Cancer Registries and Rare Cancers: Data quality and supplementary information Carmen Martínez-García. Granada Cancer Registry. Andalusian School of Public.

Slides:



Advertisements
Similar presentations
High Resolution data for rare cancers Annalisa Trama Fondazione IRCCS Istituto Nazionale dei Tumori, Milan (Italy ) WORKSHOP FOR A EUROPEAN HIGH RESOLUTION.
Advertisements

Instructions and Reporting Requirements Module 2 Electronic Reporting For Facilities March 2014 North Carolina Central Cancer Registry State Center for.
Nadya Dimitrova Marieta Petkova. 13 Regional cancer registries BNCR: -Established in 1952; cases a year; million population;
National Institute of Oncology Rabat-Morocco. National Institute of Oncology I.N.O. Rabat, Morocco : New Cases.
Tumour Matching N.Ireland Experience Colin Fox (IT Manager) Richard Middleton (Data Manager)
The challenges of coding cancer of unknown primary A survey of registration and reporting practices in the UK, Ireland and Australia Claudia Oehler 1,
EUROCHIP - EUROpean Cancer Health Indicators Project A fight against disequalities in managing cancer HMP HMP: Health Monitoring Programme Andrea Micheli.
Prostate Cancer Craig Blundred. Overview Disease Definition  Epidemiological Classification  Symptoms Disease Burden  Incidence  Mortality  Health.
National Cancer Registry Luxembourg EUROCHIP-3 Meeting Ispra, 27 th February 2012 Olivier Collignon, PhD, Sophie Couffignal, MD, CRP-Santé.
NATIONAL POPULATION BASED- CANCER REGISTRY- Dr. G.Z. Mutuma Principal Research Officer, Head, Non-Communicable Diseases Research Programme, Kenya Medical.
Cancer Card Game Answers etc.
8 April,2009 Planning a Community based Cancer Registry Cancer Registration: Principles and Methods Edited by Jensen O. M. et al IARC 1991; pages 22 –
EUROCHIP - EUROpean Cancer Health Indicators Project A project supported by the European Commission Andrea Micheli 1, Paolo Baili 1, Carmen Martinez 2,
Cancer registries and rare cancers: quality of data, supplementary information RARECARE WP6 3rd meeting National Institute of Public Health Warsaw 25th.
CANCER INCIDENCE IN THE UK, 2010 AUGUST All Cancers Excluding Non-Melanoma Skin Cancer (C00-97 Excl. C44): 2010 Number of New Cases, Crude and European.
Review of Country Specific Evidence to Strengthen Early Detection of Breast Cancers in Sri Lanka Dr. Suraj Perera MBBS, MSc, MD Consultant Community Physician.
RARECARE project Cancer registries and rare cancers: quality of data, supplementary information RARECARE WP6, 3 rd meeting th National Institute of Public.
Kenya Field Epidemiology and Laboratory Training Program (KFELTP)
Epidemiology of Oral Cancer Module 1:. Epidemiology of Cancer, U.S.
Overview of All SEER-Medicare Publications Through 2012 Mark D. Danese, MHS, PhD July 24, 2012.
RARECARENet project High-resolution study in the Finnish Cancer Registry Maarit Leinonen Chief Medical Officer Finnish Cancer Registry, Helsinki.
High Resolution Studies within the European Cancer Information System Cooperation with EPAAC Riccardo Capocaccia Istituto Superiore di Sanità (ISS), Italy.
Difficulties for the analysis of rare cancers Missing cases Example: angiosarcoma of liver Including false cases Example: malignant digestive endocrine.
Epidemiology of a Chronic Disease Exercise By Mary Murphy April 2008
Work Package 5 Information on centres of expertise for rare cancers WP leader: Sabine Siesling.
Objectives of Work Package 5 objectives for today Information on centres of expertise for rare cancers WP leader: Sabine Siesling.
Information network on rare cancers RARECARENet Annalisa Trama, Gemma Gatta Fondazione IRCCS Istituto Nazionale dei Tumori, Milan (Italy)
GM Monawar Hosain State Cancer Epidemiologist Bureau of Public Health Statistics and Informatics NH Division of Pubic Health Services.
Head and Neck MP/H Task Force Multiple Primary Rules
Statistics about unknown primary tumors Riccardo Capocaccia National Centre for Epidemiology, Surveillance and Health Promotion Istituto Superiore di Sanità,
CANCER INCIDENCE IN NEW JERSEY BY COUNTY, for the Comprehensive Cancer Control Plan County Needs Assessments August 2003 Prepared by: Cancer.
Information network on rare cancers INFORMATION NETWORK ON RARE CANCERS (RARECARENet) Kick-off meeting - Friday, July Gemma Gatta Fondazione IRCCS,
1 Head and Neck. 2 Equivalent Terms, Definitions, Charts, Tables and Illustrations Primary site –Do not code biopsy site.
KCR SPRING TRAINING 2014 New ICD-O-3 Terminology.
The “Sastipen Network Information System” Facing Drugs within the Roma Community: Gathering of Information for the development of indicators “The Sastipen.
RARECARE project Data quality and supplementary information Granada, March 25 th 2009 Andalusian School of Public Health.
Associated Web sites CustomizableMaps The Atlas On-Line.
13 site specific articles 13 site specific articles Adult patients (age 15+) Adult patients (age 15+) Survival by subsite, tumour morphology, stage Survival.
EEOICPA Compensation Results (through March 2004) Russ Henshaw, MS Epidemiologist NIOSH/Office of Compensation Analysis & Support Cincinnati, OH.
Tools to Access the Latest Cancer Statistics Paul Miller Washington Reporting Fellowships program presentation April 15, 2013.
Recognition & Reporting of Occupational Diseases.
Dr Heather O Dickinson Department of Child Health University of Newcastle
Information network on rare cancers Work Package 4 Information on epidemiology of rare cancers Riccardo Capocaccia and Sandra Mallone Cancer Epidemiology.
© Cancer Research UK 2002 Registered charity number Figure One: Numbers of new cases and rates by age and sex, brain and other central nervous.
National Cancer Intelligence Network data usage 17 November 2015 – Veronique Poirier – Principal Cancer Analyst – NCIN.
I’m not just a child. I’m a daughter. I’m a son. I’m also a friend, a parent, a wife, a husband…
Vicki LaRue, CTR KCR Abstractor’s Training February 12,
National Cancer Intelligence Network Outcome and the effect of age in 1318 patients with synovial sarcoma: Report from the National Cancer Intelligence.
* Cases diagnosed from 1992 to 1995 Childhood and adolescent cancer survival: A period analysis of data from the Canadian Cancer Registry Larry F. Ellison,
The Cancer Registry of Norway Jan F Nygård Head of the IT-department.
Cancer in Ontario: Overview A Statistical Report.
Gary M. Levin, BA, CTR Florida Cancer Data System NAACCR 2008 Annual Conference 2007 Multiple Primary Rules: Impact on Tumor Counts.
RARECARE project Proposal for improving data quality on rare cancers with high priority Granada, March 25 th 2009 Andalusian School of Public Health.
Scottish Renal Cancer Forum National Meeting 31st March 2016 Renal cancer survival Period of diagnosis: Roger Black.
SWAG SSG Lung Cancer Meeting
SWAG SSG Skin Meeting Thursday 22nd September 2016 Maxine Taylor
Incidence and Treatment Patterns in Hospitalizations for Malignant Spinal Cord Compression in the United States, 1998–2006  Kimberley S. Mak, B.A., Leslie.
Analysis 26,980 cases sent for revision to 36 registries
WP 4 – EPIDEMIOLOGY GEMMA Gatta
Childhood Cancer Statistics, England, Annual report 2018.
5 Prevalence Ontario Cancer Statistics 2016 Chapter 5: Prevalence.
Selected Common Cancers, Percentage Change in European Age-Standardised Mortality Rates, Females, UK, *Brain and central nervous system (CNS)
Selected Common Cancers, Percentage Change in European Age-Standardised Mortality Rates, Persons, UK, *Brain and central nervous system (CNS)
STEERING COMMITTEE MEETING
General Assembly, 26th October, 2018, Milan
RARE CANCERS ARE ALSO NOT RARE IN ASIA :THE RARE CANCER BURDEN IN EAST ASIA Tomohiro Matsuda 1, Young-Joo Won 2 RuRu Chun-Ju Chiang 3, Kumiko Saika 1,
Trends in cancer Incidence in the Republic of Mauritius,
Incidence and Mortality of Childhood Cancer in China
How to interpret the geographical variations in the incidence of bladder tumours in Europe
Presentation transcript:

