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Abstract
Background Philip Morris International (PMI) currently claims that its heated tobacco product, IQOS, reduces health risk by reducing users’ exposure to harmful and potentially harmful constituents present in tobacco smoke. Given the tobacco industry’s long history of misrepresenting and obfuscating research, independent assessment of PMI’s claims is important. Analysis of Accord, a failed but strikingly similar precursor to IQOS, may help contextualise PMI’s claims in its Modified Risk Tobacco Product (MRTP) application.
Methods We analysed previously secret internal Philip Morris (PM) and PMI documents, public communications and MRTP application.
Results PM marketed Accord as a ‘cleaner’ tobacco product in an attempt to address smokers’ growing health concerns without making explicit health claims. While PM communications asserted that Accord reduced users’ exposure to harmful constituents, company scientists and executives consistently stressed to both regulators and the public that such reductions did not render Accord safer. IQOS’s design and marketing are similar to Accord’s. On the basis of aerosol chemistry data, IQOS reduces user exposure to some compounds compared with Accord but raises them for others.
Discussion IQOS appears to be a variant of Accord without consistent improvements in exposure to aerosol toxic compounds. In contrast to PM’s past claims for Accord, PMI now claims in its MRTP application that IQOS reduces health risk. This shift in stance is likely not the result of any toxicological difference between Accord and IQOS, but rather a change in the social and regulatory landscape permitting these claims.
- advertising and promotion
- tobacco industry documents
- toxicology
- non-cigarette tobacco products
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Background
The tobacco industry has developed heated tobacco products since the 1960s.1 When these ‘safer’ offerings have been marketed, consumers have generally rejected the products’ poor taste, smell and user experience.2 As of May 2018, however, a heated tobacco product from Philip Morris International (PMI), IQOS, had won at least moderate consumer acceptance in several of the 31 countries in which it was available.3 By early 2018, IQOS had captured nearly 15% of the national tobacco market share in Japan, 2 years after its introduction.4 Despite the continued predominance of conventional cigarettes to company profit,3 PMI publicly frames IQOS as presaging the company’s supposed departure from the cigarette business altogether.5
In promoting IQOS, PMI has attempted to foster a perception of the product as reduced risk. The company’s public communications and warning label statements claim that switching completely to IQOS is a safer alternative to smoking cigarettes.6 In an attempt to court favourable regulation, taxation and exemptions from smoke-free ordinances for IQOS, PMI has begun promoting the product’s purported benefits in meetings with national health authorities.7 In December 2016, PMI submitted a multi-million page Modified Risk Tobacco Products (MRTP) application to the US Food and Drug Administration (FDA).8 If approved, PMI will be able to market IQOS in the USA as a reduced risk alternative to conventional cigarettes.
Given the tobacco industry’s well-documented history of misrepresenting and obfuscating its research,2 independent assessment of PMI’s claims is important. While PMI’s internal data and business strategy on IQOS are largely unknown, internal Philip Morris (PM) documents discussing Accord—a failed, but similar heat-not-burn precursor to IQOS—are available in public archives. We compared available documents detailing product design, exposure data and safety claims PM made for Accord to data and claims submitted as part of the IQOS MRTP application. Our aims were to compare product design characteristics; determine if IQOS exposure levels were demonstrably and consistently improved compared with Accord; and learn how PM understood the extent to which reductions in exposure to harmful constituents reduced harm to users.
Methods
Between October 2013 and January 2016, we searched industry documents (available through the Truth Tobacco Industry Document Library; https://industrydocuments.library.ucsf.edu/tobacco/) detailing tobacco companies’ development of various heat-not-burn tobacco product prototypes. Between January 2017 and May 2018, this dataset was expanded with additional iterative searches9–11 focused specifically on Accord, with initial keyword searches including "Accord market*,” "Accord research," "Accord consumer," "Accord science," and related terms drawn from earlier searches, such as "electrically heated cigarette smoking system" (EHCSS) and "EHCSS." We then conducted snowball searches to locate related documents using reference (Bates) numbers, file locations, dates and individuals mentioned in pertinent documents, and by refining subsequent searches with Boolean operators and year and publication type filters. Iterative searches were repeated until keywords and documents yielded only previously viewed documents, suggesting saturation.
