Tag Archive for: endometrial cancer screening

Overcoming Barriers: Empowering Underrepresented Groups With Endometrial Cancer

Overcoming Barriers: Empowering Underrepresented Groups with Endometrial Cancer from Patient Empowerment Network on Vimeo.

 How can endometrial cancer care barriers be overcome for underrepresented groups? Expert Dr. Emily Hinchcliff from Northwestern Medicine discusses racial and cultural barriers and advice to patients to be proactive toward receiving optimal care.

[ACT]IVATION TIP

“…know the genetic status of your tumor, specifically something called the mismatch repair status of your tumor. And then not only how does that status impact your own treatment, but also how that may impact your family members…understand what resources are out there for you as a patient, especially for women in underserved groups and minority populations.”

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See More from [ACT]IVATED Endometrial Cancer

Related Resources:

Overcoming Geographical Barriers in Endometrial Cancer Care

Overcoming Geographical Barriers in Endometrial Cancer Care

Innovative Approaches to Endometrial Cancer Care in Underrepresented Communities

Innovative Approaches to Endometrial Cancer Care in Underrepresented Communities

Endometrial Cancer Care Disparities | The Impact of Rural Residence

Endometrial Cancer Care Disparities: The Impact of Rural Residence

Transcript:

Lisa:

Dr. Hinchcliff, in your research, you dive deeply into the significant disparities that exist within medically underserved and minority populations in the U.S. when it comes to awareness of, access to, and the use of genetic services in endometrial cancer. Can you speak to the research and provide tips to these patients and families?

Dr. Emily Hinchcliff: 

Yeah, so I think that there are sort of two different pieces that go on here. First is the relationship of endometrial cancer, that some of it can be, I guess, at random, and some of it can be genetic. So understanding, especially for those who have a strong family history, that there are hereditary forms of endometrial cancer. I think that’s a really important point for patients to take away. And then we, as a society, as a field, now recommend kind of routine screening for those tests to determine, Is an endometrial cancer hereditary or not? So make sure that you, as a patient, know your results and know if your family members should be tested in any way.

The second is regarding the significant disparities that exist. We know, as a field, as a kind of medical subspecialty, that there is a racial disparity in endometrial cancer mortality. While there is a lot of research going on to address the kind of potential biologic component there, is there something different about the cancers that are developed in different racial groups? I think there’s also really important research going on about the kind of systemic and cultural barriers and differences that women of different races experience that also can dramatically impact their cancer care.

Lisa:

And do you have an activation tip for this question?

Dr. Emily Hinchcliff:  

I’ll give you two different activation tips. I think that the first is to know the genetic status of your tumor, specifically something called the mismatch repair status of your tumor. And then not only how does that status impact your own treatment, but also how that may impact your family members. And then I think the second is to understand what resources are out there for you as a patient, especially for women in underserved groups and minority populations. Simply obtaining support can often be a really important key first step to gaining access and understanding of your disease.


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Endometrial Cancer Care Disparities: The Impact of Rural Residence

Endometrial Cancer Care Disparities: The Impact of Rural Residence from Patient Empowerment Network on Vimeo.

What kind of care disparities do endometrial cancer patients from rural areas face? Expert Dr. Emily Hinchcliff from Northwestern Medicine shares her perspective on obstacles for patient care in rural areas and patient advice to help ensure optimal care.

Download Guide | Descargar Guía en Español

See More from [ACT]IVATED Endometrial Cancer

Related Resources:

Which Endometrial Cancer Clinical Trials Are Showing Promise

Which Endometrial Cancer Clinical Trials Are Showing Promise?

Understanding Endometrial Cancer Risk: Factors Influencing Incidence and Mortality

Understanding Endometrial Cancer Risk: Factors Influencing Incidence and Mortality

Overcoming Geographical Barriers in Endometrial Cancer Care

Overcoming Geographical Barriers in Endometrial Cancer Care

Transcript:

Lisa:

Dr. Hinchcliff, can you speak to barriers faced by rural endometrial cancer patients, those living in rural areas, and are there specific challenges that these women in rural areas face in accessing timely and quality healthcare services for endometrial cancer screening and treatment?

Dr. Emily Hinchcliff: 

Absolutely. So, when I think of barriers, I think that barriers can be broken into some really key steps along the kind of diagnosis continuum. So certainly, a patient needs to understand that the symptom that they’re having is a problem. Then they need to see that problem and seek care. Then once they have established care they need to obtain a diagnosis. And then once you have a diagnosis, you need to get treated. And so I would suspect that those living remote from major hospital centers or from subspecialty care probably experience delays at each single one of those time points.

First, I think a knowledge gap probably exists about what bleeding should be, especially for postmenopausal women. Postmenopausal bleeding is not normal. And so even a small episode of spotting should warrant a visit to your physician. And then I think for those who see their physician, who have a less kind of either geographic or less access for whatever reason, there’s probably a greater prolongation of the series of visits that are required before they get the necessary endometrial sampling and a transvaginal ultrasound, which are really core tests when it comes to diagnosis.

Once the diagnosis is obtained, I think that the further referral and potential delay to someone like myself, like a GYN oncologist, is also a key barrier for those who are rural. There’s actually a really good study in gynecologic specifically in the Midwest that showed that rural women were significantly less likely to receive care from a subspecialist like myself.  I think that particular study was in endometrial, sorry in ovarian cancer, but it showed that those who receive care by a specialist are more likely to get optimal surgery and to get guideline-inherent care. So getting yourself to that subspecialist, I think is really key, but can be difficult for women who live remote from subspecialty care.


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