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Increasing Frequency of Soft Tissue Sarcomas in Vojvodina - Comparison with the Literature

  • Published : 2014.01.30

Abstract

Background: Soft tissue sarcomas (STS) represent 1% of all malignant lesions. In this study the authors analyzed the incidence of STS in Vojvodina (the north region of Serbia) in the period from 1985 to 2009. A number of studies conducted worldwide indicate that STS incidence rates are tending to increase. Materials and Methods: On the basis of data from the Cancer Registry of Vojvodina, age standardized STS incidence rates were established as well as their linear trend, with data on histological structure, age, gender and STS distribution at specific locations. Results: The total number of registered patients was 1,308. Average age standardized rate was 1.90/100,000 per year. The investigated period showed a slight increase in the incidence rate (average annual percent increase=0.77%). The most frequent histological type was sarcoma not otherwise specified-NOS (27%), followed by leiomyosarcoma (21%), liposarcoma (14%), rhabdomyosarcoma (11%) and malignant fibrous histiocytoma (9%). The male/female ratio was 0.73:1. Every fifth patient was younger than 39. Conclusions: Comparison among eight international STS epidemiology studies show that the incidence rate range is between 1.4/100,000-5.0/100,000, though our finding is closer to the lower limit. Furthermore, the incidence rate increase was lower than that characteristic for the half of the analyzed studies. A partial explanation for that should be looked for among changes in diagnostic criteria and STS classifications.

Keywords

References

  1. Aqaimy A, Vassos N, Croner RS (2012). Gastrointestinal manifestations of neurofibromatosis type 1 (Recklinghausen's disease): clinicopathological spectrum with pathogenetic considerations. Int J Clin Exp Pathol, 5, 852-62.
  2. Bhatia K, Shiels MS, Berg A, Engels EA (2012). Sarcomas other than Kaposi sarcoma occurring in immunodeficiency: interpretations from a systematic literature review. Curr Opin Oncol, 24, 537-46. https://doi.org/10.1097/CCO.0b013e328355e115
  3. Fletcher CD, Krishnan Unni K, Mertens F (2002). Pathology and genetics of tumours of soft tissue and bone. In Kleihues PM, Sobin LH (eds), World Health Organization Classification of Tumours, 4th edition. Lyon, France: IARC Press 2002; 10-6, 120-4.
  4. Gladdy RA, Qin LX, Moraco N, et al (2010). Do radiationassociated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas? J Clin Oncol, 28, 2064. https://doi.org/10.1200/JCO.2009.25.1728
  5. Gustafson P (1994). Soft tissue sarcoma. Epidemiology and prognosis in 508 patients. Acta Orthop Scand, 259, 1-31.
  6. Hoppin JA, Tolbert PE, Herrick RF, et al (1998). Occupational chlorophenol exposure and soft tissue sarcoma risk among men aged 30-60 years. Am J Epidemiol, 148, 693. https://doi.org/10.1093/aje/148.7.693
  7. Ji J, Eng C, Hemminki K (2008). Familial risk for soft tissue tumors: a nation-wide epidemiological study from Sweden. J Cancer Res Clin Oncol, 134, 617-24. https://doi.org/10.1007/s00432-007-0327-5
  8. Latchford A, Volikos E, Johnson V, et al (2007). APC mutations in FAP-associated desmoid tumours are non-random but not “just right”. Hum Mol Genet, 16, 78.
  9. Levi F, La Vecchia C, Randimbison L, Te VC (1999). Descriptive epidemiology of soft tissue sarcomas in Vaud, Switzerland. Eur J Cancer, 35, 1711. https://doi.org/10.1016/S0959-8049(99)00179-3
  10. Muller R, Hajdu SI, Brennan MF (1987). Lymphangiosarcoma associated with chronic filarial lymphedema. Cancer, 59, 179. https://doi.org/10.1002/1097-0142(19870101)59:1<179::AID-CNCR2820590134>3.0.CO;2-D
  11. Neter J, Wasserman W, Kutner M (1985). Applied Linear Statistical Methods. R.D. Irwin, 2nd edition, p 167-220.
  12. Radu O, Pantanowitz L (2013). Kaposi Sarcoma. Arch Pathol Lab Med, 137, 289-94. https://doi.org/10.5858/arpa.2012-0101-RS
  13. Ross JA, Severson RK, Davis S, Brooks JJ (1993). Trends in the incidence of soft tissue sarcomas in the United States from 1973 through 1987. Cancer, 72, 486. https://doi.org/10.1002/1097-0142(19930715)72:2<486::AID-CNCR2820720226>3.0.CO;2-R
  14. Samartzis D, Nishi N, Cologne J, et al (2013). Ionizing radiation exposure and the development of soft-tissue sarcomas in atomic-bomb survivors. J Bone Joint Surq Am, 95, 222-9. https://doi.org/10.2106/JBJS.L.00546
  15. Schuurman B, Meyer S, Cuesta MA, Nauta JJ (1992). Increasing frequency of soft tissue sarcomas in The Netherlands. Ned Tijdschr Geneeskd, 136, 1556-60.
  16. Steenland K, Piacitelli L, Deddens J, Fingerhut M, Chang LI (1999). Cancer, heart disease, and diabetes in workers exposed to 2,3,7,8-tetrachlorodibenzo-p-dioxin. J Natl Cancer Inst, 91, 779. https://doi.org/10.1093/jnci/91.9.779
  17. Storm HH (1994). Cancers of the soft tissues. Cancer Surv, 197, 19-20.
  18. Svajdler M, Andrasina I, Ilencikova D, Rychly B, Piackova B (2012). Recurring multifocal leiomyosarcoma of the urinary bladder 22 years after therapy for bilateral (hereditary) retinoblastoma: a case report and review of the literature. Cesk Patol, 48, 44-8.
  19. Toro JR, Travis LB, Wu HJ, et al (2006). Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978-2001: an analysis of 26758 cases. Int J Cancer, 119, 2922. https://doi.org/10.1002/ijc.22239
  20. Visuri T, Pukkala E, Pulkkinen P, Paavolainen P (2003). Decreased cancer risk in patients who have been operated on with total hip and knee arthroplasty for primary osteoarthrosis: a meta-analysis of 6 Nordic cohorts with 73000 patients. Acta Orthop Scand, 74, 351. https://doi.org/10.1080/00016470308540852
  21. Wibmer C, Leithner A, Zielonke N, Sperl M, Windhager R (2010). Increasing indicence rates of soft tissue sarcomas? A population-based epidemiological study and literature review. Ann Oncol, 21, 1106-11. https://doi.org/10.1093/annonc/mdp415
  22. Zahm SH, Fraumeni JF Jr (1997). The epidemiology of soft tissue sarcoma. Semin Oncol, 24, 504.

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