To ensure documents’ internal consistency, all documents were organised thematically and chronologically, and relevant documents were compared with relevant sections of PMI’s MRTP application available on the FDA’s website.8 Triangulation with online search engines, news coverage, public statements made by PMI (most often found at http://www.pmi.com) and internal PMI documents obtained by Reuters (accessible at https://www.documentcloud.org/public/search/projectid:_2033738) generated data that helped resolve and contextualise questions raised by the documents. Having reviewed over 1,000 documents, this analysis is based on a final collection of 200 documents.
Results
Accord origins and specifications
Through the late 1980s and early 1990s, public health consensus on the negative health effects and addictiveness of smoking led to smoke-free policies and the broader social denormalisation of smoking.12 In response to these pressures, RJ Reynolds introduced its ‘clean smoke’ heated tobacco product, Premier, in 1988.13 Although similar to a conventional cigarette, Premier heated tobacco, instead of burning (combusting) it, producing an aerosol for inhalation.14 15 Industry scientists hypothesised that such products presented a lower health risk to users: because tobacco was not combusted, smokers might beexposed to fewer respiratory irritants and carcinogens.1 Marketed as a ‘smokeless’, ‘cleaner’ cigarette, Premier was widely rejected by consumers and pulled from shelves within 4 months of its release.
In response to Premier, PM began developing reduced-risk tobacco products of its own.2 13 16 A 1990 presentation introduced Project Beta, a battery-operated device that would heat rather than burn tobacco.17 Through Project Beta, PM developed the heat-not-burn product, Accord (internally referred to as an electrically heated smoking system (EHCSS)).18 Accord comprised a short, low-tar cigarette (in 3 and 6 mg tar versions) and a battery-powered lighter into which the user inserted the short cigarette. On the user’s puffing, the tobacco in the cigarette would heat, generating a tobacco-flavoured aerosol for inhalation. Retailing at US$77 (inflation-adjusted to 2018), Accord was packaged for sale as part of a kit that included Accord’s special cigarettes (sold at prices comparable to regular cigarettes), the product’s heating device and an instructional video (table 1).16
Component comparison: Accord and IQOS
Accord marketing
In October 1998, PM introduced Accord in 16–20 stores in Richmond, Virginia (the location of a major PM manufacturing facility), expanding to 120 stores within 3 months.19 In the same year, PM released Accord in Osaka, Japan, under the name ‘Oasis’. The tobacco industry has long marketed its ‘cleaner’ (eg, low-tar) products in Japan due to perceptions that Japanese smokers value cleanliness and are more willing than consumers in other countries to embrace new technologies.13 20 During Accord’s first three years on the market, consumer awareness remained limited, and sales and retention were low.21 Dual use of Accord with conventional cigarettes was also high: 86% of those who smoked Accord used the product for between one-quarter and one-half of their tobacco use; and only 9% of Accord users used the product for 75% or more of their tobacco use.22 PM attributed this ‘situationa[l]/occasiona[l]’ use to the product’s poor taste, higher price than conventional cigarettes, unfamiliar operating system and unconventional appearance.21 22
PM characterised Accord smokers as favouring product characteristics related to ‘hygiene or consideration of others,'23 and attributed the little success that Accord enjoyed to its perception as a ‘cleaner’ product that would not irritate others.21 To attract hygiene-conscious consumers, one Accord advertisement read, ‘Less smoke around you. Virtually no lingering odor. And no ashes’, all of which rendered Accord ‘a whole new way to smoke'.24 Another ad (figure 1) showed a couple sitting together on the same lounge chair while the man holds an Accord device, the woman seemingly unperturbed by any foul smell or smoke.
Visual comparison of Accord and IQOS tobacco stick, heating device structure, advertising and product demonstration. Photo credit for Product in Use images: www.vaping360.com and WGBH Educational Foundation.
