Early Colorectal Cancer: Missing the Clues? Third Annual Early Age Onset – Colorectal Cancer Symposium; March 12, 2017

“Colorectal problems can occur at any age. Here’s an article that will tell you more.”
— Dr. Dale

From Early Colorectal Cancer: Missing the Clues? Third Annual Early Age Onset – Colorectal Cancer Symposium; March 12, 2017 

In 2012, teacher Kristen McRedmond was the picture of health; by February 2017 she was deceased. Given that snippet of information alone, the story does not seem all that uncommon, but Kristen was only 38 years old when she died, and the cause of death was colorectal cancer (CRC).[1]

Josh Lambeth returned to his family doctor many times over the course of 3 years with the same rectal bleeding symptoms. The doctor told him he was healthy, chalked it up to hemorrhoids, and said that at age 30 he was too young for it to be anything serious. Even the gastroenterologist thought it would be nothing more than irritable bowel syndrome or ulcerative colitis. But the results of his colonoscopy proved far more devastating—stage II rectal cancer. And Josh was only 31 years old.[2]

Of course, virtually any disease can present outside the usual patient cohort, but CRC in younger adults is no longer unusual and has, in fact, become common enough to have earned its own name. In fact while CRC overall has been on the decline in the United States for decades, its incidence has increased dramatically in those under 50.

"[F]oremost for all of the attendees was the absolute necessity of early detection."

The Third Annual Early Age Onset-Colorectal Cancer (EAO-CRC) Symposium, which was held at New York's NYU Langone Medical Center on March 12, provided an opportunity for patients, clinicians, researchers, and caregivers to discuss and brainstorm a number of issues related to care and treatment. But foremost for all of the attendees was the absolute necessity of early detection.

A February 2017 article in the Journal of the National Cancer Institute (JNCI) [3]provides some sobering figures:

"...colon cancer incidence rates increased by 1.0% to 2.4% annually since the mid-1980s in adults age 20 to 39 years and by 0.5% to 1.3% since the mid-1990s in adults age 40 to 54 years; rectal cancer incidence rates have been increasing longer and faster (e.g., 3.2% annually from 1974–2013 in adults age 20–29 years)."

Since 1974, the incidence of rectal cancer in adults 55 years of age or older has declined. Since the mid-1980s, the same is true of colon cancer. But between 1989-1990 and 2012-2013, incidence rates of rectal cancer in adults 50-54 years old increased from half that of the 55-59 rate, to the equivalent (24.7 vs 24.5 per 100,000 persons: incidence rate ratio (IRR), 1.01; 95% confidence interval [CI], 0.92-1.10). At the same time, the number of rectal cancer diagnoses in those younger than 55 doubled, from 14.6% (95% CI, 14.0%-15.2%) to 29.2% (95% CI, 28.5%-29.9%).[3]

"CRC is up significantly in those under age 50."

As a result, people born after 1990 have about double the risk of getting colon cancer at a younger age than those born in 1950 (IRR, 2.40; 95% CI, 1.11-5.19) and quadruple the risk of early rectal cancer (IRR, 4.32; 95% CI, 2.19-8.51).[3]

The conclusions? Although the cause or causes of the increase are unknown, CRC is up significantly in those under age 50, and the increase of CRC in young adults in their 20s and 30s is alarming.

The Primary Care Connection

Early detection is where the primary care doctor plays a critical role.

For primary care doctors, the increase in the number of CRC diagnoses raises many questions and concerns: when to screen, how to increase awareness of symptoms, the need for better and more detailed family medical histories, and the recognition that a referral to a gastroenterologist for a colonoscopy should not be ruled out even when the patient is young.

The symposium's takeaway was this: When CRC-like symptoms are present, regardless of a patient's age, it is important not to dismiss them or chalk them up to more benign causes simply because the patient is under 50, 30, or, sadly, even under 20.

Dr Joshua Raff, director of the Digestive Cancer Program at White Plains Hospital in New York, who attended the symposium, told Medscape that "attitudes toward symptomatic young patients—for example, those with gastrointestinal bleeding or change in bowel habits—are important. This requires more attention on the part of primary care doctors, to allow them to consider a GI referral more readily." In addition, said Raff, "gastroenterologists need to be more considerate of the possibility of a GI malignancy in younger patients once referred." Family history must be taken more thoroughly too and updated on a regular basis, perhaps annually. But a negative family history does not obviate the need to proceed with a workup for concerning symptoms.

Making Connections for Early Detection

Lynch syndrome. In the case of CRC, family history is vital.

While "most colorectal cancer is sporadic," some "3% to 5% of all cases of colorectal cancer are thought to be due to Lynch syndrome," according to Cancer.Net.[4]

  

National Youth HIV & AIDS Awareness Day

“A day which we highlight the impact HIV/AIDS has on the youth and the impact the young people have in the fight against HIV/AIDS.”
— Dr. Dale

From National Youth HIV & AIDS Awareness Day  

April 10th is National Youth HIV & AIDS Awareness Day (NYHAAD). NYHAAD is the first annual observance day set aside to recognize the impact of the HIV/AIDS epidemic on young people.

