Infection and cancer: a significant part of the global cancer - - PowerPoint PPT Presentation

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Infection and cancer: a significant part of the global cancer - - PowerPoint PPT Presentation

Infection and cancer: a significant part of the global cancer burden David Forman Section of Cancer Information Cancer & Infection Session Global burden of cancers attributable to infections in 2008 Goals Estimate the number of


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Infection and cancer: a significant part of the global cancer burden

David Forman Section of Cancer Information

Cancer & Infection Session

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Global burden of cancers attributable to infections in 2008

Goals

  • Estimate the number of incident cancers attributable to

infection worldwide: – Geographic distribution. – Relation to total cancer burden – Assess global cancer impact of most important infectious agents

  • Help set regional priorities for cancer control
  • Update previous estimates for 1990 and 2002
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Monograph 100. A review of human carcinogens Part B: Biological agents (February 2009) http://monographs.iarc.fr/ENG/Monographs/vol100B/

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Global burden of cancers attributable to infections in 2008

  • GLOBOCAN 2008 (globocan.iarc.fr) estimates of cancer

incidence, mortality and prevalence in the year 2008 – 184 countries – 27 cancer sites

  • We extended estimates to include sub-sites associated

with infection.

  • Incidence estimates were aggregated into eight

geographic regions.

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Global burden of cancers attributable to infections in 2008

  • 12.7 million cancer cases (Globocan 2008)
  • 2.0 million (16%) attributable to infection

– 22.9% in less developed countries – 7.4% in more developed countries

  • 10-fold variation between regions

– 32.7% in Sub-Saharan Africa – 3.3% in Australia and New Zealand

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Fraction of new cancer cases attributable to infection: Population attributable fraction (PAF) by world regions

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  • Number of new cancer cases occurring in 2008

attributable to infectious agents by anatomic site

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Global burden of cancers attributable to infections in 2008

Cancer site Global incidence estimate Number attributable to infection Population Attributable Fraction (%)

Gastric (non-cardia) 870,000 650,000 74.7 Liver 750,000 580,000 76.9 Cervix uteri 530,000 530,000 100 Nasopharynx 84,000 72,000 85.5 Kaposi’s sarcoma 43,000 43,000 100 All other 893,000 168,000 Total 2 million

de Martel et al. (Lancet Oncol, 2012)

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Numbers are rounded to two significant digits

Number of new cancer cases attributable to infection in 2008 by development status

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Number of new cancer cases attributable to infection in 2008 by development status

Less developed regions More developed regions

Thousands new cases

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Relative percentage of new cancer cases attributable to infection by sex, age group, and development status

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Human papillomavirus

  • HPV is a necessary cause of cervical cancer
  • Prevalent in other anogenital cancers:

– Penis: 50% – Anus: 88% – Vulva: 43% – Vagina: 70%

  • Found in a sub-set of oropharyngeal cancers

(oropharynx, including tonsils and base of tongue)

– Prevalence from 56% (N America) to 13% (Outside Europe, N America, Australia & New Zealand, Japan)

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Cancers attributable to HPV

Worldwide, cervical cancer dominates the HPV-associated cancers In N America, where cervical cancer is controlled by screening, HPV-associated cancers at other sites are equally important.

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Hepatitis viruses

  • Both HBV and HCV are strong risk factors

for liver cancer (R ~ 20)

  • HCV is also associated with non-Hodgkin

lymphoma (PAF=8%)

  • Strong geographical variation in

prevalence of both HBV and HCV in liver cancer cases.

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Prevalence of HBV in cases of hepatocellular carcinoma

86.1

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Prevalence of HCV in cases of hepatocellular carcinoma

78.7

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Helicobacter pylori

  • H. pylori is a risk factor for gastric cancer, but

risk is restricted to non-cardia location.

  • H. pylori is also associated with non-Hodgkin

lymphoma of gastric location (MALT and DLBC), PAF=74%

  • Once acquired (usually in childhood), infection

tends to be lifelong

  • Treatment is c. 90% effective with a combination
  • f antibiotics and acid lowering drugs
  • Screen and treat is a policy that may be an

effective means of preventing gastric cancer – not yet adequately evaluated

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Comparison of other estimates of proportion

  • f cancers attributable to infection
  • World (2002)

– 17.8% (Parkin 2006) vs 16.1%

  • China

– 25.9% (Xiang et al 2011) vs 26.1%

  • South Korea

– 21.2% (Shin et al 2011) vs 22.5% (E Asia)

  • UK

– 3.1% (Parkin 2011) vs 7.0% (Europe) or – vs 4.0% (N America)

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Global burden of cancers attributable to infections in 2008

Conclusions

  • Wide geographic variation in the fraction of cancers

attributable to infection.

