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Fakultät für Gesundheitswissenschaften School of Public Health WHO Collaborating Center Other Immigrant Studies: Cancer and Cancer Registration Prof. Oliver Razum Melina Arnold EUNAM Meeting Ferrara, 9 Sep 2011 1
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Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Other Immigrant Studies:

Cancer and Cancer Registration

Prof. Oliver Razum

Melina Arnold

EUNAM Meeting

Ferrara, 9 Sep 2011 1

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Outline

• Examples of „typical“ projects• MigHealthNet

• MEHO

• MEHO: WP Cancer in Migrants• Migrant health from a lifecourse perspective

• Migration-sensitive Cancer Registration• Survey

• Building migration-sensitive health indicators in

cancer research

• Country Reports2

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

MigHealthNet (1)

• Supported by the EC's Directorate-General Health and

Consumer Protection (DG SANCO) and the Stavros

Niarchos Foundation (completed in April 2009)

Objectives

• to stimulate the exchange of knowledge and the formation

of networks on migrant and minority health through the

development of interactive databases in each of the

participating countries

• to give professionals, policy makers including health

authorities, researchers, educators and representatives of

migrant and minority groups easy access to a virtual

network of expertise3

See also: http://mighealth.net/

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

MigHealthNet (2)

• Implementation of 20 country-specific wikis and one

general wiki

• Participating countries:

• Austria

• Belgium

• Bulgaria

• Czech Republic

• Denmark

• Finland

• France

4

• Germany

• Greece

• Hungary

• Lithuania

• Netherlands

• Norway

• Poland

• Portugal

• Romania

• Sweden

• Switzerland

• Turkey

• United Kingdom

See also: http://mighealth.net/

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

MEHO (1)

• Migrant and Ethnic Health Observatory

• Funded under the framework of the Public Health

Programme 2003-2008 of the European Commission

Objectives

• to develop indicators to monitor the health status of

immigrants and ethnic minorities

• to approach the conceptual, methodological, ethical and

practical issue of identifying immigrants and ethnic

minorities in health databases

• to conduct valid comparisons between these groups within

and between European countries and migrant groups 5

See also: http://www.meho.eu.com/

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

MEHO (2)

• Five critical health areas/ workpackages

• Mortality

• Cardiovascular Disease and Diabetes

• Cancer

• Infectious Diseases

• Self-perceived health and health care use

• Partners

• Erasmus MC Rotterdam, The Netherlands

• Amsterdam Medical Center/ University of Amsterdam, The Netherlands

• University of Edinburgh, Scotland

• Bielefeld University, Germany

• University of Copenhagen, Denmark

• University of P.J. Safarik Kosice, Slovakia6

See also: http://www.meho.eu.com/

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Cancer in Migrants (I)

• Cancer risks vary

• geographically

• within and between populations

• Assessing the relevance of

• environmental („nurture“) components

• genetic („nature“) components

Lifecourse perspective

Allowing progress in etiology research

Allowing migrant-specific prevention means

7

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Cancer in Migrants (II)

• Greater likelihood to develop cancers with a relation to infectious diseases

• Oral cavity, nasopharynx, stomach, liver, gallbladder, cervix uteri, lymphoma

• Decreased risk for cancers associated with a ‚Western‘ lifestyle

• Colorectum, pancreas, lung, breast, ovary, kidney, bladder

8

Arnold, M., O. Razum, and J.W. Coebergh, Cancer risk diversity in non-western migrants to Europe: An overview of the

literature. European journal of cancer (Oxford, England: 1990), 2010. 46(14): p. 2647-59.

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Cancer in Migrants (III)

1. Lower all-cancer risk coincide in most studies

irrespective of exact migrant origin

health/epidemiologic transition

2. Susceptibility to certain cancers

life-course perspective can help to identifyimportant exposures during life

3. Cancer risks in migrants converge over time

to be investigated

9

Arnold, M., O. Razum, and J.W. Coebergh, Cancer risk diversity in non-western migrants to Europe: An overview of the

literature. European journal of cancer (Oxford, England: 1990), 2010. 46(14): p. 2647-59.

