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			 Results of a trial in 413 patients showed that the drug, which is 
			activated with a laser to destroy tumor tissue in the prostate, was 
			so effective that half the patients went into remission, compared 
			with 13.5 percent in a control group. 
			 
			"These results are excellent news for men with early localized 
			prostate cancer, offering a treatment that can kill cancer without 
			removing or destroying the prostate," said Mark Emberton, a 
			University College London consultant urologist who led the trial. 
			"This is truly a huge leap forward." 
			 
			The treatment, called vascular-targeted photodynamic therapy or VTP, 
			was developed by scientists at the Weizmann Institute of Science in 
			Israel in collaboration with the privately-owned STEBA Biotech. 
			
			  
			The light-sensitive drug used, called WST11, is derived from 
			bacteria found at the bottom of the ocean. To survive with very 
			little sunlight, they have evolved to convert light into energy with 
			incredible efficiency, Emberton's team said in a study published in 
			the journal Lancet Oncology. 
			 
			The Weizmann scientists exploited this feature to develop WST11, a 
			compound that releases free radicals to kill surrounding cells when 
			activated by laser light. 
			 
			Men with low-risk prostate cancer are currently put under active 
			surveillance, where the disease is monitored and only treated when 
			it becomes more severe. Radical therapy, which involves surgically 
			removing or irradiating the whole prostate, has significant 
			long-term side effects so is only used to treat high-risk cancers. 
			 
			
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			While radical therapy causes lifelong erectile problems and 
			incontinence, VTP only caused short-term urinary and erectile 
			problems which resolved within three months, the researchers said. 
			No significant side-effects remained after two years. 
			 
			In the trial, only 6 percent of patients treated with VTP needed 
			radical therapy compared with 30 percent of patients in the control 
			arm who were under active surveillance. 
			 
			The trial involved 47 treatment sites in 10 European countries, most 
			of which were performing VTP for the first time. 
			 
			"The fact that the treatment was performed so successfully by 
			non-specialist centers in various health systems is really 
			remarkable," Emberton said. 
			 
			The VTP treatment is now being reviewed by the European Medicines 
			Agency (EMA) for possible license, but it likely to be several years 
			before it can be offered to patients more widely. 
			 
			(Reporting by Kate Kelland, editing by John Stonestreet) 
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