National Youth HIV & AIDS Awareness Day (NYHAAD) serves as a reminder that investing in young people's health and education is a critical step to achieving an AIDS-free generation. This annual observance was created in 2013 by Advocates for Youth and other partners to educate the public about the impact of HIV/AIDS on youth.

Teens in the United States

In the United States, more than 1 in 5 new HIV diagnoses were in young people aged 13-24 years. Despite the disproportionate number of new HIV infections occurring among youth, the percentage tested for HIV is low compared to other age groups. Only 10% of sexually experienced U.S. high school students have ever been tested for HIV.

From 2005 to 2015, CDC data show declines in sexual risk behaviors among teens, including fewer currently sexually active high school students. Still, the prevalence of some behaviors remains high and puts young people at risk. For instance, condom use has decreased among teens, with more than 40% of sexually active high school students not using a condom the last time they had sex.

Additionally, some teens, including lesbian, gay, and bisexual (LGB) teens, often remain at greater risk for negative health outcomes. It is critical to use tailored approaches to reach the highest risk teens with the right interventions, in the right way, at the right time.

Addressing HIV in youth requires that young people are provided the tools they need to reduce their risk, make healthy decisions, and get treatment and care if needed.

The Role of Schools

Schools can play a critical role in promoting the health and safety of young people. The nation's schools provide an opportunity for 56 million students to learn about the dangers of unhealthy behaviors and to practice skills that promote a healthy lifestyle.

Schools and other youth-serving organizations can help young people adopt behaviors that reduce their risk for HIV, sexually transmitted diseases (STDs), pregnancy, and other related health problems. Some ways to encourage youth to stay healthy is to teach them about HIV/AIDS and other STDs, promote communication between youth and their parents, and support student access to confidential HIV counseling and testing services.

What CDC is Doing

CDC works with an established network of leaders in school-based HIV prevention, funding 18 state and 17 local education agencies that reach 1.8 million students nationwide. These funded partners:

  • deliver HIV, STD, and pregnancy prevention programs grounded in the latest research
  • select effective health education curricula
  • build local capacity to connect students to school-based and school-linked health services
  • engage parents to promote a positive school environment that’s safe and supportive for all students

Six national organizations also are funded to help state and local agencies with training, technical assistance, and resource development.

CDC uses three state-of-the-art monitoring systems designed to collect, analyze, and disseminate data on youth risk behaviors and school health policies and practices. These systems provide state and district level educators with information that they can translate into programs, policies, and practices that reduce health costs and improve teens’ lives.

This year marks the 5th year of NYHAAD-an observance that highlights the exceptional work young people are doing across the country to stregthen the fight against the HIV/AIDS epidemic.

What Can You Do?

CDC recognizes the impact of the HIV/AIDS epidemic on youth and the importance of HIV prevention. On NYHAAD, CDC joins with partners across the country to work to ensure young people know how to protect themselves against HIV. NYHAAD encourages everyone to:

  • Get educated. Learn the basic facts about HIV transmission, testing, and prevention.
  • Get tested for HIV. CDC recommends that everyone between the ages of 13 and 64 years get tested for HIV at least once as part of routine health care. Contact your health care provider about testing.

To have the most positive impact on adolescent health, parents, schools, and community- and school-based organizations and health centers must work together to help provide safe and nurturing environments for youth.

Help raise awareness about this important day by sharing communication messages and resources.

  • NYHAAD Resources Web page: This page contains information that is helpful in planning communication activities to inform and educate partners, stakeholders, and media about HIV in youth and the importance of recognizing the impact of the disease on young people. Included are graphics, sample social media posts, and links to additional resources for state and local education agencies, healthcare providers, and parents.
  • NYHAAD button: Post this web button on your site.

April is IBS Awareness Month

“A month aimed to reduce the stigma with IBS and encourage individuals who have symptoms to get help.”
— Dr. Dale

From April is IBS Awareness Month 

If you have irritable bowel syndrome (IBS), you are not alone – IBS is common with prevalence estimated at 10% to 15%. Yet many people remain undiagnosed and unaware that their symptoms indicate a medically recognized disorder.

In 1997, IFFGD designated April as IBS Awareness Month. During this time, we work to focus attention on important health messages about IBS diagnosis, treatment, and quality of life issues.

IBS Awareness Month is listed on the U.S. National Health Observances calendar. Health observances are days, weeks, or months devoted to promoting particular health concerns. Individuals, health professionals, teachers, community groups, and others can use these special times to sponsor health promotion events and stimulate awareness of health issues.

How you can get involved

The more we work together to raise awareness for IBS, the greater our ability to impact positive outcomes, such as additional research, increased educational opportunities and improved patient care, for the functional GI community. Here are a few tools for you to raise the visibility of IBS in your community.

  • Send our 2016 IBS Awareness Month press release to your local media outlet or share a link to it on social media.
  • Read Some Take Things to Heart, Others to their Belly – Irritable Bowel Syndrome: What is it and how is it treatedby Ami D. Sperber, MD. Available online at Amazon.com.
  • Join with IFFGD and use your voice to make a difference.
  • Find other resources to raise awareness for IBS in your community, including flyers and a link to contact your legislator at Advocate for Digestive Health.
  • Find IFFGD on Facebookand Twitterand join the conversation.