  • Almost a quarter of all cancers in less developed

countries have an infectious cause.

  • Importance of HPV, H. pylori, HBV, and HCV as main

cancer-related infectious agents.

  • Available strategies for prevention

– vaccination against HBV and HPV – use of safe injection practices and avoidance of parenteral treatment for HCV – antibiotics for control of H. pylori (requires evaluation)

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Global burden of cancers attributable to infections in 2008

Infection and Cancer Epidemiology Group

  • Catherine de Martel
  • Martyn Plummer
  • Jerome Vignat
  • Silvia Franceschi

Section of Cancer Information

  • Jacques Ferlay
  • Freddie Bray
  • David Forman

De Martel C, Ferlay J, Vignat J, Franceschi S, Bray F , Forman D, and Plummer M. Global burden of cancers attributable to infections in 2008: A review and synthetic

  • analysis. Lancet Oncology,13:607-15, 2012
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GAVI’s mission

Strategic goals 2011–2015

! Accelerate the uptake and use of underused and new vaccines ! Contribute to strengthening the capacity of integrated health systems to deliver immunisation ! Increase the predictability of global financing and improve the sustainability of national financing for immunisation ! Shape vaccine markets

To save children’s lives and protect people’s health by increasing access to immunisation in poor countries

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The power of partnership: the GAVI Alliance Board

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What countries have achieved with GAVI support

! Immunised 326 million children ! Prevented over 5.5 million future deaths ! Accelerated vaccine introductions in over 70 countries ! Strengthened health systems to deliver immunisation ! Helped shape the market for vaccines

Source: These estimates and projections are produced by the WHO Department of Immunization, Vaccines and Biologicals, based on the most up-to-date data and models available as of 30 September 2011. *Includes deaths averted by GAVI-supported vitamin A supplementation programmes.

Future deaths averted

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Accelerating Hepatitis B vaccine introduction in low-income countries

4

Source: WHO, Vaccine introduction database

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Driving equity in vaccine access

Source: WHO, Vaccine introduction database.

Hepatitis B Routine use of vaccines in high- and low-income countries

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GAVI support 2000-2011

Source: GAVI Alliance 2012

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Increased competition reduces vaccine price

Price decline of pentavalent vaccine and number of manufacturers

Source: UNICEF Supply Division, 2012

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Pentavalent vaccine - 5 in one shot - diptheria tetanus pertussis hep B and hib

Source: GAVI Alliance data as of 13 April 2012

Approved for pentavalent vaccine support 2000 – April 2012

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China hepatitis B vaccine success story

! US$ 76 million project equally funded by GAVI and the Government of China ! Aim: accelerate integration of hep B vaccine into EPI and ensure injection safety ! Focus: W. China and poor areas in Central China ! Results: 2001-2009 in project counties

! Hep B 3 coverage - 40% to 95% increase ! Hep B at birth coverage - 50% to 88% increase ! 90% use of autodisable syringes

! Carrier rate in children under 5 dropped 10% to 1% ! Catalytic: Government fully funding Hep B vaccines

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rop in chronic carrier rate between 1979 - 2006

0.00 2.00 4.00 6.00 8.00 10.00 12.00

1~4 5~9 10~14 15~19 20~24 25~29 30~34 35~39 40~44 45~49 50~54 55~49 HBsAg (%) Age Group (year) 1979 1992 2006

1.Qu Z. An epidemiological study on the distribution of HBsAg and anti-HBs in China. Chine Journal of Microbiogy Immunology. 1986; Suppl(20-40). 2.Dai ZC, G.M. Q. Seroepidemiological Survey in Chinese population (part one), 1992–1995. Beijing. Sci Tech Exp. 1996: 39-59. 3.Liang X, Bi S, Yang W, Wang L, Cui G, Cui F, et al. Epidemiological serosurvey of hepatitis B in China--declining HBV prevalence due to hepatitis B vaccination.

  • Vaccine. 2009; 27(47): 6550-7.!

14 0.96% 514 2.42% 1559 8.57%

Courtesy: Dr Cui Fuqiang

!!!!!!!!!!!!Prevalence!of!HBsAg!in!age!groups!surveyed!in!the!year!of!1979,!1992!&!2006!

