Friday, October 29, 2021

Trial Drug Reduces Recurrence of Genetic Breast Cancer in Women, New Study Shows

A trial drug was found to slow down and reduce the recurrence of genetic breast cancer in women with an early but aggressive form of the disease, a major study shows. 

The BRCA1 and BRCA2 genes in women offer protection from getting certain cancers. But abnormal mutations in the gene, if inherited, increase an individual’s risk of breast and other cancers. BRCA1 and BRCA2 gene mutations account for about 10% of all breast cancer cases globally. In India, this number is higher, and a lack of awareness about the disease leads to a higher death toll from t

he disease.

“Women with early-stage breast cancer who have inherited BRCA1 or BRCA2 mutations are typically diagnosed at a younger age,” said Andrew Tutt, the lead author of the study, from the Institute of Cancer Research, London. For most, the risk of relapse persists.

Experts point out the “breakthrough” potential of the study published in the New England Journal of Medicine. Where there were previously no options to prevent recurrence of cancer in patients with these mutations, the drug reportedly increases the recovery and survival rate among women. Notably, the researchers conducting the study stopped the trial period early — in 2.5 years, as opposed to the initial 10 years — in light of the drug’s benefits. They also noted the advancement in cancer treatment by targeting genetic sources.

The drug, named olaparib, was administered to 1,836 women during their post-treatment period — that is, after they had received rounds of chemotherapy or surgery. The aim was to determine the efficacy of the drug in preventing recurrence of cancer. During the trial, researchers found that the chances of recurrence of both invasive (cancer which spreads to the surrounding breast tissue) and distant (cancer which spreads to other parts of the body) types of disease were lower for those who took the drug, as compared to those who did not. After three years, 86% of those treated with the drug were free of invasive breast cancer, compared with 77% given placebo pills.

The drug significantly decreased the relative risk of recurrence, second cancers, or death by 40%. These numbers are “clinically meaningful and practice changing,” Sayeh Lavasani, an assistant clinical professor at City of Hope’s Department of Medical Oncology & Therapeutics Research, who wasn’t involved in the trial, told Biopharma Dive. 

The findings are also important in the context of ramping up genetic testing among women. It is possible to test for the BRCA1 and BRCA2 mutations early on, depending on certain risk factors among women. For early detection of hereditary breast cancer, especially in young women with a history of mutations, screenings can begin at the age of 25. Given that breast cancer in young women is aggressive and that this demographic is more likely to have the BRCA mutation, better awareness about breast cancer is recommended as a means of controlling the cancer in young women. By increasing breast MRIs, “cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation could be reduced,” concluded one study. 

Among women, breast cancer is the second-leading cause of cancer-related death — and scientists say better early cancer detection makes a big difference. 

The research on the drug was collaboratively conducted by the Breast International Group along with various global organizations. The drug’s clinical trial was funded by AstraZeneca outside the United States and by NRG Oncology in the United States.

“Up to now, there has been no treatment that specifically targets the unique biology of these cancers to reduce the rate of recurrence, beyond initial treatment such as surgery, hormone treatment, radiotherapy and chemotherapy,” Tutt added.

The trial did not observe adverse or unexpected side effects outside the known side effects associated with olaparib.

More research is, however, needed to study the recovery of patients taking the drug. There is also no comparative study yet between this drug and chemotherapy in the long run. Further, the drug is part of a range of pharmaceutical offerings that are on the higher side cost-wise — making affordability and access a challenge.

For now, the drug offers a promising outcome. “Finishing active hospital treatment can be an incredibly difficult time, with many women calling our helpline to share their anxiety and fears of their breast cancer coming back,” said Dr. Simon Vincent, director of Breast Cancer Now, who took part in the study. “Finding effective new ways to prevent recurrence is vitally important.”

 

This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   

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Sunday, December 01, 2019

Six health conditions you can inherit from your mother


Genetics have a huge role to play in our health and well-being. As per the research from the Institute of Cancer Research at the University of London, there are 57 per cent chances that a girl will start menstruating within three months of the date when her mother first began to menstruate. So, yes genes do play a role.

Here are six health conditions that you can inherit from mother.
​Heart disease
If your mother had a heart attack, your chances of getting it increases by 20 per cent. A study from Oxford University showed that your chances of getting a stroke also increase if your mother has suffered one. This happens because the inherited vascular disease affects the coronary artery in the heart as well as the cerebral artery in the brain.

​Breast cancer
Women carrying mutated gene BRCA1 or BRCA2 are more at risk of developing breast cancer. Most women who have this defective gene develop breast cancer at an early age.

It’s extremely important for women to get mammograms after the age of 40. If any of your relatives have breast cancer, you should get genetically screened. Women who have a family history of breast cancer get prophylactic mastectomies to reduce their chances of developing cancer.

​Alzheimer’s
The Alzheimer Society has found that the Alzheimer gene can be passed on. If your mother is suffering or has suffered from Alzheimer, your chances of getting dementia increase by 30 – 50 per cent.

Keeping a check on your weight, getting your blood pressure and cholesterol monitored regularly and leading an overall healthy lifestyle can help reduce your risk of developing dementia by almost 20 per cent.

​Depression
Mental illnesses are known to run in families. There is a 10 per cent chance of you inheriting depression if you have a family history of it.
Take proper sleep, watch your alcohol intake and manage stress levels to reduce your chances of getting depression.

