World Summit Against Cancer for the New Millenium
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The
fight against the increasing threat of cancer is a challenge that cannot
successfully be fought in isolation.
The World Summit Against Cancer for the New Millennium, held in Paris, outlined
the need for a global commitment aiming at co-ordinating and harmonising the
efforts and actions of Research Centres, Hospitals, Voluntary and Patients
Associations, Schools and Public Institutions involved in fighting cancer.
This is the content of the Charter of Paris, signed on February 4th,
2000, by over 100 oncology experts and Anti-Cancer Associations:
a great effort
to work and grow together
for the improvement of health and quality of life
of patients affected by cancer
Preamble
Deeply
troubled by the profound and universal impact of cancer on human life, human
suffering, and on the productivity of nations,
Committed
to the humanitarian treatment and equal partnership of people with cancer in the
ongoing effort against this disease,
Anticipating
the rapidly rising tide of cancer incidence throughout the globe, in developed
and developing nations alike,
Recognizing
the need for intensified innovation in all avenues of cancer research,
prevention and healthcare delivery,
Believing
that quality healthcare is a basic human right,
Acknowledging
that currently achievable improvements in cancer survival remain unrealized, due
to inadequate emphasis on prevention, inadequate funding and unequal access to
quality cancer care,
Certain
that lives can and will be saved by increased access to existing technologies,
Aspiring to nothing less than an invincible alliance --
between researchers, healthcare professionals, patients, government, industry
and media -- to fight cancer and its greatest allies, which are fear, ignorance
and complacency…
We, the undersigned, in order to prevent and cure cancer, and to maintain the
highest quality of life for those living with and dying from this disease, fully
commit and hold ourselves accountable to the principles and practices outlined
herein.
Articles
Article I
Cancer patient rights are human rights. The currently
evolving movement to define and adopt cancer patients' rights is critical to
recognizing and protecting the value and dignity of individuals with cancer
throughout the world.
Article II
The
stigma associated with cancer is a significant barrier to progress in both
developed and developing nations, often causing:
- undue
emotional trauma for patients and their families
- bias and discrimination against employment of people with cancer
and/or their meaningful participation in and contribution to society
- related financial hardship and loss of productivity
- poor communication and insufficient public education
- an undue sense of fatalism that can adversely impact the
commitment of governments, health agencies and private institutions
in the war against cancer.
The
parties to this charter undertake to better understand and eradicate the stigmas
associated with cancer, to assertively redefine the disease as a treatable
biological pathology and not a social condition.
The positive realignment of popular opinion, perception,
and concern regarding cancer and the millions of lives it affects will enable
the full realization of each of the following priorities.
Article III
The
parties undertake a vigorous commitment to create an optimal environment for
anti-cancer research innovation.
1.
Knowledge of the biology of cancer and the fundamental mechanisms by which
cancers emerge and progress is the origin of all advances that have increased
and will further increase the rate of cure and the quality of life of millions
of people worldwide. The identification of new targets for detection, diagnosis
and treatment must accelerate if we are to win the war against cancer.
The parties agree to aggressively build the case for
enhanced government and industry funding of basic research, to encourage,
protect and incentivize those who innovate, and to increase the means by which
scientists may labor in intellectual freedom to constantly advance the frontiers
of current knowledge.
2.
Clinical research is the sole means by which basic research becomes
meaningful to the lives of human beings. Breakthroughs in molecular biology
or genetics can have no impact on cancer prevention, screening, diagnosis
and treatment unless they are carefully evaluated and developed in clinical
trials.
Research
in the clinic also can immediately inform ongoing basic research
efforts. This kind of translational research, commonly conducted by
institutions with both a basic and clinical research capability, rapidly tests
hypotheses generated in the laboratory. Immediate feedback from the clinic
obtained through translational research can meaningfully redirect basic
research efforts and stimulate the generation of important new hypotheses.
Despite
its importance, clinical research is significantly challenged not only by
a lack of funding, but often by a lack of involvement on the part of healthcare
professionals and institutions -- and a lack of awareness among patients of
the purpose and benefits of participating in clinical studies. Inadequate legal
and regulatory harmonization between countries also means that large
international clinical trials - the kind that are statistically powerful and can
rapidly advance medical practice - can be extremely difficult and costly to
conduct.
The parties pledge to elevate awareness and commitment
to clinical research
among all constituencies they represent and to seize every opportunity to
strengthen the international research infrastructure. The parties further
pledge to advance universal recognition of informed consent - the process
by which patients are fully advised of the purpose, risks, and benefits of any
clinical study. In so doing, the parties seek to enable rapid, powerful and
inclusive clinical trials that ethically engage and also empower people with
cancer.
Article IV
Despite
the considerable strides that have been taken in the fight against cancer,
survival outcomes vary dramatically throughout the world - not just between
countries, not just between cities, but even between institutions within the
same city. Wide variations in standards of care and access to quality cancer
care are a major cause of these discrepancies -- and the often unnecessary
morbidity and mortality that result.