While PM emphasised Accord’s ‘cleanliness’ in consumer communications,25 the company also went to great lengths to clarify that such ‘cleanliness’ did not render the product safer than conventional cigarettes. In an advertisement accompanying the Accord Kit, PM stated that while ‘Accord reduces certain harmful smoke compounds you inhale … [(such] reductions … have not been proven to lead to a reduction in smoking-related diseases'.26 After asserting that Accord reduces carbon monoxide exposure by 98% compared with an ultra-light cigarette, PM asked rhetorically in the same brochure, ‘Are we saying that Accord is a "safer" cigarette? No.'26 The brochure also stated that ’public health authorities do not endorse either smoking fewer cigarettes or switching to lower-yield brands or a cigarette that heats rather than burns tobacco as a satisfactory way of reducing risk'.26 27 This is consistent with past and current research showing that the extent to which reduced exposure leads to reduced harm is unclear.28 29 Despite these clarifications, a 2003 PM presentation to the company’s ‘New Products Committee’ reported that on average 11% of consumers exposed to Accord advertisements believed Accord to be less harmful than other cigarettes.30
Outside of PM, research on Accord’s safety was limited. Two independent studies compared Accord smokers’ CO intake and heart rate to those of cigarette smokers, and found both levels to be lower in the Accord users.31 32 However, nicotine uptake for Accord smokers was slower than conventional cigarettes, leading smokers to ‘compensate’; that is, inhale more deeply to extract more nicotine, thereby negating any health benefits of lower tar cigarettes.31
The significance of these findings, however, was undercut by the product’s scant adoption. By 2003, PM had spent over $400 million in operating expenses and almost $70 million (inflation-adjusted to 2018) in capital expenses in developing subsequent versions33 of Accord.34 One PM study found that both Japanese and American consumers rejected Accord (although acceptance was higher in Japan) because of its taste (‘hard to draw, perceived harshness, not enough taste, not enough puffs per cigarette’) and inconvenience (‘charging time, cigarettes per charge’).35 Accord also required smokers to adopt a new routine (eg, buying a new brand of cigarettes, recharging the battery pack), while the device itself required ‘enhanced consumer support, product maintenance, spare parts, technology acceptance and product education’, which most users found burdensome.22 PM discontinued Accord in 2006 after 8 years on the market.
PM’s pursuit of normalisation
Accord was designed as a potentially reduced exposure product (PREP), with PM clarifying in external company communications that reduced exposure did not indicate reduced risk.36 While PM contracted an advertising company to draft harm reduction advertisements for Accord in the USA, these advertisements were ultimately not used,12 perhaps because tobacco companies were legally barred from making reduced risk or reduced exposure claims while Accord was available.37 PM marketed the product instead as a low-smoke alternative,16 likely hoping to imply to consumers that Accord was safer than conventional cigarettes.
In 2000, as part of efforts to improve the company’s beleaguered image, PM began lobbying for legislation that would grant the FDA authority over tobacco.38 In 2001, 3 years after PM introduced Accord, the Institute of Medicine (IoM, now National Academies of Sciences, Engineering and Medicine) conditionally endorsed PREPs as potentially capable of reducing user risk.39 Believing that reduced risk products could help ‘normalise’ the company,27 40 PM echoed IoM policy recommendations in arguing that potential legislation should create separate classifications for reduced exposure products and reduced risk products. This distinction would enable PM to make reduced exposure claims for products like Accord, without having to wait for long-term evidence finding exposure reduction sufficient to indicate risk reduction.27 The proposed legislation failed to pass Congress in 2004.
In 2007, a year after PM discontinued Accord , Kenneth Podraza, Vice President of Research and Development at PM USA, wrote to the Surgeon General in an effort to gain government endorsement of Accord. ‘In the absence of FDA regulation’, Podraza stated that PM ‘now turn[ed] to you for guidance’, asking that the Office of the Surgeon General determine if Accord is a PREP,41 likely in the hopes that the Surgeon General’s designation of Accord as reduced exposure would generate increased consumer acceptance of either Accord (should it be reintroduced), or of future, similar products. The tobacco industry has long viewed third-party endorsements of industry products as crucial to those products’ success.2 42 Podraza attributed Accord’s commercial failure to both consumer rejection and the company’s ‘inability to communicate a potential reduced exposure message'.41
Reiterating PM’s previous communications on Accord, Podraza clarified that while Accord may be a PREP it nonetheless ’has not been proven safer [as] substantial reductions in certain harmful compounds have not been proven to lead to a reduction in smoking-related diseases'.41 Podraza concluded his letter stating that PM would continue to develop future potentially reduced-risk products that smokers would hopefully accept.41 We found no evidence that the Surgeon General responded to Podraza. In 2008, PM briefly test-marketed a near-identical product, ‘Heatbar’ in Switzerland and Australia.16 43 44
IQOS and Accord product design
In 2014, PMI introduced a new heated tobacco product, IQOS, in Italy and Japan. IQOS’s moderate success in several markets as of 2018 is at least partly attributable to the current social and regulatory landscape. When Accord was available, public health authorities were unwilling to deem safe, new, unpopular products designated as ‘cleaner’ by the industry.2 Since 2007, however, as the popularity of electronic cigarettes (e-cigarettes) increased,45–47 several prominent public health organisations48–51 and health authorities52 53 have promoted e-cigarettes as safer alternatives to cigarettes. In the USA, the 2009 Family Smoking Prevention and Tobacco Control Act granted the FDA authority to regulate all tobacco products.54 As part of this legislation, tobacco manufacturers could, for the first time, market preapproved products as ‘modified risk tobacco products’.
