K Hemminki1, X Liu, J Ji, J Sundquist, K Sundquist. 1. Division of Molecular Genetic Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany. k.hemminki@dktz.de
Abstract
BACKGROUND: Patients with some autoimmune diseases (AIDs) are at increased risk of cancer, possibly a result of an underlying dysregulation of the immune system, medication, treatment or, probably, surveillance bias. Data on cancer mortality and survival in patients previously diagnosed with AIDs would provide novel information on these comorbidities and their clinical implications. PATIENTS AND METHODS: Standardized mortality ratios (SMRs) and hazard ratios (HRs) were calculated for subsequent deaths from seven digestive tract cancers between 1964 and 2008 in patients hospitalized for any of 33 AIDs. RESULTS: There were 33 increased SMRs for specific cancers after a defined AID; similarly, 21 HRs were increased. Both the SMR and HR were increased after 10 autoimmune disorders, including pernicious anemia, systemic lupus erythematosus and psoriasis. Increased SMRs and unchanged HRs were noted for 23 cancers. Myasthenia gravis was associated with SMRs for five cancers but no increases in HRs. For nine cancers, including esophageal cancer after ulcerative colitis and rheumatoid arthritis, the SMR was unchanged but the HR increased. CONCLUSIONS: The increases in SMRs provide evidence that cancer risks were truly increased and largely unaffected by surveillance bias. The prognostic survival data should contribute to clinical evaluation and therapeutic planning.
BACKGROUND:Patients with some autoimmune diseases (AIDs) are at increased risk of cancer, possibly a result of an underlying dysregulation of the immune system, medication, treatment or, probably, surveillance bias. Data on cancer mortality and survival in patients previously diagnosed with AIDs would provide novel information on these comorbidities and their clinical implications. PATIENTS AND METHODS: Standardized mortality ratios (SMRs) and hazard ratios (HRs) were calculated for subsequent deaths from seven digestive tract cancers between 1964 and 2008 in patients hospitalized for any of 33 AIDs. RESULTS: There were 33 increased SMRs for specific cancers after a defined AID; similarly, 21 HRs were increased. Both the SMR and HR were increased after 10 autoimmune disorders, including pernicious anemia, systemic lupus erythematosus and psoriasis. Increased SMRs and unchanged HRs were noted for 23 cancers. Myasthenia gravis was associated with SMRs for five cancers but no increases in HRs. For nine cancers, including esophageal cancer after ulcerative colitis and rheumatoid arthritis, the SMR was unchanged but the HR increased. CONCLUSIONS: The increases in SMRs provide evidence that cancer risks were truly increased and largely unaffected by surveillance bias. The prognostic survival data should contribute to clinical evaluation and therapeutic planning.
Authors: Kevin A Bockerstett; Scott A Lewis; Christine N Noto; Eric L Ford; José B Saenz; Nicholas M Jackson; Tae-Hyuk Ahn; Jason C Mills; Richard J DiPaolo Journal: Gastroenterology Date: 2020-08-21 Impact factor: 22.682
Authors: Thanh-Long M Nguyen; Shradha S Khurana; Clifford J Bellone; Benjamin J Capoccia; John E Sagartz; Russell A Kesman; Jason C Mills; Richard J DiPaolo Journal: Cancer Res Date: 2013-02-01 Impact factor: 12.701
Authors: Jin Kyun Park; Ji Ae Yang; Eun Young Ahn; Sung Hae Chang; Yeong Wook Song; Jeffrey R Curtis; Eun Bong Lee Journal: BMC Cancer Date: 2016-07-04 Impact factor: 4.430
Authors: Ebba K Lindqvist; Ola Landgren; Sigrún H Lund; Ingemar Turesson; Malin Hultcrantz; Lynn Goldin; Magnus Björkholm; Sigurdur Y Kristinsson Journal: Ann Hematol Date: 2016-11-02 Impact factor: 3.673
Authors: Richard Partington; Toby Helliwell; Sara Muller; Alyshah Abdul Sultan; Christian Mallen Journal: Arthritis Res Ther Date: 2018-11-20 Impact factor: 5.156