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			 Researchers looked at the 62 cancer drugs approved in the U.S. and 
			Europe between 2003 and 2013 and found they extended survival by an 
			average of about 3.5 months. 
			 
			But nearly a third of the drugs lacked evidence to suggest they 
			increased survival when compared to alternative treatments. 
			 
			"Our results point to the notion that new cancer treatments may not 
			always provide patients with greater clinical benefits, or lower 
			risks, over existing treatments," wrote senior researcher Dr. Elias 
			Mossialos, of the London School of Economics and Political Science, 
			in an email to Reuters Health. 
			 
			The risk-benefit ratio of new drugs is especially important if 
			people are concerned, for example, about whether the cost of a drug 
			would make it difficult for a person to complete the treatment 
			regimen. 
			 
			Writing in JAMA Oncology, Mossialos and colleagues point to growing 
			questions about the value of new cancer medicines. While the drugs' 
			high costs may be a barrier to access, they note, some people argue 
			the high prices are justified if the treatments offer large 
			benefits. 
			
			  
			  
			A lack of solid data on new drugs' benefits and risks makes it 
			difficult to evaluating their value. 
			 
			For the 62 medicines they wanted to study, the researchers found 
			data from England, France and Australia evaluating 53 drugs. Nearly 
			80 percent were tied to improvements in survival, quality of life or 
			safety. 
			 
			The drugs increased survival - with or without recurrence - by about 
			3.5 months on average, compared to other treatments available in 
			2003. 
			 
			Twenty-three drugs were individually tied to an increase in survival 
			of three months or more. Six drugs extended survival by less than 
			three months. Eight drugs increased survival by an unknown amount. 
			And for 16 of the approved drugs, there was no evidence to suggest 
			they were better than alternative treatments at extending survival. 
			
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			The researchers point out in an email that overall survival benefits 
			differed by the type of drug. For example, drugs for thyroid cancer 
			were tied to no increase in overall survival, while drugs to treat 
			breast cancer were linked to an average increase of about 8.5 
			months. 
			Twenty-two of the drugs were tied to an improved quality of life, 
			but 24 were linked to worse patient safety, which include side 
			effects and whether a person could tolerate the treatment. 
			 
			The researchers write in their email that they extending the study 
			to look at newer drugs. They are also working to link their evidence 
			with the cost of individual medicines. 
			 
			Mossialos said the study should remind people of the importance of 
			the relationship between doctors and patients. He said, "Patients 
			should work with their physicians to consider all available evidence 
			that exists in support of individual treatments, and use this 
			alongside any inputs from their clinician to identify the treatment 
			that would best correspond with their own medical and personal 
			circumstances." 
			 
			SOURCE: http://bit.ly/2iXJ2QR JAMA Oncology, online December 29, 
			2016. 
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