Probiotics and Breast Health

Titre officiel

Re-setting the Breast Microbiome to Lower Inflammation and Risk of Cancer.

Sommaire:

Le cancer du sein demeure une importante cause de décès chez les femmes et, malgré les avancées importantes réalisées dans le domaine de soins, le rôle des « facteurs environnementaux » dans la maladie demeure encore mal compris. Les chercheurs ont démontré que les bactéries présentes dans les tissus mammaires figurent parmi ces facteurs. Ces bactéries ne causent pas d’infections proprement dites, mais elles peuvent produire de faibles quantités de substances connues pour causer le cancer. Les chercheurs ont ainsi découvert que les bactéries présentes dans les seins de femmes atteintes de cancer sont très différentes de celles présentes dans le tissu mammaire des femmes en bonne santé. Les chercheurs aimeraient vérifier leur théorie selon laquelle la prise de lactobacilles probiotiques par voie orale pourrait permettre la progression de ces probiotiques dans le tissu mammaire et aider à déloger les bactéries nocives et à réduire l’inflammation qui est étroitement liée au cancer.

Description de l'essai

Primary Outcome:

  • Change in breast microbiota
Secondary Outcome:
  • Testing of inflammatory markers and pollutants
  • Testing for environmental pollutants - heavy metals.
  • Testing for environmental pollutants - pesticides.
Certain bacteria, particularly Gram negatives, are major causes of inflammation. In fact, the lipopolysaccharides from these bacteria are used in vast numbers of studies to induce inflammation and study disease. Many cancers are the result of inflammatory processes. Breast cancer is a major cause of illness and death in women and inflammatory processes are one of the foci of investigation; however, not yet from the stand point that bacteria in the breast may be the instigators of cancer development. The investigators were the first in the world to describe the breast microbiota and show that the bacterial profiles are more pathogenic in women with cancer than in tissues of healthy controls. This work has been validated by others. Although this does not prove a cause-and-effect link with breast cancer, such linkages have been shown in stomach and colon cancers. If researchers assume there is a link, then how can the inflammatory microbiota be re-set to one that is somehow beneficial and able to reduce inflammation and potential cancer induction? The concept of probiotics emerged from the quest to reset the disrupted microbiota of the gut and upper respiratory tract. This investigational group has led the world in doing the same in the urogenital tract of women. The researchers would like to test their theory that taking probiotic lactobacilli by mouth can lead to these organisms reaching the breast tissue and helping displace the harmful bacteria and reducing inflammation. A study in Spain has shown that oral intake of probiotic lactobacilli can not only cure mastitis, but lead to the lactobacilli reaching the milk glands. Women who breast feed for more than six months (and thereby pass along lactic acid bacteria to the infant from the breast milk) have a reduced risk of breast cancer. The investigators hypothesize that the breast microbiome of women at risk of cancer has the same profile as women with cancer and that oral administration of probiotic lactobacilli can reset this to one found in healthy women. They also hypothesize the breast tissue of these at-risk patients is contaminated by environmental toxins. The project plan is to test the concept of re-setting the breast tissue microbiota in women at risk of cancer, to one more aligned with health. Samples will be tested for relative bacterial abundance to determine any shift in bacterial breast tissue composition by next-generation sequencing and bioinformatics. Samples will also be tested for inflammatory markers using Luminex technology, and for mercury, arsenic and pesticides using LC-MS as described in previous studies. Twenty women at high-risk for breast cancer (See Inclusion Criteria) will be randomized (10 each) to receive either probiotic or placebo, once a day for 90 days. This capsule is approved in Canada and widely available and contains 2.5 billion CFU viable bacterial cells of each of the following strains: Lactobacillus rhamnosus GR-1 and Lactobacillus reuteri RC-14. Both active capsules and placebo will be provided by the manufacturer Chr Hansen (Denmark). Samples will be collected at t=0 (enrollment), t=1 (end of 90 days) and t=2(30 days post-treatment). Twenty women will act as healthy controls (See Inclusion Criteria) and will be randomized (10 each) as described above for the high-risk group. At each time point, samples collected will include:
  • Breast skin swab
  • a cotton tipped swab with be moistened with sterile water and the passed over the skin on the breast 10 times.
  • Needle aspirate
  • a 22-gauge needle into the breast tissue with repeated passage under suction until aspirate material is identified in the needle hub. This material would then be placed in normal saline.
  • Nipple aspirate
  • the participant will be asked to massage their breast from chest wall to nipple for several minutes as needed. Using a hand-held modified breast pump placed over the nipple, nipple aspirate fluid will be drawn out and into a capillary tube.
  • Blood draw
  • one 6mL EDTA plasma tube using standard phlebotomy procedures. Samples will be analyzed for relative bacterial abundance (next-generation sequencing), inflammatory markers (Luminex technology).
  • Urine
  • 100mL sample that will be tested for heavy metals and pesticides using LC-MS.

Voir cet essai sur ClinicalTrials.gov

Intéressé(e) par cet essai?

Imprimez cette page et apportez-la chez votre médecin pour discuter de votre admissibilité à cet essai et des options de traitement. Seul votre médecin peut vous recommander pour un essai clinique.

Ressources

Société canadienne du cancer

Ces ressources sont fournies en partenariat avec Société canadienne du cancer