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21 Mar 2005 15:44:52 -0000

 

No Biotech Revolution in Sight

 

press-release

 

 

The Institute of Science in Society Science Society

Sustainability http://www.i-sis.org.uk

 

General Enquiries sam Website/Mailing List

press-release ISIS Director m.w.ho

========================================================

 

 

 

ISIS Press Release 21/03/05

 

Gene gold turning to dust?

 

No Biotech Revolution in Sight

***********************

 

Governments are sinking further billions into genomics and

related research but a new study finds no sign of revolution

in healthcare Dr. Mae-Wan Ho

 

The sources for this article are posted on ISIS members'

website http://www.i-sis.org.uk/full/NBRISFull.php. Details

here http://www.i-sis.org.uk/membership.php

 

What revolution?

 

Over the past decade, consultants, policy makers, academics

and industrialists have united in telling the world how

biotechnology, and genomics in particular, are

" revolutionizing " drug discovery and bringing about radical

changes in healthcare involving predictive and even

personalized medicine. These euphoric expectations underpin

science and technology policy not only in the rich countries

of the OECD and the European Union, but also some of the

less rich countries such as Malaysia (see " Biotech fever

grips Asia " SiS 16

http://www.i-sis.org.uk/isisnews/sis16.php).

 

UK's Prime Minister Tony Blair had described the human

genome map as " a revolution in medical science whose

implications far surpass even the discovery of antibiotics " ;

and said his government had made available an extra £100

million in 2003 to speed the introduction of new drugs, and

would boost investment in research.

 

But a study on the impact of biotechnology on medical

treatments published at the end of 2004 concluded that the

objective evidence provides no support for the idea of a

biotechnology revolution, and warned of " substantial

mismatch between the real world and the unrealistic

expectations of policy-makers " .

 

The tens of billions invested produced only a handful of

useful drugs over the past 20 years; and despite a 10-fold

increase in research spending worldwide, the total number of

new drugs has remained virtually unchanged.

 

The " breakthroughs " that weren't

 

The scientific " breakthroughs " have been equally

disappointing: Dolly the cloned sheep was supposed to bring

identical " elite herds " as `bio-factories' for

pharmaceuticals; but the cloning process proved extremely

difficult. Dolly became seriously ill and had to be put

down, extinguishing any hope of animal pharming (see " Animal

pharm folds " SiS 19

http://www.i-sis.org.uk/isisnews/sis19.php).

 

Dolly's creator Ian Wilmut gave up cloning animals (see

" Death sentence on cloning " , SiS 19

http://www.i-sis.org.uk/isisnews/sis19.php).

He applied instead to the Human Fertilisation and Embryology

Authority (HFEA) and was awarded a licence to clone human

embryos for stem cells research, holding out hope of curing

diseases by embryonic stem cell transplant.

 

But there is little moral or scientific justification for

such `therapeutic' human cloning, especially given the

technical difficulties of the cloning process and the known

risks in using embryonic stem cells for transplant, in

contrast with the proven successes and promise of adult stem

cells that can easily be obtained from patients requiring

the transplant (see " Human cloning & the stem cell debate " ,

SiS 16 http://www.i-sis.org.uk/isisnews/sis16.php).

 

The clinical successes of the patient's own adult stem cells

have been amply confirmed recently (see " Which stem cells "

series, SiS 25 http://www.i-sis.org.uk/isisnews/sis25.php),

at the same time that the technical, economic, safety and

ethical concerns over embryonic stem cell have multiplied

(see " No case for human embryonic stem cells research " , SiS

25 http://www.i-sis.org.uk/isisnews/sis25.php).

 

Gene therapy has yet to cure any person of major genetic

disorders such as cystic fibrosis or sickle cell anaemia.

To-date, nine children with X-linked severe combined immune

deficiency had apparently been successfully treated, by re-

implanting the patient's bone marrow cells that were

genetically modified in the lab. But three of the treated

children have developed leukaemia; and the full risks of

gene therapy are coming to light.

 

Gene therapy vectors provoke immune reactions that target

viral gene products, transgene products as well as plasmid

DNA (see " Gene therapy woes " this series). It was an acute

immune reaction that killed a healthy teenage volunteer in a

gene therapy clinical trial in 1999 (see " Failures of gene

therapy " , SiS 16

http://www.i-sis.org.uk/isisnews/sis16.php).