The
parties reaffirm Article 25 of the Universal Declaration of Human Rights, which
states that every individual "has the right to a standard of living
adequate for the health and well-being of himself and of his family, including
food, clothing, housing and medical care." The parties further assert that
given the ubiquitous presence of cancer and its impact on society, the provision
of quality cancer care within the local economic context is a basic human right.
The parties therefore endeavor to promote:
1.
Evidence-based medical practice and clear definition of "quality care"
according to all available scientific evidence.
2.
Systematic development of guidelines based on the best available evidence for
prevention, diagnosis, treatment and palliative care.
3.
Appropriate prioritization of quality anti-cancer care at every level of
healthcare provision, consistent with the total burden of disease.
4.
Intensified cancer specialization and better integration of care among
medical disciplines.
5. Widespread patient access to high quality clinical
trials.
Article V
The
World Health Organization estimates that by the year 2020, 20 million new cases
of cancer will emerge each year. 70% of these patients will live in countries
that between them will have less than 5% of the resources for cancer control.
Cancer will continue to become an increasingly important contributor to the
global burden of disease as we enter the next millenium, despite the fact that
many cancers are preventable through control of tobacco use, diet, infection and
pollution. It is estimated, for instance, that infections -- many potentially
preventable -- cause 15% of cancer worldwide and 22% of cancers in the
developing world. The use of tobacco similarly causes millions of new cancers
and cancer deaths each year, in both the developed and the developing world.
This
reality emphasizes the need for development of public policies that support the
fight against cancer and urgent deployment of existing knowledge and
technologies in the basic prevention of cancer to stem the rising tide of
disease. The parties undertake to:
1.
Actively support existing cancer prevention programs globally and build
awareness and commitment to cancer prevention across all constituencies they
represent.
2.
ldentify opportunities to accelerate public education in tobacco control, diet
modification, infection control and environmental protection.
3.
Organize the support of industry and governments to enhance the delivery of
cancer prevention through medical technology wherever possible
Article VI
It is an
uncontested fact that early detection of cancer for any or all of the two
hundred or more varieties, leads to a better outcome for the patient.
Importantly, the treatment of several recognizable pre-cancerous conditions also
can prevent cancer. Fear and ignorance of signs and symptoms of cancer or
precancerous conditions are common, however, and by its nature cancer can be
insidious and difficult to detect without a screening intervention. It is also
known that early detection is particularly important for those people at high
risk of cancer, due to lifestyle, environment, occupation, family predisposition
or low socio-economic status.
Recognition
that the earliest symptoms of cancer can be confused with common illnesses
further emphasizes the need for effective screening and attentive medical
diagnosis. Screening methodology to identify cancer early can extend from simple
observation, laboratory tests and x-ray examinations to more sophisticated
examinations, all of which have proven value in the early detection of several
cancers. In addition to education about cancer prevention, implementation of
screening programs -- within economic possibilities -- should be a prime
objective to reduce the cancer burden. These screening programs must be coupled
with access to quality treatment in order to be effective.
The parties undertake to accelerate the development and
widespread application of proven and emerging screening technologies, such that
all individuals who might benefit from screening will do so, irrespective of
race or socio-economic status.
Article VII
Individual
and constituency-based patient advocacy has directly and favorably impacted the
war against cancer in instances in which it is well informed and rooted in an
understanding of and commitment to quality science and evidence-based medical
practice. As the primary stakeholder in the anti-cancer effort, the patient is
uniquely positioned to focus the overall anti-cancer effort on eradication of
disease and on the optimal use of resources to benefit people at risk of cancer
and people living with and fighting the disease.
The
parties undertake to strengthen the position of the cancer patient as an active
partner in the fight against cancer and will actively promote the following
principles:
1. All
people affected or potentially affected by cancer should have free and equal
access to information on disease origin, prevention and current standards for
detection, diagnosis and treatment.
2. Open
and collaborative communication between people with cancer and health care
professionals and scientists is essential.
3. A
commitment to total patient well being includes not only clinical care but also
information and psychosocial support. Health care professionals and people with
cancer share the responsibility to ensure that total patient needs are met.
4.
People with cancer throughout the world have the opportunity to become informed,
organized and influential.
5. The
professional medical community, recognizing the power and
benefit of an informed and active public, will help facilitate popular
commitment to both the scientific process and the practice of evidence-based
medicine.
6. The medical research, industry and policy
communities will regard informed patient advocates as key strategic partners in
all aspects of the fight against cancer, including the advancement of standards
of care and survival.
Article VIII
Improving
patients' quality of life is a primary objective in the effort against cancer.
Both the physical and emotional burdens of cancer can be significant, and often
they are compounded by the side effects of treatment. Because clinical outcomes
can be affected by the overall state of a patient's mental and physical well
being, the preservation of quality of life -- including physical, psychological
and social functioning -- should be a medical as well as a humanitarian priority.
