Tag Archive for: cancer risk factors

What Are Common Bladder Cancer Myths and Resolutions for Underrepresented Patients?

Dr. Randy Vince from University Hospitals Cleveland Medical Center addresses and dispels four of the most common misconceptions: that bladder cancer only affects older adults, only smokers, or only men and that a diagnosis is always fatal. He also emphasizes the importance of education and early detection, and shares insights into risk factors and hereditary concerns. Learn more about Dr. Randy Vince

See More from [ACT]IVATED Bladder Cancer

Download Resource Guide

Related Programs:

Exciting Developments in Bladder Cancer Treatment Advances | Muscle-Invasive and Non-Muscle-Invasive Care

More Than Medicine_ Breaking Barriers in Bladder Cancer Care

More Than Medicine | Breaking Barriers in Bladder Cancer Care

Bladder Cancer Diagnosis and Treatment: Barriers to Timely Response

Bladder Cancer Diagnosis and Treatment: Barriers to Timely Response


Transcript:

Lisa Hatfield:

Vince, what are some common myths about bladder cancer that people in underrepresented communities might believe, and how can we clear up these misunderstandings to help improve outcomes?

Dr. Randy Vince:

Yeah, so if it’s okay, I’m probably going to answer that question in reverse. And the reason why is because, again, I’m a big believer in education, education, education. So, whether it’s at a physician’s appointment or whether it’s at a local community group or, you know, attending a health talk that is local to you, really educating yourself about health conditions can lead to increased awareness, which can dispel a lot of these myths.

But in my experience, I would say there’s probably about four common myths that I’ve heard. The first one is only old people get bladder cancer, which is just simply not true. While it is more common for bladder cancer to be developed in older individuals, it can happen in the younger population as well. I personally treated people who are in their 30s and 40s for bladder cancer.

So again, it’s not a disease that only impacts elderly patients. The next thing that I’ve heard is that only smokers get bladder cancer. So, while it is a major risk factor, and I mean smoking is a major risk factor for bladder cancer, there are other environmental exposures that you can have, especially in the workplace, whether it’s chemicals or paints or plastics.

So, these can also increase the risk of developing bladder cancer. And there are other treatments for pelvic conditions. Specifically, I’m thinking of radiation that can have a delayed onset of bladder cancer in patients.

Thirdly, bladder cancer diagnosis is equal to death, and that’s just simply not the case. Like many cancers, we know that early detection is key because when we have early detection, our survival rates go up. We talked about non-muscle-invasive bladder cancer versus muscle-invasive bladder cancer. What we know is that five-year survival rates for non-muscle-invasive bladder cancer, which is an earlier diagnosis of earlier detection, five-year survival rates exceed 90 percent.

So again, cancer, bladder cancer diagnosis does not equal a death sentence. And then lastly, that only men get bladder cancer. Again, it’s more common in men, but women get bladder cancer as well. But the difference that we’ve seen is that women in minority communities are actually more likely to succumb to that bladder cancer diagnosis. Which again, just points to why that increased awareness is so important in early detection efforts remain critical.

Lisa Hatfield:

Okay, thank you. And I have one follow-up question to that. You talked about some risk factors for bladder cancer. Is there any type of genetic or hereditary component to bladder cancer?

Dr. Randy Vince:

Yeah. So, the vast majority of bladder cancers do not have an inherent genetic risk. There are some very rare bladder cancers that are associated with a genetic link. But for the vast majority of patients who develop bladder cancer, there is not a hereditary link to that.

What Are Colon Cancer Screening Guidelines?

What Are Colon Cancer Screening Guidelines? from Patient Empowerment Network on Vimeo.

What are the guidelines for colon cancer screening? Dr. Suneel Kamath explains the current recommendations, including the appropriate screening age and reviews risk assessment based on factors such as family history and race. 

Dr. Suneel Kamath is a medical oncologist at the Cleveland Clinic Cancer Institute. Learn more about Dr. Kamath.

Download Resource Guide

See More from DETECT Colon Cancer

Related Resources:

Research Advances in Colon Cancer Screening and Detection

Research Advances in Colon Cancer Screening and Detection

What Can Patients Do to Access Better Colon Cancer Care?

What Can Patients Do to Access Better Colon Cancer Care?

What Is the Role of Genetic Testing in Colon Cancer Care?

What Is the Role of Genetic Testing in Colon Cancer Care?


Transcript: 

Katherine:  

It seems like the suggested ages for screening may vary based on gender and race and family history. What are the current screening guidelines?

Dr. Kamath:

The current screening guidelines that are unfortunately due this rise, there is now recommendation for starting colon cancer screening at age 45. That’s really for everybody. There are certain people that really should be screened even earlier. We definitely know that the black community is affected at a higher rate. There are some professional societies, like the AGA or ACG, that actually recommend starting even earlier in the black community, maybe even by age 40. 

And then, the other thing I always try to emphasize is with this is the usual screening guidelines that we talk about are for what we call the average risk population. I do think that we overestimate how many people are average risk. One of the things that I think is not talked about as much is that if you have a family history of even polyps – high risk polyps – that also means that your family members should get screened earlier, 10 years earlier, than the age that you were found to have a high-risk polyp.  

But my experience has been most people don’t share with their families that they had those. Let’s say I had a colonoscopy done one day and they found those, they get taken out, and they just say, “Oh, come back in three years,” instead of 10. As far as I’m concerned, that’s where it ends. But actually, the fact that I had those polyps has implications for my siblings, for children, and everything. I don’t think most people are in the habit of disseminating that information. As a result of that, a lot of people are probably at increased risk and they’re really not aware of it.

Katherine:

Yeah. Where can patients find the most up-to-date information regarding screening?

Dr. Kamath:

The best resource, to me, is the American Cancer Society, their websites. They’re highly reliable, they’re easy to understand, and I find that they’re very balanced. They’re not going to be overly pushing one side or the other. But they’re going to be evidence-based. As we all know, there is so much fake news and misinformation out there, especially when it comes to health. I think having a resource you could really trust and understand is key and the American Cancer Society, you find, is an excellent resource.