the good cholesterol, have been shown to increase the risk of heart attack and stroke. While we found that exemestane lowers good cholesterol levels, the clinical significance of this decrease is unknown," says a study investigator, Margaret Gatti-Mays, M.D. an intern in internal medicine at Georgetown.

The results come from a phase II multi-institutional study of women at increased risk for breast cancer that evaluated the safety and efficacy of exemestane over two years of therapy. The findings, from 31 patients, showed that the absolute change from the baseline HDL level at 3, 12, and 24 months were -8.0 mg/dL, -8.5 mg/dL, and -9.9 mg/dL, respectively. The rest of the lipid panel, including LDL (the bad cholesterol) was relatively unchanged.

"It is notable that both women taking and not taking lipid-lowering medication had decreases in HDL," Gatti-Mays says.

"Lower HDL levels are associated with an increased risk of heart disease, so if a patient has a low HDL level, exemestane may not be the best choice as a breast cancer prevention agent," says the study's senior investigator, Jennifer Eng-Wong, M.D., senior medical director of the Capital Breast Care Center at Georgetown Lombardi Comprehensive Cancer Center.

She adds that other anti-estrogen therapies designed to prevent breast cancer don't appear to lower HDL. "Less data is available on anastrozole and letrozole, which are other aromatase inhibitors, but they do not appear to lower HDL. Conversely, tamoxifen has an overall favorable effect on cholesterol."

"Exemestane has been shown to be an effective therapy in the prevention of breast cancer in postmenopausal women who have an increased risk of developing it. This study adds information that will help individualize care for these women though larger studies are needed to more fully evaluate the impact of exemestane on cholesterol and cardiovascular health," says Gatti-Mays.

The research was conducted at Georgetown and the National Cancer Institute (NCI), and was supported by both institutions, as well as the National Institutes of Health, and Pfizer Inc. (which supplied exemestane). (OVER)

A recipient of the ACCR Scholar-in-Training Award, Gatti-Mays' travel to the SABCS conference was funded by this award which is supported by Susan G. Komen for the Cure. She reports no personal financial interests related to the study.

The 2011 CTRC-AACR San Antonio Breast Cancer Symposium is presented by the Cancer Therapy & Research Center at UT Health Science Center San Antonio, the American Association for Cancer Research, and Baylor College of Medicine.

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Breast Cancer Prevention - Part Time Low Carb Diet Better Than Standard Full Time Diets

Breast Cancer Prevention - Part Time Low Carb Diet Better Than Standard Full Time Diets@import "/css/pagelayout.css";@import "/css/default.css";@import "/css/defaultnews.css";Medical News Today Follow us on FacebookFollow us on TwitterOur RSS feedsYour MNT
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Main Category: Breast Cancer
Also Included In: Nutrition / Diet;  Diabetes
Article Date: 10 Dec 2011 - 10:00 PST

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Current Article Ratings:
Patient / Public:4 stars4 (16 votes)

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Article Opinions: 2 posts
Women who go on a low carb diet just two days per week have a lower risk of developing breast cancer compared to those who follow a standard calorie-restricted diet every day of the week, in order to lose weight and lower their insulin blood levels. Long-term high blood insulin levels are known to raise cancer risk. These findings were presented by scientists from Genesis Prevention Center at University Hospital in South Manchester, England, at the 2011 CTRC-AACR San Antonio Breast Cancer Symposium.

The researchers stressed that a larger, longer-term additional study is required.

Michelle Harvie, Ph.D., SRD, a research dietician at the Genesis Prevention Center, who presented the study said:

"Weight loss and reduced insulin levels are required for breast cancer prevention, but [these levels] are difficult to achieve and maintain with conventional dietary approaches."


Harvie and her team set out to compare three different 4-month-long diets to assess the effects on weight loss and blood markers of breast cancer risk in 115 women who had a family history of breast cancer. The researchers randomly assigned patients into three groups:The low cal/carb group - they followed a calorie-restricted, low-carbohydrate dietThe part-time low-carb group - they followed an "ad lib" low-carbohydrate diet whereby patients were allowed to consume unlimited proteins and healthy fats, like lean meats, olives and nuts for 2 days per weekThe Mediterranean diet group - a standard, calorie-restricted daily Mediterranean diet for seven days per weekBoth low-carb diets were found to be more effective than the Mediterranean diet in achieving weight loss, reducing body fat, and lowering insulin resistance.Weight loss - in the two low-carb groups the participants lost an average of 4kg (approx. 9 pounds) compared to 2.4kg (approx 5 pounds) in the Mediterranean diet group.Insulin resistance - this went down 22% in the low cal/carb group, 14% in the part-time low-carb group, and 4% in the Mediterranean diet group.Harvie said:


"It is interesting that the diet that only restricts carbohydrates but allows protein and fats is as effective as the calorie-restricted, low-carbohydrate diet."


Harvie and her team are planning on studying carbohydrate intake and breast cancer.

