Author:
Klangjorhor Jeerawan,Pongnikorn Donsuk,Sittiju Pattaralawan,Phanphaisarn Areerak,Chaiyawat Parunya,Teeyakasem Pimpisa,Kongdang Patiwat,Moonmuang Sutpirat,Waisri Narate,Daoprasert Karnchana,Wisanuyotin Taweechok,Santong Chalongpon,Sitthikong Siriphon,Tuntarattanapong Pakjai,Prechawittayakul Paradee,Pruksakorn Dumnoensun
Abstract
AbstractThis study aimed to analyze burden of STS and GIST in population and survival rate which represented the current situation of treatment in Thailand. The data was collected from five population-based cancer registries around the country for the period 2001 through 2015. The Segi world standard population was used to calculated age-standardized incidence rates (ASR). Standardized rate ratios (SRR) were used to compare populations. Joinpoint Trend Analysis was used to assess changes in incidence. STATA was used to examine patient survival rates. During the study period, 4080 cases of STS and 457 cases of GIST were reported. The ASR of STS and GIST was 2.14/100,000 person-years and 0.22/100,000 person-years, respectively. The most common histological types of STS were unspecified sarcoma (24.8%), leiomyosarcoma (19.0%) and liposarcoma (11.4%). The overall ASR of STS in Thailand was relatively low compared to Western countries. The five-year survival rate was 62.6% for STS and 63.4% for GIST, which was comparable to the rates reported in other countries. This is the first report of STS and GIST from PBCRs in Thailand. Based on current healthcare service, an overall survival rates of STS and GIST are comparable to those reported from others.
Funder
National Science and Technology Development Agency
Health Systems Research Institute, Thailand
Publisher
Springer Science and Business Media LLC
Reference34 articles.
1. Fletcher, C. D., Unni, K. K. & Mertens, F. Pathology and Genetics of Tumours of Soft Tissue and Bone (Iarc, 2002).
2. American Cancer Society. What is a soft tissue sarcoma? Available: https://www.cancer.org/cancer/soft-tissue-sarcoma/about/soft-tissue-sarcoma.html. (Accessed 28 June 2020).
3. Fletcher, C., Bridge, J. A., Hogendoorn, P. C. W. & Mertens, F. WHO Classification of Tumours of Soft Tissue and Bone: WHO Classification of Tumours Vol. 5 (World Health Organization, 2013).
4. Amadeo, B. et al. Incidence and time trends of sarcoma (2000–2013): Results from the French network of cancer registries (FRANCIM). BMC Cancer 20, 1 (2020).
5. Toro, J. R. et al. Incidence patterns of soft tissue sarcomas, regardless of primary site, in the surveillance, epidemiology and end results program, 1978–2001: An analysis of 26,758 cases. Int. J. Cancer. 119, 12 (2006).
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