2020 Cancer Experience Registry Report

illustration multicultural women standing by tree

What is the Cancer Experience Registry?

The Cancer Experience Registry® is an opportunity for any adult touched by cancer to share their experience so that others may learn. This online survey captures several parts of the patient and caregiver experience including physical, emotional, social, practical, and financial aspects of cancer. Doctors, nurses, researchers, policymakers, and others in the health care field use the findings in this report to help improve the cancer care journey.

Learn More or Take the Survey
illustration woman with document

What is the 2020 Cancer Experience Registry Report?

The 2020 Cancer Experience Registry Report describes general findings among patients with any cancer type, findings among patients living with specific cancers, and findings among caregivers. Below are some key highlights.

Read the Full Report

This is what people in the report tell us about living with cancer:

 

SIDE EFFECT AND SYMPTOMS

4 out of 10 
felt inadequately prepared to manage side effects of treatment

4 out of 10 
did not recall receiving information about long-term side effects of treatment

1 out of 3 
held back from telling their health care team about side effects and symptoms

 

TREATMENT DECISION-MAKING

9 out of 10 
rated quality of life as a very important factor when weighing treatment options 

1 out of 3 
were not satisfied with how much they participated in making the treatment decision 

1 out of 2 
did not feel prepared to discuss treatment options with their doctor

 

COST OF CARE

1 out of 10 
postponed filling prescriptions to reduce cost 

7 out of 10 
reported that no one from their health care team talked to them about the cost of their care 

1 out of 3 
depleted savings or used money from retirement to cover treatment costs

 

PRACTICAL CONCERNS

41% were moderately to very seriously concerned about changes or disruptions in work, school, or home life 

40% were moderately to very seriously concerned about thinking clearly (“chemo brain” or “brain fog”)  

13% were moderately to very seriously concerned about transportation to treatment and appointments

 

This is what people who were caregivers tell us:

 

CAREGIVER ROLES

89% were quite a bit/very much involved in providing emotional support 

80% were quite a bit/very much involved in going to medical appointments with the patient 

20% spent more than 100 hours per week caregiving 

16% reported having received formal caregiving training 

41% of those trained wanted additional training

 

CAREGIVER NEEDS 

3 out of 4 
wanted help with understanding the patient’s medical condition and treatment

More than 1 out of 2 
wanted help managing health benefits and financial services   

Nearly 1 out of 2 
reported at least sometimes experiencing a sense of loss of control over their own life

Do you have questions about the findings or the report?

Email Us
illustration four people chatting at a table

Join the Cancer Experience Registry

Join now. Take the survey. Together we can improve cancer care.

Learn More or Take the Survey