In addition to its distinct context, IQOS has several notable design differences from Accord. IQOS cigarettes have more nicotine and more than six times as much tar per cigarette as Accord cigarettes. IQOS’s HeatSticks are shorter than Accord’s cigarettes (45 mm vs 62 mm), as is its tobacco plug (12 mm vs 32 mm). IQOS cigarettes also have less tobacco per cigarette than Accord (314 mg vs 407.6 mg), are burned at a lower temperature (~350°C vs 500°C) and the product kit is approximately US$40 more expensive (inflation adjusted to 2018) than Accord’s (table 1).
The products also share a number of similarities. Like Accord, IQOS maintains the core technology of heating rather than burning tobacco, which purportedly lowers users’ exposure to harmful or potentially harmful constituents (HPHCs)—constituents linked to the most serious effects of tobacco use (eg, cancer, cardiovascular disease, respiratory effects, addiction). Both products work by activating a heating blade (eight iron-aluminide alloy blades for Accord and one ceramic blade for IQOS), which then warm(s) the adjacent tobacco, and both products’ electronic systems control the temperature of the blade and delimit the amount of puffs the user takes per cigarette (figure 1).
IQOS and Accord advertising
IQOS’s marketing has also resembled Accord’s. A 2016 internal training for employees managing IQOS’s social media presence revealed that, like Accord, IQOS is partially targeted at the hygiene-conscious, particularly ‘those who want to reduce risks to their young families'.55 PMI alerted employees that, as occurred with Accord, consumers may be turned off by the product’s ‘learning curve’, different ‘taste and satisfaction levels’ and the required time commitment, estimated at 3 weeks, to become accustomed to the product experience.55 Nonetheless, PMI stated in the same document that IQOS would ‘change the way legal-age smokers smoke for the better'.55
PMI also expects a number of indirect benefits to accrue to the company if consumers perceive IQOS to be safer than cigarettes. This is consistent with PM’s hopes for earlier reduced risk products.27 40 A 2014 internal PMI document entitled ‘10 year Corporate Affairs Objectives and Strategies’ frames IQOS as a key component in ‘normalising’ PMI’s business more broadly, transforming the company into a ‘trusted and indispensable partner … bringing solutions to the table'.56 In gaining the trust of the public and regulators, PMI hoped to both regain access to broader regulatory discussions from which it is currently excluded and reverse the trend of ‘PMI/industry de-normalization … [so as] to drive future growth'.56
Such normalisation efforts will be most successful if smokers switch completely to IQOS. Nonetheless, research on corporate social responsibility programmes has shown that tobacco companies can use purported gestures of goodwill (such as developing ‘safer’ products) to increase access to policymakers and generate support for industry activity regardless of a given programme’s effectiveness.38 57 58 In IQOS’s case, the mere manufacture of a potentially safer product may be enough to earn PMI influence.59 60
Comparing IQOS and Accord aerosol chemistry
In December 2016, PMI submitted a multi-million-page MRTP application to the FDA for the company to market IQOS in the USA with reduced-risk claims.8 While PM consistently clarified that reductions in exposure did not reduce user risk , PM’s spin-off company, PMI, now claims that such reductions in exposure do indeed reduce user risk, asserting that ‘switching completely [from cigarettes to IQOS] presents less risk of harm than continuing to smoke cigarettes'.61
Internal documents and statements by PMI scientists contradict these reduced risk claims about IQOS. In October 2015, an internal newsletter for Philip Morris Japan stated that while ‘the ‘Tobacco Vapor’ generated by the use of iQOS contains significantly lower levels of harmful or potentially harmful compounds’, PMI has nonetheless ‘not reached the point where we can say that it is ‘less harmful for adult smokers and those around them'62 (figure 2). In 2018, four former PMI scientists and researchers that worked on IQOS also claimed that the product’s reduction of certain compounds does not necessarily render IQOS safer.63
Excerpt from an internal October 2015 Philip Morris Japan newsletter. To clarify employee understanding of IQOS, a mock employee asks: '… iQOS has a less harmful impact on health, right?' The company expert replies, ’No no no! While these [ambient air reductions] are important results, we have not reached the point where we can say that it is “less harmful” for both adult smokers and those around them.'74