​Migraine
You might be shocked to know but there are 70 – 80 per cent chances that you might suffer from migraine if your mother did. The flawed gene that causes headache can be passed on.
Some common migraine triggers include sensitive foods like chocolate, cheese, coffee, citrus fruit and red wine. Also, girls need to really take care of their hormones during the menstrual cycle as it can set them off.

​Early menopause
If your mother had early menopause, your chances of following her footsteps increase by 70 – 85 per cent. The average age of menopause is 51, but one in every 20 women gets it even before the age of 46.
There is nothing you can do to prevent early menopause, though you can meet your doctor to get advice. 


this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.     
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Wednesday, October 09, 2019

Worried About Breast, Ovarian Cancer? Genetic Testing Could Help

India accounts for the third highest number of breast cancer and second highest number of ovarian cancer cases among women, globally. Also, three times more cases of familial breast and ovarian cancers are recorded in India, as compared to western countries. It is projected that cancer incidence in Indian women will increase to 190-200 cases per lakh by 2025. Mortality to incidence ratio is worst in India for breast and ovarian cancers with one in every 28 women likely to develop it during her lifetime and one in every two women diagnosed with it, succumbing to it.

Harmful mutations (multiple changes in DNA sequence) in BRCA1 and BRCA2 genes are known to be associated with high risk of developing hereditary breast and ovarian cancer (HBOC) syndrome (Table 1).
  Table 1: Lifetime risk of developing Breast and Ovarian Cancer in BRCA1/2 mutation carriers and non-carriers
About 20-25 percent of breast cancer cases are attributed to mutations in BRCA1 and BRCA2 genes. There is also an increased risk of developing cancer in other breast and/or ovarian cancer, after the first onset of breast cancer, in women who carry mutated BRCA1 or BRCA2 genes.

The harmful germline mutations in other genes such as TP53, CHEK2, STK11, BARD1, ATM, BRIP1, CDH1, PALB2, RAD51C, RAD51D, RAD50, NBS1, PTEN accounts for about 10 percent of familial breast and ovarian cancer cases.

Next Generation Sequencing based genetic test is a blood test that uses technique to analyse genomic DNA for detecting mutations in the multiple genes in a single assay. This is a  highly sensitive and robust sequencing method that generates more reliable results. It is a comprehensive assay covering single nucleotide variations (SNVs) and short insertions and deletions (InDels) and a cost-effective alternative to other available techniques with a shorter turnaround time.

BRCA1 and BRCA2 genetic test helps to identify the hereditary risk (presence of personal or family history) accurately and also helps to recognise the disease prognostication (impact on overall survival rate of breast cancer patients) and adds theragnostic value (deciding the best drug treatment). One of the most important utilities of the test is to improve early detection by 1.5 to 2.5 times and, therefore, increase the overall survival and reduce the cost of treatment.

Who Should Get Tested?

Genes are inherited, therefore, knowing your family history is significant when determining breast cancer risks. If either of your parents has a BRCA1 or BRCA2 mutation, you have a 50 percent chance of inheriting the mutated gene. One should consider gene testing if any one of the following conditions are predominant:
  • A personal history of breast or ovarian cancer diagnosed at young age (pre-menopausal), bilateral breast cancer (affecting both breasts) or presence of both ovarian and breast cancer
  • A family history of breast, ovarian, fallopian tube, peritoneal, prostate, or pancreatic cancer
  • A male family member having breast cancer
  • A relative with a known deleterious mutation in BRCA1 or BRCA2 genes
  • A history of breast cancer diagnosed below the age of 45 years
  • A family member with bilateral breast cancer below the age of 50
  • An individual with triple negative breast cancer below the age of 60 years with or without family history
  • Two or more relatives with ovarian cancer
  • Both breast and ovarian cancers in either the same woman or the same family
  • Ashkenazi Jewish ethnicity
BRCA1 and BRCA2 gene test has different implications on asymptomatic individuals and newly diagnosed patients.

i) A positive test result in an asymptomatic individual would help in disease prevention, early detection and better management of the disease by increased surveillance, using risk reducing chemoprevention and/or surgical interventions. Bilateral total mastectomy and oophorectomy may also reduce the risk of breast cancer and ovarian cancer in mutation carriers.

ii) A negative test result means there is no mutation in BRCA1 and BRCA2 genes. A person with negative test result holds same risk of developing breast cancer as someone in the general population.
iii) An ambiguous result occurs when a genetic test finds a change in BRCA1 or BRCA2 that has not been reported to be directly associated with breast cancer till date. This type of test result may be described as “a genetic variant of uncertain significance” because it is not known whether this specific genetic change is harmful. A study in Asian women found that 7.8 percent of women who underwent BRCA1 and BRCA2 mutation testing had this type of ambiguous result.

In newly diagnosed patients with breast or ovarian cancer, gene test results help to guide disease management and drug treatment decisions.

Genetic counseling is highly recommended before undergoing genetic test (pre-test counseling) and after the results are disclosed (post-test counseling). Genetic counselor can help decide whether genetic testing is needed based on the personal and family history and various other risk factors. If genetic testing is indicated, it should occur early in the cancer trajectory as patients who carry a mutation may receive more aggressive treatment.

this is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   
https://gscrochetdesigns.blogspot.com. one can see my crochet creations  

https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes    
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