Five years later, serious safety concerns have emerged over

a new gene therapy technique hailed as a breakthrough in

2002 (see " Controversy over gene therapy breakthrough " ,

this series).

 

Mapping the human genome and the enormous expansion in `bio-

informatics' brought little in the way of miracle cures or

wonder drugs. In October 2004, another draft of the human

genome map was announced; and we are told it is only " the

end of the beginning " . But even that is not certain; for the

new genome map, though much improved in accuracy, is still

not complete. The `finishing' procedure roughly doubled the

total time and cost of the human genome project. And a lot

more investment is necessary to really bring about the

revolution in healthcare. `Health genomics' is indeed in

danger of being the " financial and scientific black hole " I

had predicted five years ago.

 

Facing the stark evidence

 

Paul Nightingale from the Science Policy Research Unit,

University of Sussex, and Paul Martin from the Institute for

the Study of Biorisks and Society, Nottingham, looked at

relevant indicators that might support the idea of there

being a biotechnology revolution.

 

The explosive increase of scientific publications in

genomics between 1978-2002 clearly indicated a major, and

possibly revolutionary, change in some of the scientific

inputs that may lead to drug discovery. But data from the US

Patent Office (USPTO) in the same period showed only a

steady rise in the number of patented compounds. Patenting

increased approximately seven-fold, while R and D spending

increased roughly ten-fold.

 

So, even if one takes into consideration the expected lag of

4–8 years between R and D investments and patenting, there

is no evidence of dramatic improvement in drug discovery. On

the contrary, there is a decline in R and D productivity as

measured by the number of patents per dollar spent on R and

D, and hence, a possible decline in research productivity,

at least in the short term.

 

Several other indicators followed the same trend.

 

The number of drugs approved by the FDA in the period

1983–2003 showed an increase until the mid 1990s, followed

by a sharp decline, so that roughly the same number of drugs

was approved in 2002 as two decades earlier. Set against the

substantial increase in R and D expenditure that took place

between 1970 and 1992 (i.e. allowing for the 8–12 year lag

between research investment and new product launches) there

is further evidence of a decrease in productivity rather

than the revolutionary increase we have been told to expect.

 

In terms of therapeutic proteins and antibodies that have

reached the market since 1980 and sold more than $500m a

year in 2002 and 2003, there are only 12 recombinant

therapeutic proteins and three monoclonal antibodies.

Moreover, three of the therapeutic proteins were already

characterized in 1980, with biotechnology simply leading to

new production techniques.

 

Other researchers in Edinburgh University and the Open

University using data that evaluate the performance of new

drugs, found only 16 drugs evaluated between January 1986

and April 2004 that were better than `minimal improvements'

over pre-existing treatments.

 

In short, the evidence provides no support for a

biotechnology revolution.

 

The biotechnology bubble

 

" The emergence of the biotechnology industry has rested

heavily on the creation of these high hopes and many people

in the sector have been active in promoting the idea of a

biotech revolution. " Nightingale and Martin wrote,

" Management consultants, financial analysts and venture

capitalists all clearly have a vested interest in hyping new

technologies. Similarly, the promise of a biotechnology

revolution provides government policy makers with simple,

but as our analysis suggests, probably ineffective ways of

promoting regional development, improved healthcare delivery

and economic growth. "

 

Nightingale and Martin continued: " Unrealistic expectations

are dangerous as they lead to poor investment decisions,

misplaced hope, and distorted priorities, and can distract

us from acting on the knowledge we already have about the

prevention of illness and disease. "

 

We remain caught in the biotechnology bubble created around

the scientific myth of genetic determinism that was

untenable even before the human genome was mapped, and

thoroughly exposed as such since then. The vast domains of

complexity that connects the genome to the rich tapestry of

life are refusing to yield to mechanistic analysis ( " Biotech

wonder tool in disarray " , this series). But the scientific

establishment and our policy-makers lack the moral and

intellectual courage to admit that to themselves or to the

public. So, governments continue to sink billions of

taxpayer's money into raising false hopes of gene therapy

and personalized medicine and putting society at risk from

eugenics. This money can be much more effectively invested

instead to address the real causes of ill-health, which are

overwhelmingly social and environmental ( " Why genomics won't

deliver " , this series).

 

 

 

========================================================

This article can be found on the I-SIS website at

http://www.i-sis.org.uk/NBRIS.php

 

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press-release ISIS Director m.w.ho

 

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