To assess one measure on which PMI bases IQOS’s claims of reduced exposure and thus reduced risk, we compared aerosol chemistry data from PM’s Scientific Data Summary (SDS) of Accord with information provided in PMI’s MRTP application for IQOS. PM assembled the SDS to detail Accord’s product specifications and clinical and non-clinical research findings. An ‘evolving document … intended for scientific and regulatory discussions',36 PM compiled the report from 2002 to 2006 to support reduced-risk claims for the Accord,64 perhaps anticipating US governmental regulation of tobacco and the creation of a regulatory mechanism through which manufacturers could make reduced-exposure and/or reduced-risk claims for preapproved products.27 Despite detailing reductions in HPHC exposure compared with reference cigarettes, PM stated in later versions of the SDS that the company made neither a reduced exposure claim for Accord,36 nor a reduced risk claim, stating that ‘reduc[ing] exposure to potentially harmful smoke constituents [did] not … establis[h] whether the product decreases the hazard of smoking.'36
In both PM’s SDS for Accord and PMI’s MRTP application for IQOS, industry scientists quantified levels of HPHCs in the products’ mainstream aerosol. PMI frames IQOS as safer than conventional cigarettes partly because levels of 58 constituents (PMI-58) were lower in IQOS mainstream aerosol relative to 3R4F reference cigarette mainstream smoke. The MRTP application for IQOS does not report data on 18 compounds included in the SDS for Accord, many of which are nitrosamines and polycyclic aromatic hydrocarbons, all of which are known toxicants (table 2).
Compounds listed in Philip Morris’ Scientific Data Summary for Accord but not Philip Morris International’s modified risk tobacco product application for IQOS
The MRTP application presents percent reduction of HPHC yields from IQOS compared with that of 3R4F reference cigarette on a per cigarette/stick basis as well as normalised by nicotine yields (per nicotine basis). The SDS for Accord provides only absolute HPHC yields. In addition, because Accord and IQOS were compared to different reference cigarettes (2R4F and 3R4F, respectively), which have different smoke constituent yields, the percent reductions of Accord and IQOS to their respective reference cigarettes are not comparable. Thus, we compared constituent yields from Accord and IQOS on a per stick basis, using values reported in the SDS for Accord and MRTP for IQOS (table 3). Based on levels of 25 constituents measured in both Accord and IQOS mainstream aerosol, 8 constituents appeared to be higher in Accord emissions while 17 appeared to be higher in IQOS emissions. When normalized by the weight of tobacco in the product, IQOS exposures were higher for 12 constituents and lower for 13 compared to Accord.
Comparison of Accord and IQOS constituent yields on a per cigarette basis based on data from Philip Morris' Scientific Data Summary and Philip Morris International’s modified risk tobacco product application
Discussion
While Accord was a commercial failure, IQOS is situated in a distinct social and regulatory landscape, which may increase its chances of success. The decline of cigarette consumption in developed markets, the increased popularity of e-cigarettes, select public health endorsements of e-cigarettes and the creation of a legal mechanism in the USA through which manufacturers can now make reduced risk claims may all have increased both consumers’ willingness to try new tobacco products, and PMI’s willingness to designate new products as safer than conventional cigarettes. In 2017, PMI announced the establishment of a US$1 billion foundation dedicated to partnering with public health and promoting PMI’s portfolio of reduced harm products, chiefly IQOS.65
Despite PMI’s claims of IQOS’s novelty,66 the product appears to be a successor of Accord on the basis of product design, marketing and aerosol chemistry. Both products work by inserting a modified cigarette into a holder that heats, rather than burns tobacco. Both products’ marketing implies reduced harm relative to cigarettes. While PMI claims that IQOS is reduced risk largely because it reduces users’ exposure to harmful constituents, IQOS does not drastically improve users' exposure to toxic compounds than relative to Accord. PMI’s claims for IQOS’s comparative safety on the basis of reduced exposure are further undermined by internal documents from PMI’s parent company: as late as 2007, PM executives and scientists claimed that reductions in exposure did not render Accord safer than conventional cigarettes.
