open access

Vol 72, No 3 (2022)
Review paper
Published online: 2022-04-12
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Cancer and rheumatic diseases. Methodological and clinical pitfalls in searching links between these diseases

Krzysztof Jeziorski12
·
Nowotwory. Journal of Oncology 2022;72(3):190-194.
Affiliations
  1. Department of Gerontology, Public Health and Didactics, National Institute of Geriatrics, Rheumatology and Rehabilitation, Warsaw, Poland
  2. Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland

open access

Vol 72, No 3 (2022)
Review article
Published online: 2022-04-12

Abstract

Results of studies on coexistence of rheumatic and oncological diseases are somewhat conflicting in the literature. This is probably due to various methodological problems of the conducted research such as: small groups of patients, possible Berkson’s bias, lack of information about the most important factors affecting the risk of developing cancer including lifestyle, body mass index, use of tobacco and alcohol, family history of cancer and autoimmune diseases, misclassification of diseases in administrative registries, differences including geographical, racial factors, and a relatively short observation period. The risk of cancer development or recurrence in patients treated for rheumatic disease is very low, estimated as 2–5 cases per 1000 patients treated annually, and even lower in patients with cured cancer and 5 years after completion of oncological treatment. In the absence of clear recommendations for cancer screening of patients with rheumatic diseases, there is a need to develop guidelines for screening.

Abstract

Results of studies on coexistence of rheumatic and oncological diseases are somewhat conflicting in the literature. This is probably due to various methodological problems of the conducted research such as: small groups of patients, possible Berkson’s bias, lack of information about the most important factors affecting the risk of developing cancer including lifestyle, body mass index, use of tobacco and alcohol, family history of cancer and autoimmune diseases, misclassification of diseases in administrative registries, differences including geographical, racial factors, and a relatively short observation period. The risk of cancer development or recurrence in patients treated for rheumatic disease is very low, estimated as 2–5 cases per 1000 patients treated annually, and even lower in patients with cured cancer and 5 years after completion of oncological treatment. In the absence of clear recommendations for cancer screening of patients with rheumatic diseases, there is a need to develop guidelines for screening.

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Keywords

cancer; rheumatologic diseases; screening; coexisting diseases and malignancies; multi-disease phenomenon

About this article
Title

Cancer and rheumatic diseases. Methodological and clinical pitfalls in searching links between these diseases

Journal

Nowotwory. Journal of Oncology

Issue

Vol 72, No 3 (2022)

Article type

Review paper

Pages

190-194

Published online

2022-04-12

Page views

4350

Article views/downloads

695

DOI

10.5603/NJO.a2022.0023

Bibliographic record

Nowotwory. Journal of Oncology 2022;72(3):190-194.

Keywords

cancer
rheumatologic diseases
screening
coexisting diseases and malignancies
multi-disease phenomenon

