Carolina BioOncology Institute
About CBI Our Clinic Understanding Cancer Clinical Trials Personalized Medicine Contact Us
   
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 

 

 

 

 

 

 


 

Only 3% of US Cancer Patients Participate in Clinical Trials

Despite the plethora of new drugs and increasing trial access, cancer trials are woefully undersubscribed.  Only 3% of U.S. adults with cancer enroll in trials, and 86% of all U.S. cancer trials do not even meet their original accrual goals (enrollment goals for participation).  Many trials close due to lack of enrollment. At that rate, the war on cancer will never leave the lab rat.  These idle clinical trails cost millions of dollars a day from taxpayers’ federally funded NIH research as well as significant costs to pharmaceutical companies and their investors.  On average, a pharmaceutical company loses $1.3 million for each day’s delay in a drug gaining FDA approval. 

            By comparison, in Scandinavia 70% of cancer patients enroll in clinical cancer research trials, and the Netherlands has become the first country to fund and offer 100% tumor banking for gene array research.  In general, trials accrue faster outside the U.S. and drug development and approval is faster outside the U.S.  One exception in the U.S. is pediatric cancer, of which 75% participate in clinical trials.  This may be due to the probability that parents are more motivated about their children’s health than their own.  Due to the large 75% enrollment in pediatric cancer trials, the past few decades have witnessed a massive improvement of 75% cure rate in childhood cancer. 
           

            Some estimates predict that if U.S. adult participation in trials doubled to 6% nationwide, we could have a doubling of the length of survival and cure rate in the adult population over the next decade.  If no one participates in clinical trials today, cancer research will stay in the lab, new treatments and a cure will be delayed.  Additionally, if enrollment is slow for a particular trial, the patients who are participating are more at risk than stated because adverse event trends are difficult to recognize in a small group.   At major cancer conferences, it is sad to hear research trials frequently presented that are not statistically powered for conclusions because of poor trial enrollment.            

 

 
Home | About CBI | Out Clinic | Understanding Cancer | Clinical Trials
Personalized Medicine | Contact | Privacy
© 2007 Carolina BioOncology Cancer Therapy & Research Center