| 
			
			 Writing in Annals of Internal Medicine, researchers at the 
			University of California, San Francisco (UCSF) call the industry’s 
			push into the smoking-cessation market “the pharmaceuticalization of 
			the tobacco industry.” 
 “The same hand that’s creating the problem is attempting to create 
			the solution,” lead author Yogi Hendlin said in a phone interview. 
			“But their solution is long-term nicotine maintenance, rather than 
			total tobacco cessation.”
 
 Marketing tobacco-industry merchandise as pharmaceutical products 
			and devices threatens to endanger public health and to derail 
			decades of progress in educating the public about the risks of 
			smoking, his team's opinion piece says.
 
 “Tobacco companies see their future as pharmaceutical companies. 
			They’ve already begun to acquire pharmaceutical subsidiaries, and 
			they’re producing tobacco products that look and feel like 
			medicines,” senior author Dr. Pamela Ling, a professor of medicine 
			at UCSF, said in a phone interview.
 
			 
			The authors define “pharmaceuticalization” as the tobacco industry’s 
			“actual and perceived transition into a pharmaceutical-like industry 
			through the manufacture and sale of noncombustible tobacco and 
			nicotine products for smoking cessation or long-term nicotine 
			maintenance without the testing and oversight required of 
			traditional pharmaceutical products.”
 The effort confuses consumers, complicates the regulatory process 
			and legitimizes the tobacco industry as a healthcare partner, they 
			say.
 
 In response, Philip Morris International told Reuters Health in a 
			statement that it understood that some might question its motives.
 
 “At the same time we are very encouraged by the growing number of 
			experts and health authorities who believe that tobacco companies 
			like us have a key role to play in reducing the harm caused by 
			smoking,” the statement said.
 
 “We are making significant efforts so that all those who would 
			otherwise continue smoking switch to scientifically substantiated 
			smoke-free alternatives as soon as possible,” it said. “We do not 
			ask to be trusted but to be judged based on facts.”
 
 Ling, Hendlin and their coauthor Jesse Elias say the 
			pharmaceuticalization of tobacco relies on two false assumptions: 
			substantial numbers of smokers cannot quit, and the only way most 
			smokers could quit would be with the help of pharmacotherapy.
 
			
			 
			As many as 90 percent of smokers who stop smoking do so cold turkey, 
			without cessation aids, said Hendlin, a postdoctoral fellow at 
			UCSF’s Center for Tobacco Control Research and Education.
 But quitting cold turkey is easier said than done for a substantial 
			group of smokers, particularly smokers coping with substance abuse 
			and other mental health issues, said Donna Vallone, chief research 
			officer at Truth Initiative’s Schroeder Institute, a Washington, 
			D.C. nonprofit dedicated to ending youth smoking.
 
			
            [to top of second column] | 
 
			“Believe me, it’s right to worry about the industry’s objectives 
			here,” she said by phone.
 “On the other hand, we do believe that harm reduction is a 
			legitimate public-health strategy. When you’re a lifetime committed 
			smoker and you’re trying to quit, these products can be helpful to 
			you,” said Vallone, who was not involved in the commentary.
 
			All the major transnational tobacco companies have invested in 
			so-called pharmaceuticalized tobacco products, according to the 
			commentary authors.
 In December, Philip Morris submitted a multimillion-page application 
			to the U.S. Food and Drug Administration (FDA) seeking to certify a 
			new product – I Quit Ordinary Smoking, or IQOS – as having “modified 
			risk” compared to cigarettes.
 
 IQOS includes short, disposable tobacco sticks soaked in propylene 
			glycol and inserted in a heat-not-burn cigarette, which, like 
			e-cigarettes, exempts it from smoking laws in many countries. A 
			recent study in JAMA Internal Medicine found that the product 
			releases chemicals linked to cancer, sometimes in higher 
			concentrations than conventional cigarettes.
 
			If approved by the FDA, IQOS would become the country’s first 
			modified-risk, or reduced-harm, tobacco product.
 Smoke from IQOS cigarettes releases 84 percent of the nicotine found 
			in traditional cigarettes, the JAMA Internal Medicine study found.
 
			
			 
			“While the tobacco industry seeks to glamorize, normalize and 
			rationalize nicotine addiction, don’t be fooled: nicotine is a 
			potently addictive and harmful drug,” said Mark Travers, a 
			researcher at the Roswell Park Cancer Institute in Buffalo, New 
			York.
 “Our ultimate goal will always be to end tobacco use AND nicotine 
			addiction,” said Travers, who was not involved with the commentary, 
			in an email. “Yes, pharmaceutical nicotine, as approved by the FDA, 
			is an effective way to assist in stopping smoking, but complete 
			abstinence of tobacco and nicotine use is the best outcome.”
 
 SOURCE: http://bit.ly/2tkmP93 Annals of Internal Medicine, online 
			July 17, 2017.
 
			[© 2017 Thomson Reuters. All rights 
				reserved.] Copyright 2017 Reuters. All rights reserved. This material may not be published, 
			broadcast, rewritten or redistributed. 
			
			 |