Authors

Krzysztof Jeziorski

References (52)
  1. Stertz O. Polymyositis. Berl Klin Wochenschr. 1916; 53: 489.
  2. Bernatsky S, Ramsey-Goldman R, Clarke A. Malignancy and autoimmunity. Curr Opin Rheumatol. 2006; 18(2): 129–134.
  3. Chang SH, Park JK, Lee YJ, et al. Comparison of cancer incidence among patients with rheumatic disease: a retrospective cohort study. Arthritis Res Ther. 2014; 16(4): 428.
  4. Karmacharya P, Shahukhal R, Ogdie A. Risk of Malignancy in Spondyloarthritis: A Systematic Review. Rheum Dis Clin North Am. 2020; 46(3): 463–511.
  5. Ioannidis JPA, Karassa FB, Druyts E, et al. Biologic agents in rheumatology: unmet issues after 200 trials and $200 billion sales. Nat Rev Rheumatol. 2013; 9(11): 665–673.
  6. Kwiatkowska B, Przygodzka M, Filipowicz-Sosnowska A. Rheumatic symptoms in malignant disease. NOWOTWORY J Oncol. 2006; 56: 693–699.
  7. Cioffi G, Viapiana O, Tarantini L, et al. The troubling liaison between cancer and metabolic syndrome in chronic inflammatory rheumatic diseases. Arthritis Res Ther. 2021; 23(1): 89.
  8. Ytterberg SR, Bhatt DL, Mikuls TR, et al. ORAL Surveillance Investigators. Cardiovascular and Cancer Risk with Tofacitinib in Rheumatoid Arthritis. N Engl J Med. 2022; 386(4): 316–326.
  9. Davis JM. Overview of the Associations Between Cancer and Rheumatic Disease. Rheum Dis Clin North Am. 2020; 46(3): 417–427.
  10. Penn I. The effect of immunosuppression on pre-existing cancers. Transplantation. 1993; 55(4): 742–747.
  11. Bhandari B, Basyal B, Sarao MS, et al. Prevalence of Cancer in Rheumatoid Arthritis: Epidemiological Study Based on the National Health and Nutrition Examination Survey (NHANES). Cureus. 2020; 12(4): e7870.
  12. Simon TA, Thompson A, Gandhi KK, et al. Incidence of malignancy in adult patients with rheumatoid arthritis: a meta-analysis. Arthritis Res Ther. 2015; 17(1): 212.
  13. Klein A, Polliack A, Gafter-Gvili A. Rheumatoid arthritis and lymphoma: Incidence, pathogenesis, biology, and outcome. Hematol Oncol. 2018; 36(5): 733–739.
  14. Khurana R, Wolf R, Berney S, et al. Risk of development of lung cancer is increased in patients with rheumatoid arthritis: a large case control study in US veterans. J Rheumatol. 2008; 35(9): 1704–1708.
  15. Nayak P, Luo R, Elting L, et al. Impact of Rheumatoid Arthritis on the Mortality of Elderly Patients Who Develop Cancer: A Population-Based Study. Arthritis Care Res (Hoboken). 2017; 69(1): 75–83.
  16. Park JK, Yang JiAe, Ahn EY, et al. Survival rates of cancer patients with and without rheumatic disease: a retrospective cohort analysis. BMC Cancer. 2016; 16: 381.
  17. Giat E, Ehrenfeld M, Shoenfeld Y. Cancer and autoimmune diseases. Autoimmun Rev. 2017; 16(10): 1049–1057.
  18. Igoe A, Merjanah S, Scofield RH. Sjögren Syndrome and Cancer. Rheum Dis Clin North Am. 2020; 46(3): 513–532.
  19. Tseng HW, Huang WC, Lu LY. The influence of immunosuppressants on the non-melanoma skin cancer among patients with systemic lupus erythematosus and primary Sjögren's syndrome: a nationwide retrospective case-control study in Taiwan. Clin Exp Rheumatol. 2019; 37(6): 946–952.
  20. Ladouceur A, Tessier-Cloutier B, Clarke AE, et al. Cancer and Systemic Lupus Erythematosus. Rheum Dis Clin North Am. 2020; 46(3): 533–550.
  21. Bernatsky S, Ramsey-Goldman R, Labrecque J, et al. Cancer risk in systemic lupus: an updated international multi-centre cohort study. J Autoimmun. 2013; 42: 130–135.
  22. Bernatsky S, Ramsey-Goldman R, Foulkes WD, et al. Breast, ovarian, and endometrial malignancies in systemic lupus erythematosus: a meta-analysis. Br J Cancer. 2011; 104(9): 1478–1481.
  23. Zard E, Arnaud L, Mathian A, et al. Increased risk of high grade cervical squamous intraepithelial lesions in systemic lupus erythematosus: A meta-analysis of the literature. Autoimmun Rev. 2014; 13(7): 730–735.
  24. Chang SL, Hsu HT, Weng SF, et al. Impact of head and neck malignancies on risk factors and survival in systemic lupus erythematosus. Acta Otolaryngol. 2013; 133(10): 1088–1095.
  25. Song L, Wang Yi, Zhang J, et al. The risks of cancer development in systemic lupus erythematosus (SLE) patients: a systematic review and meta-analysis. Arthritis Res Ther. 2018; 20(1): 270.
  26. Ni J, Qiu LJ, Hu LF, et al. Lung, liver, prostate, bladder malignancies risk in systemic lupus erythematosus: evidence from a meta-analysis. Lupus. 2014; 23(3): 284–292.
  27. Cao L, Tong H, Xu G, et al. Systemic lupus erythematous and malignancy risk: a meta-analysis. PLoS One. 2015; 10(4): e0122964.