Cancer Registries and Rare Cancers: Data quality and supplementary information Carmen Martínez-García. Granada Cancer Registry. Andalusian School of Public Health. Spain WP6 Second Meeting. Andalusian School of Public Health Granada, 25 March 2009

WP6. Objectives To assess the validity, completeness and inter- registry standardisation of population-based cancer registry data on rare cancers. To improve the data quality and comparability of incidence, prevalence and survival of rare cancers among European population-based cancer registries (PBCR).

WP6 Partners Gemma Gatta, INT, Project LeaderItaly Franco Berrino, INT, EUROCAREItaly Ricardo Capocaccia, ISSItaly Stefano Ferreti FCR Italy Adriano Giacomin, BCRItaly Torgil Möller, Lund UHSweden Maja Primic Žakelj, IOLSlovenia Jean Michel Lutz, NICERSwizerland Juan A Virizuela (Oncologist), SASSpain Ricardo González-Cámpora (Anatomopath), SASSpain María José Sánchez (Epidemiologist), EASPSpain Juan Manuel Melchor, EASPSpain Carmen Martínez García, EASPSpain Samba Sowe INT

To select the same data quality indicators from the PBCR participating in RARECARE To be able to interpret the variability in incidence and survival among these PBCR To propose actions that improve the data’s quality and comparability What do we want?

