APPENDIX 11
Memorandum by Imperial Cancer Research
Fund (TB 24)
The Imperial Cancer Research Fund welcomes this
opportunity to submit evidence to the Select Committee on Health's
inquiry into the tobacco industry's response to evidence of tobacco
harms. Our mission is to contribute knowledge leading to reductions
in cancer morbidity and mortality. Our research scientists have
made important contributions to knowledge in key areas of tobacco
research: finding out the true extent of the burden of ill health
and premature death caused by cigarette smoking in the UK and
worldwide; and unravelling the underlying role of nicotine in
motivating smoking behaviour. It is now abundantly apparent that
nicotine is a powerfully addictive drug, in many respects on a
par with drugs such as heroin and cocaine, and in terms of its
intractability to change perhaps the most addictive of all the
drugs that are widely used in society. Nicotine addiction currently
leads to the premature deaths of about 120,000 people each year
in the UK, and is responsible for one in five of all deaths, and
one in three deaths from cancer.
The surest way to reduce the burden of tobacco
related disease is to persuade fewer young people to take up smoking
in the first place and more established smokers to give it up.
We fully support policies aimed at achieving this, including year-on-year
real increases in the price of cigarettes, school and public education
campaigns, provision of smoking cessation treatment under the
NHS, and greater restrictions on smoking in public places. However,
in addition to policies targeting smoking uptake and cessation,
a complementary approach is to attempt to reduce the hazards of
ongoing smoking for those who cannot or will not give up. This
has so far received less attention. If people smoke for nicotine,
but die from the effects of tar and harmful gases, then a logical
strategy would be to provide smokers with the nicotine they seek
with as little of other smoke toxins as possible. From this perspective,
the cigarette is viewed simply as a nicotine delivery deviceone
which is uniquely contaminated by carcinogens and other noxa in
the tar and gas produced by combustion.
For the past 25 years efforts to reduce the
harmfulness of cigarettes have focused on lowering machine-smoked
yields of tar and nicotine. Tar yields are now about half the
levels they were in 1970. These reductions may have initially
contributed to some lowering of risks from cigarette smoking,
but it is now apparent that further reductions in nominal yields
will confer no public health benefit, while actively confusing
and misleading smokers.
Cigarette yields are measured by smoking cigarettes
in a machine in a conventional way. Lowered deliveries are achieved
principally by diluting the smoke with air drawn in through filter
ventilation holes. In some ultra-low yielding brands the extent
of filter ventilation can be over 80 per cent. The underlying
tobacco in low yield brands is not low yieldin fact the
total nicotine content of the tobacco used in lower and higher
yielding brands is very similar. This means that smokers can (and
do) readily compensate for lower nicotine from low-yielding brands
by manoeuvres such as increased intensity of puffing, and blocking,
intentionally or otherwise, of filter ventilation holes. There
is a wealth of evidence which shows that actual intakes are reduced
little if at all in smokers of lower yielding brands. Compensation
for nicotine is essentially complete, with the implication that
tar exposures from brands of widely differing nominal yields are
also similar.
If lowered nominal tar yields do not lead to
lowered dose, they certainly do serve to confuse smokers. It would
not be unreasonable for cigarette consumers to infer that a cigarette
listed as yielding, say, 10mg of tar should produce a tar dose
10 times higher than one yielding 1mg.
Internal tobacco company documents show that
the industry has understood for over 20 years that the reduction
of machine-smoked yields offers no meaningful reduction in dose
and hence no meaningful health benefits. They have nevertheless
exploited low delivery cigarettes, which they term elastic or
compensatible products, to provide health reassurance to smokers.
In so doing they may have dissuaded some health-concerned smokers
from giving up, and deflected company research efforts from developing
alternative nicotine delivery devices which offer real health
gains.
It is clear that the tobacco industry cannot
be relied upon to make serious moves of its own accord towards
less toxic products. It is constrained both by its failure to
acknowledge the reality and extent of the burden of disease caused
by tobacco and by its unwillingness to openly acknowledge the
underlying role of nicotine addiction. Regulatory control by government
in the UK has been extremely weak. There is now scope for a fresh
and more effective approach to regulation. In the United States
the Federal Trade Commission has publicly recognised the misleading
nature of its test for cigarette yields, and the Food and Drug
Administration has asserted jurisdiction over tobacco products,
thus opening the way for consumer productssuch as cigarettes to
be brought under similar regulatory scrutiny to pharmaceutical
nicotine delivery products such as nicotine gum and transdermal
patches. The committee might well consider that there is a strong
case for a similar nicotine regulatory authority in the UK, either
freestanding or under the aegis of the Medicines Control Agency.
October 1999
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