Continuous Update Project A basis for cancer prevention and control - - PowerPoint PPT Presentation

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Continuous Update Project A basis for cancer prevention and control - - PowerPoint PPT Presentation

Continuous Update Project A basis for cancer prevention and control worldwide MARTIN WISEMAN World Cancer Research Fund International World Cancer Congress August 2012 Journal citations - WCRF/AICR Reports 500 450 400 350 Number of


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MARTIN WISEMAN World Cancer Research Fund International World Cancer Congress August 2012

A basis for cancer prevention and control worldwide

Continuous Update Project

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Journal citations - WCRF/AICR Reports

50 100 150 200 250 300 350 400 450 500 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 Number of citations Doll & Peto 1981 1997 EXPERT REPORT 2007 EXPERT REPORT

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Breast

Global variation in cancer incidence

Colorectum

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Migration data

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Around one third of the commonest cancers estimated avoidable through appropriate food, nutrition and physical activity

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Number of papers from cohort studies by year and cancer type

0" 20" 40" 60" 80" 100" 120" 140" 160" 180" 200" 1980" 1982" 1984" 1986" 1988" 1990" 1992" 1994" 1996" 1998" 2000" 2002" 2004" 2006" 2008" 2010" Number Breast" Colorectum" Prostate" Pancreas" Endometrium" Ovary"

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Everybody has a role to

play Action needs to be coherent Leadership from Government Health professionals

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Examples of 2007 WCRF/AICR Expert Report impact

q Norwegian Dietary Guidelines q CRUK Prevention estimates

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Novel aspects of CUP

q Breast Cancer Survivors q Mechanisms

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Novel aspects of CUP

q Breast Cancer Survivors q Mechanisms

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Inclusion criteria

q Survivors of prim

Survivors of primary bre ry breast c st canc ncer r

q Food, nutrition, physic

Food, nutrition, physical a l activity, nutrition- tivity, nutrition- re rela late ted c d com

  • mple

plementa ntary m ry medic dicine ine

q R

Random ndomise ised c d controlle

  • ntrolled tria

d trials ls

  • during a

during and a nd afte fter the r thera rapy for prim py for primary bre ry breast st canc ncer r

q Obse

Observa rvationa tional studie l studies - s - exposure

xposure a asse ssessm ssment nt

  • be

before fore prim primary bre ry breast c st canc ncer dia r diagnosis gnosis (c (childhood, a hildhood, adole dolesc scenc nce, a , adulthood) dulthood)

  • at dia

t diagnosis gnosis

  • during the

during thera rapy py

  • afte

fter the r thera rapy py

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Outcomes

q All-c

ll-cause use m morta

  • rtality

lity

q Bre

reast c st canc ncer m r morta

  • rtality

lity

q Se

Second prim

  • nd primary bre

ry breast c st canc ncer r

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Novel aspects of CUP

q Breast Cancer Survivors q Mechanisms

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Raise standards for preclinical cancer research

  • C. Glenn Begley and Lee M. Ellis propose how methods, publications and

incentives must change if patients are to benefit.

Many landmark findings in preclinical oncology research are not reproducible, in part because of inadequate cell lines and animal models.

  • S. GSCHMEISSNER/SPL

29 MARCH 2012 | VOL 483 | NATURE | 531

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Mechanisms Protocol Development Group

External Experts

q Stephen Hursting (chair) q Andrew Dannenberg q Johanna Lampe q Henry Thompson q Steven Clinton q Nikki Ford - associate

member

WCRF Team

q Martin Wiseman q Susan Higginbotham q Rachel Thompson q Rachel Marklew q Kate Allen q Deirdre McGinley-Gieser

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Cancer: A Complex Process

Inflammation Genomic instability Tissue invasion and metastasis Limitless replicative potential Sustained angiogenesis Evading growth suppression, apoptosis and immune surveillance Dysregulated growth signals and cellular energetics

Adapted from: Hanahan & Weinberg, Cell (2000) and Cell (2011)

✔ ✔ ✔ ✔ ✔ ✔ ✔

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Adapted from: IARC List of Mechanistic Targets

Revised IARC List of Mechanistic Targets (with Hanahan and Weinberg)

1. Genomic instability 2. DNA damage/repair (specify) 3. Gene mutation (specify) 4. Epigenetic markers (specify) 5. Gene expression/miRNA changes (specify) 6. Serum hormones/growth factors (specify) 7. Urinary or tissue metabolite 8. Inflammation

  • a. Cytokines (specify)
  • b. Tissue markers (specify)
  • c. Histological classification (specify)
  • 9. Cell proliferation markers (specify)
  • 10. Immunologic effects (specify)
  • 11. Invasion/metastasis process (specify)
  • 12. Angiogeneic effects (specify)
  • 13. Cell signaling effects (specify)
  • 14. Cell energetics effects (specify)
  • 15. Differentiation (specify)
  • 16. Cell death (apoptosis/autophagy/necrosis)
  • 17. Replicative potential/ Stem cell enrichment
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Mechanisms

q Reviews to be systematic and peer

reviewed

q Reviews conducted by exposure q Pre-feasibility pilot q Feasibility test of final draft protocol by

external group, including peer review

q External review team should have

expertise in informatics, stats, cancer biology, cancer site, nutrition

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How to manage vast body of evidence

q Consider limiting reviews to more

recent publications when abundant evidence

q Consider early exclusion of

inappropriate models

q Use informatics expert

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Timeline

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Conclusions

q The 2007 WCRF/AICR Report remains the

most authoritative review in the area

q The CUP maintains the currency of the

conclusions and recommendations

q Together these provide a firm basis for

public health and policy actions to prevent cancer, and other chronic diseases, worldwide

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http://www.dietandcancerreport.org