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Migrant health from a lifecourse perspective

10

Spallek J., Zeeb H., Razum O. What do we have to know from migrants‘ past exposures to understand their health status?

A lifecourse approach. Emerg. Themes Epidemiol. 2011. Aug 15;8(1):6.

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Migration-sensitive

Cancer Registration

11

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Migration-sensitive Cancer Registration

• Questionnaire-based survey among all European

Cancer Registries (n=191)

• Categorization into ‚exemplary‘ and ‚less than

exemplary‘ registries

• Exemplary = Used indicator of ethnicity: country of birth

• Less than exemplary = Used indicators of ethnicity: nationality or race or country of birth of father or country of birth of mother

12

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Survey Results (I)

13

191 cancer

registries

contacted

182 registries got an

online questionnaire

25 emails

returned

9 registries got a paper

questionnaire

21 registries

got a paper

version

39 registries

answered

4 registries

with wrong

email address

2 answered

118

registries

reminded

78 cancer registries answered response: 40.8 %

3 answered 34 answered

191 cancer

registries

contacted

182 registries got an

online questionnaire

25 emails

returned

9 registries got a paper

questionnaire

21 registries

got a paper

version

39 registries

answered

4 registries

with wrong

email address

2 answered

118

registries

reminded

78 cancer registries answered response: 40.8 %

3 answered 34 answered

Reeske, A., J. Spallek, and O. Razum, Migrant and Ethnic Health Observatory (MEHO): Migrant-sensitive cancer registration in Europe – Results of a survey

conducted among European cancer registries., in Network Eurolifestyle, Neumann G and Kirch W, Editors. 2008, Thieme Verlag: Stuttgart. p. 11-18.

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Survey Results (II)

14

Indicator of migrant background No migrant-

specific data

Country of birth Nationality Race

Total 35 (44.9 %) 6 (7.7 %) 3 (3.8 %) 34 (43.6 %)

Possibility to conduct

migrant-specific analyses

Yes 9 (11.5 %) 0 (0.0 %) 1 (1.3 %) 4 (5.1 %)

Migrant-specific analyses

actually carried out

Routine analyses 1 (1.3 %) 0 (0.0 %) 0 (0.0 %) 0 (0.0 %)

Additional research 6 (7.7 %) 0 (0.0 %) 1 (1.3 %) 2 (2.6 %)

Numerator and

denominator population

available

Yes 2 (2.6 %) 12 (15.4 %) 0 (0.0 %)

Tab. 3.2.1: Main results of the survey conducted among European cancer registries in 2007/08 (n = 78)

Reeske, A., J. Spallek, and O. Razum, Migrant and Ethnic Health Observatory (MEHO): Migrant-sensitive cancer registration in Europe – Results of a survey

conducted among European cancer registries., in Network Eurolifestyle, Neumann G and Kirch W, Editors. 2008, Thieme Verlag: Stuttgart. p. 11-18.

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Building migration-sensitive

health indicators in cancer

research

15

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Building migration-sensitive health indicators in cancer research (I)

• For indicators we need

• Cases (numerator of an indicator, e.g. risk)

• Background population (denominator)

• Numerator: Cases are collected in cancer registries

Survey about migrant specific data in European cancer registries

• Denominator: Background population

• Registries might have data or information

• Other data sources, e.g. national statistics

• Data linkage

16

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Building migration-sensitive health indicators in cancer research (II)

• How to merge numerator and denominator:

• Direct methods

• e.g. record linkage

• Indirect methods

• data linkage (ideally using personal identifiers)

• name-based approaches

• Numerator-only approaches

• e.g. PCIR, relative survival, descriptive analyses

17

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Country Reports

18

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Country Reports: An overview

Country Migrants in

(1) General

population (%),

(2) Largest migrant

groups (origin)*

Indicators

available in

(1) Population

data,

(2) Cancer

registry data

Routine

analyses?