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India: Pentavalent vaccine introductions 2011– 2012

Introduced 2011 Introductions 2012

Courtesy: WHO and UNICEF, India

11

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Thank you

UNICEF/2006/Josh Estey

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13

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Source: UNICEF Supply Division, 2010

Hepatitis B price decline

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HPV vaccine: a critical component in a comprehensive cervical cancer prevention program

UICC World Cancer Congress Montreal, August 27-30, 2012

Vivien Tsu

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Background on cervical cancer

  • Estimated to increase from

529,828 cases in 2008 to 776,032 in 2030*

  • Failure of cytology

screening to have impact in low- or middle-income countries

  • New prevention opportunity

in form of vaccines against primary causal agent— human papillomavirus (HPV)

Incidence highest in low and middle income countries

*Globocan, 2008

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Two vaccines available

  • Both highly effective

against HPV types 16 and 18—responsible for ~70% of cervical cancer*

  • Both very safe—no

deaths, rare serious adverse events (for women with other risk factors)

*One also protects against non-

  • ncogenic types, HPV 6 and 11
  • Both registered in >120

countries

  • Both pre-qualified by

WHO (i.e. safe and effective for UN purchase)

  • Recommended by WHO

for girls aged 9-13

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National and pilot introductions

43 countries – national 20 countries – pilot or demo

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PATH HPV Vaccine Demonstration Projects

Vietnam

(provinces)

Thanh Hoa

Peru

(regions)

India

(states)

Uganda

(districts)

  • Ibanda
  • Nakasongola
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  • Schools
  • Community health centers
  • Outreach programs

All countries Vietnam, Peru, India (out-of-school girls) Uganda

Over 66,000 girls eligible

Vaccine delivery strategies

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Overall, coverage was high – both initial acceptance and completion

  • Little difference in coverage between strategies: greater variance

in terms of cost per vaccinated child

  • Strong community mobilization efforts; careful training of health

workers

India (Yr1) Peru (Yr1) Uganda (Yr2) Vietnam (Yr2) At least 1 dose 82% 84% 96% 97% All 3 doses 79% 82% 89% 96% Completion 1 → 3 97% 98% 93% 99%

Coverage survey data, school-based delivery

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Communication materials developed

  • Manuals
  • Leaflets
  • Posters
  • Fact book
  • Radio spots
  • Banners
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Lessons learned: Factors for success

1. Secure visible government endorsement / participation. 2. Provide training for health workers, teachers, and others involved in program. 3. Engage communities through sensitization and mobilization, with strategic use of media. 4. Use pulsed schedules to facilitate community awareness and ease health worker burden. 5. Build educational messages on positive attitudes towards vaccines, prevention of cancer. 6. Have crisis communication plan in place. 7. Tailor delivery strategy. Schools can reach majority of eligible girls, with mop-up for those not in school (or absent on vaccination day).

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Practical Experience Series from PATH

  • Lessons learned and resources for

decision-making and vaccination program planning.

– Planning – Formative research – Vaccine implementation – Evaluation – Screening

www.rho.org/HPV-practical-experience.htm

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Vaccine financing

  • Low income countries

– GAVI approved, 2011 – Contingent on final price negotiated (<$5/dose) and country ability to deliver successfully

  • Middle income

– Price drop (~$15-30/dose) – PAHO Revolving Fund (~

$13/dose)

$0 $25 $60 $120

2006 07 08 09 2010

Price per Dose

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GAVI opportunity

  • 57 countries eligible for GAVI assistance
  • 2 HPV vaccine pathways approved

– National introduction – Demonstration project

  • Demonstration project has 3 objectives
  • 1. Learn by doing, on small scale first
  • 2. Explore opportunities for integrating with other

adolescent interventions

  • 3. Strengthen or develop comprehensive national

cervical cancer control strategy

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Many resources now available

  • Online library at

www.rho.org

  • Action planner
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WHO tools for cervical cancer prevention and control

http://www.who.int/nuvi/hpv/resources/en/index.html http://www.who.int/reproductivehealth/topics/cancers/index.html

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Why a comprehensive prevention approach?

  • Vaccine not 100% effective – still need screening
  • Issue of generational equity – many women already

infected, won’t benefit from vaccine

  • In long run, vaccine will ease burden on screening as

there are fewer positives needing treatment

  • Synergies in raising awareness about cervical cancer

prevention – both screening and vaccine >> demand

  • Engages broader range of stakeholders
  • Allows countries to start from where they are and build

accordingly

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Conclusions

  • Immunization is trusted, familiar, and less

likely than other services to have inequities in coverage.

  • Many synergies for combining screening and

HPV vaccination, although timetables for introduction and scale-up may differ.

  • Options for affordable screening and HPV

vaccine now exist.

  • In the long term, a comprehensive approach
  • ffers the biggest payoff.
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Thank you

Vivien Tsu, PhD MPH Director, HPV Vaccines Project vtsu@path.org www.path.org/cervicalcancer