Written by Petra Rattue
Copyright: Medical News Today
Not to be reproduced without permission of Medical News Today

Additional References Citations Visit our breast cancer section for the latest news on this subject. "The Intermittent Diet" Please use one of the following formats to cite this article in your essay, paper or report:

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Petra Rattue. (2011, December 10). "Breast Cancer Prevention - Part Time Low Carb Diet Better Than Standard Full Time Diets." Medical News Today. Retrieved from
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Visitor Opinions In Chronological Order (2)"Calorie Restricted" low carb diet? What?posted by Bob Bramel on 10 Dec 2011 at 3:56 pm

I think it is well past time for diet researchers to adopt some standards for defining a diet. "Calorie restricted low carb" is as ambiguous as "Mediterranean". Since fuel only comes in three forms, carbs, protein and fat, how about specifying "XX calories, YY gram carb, ZZ gram fat, and AA protein". I know it isn't as glamorous as (trumpet fanfare, please) "Mediterranean" or "South Park", but come on, let's at least try to be a little scientific.
As for the selected diet protocols, where is the diet so many of us use. Every day eat as little (for precision, less than XX grams) of carbs as possible and don't worry about calories or fat.
It doesn't pass the sniff test (i.e., it doesn't make any sense) that a two-day per week eating protocol works better than a seven day per week protocol. I'm guessing that the first, calorie restricted, low carb diet was more calorie restriction and only somewhat carb restricted. Folks, cutting carbs from 90% to 50% doesn't help a lot. Carbs gotta go! (40 pounds lost in 18 months over six years ago and keeping it off takes no effort at all, just stay away from carbs)

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Alright alreadyposted by Susan on 10 Dec 2011 at 6:03 pm

Blah, blah, blah. Every day a new study on what does or does not cause/prevent/treat/cure breast cancer. Obviously, to many breast-cancer grants being given out and too many budding PhD candidates in the field. Eventually, if you tried to follow every theory that's been thrown out there, you'd end up bumping into yourself running over yourself or chasing you own tail.
Give a gal a break, please.

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joi, 8 decembrie 2011

How To Better Predict Success In HIV Prevention Clinical Trials

Main Category: HIV / AIDS
Also Included In: Preventive Medicine;  Clinical Trials / Drug Trials
Article Date: 08 Dec 2011 - 3:00 PST

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New research from the University of North Carolina at Chapel Hill schools of medicine and pharmacy may help explain the failure of some recent clinical trials of prevention of HIV infection, compared to the success of others that used the same drugs.

The study published online December 7, 2011 in the journal Science Translational Medicine, also suggests how to improve the chances for success, even before the research begins. These suggestions are reinforced in an editorial by several of the UNC authors writing in The Lancet, also published online December 7, 2011.

Over the past two years, results from several clinical trials involving pre-exposure prophylaxis (PrEP) for HIV infection have been a mixed bag of successful prevention and futility. Reports described varying degrees of successful HIV infection prevention in four trials and failure in two others. In all the PrEP trials, the drugs used were tenofovir (TFV) and emtricitabine (FTC) in daily oral and/or gel combinations.

These drugs have been shown to be protective against HIV infection in animal PrEP studies and are now being used clinically, and tenofovir is considered the backbone of HIV therapy, both used orally and topically.

The new UNC study looked at drug concentrations in the mucus membrane tissues that are most susceptible to HIV infection: the tissue lining the vagina, cervix and rectum.

The study was led by Angela D.M. Kashuba, PharmD, professor in the UNC Eshelman School of Pharmacy and director of the UNC Center for AIDS Research Clinical Pharmacology and Analytic Chemistry Core. She also is a member of the UNC Institute for Global Health & Infectious Diseases.

"We did this study to understand how much drug got into these tissues and how long they lasted over two weeks," Kashuba said. And after giving normal, healthy volunteers a single pill combination of TFV/FTC, "What we found over the next 14 days was somewhat surprising. When a person takes a drug, it doesn't end up in the same concentration in different tissues."

Indeed, concentrations of tenofovir were 100 times higher in rectal tissue than in vaginal or cervical tissue. "And FTC achieved concentrations 10 to 15 times higher in vaginal and cervical tissue than they were in rectal tissue," Kashuba said.

"And this raised some questions: because of these discrepancies can the two drugs be used equally well in both populations women at risk for HIV infection and men at risk for HIV infection? And are the concentrations achieved even after a single dose high enough to prevent HIV infections?"

According to Kashuba, it's clear from the recent clinical studies that drug concentration in tissue may make a difference in effectiveness. For example, in one of the placebo-controlled PrEP clinical trials involving men who have sex with men, the combination of these drugs provided about 44 percent effectiveness overall.

But the half the men given the active form of the drugs had no detectable drug in their system when they were sampled during the study and, therefore, were not taking it consistently every day. Thus, the high tenofovir concentrations in rectal tissue could explain the relatively high efficacy of 44 percent.

Results of a PrEP clinical trial (VOICE) conducted in heterosexual women in Uganda, South Africa and Zimbabwe, also paralleled the UNC findings. The daily tenofovir arm was stopped because no protection was seen for the drug taken daily. "If these women did not take the drug every single day, we think our study supports the fact there would not be good efficacy because tenofovir drug concentrations in the vagina and cervix are so much lower than what we see in rectal tissue, Kashuba said."

The authors of the study and the editorial say adherence to taking the drug as prescribed is crucial. They lament that the only prospective means of measuring adherence now available is what the patient reports. "And so if you ask someone did you take all your doses, most will say yes," Kashuba said "People want to be considered good study participants, and sometimes they just can't remember how many doses they took last week, or in the last month, be it almost all of the doses or half of them."

The UNC researcher points to lessons learned: "Before delving into a clinical trial, we need to keep in mind that when someone takes a pill, you can't assume that the drug gets in all places at the same amount. And before we can select the drugs and the right doses for a clinical trial, we need to know what concentrations in tissue prevent HIV infection. They could be different."

And along with the above, the authors emphasize the need to develop ways to objectively measure drug-taking behavior in clinical studies so that the research can be designed and interpreted correctly.

The study was funded in part from the National Institutes of Health, the UNC Center for AIDS Research, the UNC TraCS Clinical Translational Research Center, and the Gilead Sciences Investigator Initiated Research Program.

Article adapted by Medical News Today from original press release. Source: University of North Carolina
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