Studies on

cancer in

migrants

Main barriers Current/Future

Potentials

Finland:

Finnish Cancer

Registry

(population-

based, national

level)

(1) 4.4% (foreign

country of birth)

(2) Russia, Estonia

(1) Country of

birth,

Citizenship,

Language

(2) None

• No.

• Using linkage

procedures

• Time consuming

permission procedures

• Costs of additional data

extraction

• Small number of cancer

cases among migrants

• Data linkage

through personal

identity code PID

• Inclusion of

country of origin in

CR data

Germany:

Regional

registries (all 16

federal states

covered in 2011,

completeness

fits international

standards in 14

federal states)

(1) ~20% (migration

background)

(2) Eastern Europe

(re­settlers),

South and South

Eastern Europe

(Turkey)

(1) None (Country

of birth in

Mikrocensus

data)

(2) None.

• No.

• Using a name-

based approach

to identify

Turkish cancer

cases

• Setting up a

historical cohort

of resettlers

from the FSU

• Data protection not

officially clarified

• German history

(prosecution of ethnic

minorities)

• Organisation of CRs on

federal state level by

federal state law

lacking data comparability

• Lacking of migrant

indicators in population

data

• Indirect methods

(e.g. name-based

approaches)

• Numerator-only

analyses

• Data linkage

procedures

19

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Country Reports: An overview (cont.)

Country Migrants in

(1) General population

(%),

(2) Largest migrant

groups (origin)*

Indicators available

in

(1) Population data,

(2) Cancer registry

data

Routine analyses?

Studies on cancer in

migrants

Main barriers Current/Future

Potentials

Netherlands:

Netherlands

Cancer Registry

(population-

based, national

level)

(1) 19.5% (foreign

background)

(2) Turkey, Morocco,

Western Europe,

Suriname,

Netherlands Antilles,

Indonesia

(1) Country of birth

(2) Country of birth

• No.

• Using linkage

procedures

• No resources for routine

analyses

• Lacking completeness of

country of birth variable

in incidence analyses

• Introduction of citizen

service number (CSN)

will facilitate linkage

Scotland:

Scottish Cancer

Registry

(population-

based, national

level)

(1) 3.8% (foreign country

of birth)

(2) UK, US, Western

Europe, Pakistan,

India, Bangladesh,

China

(1) Ethnic group

(category

classification,

predefined in

Scottish census)

(2) Ethnic group

• No.

• Using name-based

approaches for

migrants from India,

Pakistan and China

• First attempts using

linkage with CHI

• Existing data often

incomplete

• Inconsistent coding of

ethnic groups between

data sources

• Only small ethnic

minority groups

• Linkage procedures

using CHI are

promising and can in

future overcome most

barriers

Sweden:

Swedish

Cancer Register

(population-

based, national

level)

(1) 13.8% (foreign

country of birth)

(2) Europe (mostly

Scandinavia), Iraq,

Iran, Former

Yugoslavia, Poland

(1) Country of birth,

foreign

background

(2) None.

• Yes.

• Using the Health

and Migration

Cohort

• Using the Family-

Cancer Database

• Lack of information on

ethnicity (variation within

the same country of

origin)

• Technical solutions are

still under development

• PIN facilitates linkage

of registers and

enables all kinds of

analyses (incidence,

mortality, survival) and

covariates (e.g. SES)

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Conclusion

• Major barriers identified

- Incompleteness of nationality data in the registries

- Naturalized immigrants

- Background population/denominator must be defined in the same way as numerator

- Heterogeneity of migrant groups and origins

- Heterogeneity of applied definitions and measures of association

- 100% overlap of catchment area of registry and statistical region for background population is needed

21

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Projects

22

Fakultät für Gesundheitswissenschaften School of Public Health – WHO Collaborating Center

Suggested readings

23


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