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.”

 

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Sunday, February 23, 2020

Study Shows This Common Cancer Drug Works Just as Well When Taken for Half the Time


Herceptin, also called trastuzumab, is a cancer drug used to treat aggressive HER2-positive early-stage breast cancer. It is credited with saving many patients’ lives, but it often has some difficult side effects, including possibly permanent damage to the heart. For most people, it is prescribed for a year or longer, meaning patients must pay a great deal of money, spend lots of time in the hospital and at doctor’s appointments, and suffer from side effects during the course of their treatment. But a recent study might change all that.

The study, which was conducted in Britain and paid for by the British government, followed thousands of women with breast cancer for several years (median of over five years) to see how their treatment plans affected their treatment outcomes and cancer recurrence rates. Researchers found that for patients with stage I, II, or III breast cancer, Herceptin is just as effective when only taken over the course of 6 months, as opposed to a year or more.

A year-long course of Herceptin costs about $76,700, so patients who elect to undergo a shorter course of Herceptin stand to save a substantial chunk of change. They’ll also likely experience less severe side effects and spend less time making trips to hospitals and other healthcare facilities for treatment.

Research like this, which aims to discover when treatment should be stopped to provide the patient with the maximum benefit and the best outcome in terms of cost and side effects, is rarer than it should be. Pharmaceutical companies are not eager to fund or conduct this type of research for obvious reasons; if they discover a drug shouldn’t be taken for as long as was previously assumed, it’s money out of their pockets.

“When drug companies do research, they’re interested in gaining knowledge such that they can make money for their shareholders,” says Dr. Otis W. Brawley, chief medical and scientific officer of the American Cancer Society. “There is a difference. You will not see drug companies doing this kind of study. They don’t mind that somebody else did it, but they will not get caught doing a study that decreases their bottom line.”

But cancer drugs and other strong medications can be toxic, so taking a medication for a longer period of time than necessary may be more than just unwarranted—it could be unsafe as well.

This issue likely extends to other cancer drugs and medications for other diseases. It is important, for the well-being of so many patients who take pharmaceutical drugs, that the efficacy of those drugs be thoroughly studied. Taking a drug for longer than needed often has an immense physical, psychological, and financial burden on patients, and it could be causing more harm than we’re even aware of yet.

Luckily, this is not the first study of its kind to find. Other research has found that stopping treatment earlier can improve patient experiences without sacrificing efficacy. A 2017 study found that many colon cancer patients would receive just as much benefit from three months of chemotherapy treatment as from six. And in 2016, research done on gene activity in breast tumors showed that some women with early-stage breast cancer could safely skip pre-surgery chemotherapy treatments. There is also an increasing understanding among doctors and researchers that some cancer cases can be simply monitored rather than being immediately treated.
The Herceptin study provides hope for better financial, emotional, and physical health for many women and men who currently have cancer or will have cancer in the future. However, many experts are reserving judgment regarding the results of the study until it has been published and peer-reviewed. The 12-month course is still the only regimen of Herceptin approved for early-stage breast cancer by the Food and Drug Administration.

A spokesperson from Genentech, the maker of Herceptin, said in a statement that her company had not found the drug to be as effective when taken for a shorter period of time.

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

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Monday, February 17, 2020

New technique holds promise for melanoma patients: Know how to deal with this condition

New technique that improves on existing methods for assessing risk of melanoma recurrence after surgical removal developed. But you need to be alert too.

There is good news for patients of skin cancer. Thanks to a new study at Brigham and Women’s Hospital, there may soon be a new melanoma test that will be able to better predict recurrence and improve patient care. Researchers have developed this new technique that improves on the current method for assessing whether primary melanoma is likely to recur and spread, following surgical removal. Nature Cancer published this study.


Most people first suspect melanoma when they see changes in the appearance of a pigmented spot like a mole or freckle. Though a primary melanoma can be cured through surgical removal, in some cases the lesion recurs and spreads. Unfortunately, there has been no major changes in the field of lesion analysis in the last hundred years. This puts patients at risk of recurrence at a disadvantage. But now, the new developments will lead to better patient care.


A treatable condition

Early stage melanoma is a treatable condition. But the problem with this disease is detecting it early. Usually, a diagnosis is made only after the cancer has progressed. A cure is difficult once the diseases has progressed. Hence, an early detection is essential for a favourable outcome from treatment. Be alert to any changes in the size of a mole or any changes on your skin. Consult your doctor to rule out this condition. Early detection can lead to a cure.


What you can do

You can bring down your risk of melanoma significantly by taking a few precautions besides being alert to any changes on your skin surface. Avoid excessive sun exposure. If you spend a lot of time in the sun, wear protective clothing. Nowadays, you can buy sun-block shirts. You can try these out. Always use sunscreen and re-apply every 8 hours.


Know the ABCDE method of detecting skin cancer
You can use the ABCDE method to determine if a mole or freckle may be melanoma. This is what you need to look out for.

A: Asymmetrical: Healthy moles are symmetrical and cancerous ones are asymmetrical. Just draw a line through the middle of your mole to see if there is any asymmetry.

B: Border: If the border of your mole is ragged, raised or notched, it may be cancerous.

C: change in colour: All healthy freckle and mole have uniform colour. If there is any color variation, it may be because of cancer. Look out for different shades of tan, red, brown, blue, white and black.

D: diameter: If your mole is bigger than 6 millimeters, it may be cancerous.

E: evolving: Keep an eye out for any new moles and marks on your body. Also check to see if there are any changes in the colour or size of existing moles.


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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