One limitation of this study is that the Truth Tobacco Industry Documents Library is fragmented and incomplete, as it primarily comprises documents released through litigation. As a result, we may have missed documents relevant to our analysis, including information contained in the archive’s many ‘restricted’ documents, which the industry protects under attorney/client privilege.67 Given these limitations, there may be unreported differences in product design, marketing and aerosol chemistry between Accord and IQOS that could have informed our analysis. Similarly, we were only able to analyse one part of PMI’s MRTP application. Nonetheless, the results of this analysis suggest that PMI’s new claims of reduced health risk for IQOS are more likely the product of the current regulatory environment rather than a substantive improvement in the tobacco product’s harm profile compared with its precursor, Accord. Scientific evidence supporting reduced harm claims based solely on reduced exposure remains in.28 29
To prove that IQOS is safer than combustible cigarettes, PMI must show that IQOS ’significantly reduce[s] harm and the risk of tobacco-related disease to individual tobacco users and benefit[s] the health of the population as a whole taking into account both users of tobacco products and persons who do not currently use tobacco products'.68 Studies related to health effects range from lab-based smoking machine studies to assess constituent concentrations in products and aerosols/smoke; in vitro and in vivo toxicology studies; clinical and human pharmacology studies to examine the subjective and health effects of product use in lab and ambulatory settings; and epidemiological studies to examine the longer-term effects of these products relative to smoking. Though PMI has conducted several of these studies with favourable results, studies must also address effects on youth uptake, and product appeal to former-smokers and never-smokers to determine population-level health effects. Given the lack of long-term data on the individual and population health effects of IQOS, we remain sceptical of PMI’s claims of reduced risk through the use of predictive models.
Other independent research on IQOS has also contested IQOS’s claims of comparative safety.69–72 In analysing PMI’s MRTP application, independent researchers have noted that PMI’s conclusions of reduced population-level risk are based on data that factor in neither concerns of gateway effects for youth,73 nor secondhand smoke and dual use.74 Despite public communications about targeting solely adult smokers who would not otherwise quit,75 PMI has so far marketed IQOS much like an upscale tech gadget,6 offered primarily in countries with declining smoking prevalence and rising cessation rates.76
At the individual level, IQOS appears to cause damage to endothelial function, and the liver and the immune system at levels comparable to conventional cigarettes.77 78 In addition to showing toxicology yields from only a limited range of HPHC’s present in IQOS’s aerosol,79 22 of the constituents in the MRTP application had yields more than 200% higher than those present in conventional cigarettes, while another 7 had yields more than 1000% higher.79 PMI’s medical tests on human subjects also demonstrate ‘no statistically detectable difference between IQOS and conventional cigarettes for 23 of the 24 biomarkers of potential harm'.80 In January 2018, the FDA’s Tobacco Products Scientific Advisory Committee concluded that PMI had not proven IQOS to be safer than conventional cigarettes.81
This paper joins these analyses in casting doubt on PMI’s health claims for IQOS. Based on product specifications, marketing and aerosol chemistry, IQOS appears to represent less of a technical breakthrough than it does an attempt to capitalise on a social and regulatory landscape more favourable than a similar precursor product’s. When the regulatory environment prohibited reduced risk claims, PMI’s parent company consistently stated that reduced exposure did not mean reduced risk. The FDA should take PM at its word.
What this paper adds
What is already known on this subject
Philip Morris International (PMI) claims that IQOS reduces users’ risk by reducing their exposure to harmful and potentially harmful constituents.
From 1998 to 2006, PMI’s parent company, Philip Morris (PM), marketed a strikingly similar heated tobacco product, Accord, with little commercial success.
What important gaps in knowledge exist on this topic
Independent assessment of PMI’s health claims for IQOS important, given the tobacco industry’s long history of misrepresented and manipulated research.
Analysis of internal communications surrounding Accord may help shed light onto PMI’s understanding of IQOS.
What this paper adds
PM scientists and executives consistently stated that Accord reduced users’ exposure to harmful constituents but that these reductions did not render Accord safer than conventional cigarettes.
IQOS’s design and marketing are similar to Accord’s.
We found that when comparing the aerosol chemistry test results between Accord and IQOS there was not a consistent reduction in exposure to toxicants, calling into question PMI’s current safety claims for IQOS, which are made on the basis of reduced exposure.
References
Footnotes
Contributors Conceptualisation, data curation, investigation, writing, original draft: JE and LMD. Formal analysis, writing, review and editing: JE, LMD, GSH and PML. Funding acquisition, resources, supervision and validation: PML. Methodology: JE, LMD and PML.
Funding This study was funded by Division of Cancer Prevention, National Cancer Institute (R01 CA87472).
Competing interests None declared.
Patient consent Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement All of the documents included in this study are publicly available through the Truth tobacco documents library at https://www.industrydocumentslibrary.ucsf.edu/tobacco/.