Grant: Operating Grant
Research Institute of the McGill University Health Centre
$117,697.00
Cancer Risk in Pediatric-Onset Rheumatic Disease
FY 2009-10
Summary
Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA) are both serious diseases caused by an overactive immune system, resulting in inflammation and damage. SLE can occur at any age; 15-20% of cases may present in childhood, often with more severe disease than adults. Similarly, RA is an serious type of arthritis in adults, with Juvenile Idiopathic Arthritis (JIA) being the currently-used term for a similar arthritis that arises in childhood. Fortunately, survival in pediatric rheumatic diseases has improved in the past two decades. This means that preventing adverse events is of increasing importance not only to clinicians, but also to patients and their families. Important types of adverse events may include osteoporosis, cardiovascular disease-and potentially, cancers. Several large studies, many of them population-based, have studied cancer risk in adults with RA and SLE. These studies have all emphasized a consistent and clinically important increased risk for lymphoma. Though much has been learnt about cancer risk for adults with rheumatic diseases, there are essentially no data about their pediatric counterparts. Despite lack of evidence, patients with pediatric-onset SLE and JIA, and their families, still fear that they too are at high risk for cancer. Our study will provide new information with a long-term study in pediatric-onset SLE and JIA. We will examine cancer occurrence in two multi-center cohorts, one with SLE and one with JIA, and determine if cancer risk is increased compared to age-and-sex specific general population cancer incidence rates. What is learnt from our work will certainly advance knowledge about cancer risk, particularly in high-risk populations.
Department
Program
Operating Grant
Location
Quebec, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
198653
Name
Bernatsky Sasha R
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Musculoskeletal Health and Arthritis
Theme2
Clinical
Prcname2
Public, Community & Population Health
Projecttitle
Cancer Risk in Pediatric-Onset Rheumatic Disease
Programtype2
Operating Grants
Orgnameinp2
Research Institute of the McGill University Health Centre
Cihramount2
$117,697
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Juvenile Idiopathic Arthritis; Lymphoma; Malignancy; Systemic Lupus Erythematosus
Abstract
Systemic Lupus Erythematosus (SLE) and Rheumatoid Arthritis (RA) are both serious diseases caused by an overactive immune system, resulting in inflammation and damage. SLE can occur at any age; 15-20% of cases may present in childhood, often with more severe disease than adults. Similarly, RA is an serious type of arthritis in adults, with Juvenile Idiopathic Arthritis (JIA) being the currently-used term for a similar arthritis that arises in childhood. Fortunately, survival in pediatric rheumatic diseases has improved in the past two decades. This means that preventing adverse events is of increasing importance not only to clinicians, but also to patients and their families. Important types of adverse events may include osteoporosis, cardiovascular disease-and potentially, cancers. Several large studies, many of them population-based, have studied cancer risk in adults with RA and SLE. These studies have all emphasized a consistent and clinically important increased risk for lymphoma. Though much has been learnt about cancer risk for adults with rheumatic diseases, there are essentially no data about their pediatric counterparts. Despite lack of evidence, patients with pediatric-onset SLE and JIA, and their families, still fear that they too are at high risk for cancer. Our study will provide new information with a long-term study in pediatric-onset SLE and JIA. We will examine cancer occurrence in two multi-center cohorts, one with SLE and one with JIA, and determine if cancer risk is increased compared to age-and-sex specific general population cancer incidence rates. What is learnt from our work will certainly advance knowledge about cancer risk, particularly in high-risk populations.
Competitiondate
201003
Approvedterm2
2 yrs 0 mth
Pinamesdelim
Bernatsky, Sasha R
Approvedterm
2 ans 0 mois
Cihrcontribution2
~ $117,697~ $0~