Honey Hireme-Smiler at 2024 CCF Annual Conference

Are you or a loved one navigating a cholangiocarcinoma diagnosis?

You don’t have to face this alone. CCF is here to help you and your loved ones find support, answers, and community.

Take our 10-minute Welcome Survey to join the Newly Diagnosed/Newly Connected program and get quick access to:

  • A Free Care Kit
  • Our Resource Roadmap Workbook
  • Newly Connected email series
  • A 1:1 meeting with a Patient Advocate
  • Info on support groups, mentors, and free books
  • Join the Newly Connected Program
  • & Get Your Free Care Kit
  • Learn more about Cholangiocarcinoma
1

Find the Right Team

If you have been diagnosed with cholangiocarcinoma, the single most important thing you can do is to see an oncologist and surgeon who specialize in this rare cancer; this may require a second opinion. When it comes to treating cancer, expertise can mean the difference between life and death.

2

Get the Right Treatment

Ask your doctor about biomarker testing (molecular profiling). This test scans the DNA of your cancer cells for genetic mutations or other molecular changes that may be driving the disease. The results can help match some patients to the most effective treatment available, whether an approved therapy or one in a clinical trial.

Comprehensive biomarker testing isn’t yet standard for everyone, but Medicare covers it for patients with advanced solid tumors. It’s also increasingly available at major cancer centers and is often included in clinical trial protocols.


When first diagnosed, most cancers have a standard treatment that is considered the best approach for treating the disease. For cholangiocarcinoma, this is outlined in the  National Comprehensive Cancer Network guidelines, which are based on the latest scientific evidence.

Patients on 5-FU or Capecitabine (Xeloda)

Be aware of potential for an adverse drug reaction if not pre-screened for DPD Enzyme deficiency

Participant Engagement & Cancer Genome Sequencing Program

Volunteers needed for “Moonshot Program”

3

Participate in Patient-Powered Research

Researchers are trying to find individuals who might have a higCholangiocarcinoma is a rare but increasingly prevalent disease; scientists are still learning about its causes and effective treatment methods. Mayo Clinic’s Genome-Wide Association Study (GWAS) compares DNA from people with and without the disease. Participation is simple, free, and involves a small blood sample and a questionnaire. Your involvement could help improve prevention, detection, and care for patients and families affected by this disease.h risk for developing cholangiocarcinoma so they can identify new ways to detect, diagnose, and treat it. 

4

Get Connected & Find Support

SURVIVOR STORIES

Matt Reidy’s Story

CCA Patient
SURVIVOR STORIES

Stephanie Kleine-Ahlbrandt’s Story

CCA Patient