It also must be noted that while giant strides have been taken to improve cure
rates in the last 20 years, the majority of the world's cancer patients today do
not experience a cure.
When
cancer is not curable, important quality of life advantages still can be
achieved through optimal anticancer treatment (chemotherapy, radiotherapy) and
supportive care, including pain and fatigue management, and end of life
palliation.
The
parties will pursue the following goals to increase commitment to quality of
life issues in the fight against cancer:
1.
Improvement in the comprehensive care of people with cancer including
supportive care and palliation through specific treatment modalities.
2.
Recognition at the clinical and also at the policy level of the importance of
patients' quality of life, regardless of the stage of the disease and prognosis,
and optimal supportive care of cancer patients, particularly in instances in
which cure is not achievable.
3.
Prioritization of quality of life as a key endpoint in the development of new
drugs and also in patient care.
4.
Aggressive, continued development of scientific tools to measure and assess
quality of life in the clinical setting.
5.
Intensive education of healthcare professionals and cancer patients regarding
both the need and the opportunity for effective cancer pain control at every
stage of disease and treatment. Cancer-related pain profoundly impacts quality
of life and is often grossly underestimated and undertreated, even when it can
be adequately controlled.
6. Pursuit of a better understanding and also a
transformation of attitudes regarding death and dying, to ensure that the end of
life is accepted as a natural experience that can and should be addressed
medically, psychologically, emotionally and spiritually. Optimal medical care of
the dying cancer patient must be effective, humane and compassionate
Article IX
Recognizing
the wide variability in resources and epidemiology throughout the world, the
parties agree that individual countries must design national anti-cancer
strategies according to local needs, and apply resources where they will have
the greatest impact. Some nations might choose, for instance, to fund as a first
priority strategies against those cancers that are preventable or curable,
including prevention education and specific treatments. Other countries might
strengthen immunization efforts as part of an overall cancer control strategy or
more aggressively support the use of adjuvant chemotherapy to improve cancer
survival outcomes. Each of these variable needs and opportunities have recently
been defined by the World Health Organization in its effort to craft a global
cancer control strategy.
It is
clear that regardless of economic circumstance, a critical assessment of
anti-cancer needs, appropriate planning and prioritization can meaningfully
curtail the impact of cancer in both developed and developing nations alike.
The
parties undertake to actively support the concept of national anti-cancer
planning according to local need and resource. They further pledge to challenge
all communities engaged in the fight against cancer to ensure such planning
sufficiently prioritizes the current and looming cancer crisis -- and optimally
captures the significant opportunity to reduce cancer-related morbidity and
mortality.
Article X
Since
cancer knows no boundaries, and individual countries cannot address the
challenges of cancer in isolation, a new cooperative approach to research,
advocacy, prevention and treatment must be established.
The parties undertake to develop unprecedented global
networks and alliances to further the goals of this charter. They further pledge
to ensure that the objectives of this charter are not abandoned after its
signing, by:
1.
Recognizing the declaration by all appropriate institutions that February 4
shall be marked as "World Cancer Day" so that each year, the Charter
of Paris will be in the hearts and minds of people around the world.
2.
Establishing standing committees that will produce annual reports, benchmarking
progress against each of the articles of the Charter.
3.
Forming a global network of advocacy groups to encourage grassroots support for
charter articles within their communities.
4.
Creating a global research organization made up of leading professional
societies around the world. This group will be dedicated to ensuring that
current knowledge is shared across borders, research gaps are identified and
promising areas are explored.
5.
Rallying one million people around the world to sign the Charter of Paris by the
year 2001, thereby showing their willingness to mobilize on behalf of those
affected by cancer.
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Dr. Alan S. Coates |
Dr. David Khayat |
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Dr. Dieter K. Hossfeld |
Dr. J. Gordon McVie |
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Dr. Thierry Philip |
Dr. Eiichi Tahara |
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Dr. Weiming CAI |
Prof.
Natale Cascinelli |
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Mrs Lilly Christensen |
Prof. Alan S. Coates |
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Dr. Margaret Foti |
Jean Claude Horiot |
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Pr. Dieter Hossfeld |
Dr. Heizaburou Ichikawa |
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Dr. Thierry Le Chevalier |
Mr. Michel Lucas |
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Dr. Ruggero Montesano |
Prof.
Pier Giorgio Natali |
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Prof. Eliezer Robinson |
Mrs Elle Stovall |
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Dr. Tetsuo Taguchi |
Ms Frances M Visco |
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Dr. Jacqueline Whang Peng |
Dr. Gerald Woolam |
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Dr. Derek Yach |
The Charter of Paris was signed by Pier Giorgio Natali,
M.D. as President of SIC (Società Italiana di Cancerologia) and
Scientific Director of the Regina Elena Cancer Institute
The document was translated by the "International
Affairs Bureau" of the Institute.