Data Quality.WP6 Indicators used to evaluate completeness and validity in cancer registries: Basis of diagnosis %Microscopically verified cases %Clinical diagnosis %Unknwon %Death Certificate only %Autopsies

Data Quality Unknown primary site: C80.0 Ill-defined site: C55.9 (uterus); C76.- (Thorax,…) Ill-defined subsite: 4th digit 8 and 9 Morphology NOS ( 8000/3, 8001/3, 8010/3...) Pathological review of specific cases/markers? Follow up indicators ?

Data Quality WP6 What have we done until now? To calculate indicators on basis of diagnosis for some layer 1 categories: Epithelial: C30-31, C11, C07- C08 Mesothelioma Central Nervous system: Glial, Non glial, Meningioma By registry, country and region

Data Quality Epithelial Tumour of the Nasal Cavity and Sinuses, by country

Data Quality Epithelial Tumour of the Nasal Cavity and Sinuses, by Area

Data Quality Glial Tumour of the CNS and Pineal Gland, by country

Data Quality Glial Tumour of the CNS and Pineal Gland, by Area

Data Quality WP6 What have we done until now? To “explore” the ill defined sites By registry and country To “explore” the morfology NOS By registry

Data Quality i ll-defined sites NumeradorNumerator Overlapping lesion of other and unspecified parts of mouth and Mouth,NOS Hypopharynx,NOS13.9 Pharynx,NOS and Overlapping lesion of lip, oral cavity and pharynx Overlapping lesion of rectum, anus and anal canal21.8 Intestinal tract, NOS and Gastrointestinal tract, NOS Overlapping lesion of heart, mediastinum, and pleura38.8 Upper respiratory tract, NOS-ILL-defined withing respiratory system Uterus, NOS55.9 Overlapping lesion of female genital organs- Female genital tract, NOS Overlapping lesion of male genital organs- Male genital tract, NOS Overlapping lesion of urinary organs-Urinary system, NOS Overlapping lesion of brain and central nervous system-Nervous system, NOS Overlapping lesion of endocrine glands and related structures-Endocrine gland, NOS Head, face or neck, NOS- Overlapping lesion of ill-defined sites Unknown primary site80.9

Data Quality ill-defined sites. Number of incident cases and percentage by site and Registry

Data Quality WP6 Morphology NOS

Data Quality

Data Quality.WP6 Proposal of short list of rare cancers of high priority: Mesothelioma: primary prevention Angiosarcoma of the liver: primary prevention Sarcoma: diagnostic accuracy Oral cavity: secondary prevention CNS: appropiateness of treatment Germ cell tumours: appropiateness of treatment Leukaemia: appropiateness of treatment Endocrine tumours: data quality Other sugestions for quality control?

Data Quality Report. WP6 The report will include: Results on quality control of rare cancers complet list priority list List of markers that may improve the accuracy of the diagnosis of selected cancers Proposal for improving the quality and comparability in terms of completeness and validity The Report (D15) will be done by October 2009

Data Quality Seminar. WP6 Seminar on classification and coding problems for selected rare cancers addressed to profesionals linked with population-based cancer registries. Linked with WP4 and WP5 Collaboration with: European Network of Cancer Registries Northern Cancer Registries Groupe pour l’Epidemiologie et l’Enregistrement du Cancer dans les Pays de Langue Latine (GRELL) The seminar will be due by April 2010

Difficulties studying rare cancers: quality and comparability Low number of cases: random variations in incidence and survival, as well as in quality indicators, for small registries Some cancers are new entities that need: technology for diagnosis (laboratory, imaging...) training of professionals training of registrars Some morphological entities in ICD-O-3 don’t exist in ICD-O-1 or ICD-O-2.

Comparing data from Population-based Cancer Registries: Art or Science?

Comparing data from population- based cancer registries Some aspects to be taken into account when interpreting results from PBCR Socioeconomic conditions and health system in the region Definition of incident case: /0, /1, /2 and /3 Rules for collecting coding and classifying data The “traditional” quality indicators Consider for each age group, site or morphology the circumstances that may be affected by a selection bias

When comparing data “each tumour” or group of tumours must be studied using different approaches; taking into account age, risk factors, diagnostic resources (more or less advanced technology), treatment (new drugs, specialized centres for treatment), screening programs in the region (neuroblastoma in children) and other circumstances that may influence incidence and survival Considerations

Some sites with special problems Bladder cancer –Not enough tissue for diagnosis of invasion: /2 or /3 ? –Different criteria for coding the cases /1, /2 /3 Ovary cancer –Borderline tumours: /1 in ICD-O-1, /3 in ICD-O-2 Neurological/ Intracranial tumours –Inclusion of /0, /1 and /3 or only /3 Uveal melanoma –Underascertainment when surgery is not performed