A common drug sitting in your medicine cabinet right now may help fight cancer

It’s been a go-to for headaches, fevers, and sore muscles for over a century. But new research suggests that aspirin—the everyday over-the-counter medication sitting in your cabinet—might also have another, far more unexpected use as an anti-cancer drug.

A 30-year study from researchers at Harvard is catching attention

By analyzing data from over 100,000 people, researchers found that taking aspirin at least twice a week was associated with a reduced risk of colorectal cancer—but especially among people who don’t follow other health guidelines, like eating well or not smoking. So, while it isn’t a mind-blowing anti-cancer drug, it could very well have some promising potential to become one.

These newest findings could point toward a future where aspirin is used strategically based on someone’s genetic makeup and lifestyle risk factors to help treat dangerous cancers. However, there’s still reason for caution (Aspirin carries several known side effects, including the risk of stomach bleeding, especially in people over the age of 70. That’s why researchers are increasingly calling for personalised guidelines rather than blanket recommendations when treating it as an anti-cancer drug)

https://bgr.com/science/a-common-drug-sitting-in-your-medicine-cabinet-right-now-may-help-fight-cancer/

Outcomes of endometrial cancer prevention strategies in Patients with Lynch syndrome: a nationwide cohort study.

Female Lynch syndrome carriers have an increased risk of developing endometrial cancer. Regardless, research on endometrial carcinoma tumorigenesis is scarce and no uniform, evidence-based gynaecological management guidelines exist. We therefore described gynaecological surveillance and surgery outcomes in a nation-wide Lynch syndrome cohort.

Interpretation: In a nation-wide cohort of Lynch syndrome carriers, nearly one-third of eligible carriers did not undergo gynaecological surveillance. Endometrial carcinomas diagnosed during surveillance were slightly more often stage FIGO IA, but this did not seem to substantially decrease the requisite for adjuvant therapy or affect overall survival, questioning effectiveness of current gynaecological management. Prospective research should further assess this, as well as patient preferences.

What is the Lynch syndrome registry? (UK)

Lynch syndrome can run in families. It increases your risk of being diagnosed with bowel cancer, as well as other cancers including endometrial (womb), ovarian, stomach, bladder, kidney, and skin cancers. This condition is diagnosed by having a genetic test.

The Lynch syndrome registry records and analyses important information about people with Lynch syndrome. This helps to understand how people with Lynch syndrome are looked after and cared for across England. All information is held on a secure and confidential computer database.

Why have a Lynch syndrome registry? 

The focus of the Lynch syndrome registry is to address the differences in access, quality and timeliness of regular check-ups that people with Lynch syndrome in England currently experience.

The registry will collect information from people with Lynch syndrome and help us to better understand how these people are currently being monitored and managed. 

https://www.40tude.org.uk/news/kevin-monahan-award-25

https://lynchregistry.org.uk/#:~:text=The%20Lynch%20syndrome%20registry%20records,secure%20and%20confidential%20computer%20database.

April is Bowel Cancer Awareness Month

According to the 2023 National Cancer Registry of Ireland (NCRI) report, around 2,500 men and women are diagnosed with bowel cancer in Ireland every year 1,452 men and 1,047 women. To learn more about the condition and some helpful advice to support you at every step of your bowel cancer journey, click below.

Navigating Patient Vulnerability During Medical Procedures

The person actually taking a sharp object to cut me open to remove my port, he never introduced himself to me.

This act of restraint heightened feelings of vulnerability and helplessness.

No one acknowledged that I was speaking.

It’s scary to be so vulnerable, no matter how old you are, no matter how many procedures you endure, especially when you’ve never met the person performing it and can’t see.

I couldn’t anticipate the impact.

The doctor who performed the procedure never came to talk to me.

New report : How can we improve the experience for people who need to be screened for Lynch syndrome?-NHS

Recommendations:

Training for GPs & oncologists in Lynch syndrome needs to be a priority. 
Improved communication between services about the Lynch syndrome pathway 
Taking a person-centred approach to Lynch syndrome 
Every patient should have a named contact in a mainstreamed clinic 
All clinicians providing mainstreamed clinics should have access to appropriate guidance. This knowledge can then be shared with patients at the point of care 
Reduce pathway variation and ensure geographical equity of care. 
Dedicated, specialist clinicians trained in Lynch syndrome mainstreaming should be provided for all patients 
Standardised patient information should be created and utilised across all regions and NHS providers 
Lynch Syndrome App should be widely promoted among healthcare providers to help increase awareness of the condition. 
Everyone diagnosed with Lynch Syndrome should be given information about Lynch Syndrome UK 
Standardised information about ‘Living with Lynch’, talking to relatives, family planning, and mental health support should be created. 
New processes around cascade testing should be considered to improve support and information provided for the patient and their families. 
Consider concerns of/about family members 
Regular, clear and consistent communication for patients whilst awaiting appointments or results is necessary. 
Increased psychological support 
Training given to all clinicians (not just those working with Lynch) about gender inclusivity and how to ensure that patients feel welcomed and respected within any NHS service.

https://southeastgenomics.nhs.uk/new-report-how-can-we-improve-the-experience-for-people-who-need-to-be-screened-for-lynch-syndrome/

National Screening Service

Annual report available at…

https://www2.healthservice.hse.ie/organisation/nss/news/operational-excellence-quality-central-to-strategy-implementation-at-nss/

Lots of lovely words and Pics…unfortunately uptake of Free Bowel screen is still very low…why?

Lynch Choices

  • Lynch syndrome is an inherited condition that increases the chance of developing certain cancers. The type of cancer depends on the genes involved.
  • This website helps people with Lynch to make choices that are right for them. It is designed to be used with support from the genetics service, GPs, healthcare teams in the community, charities and patient groups.
  • If you are concerned about Lynch but have not been diagnosed, please speak to your GP or genetics service.
  • You’ll find two sections which help you think about your choices at home, so you are ready to talk through these choices with a GP, genetics or other specialist.
  • There are also another six sections providing support and information for people with Lynch. These sections may also be useful to family members and healthcare professionals of people with Lynch.

https://lynchsyndromeireland.wordpress.com/wp-admin/post-new.php

Access to New Drugs….

Matt Cooper the Last word. Miriam Staunton Talks about UCAN Ireland launch and problems around access to New Drugs. Listen back here

https://www.goloudplayer.com/episodes/access-to-new-drugs-most-pressin-MDA3YjQ0ZjY4ZTdjNGY1MDMxMDlhMGJmZjk2OTgyMDM=

UCAN

Launched today outside Leinster House.

https://www.facebook.com/reel/1009053707324898