  28. Weeding E, Casciola-Rosen L, Shah AA. Cancer and Scleroderma. Rheum Dis Clin North Am. 2020; 46(3): 551–564.
  29. Onishi A, Sugiyama D, Kumagai S, et al. Cancer incidence in systemic sclerosis: meta-analysis of population-based cohort studies. Arthritis Rheum. 2013; 65(7): 1913–1921.
  30. Zhang JQ, Wan YN, Peng WJ, et al. The risk of cancer development in systemic sclerosis: a meta-analysis. Cancer Epidemiol. 2013; 37(5): 523–527.
  31. Bonifazi M, Tramacere I, Pomponio G, et al. Systemic sclerosis (scleroderma) and cancer risk: systematic review and meta-analysis of observational studies. Rheumatology (Oxford). 2013; 52(1): 143–154.
  32. Moghadam-Kia S, Oddis CV, Ascherman DP, et al. Risk Factors and Cancer Screening in Myositis. Rheum Dis Clin North Am. 2020; 46(3): 565–576.
  33. Yang Z, Lin F, Qin B, et al. Polymyositis/dermatomyositis and malignancy risk: a metaanalysis study. J Rheumatol. 2015; 42(2): 282–291.
  34. Stockton D, Doherty VR, Brewster DH. Risk of cancer in patients with dermatomyositis or polymyositis, and follow-up implications: a Scottish population-based cohort study. Br J Cancer. 2001; 85(1): 41–45.
  35. Buchbinder R, Forbes A, Hall S, et al. Incidence of malignant disease in biopsy-proven inflammatory myopathy. A population-based cohort study. Ann Intern Med. 2001; 134(12): 1087–1095.
  36. Chow WH, Gridley G, Mellemkjaer L, et al. Cancer risk following polymyositis and dermatomyositis: a nationwide cohort study in Denmark. Cancer Causes Control. 1995; 6(1): 9–13.
  37. Sigurgeirsson B, Lindelöf B, Edhag O, et al. Risk of cancer in patients with dermatomyositis or polymyositis. A population-based study. N Engl J Med. 1992; 326(6): 363–367.
  38. Wang J, Guo G, Chen G, et al. Meta-analysis of the association of dermatomyositis and polymyositis with cancer. Br J Dermatol. 2013; 169(4): 838–847.
  39. András C, Ponyi A, Constantin T, et al. Dermatomyositis and polymyositis associated with malignancy: a 21-year retrospective study. J Rheumatol. 2008; 35(3): 438–444.
  40. Ponyi A, Constantin T, Garami M, et al. Cancer-associated myositis: clinical features and prognostic signs. Ann N Y Acad Sci. 2005; 1051: 64–71.
  41. Prohic A, Kasumagic-Halilovic E, Simic D, et al. Clinical and biological factors predictive of malignancy in dermatomyositis. J Eur Acad Dermatol Venereol. 2009; 23(5): 591–592.
  42. Sparsa A, Liozon E, Herrmann F, et al. Routine vs extensive malignancy search for adult dermatomyositis and polymyositis: a study of 40 patients. Arch Dermatol. 2002; 138(7): 885–890.
  43. Leow YH, Goh CL. Malignancy in adult dermatomyositis. Int J Dermatol. 1997; 36(12): 904–907.
  44. Basset-Seguin N, Roujeau JC, Gherardi R, et al. Prognostic factors and predictive signs of malignancy in adult dermatomyositis. A study of 32 cases. Arch Dermatol. 1990; 126(5): 633–637.
  45. Thanarajasingam U, Abdel-Wahab N. Immune Checkpoint Inhibition-Does It Cause Rheumatic Diseases? Mechanisms of Cancer-Associated Loss of Tolerance and Pathogenesis of Autoimmunity. Rheum Dis Clin North Am. 2020; 46(3): 587–603.
  46. Szekanecz Z, Gomez I, Soós B, et al. Hungarian OncoRheumatology Network (HORN) initiative. Eight pillars of oncorheumatology: Crossroads between malignancies and musculoskeletal diseases. Autoimmun Rev. 2020; 19(11): 102658.
  47. Szekanecz Z, Haines GK, Harlow LA, et al. Increased synovial expression of the adhesion molecules CD66a, CD66b, and CD31 in rheumatoid and osteoarthritis. Clin Immunol Immunopathol. 1995; 76(2): 180–186.
  48. Szekanecz E, Sándor Z, Antal-Szalmás P, et al. Increased production of the soluble tumor-associated antigens CA19-9, CA125, and CA15-3 in rheumatoid arthritis: potential adhesion molecules in synovial inflammation? Ann N Y Acad Sci. 2007; 1108: 359–371.
  49. Szekanecz E, Szucs G, Szekanecz Z, et al. Tumor-associated antigens in systemic sclerosis and systemic lupus erythematosus: associations with organ manifestations, immunolaboratory markers and disease activity indices. J Autoimmun. 2008; 31(4): 372–376.
  50. Kimura K, Ezoe K, Yokozeki H, et al. Elevated serum CA125 in progressive systemic sclerosis with pleural effusion. J Dermatol. 1995; 22(1): 28–31.
  51. Safadi R, Ligumsky M, Goldin E, et al. Increased serum CA 19-9 antibodies in Sjögren's syndrome. Postgrad Med J. 1998; 74(875): 543–544.
  52. Wong RCW, Brown S, Clarke BE, et al. Transient elevation of the tumor markers CA 15-3 and CASA as markers of interstitial lung disease rather than underlying malignancy in dermatomyositis sine myositis. J Clin Rheumatol. 2002; 8(4): 204–207.

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