Cancer Res Treat.  2019 Oct;51(4):1380-1391. 10.4143/crt.2018.476.

Characteristics and Treatment Patterns of Patients with Advanced Soft Tissue Sarcoma in Korea

Affiliations
  • 1Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea. rha7655@yuhs.ac
  • 2Department of Preventive Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • 3Department of Preventive Medicine, Eulji University College of Medicine, Daejeon, Korea.
  • 4Department of Biomedical Systems Informatics, Yonsei University College of Medicine, Seoul, Korea.
  • 5Department of Public Health, Yonsei University Graduate School, Seoul, Korea.
  • 6Parc Sanitari Sant Joan de Déu, Fundació Sant Joan de Déu, CIBERSAM, Universitat de Barcelona, Barcelona, Spain.
  • 7Eli Lilly and Company, Seoul, Korea.
  • 8Eli Lilly and Company, Windlesham, UK. novick_diego@lilly.com

Abstract

PURPOSE
A soft tissue sarcoma (STS) is a rare type of cancer, accounting for 1% of adult solid cancers. The aim of the present study is to determine the incidence of localized and advanced STS in Korean patients, their treatment patterns, and the survival of patients by disease status.
MATERIALS AND METHODS
The STS patient cohort was defined using National Health Insurance Service medical data from 2002 to 2015. Incidence, distribution, anatomical location of tumors, survival rates (Kaplan-Meyer survival function) and treatment patterns were analyzed by applying different algorithms to the STS cohort containing localized and advanced STS cases.
RESULTS
A total of 7,813 patients were diagnosed with STS from 2007 to 2014, 4,307 were localized STS and 3,506 advanced STS cases. The total incidence of STS was 2.49 per 100,000 person- years: 1.37 per 100,000 person-years for localized STS and 1.12 per 100,000 person-years for advanced STS. The 5-year survival rate after diagnosis was 56.4% for all STS, 82.4% for localized, and 27.2% for advanced STS. Half of the advanced STS patients (49.98%) received anthracycline-containing chemotherapy as initial treatment after diagnosis.
CONCLUSION
This study provides insights into localized and advanced STS epidemiology, treatment patterns and outcomes in Korea, which could be used as fundamental data in improving clinical outcomes of STS patients in the future.

Keyword

Epidemiology; Korean population; Advanced soft tissue sarcoma; Treatment pattern; Modality

MeSH Terms

Adult
Cohort Studies
Diagnosis
Drug Therapy
Epidemiology
Humans
Incidence
Korea*
National Health Programs
Sarcoma*
Survival Rate

Figure

  • Fig. 1. Taxonomy of soft tissue sarcoma (STS) patients by treatment patterns. Localized and advanced cases were defined using a diagnostic algorithm. OP, only surgery; RT, only radiotherapy; Pre/Post-OP, surgery in combination with pre/postoperative treatment; CTx/CCRT (systemic treatment), chemotherapy±radiotherapy; CD (clinical deterioration < 1 year), patients who died within a year of diagnosis; Pre-Obs, patients who received surgery with preoperative treatment followed by observation; Pre-Tx, patients who received surgery with preoperative treatment followed by any treatment for cancer (chemotherapy, radiotherapy or surgery) 1 year after the initial surgery; Pre-Sys CTx, patients who received surgery with preoperative treatment followed by systemic chemotherapy 1 year after the initial surgery; Pre-Local Tx, patients who received surgery with preoperative treatment followed by local treatments 1 year after the initial surgery; Post-Obs, patients who received surgery with postoperative treatment followed by observation; Post-Tx, patients who received surgery with postoperative treatment followed by any treatment for cancer (chemotherapy, radiotherapy or surgery) 1 year after the initial surgery; Post-Sys CTx, patients who received surgery with postoperative treatment followed by systemic chemotherapy 1 year after the initial surgery; Post-Local Tx, patients who received surgery with postoperative treatment followed by local treatments 1 year after the initial surgery; CD-OP, patients who received only surgery and died within a year of diagnosis; CD-RT, patients who received only radiotherapy and died within a year of diagnosis; CD-Pre/Post-OP, patients who received surgery with pre/postoperative treatment and died within a year of diagnosis; CD-CTx/CCRT, patients who received systemic chemotherapy and/or radiotherapy and died within a year of diagnosis; CD-No Tx, patients who did not receive any treatment and died within a year of diagnosis. a) 1 Year; the 1-year period was chosen because in clinical practice adjuvant therapy usually lasts about 1 year after surgery in Korea.

  • Fig. 2. Annual incidence cases by subgroup. STS, soft tissue sarcoma.

  • Fig. 3. Incidence cases by age and distribution by subgroup. STS, soft tissue sarcoma.

  • Fig. 4. Incidence rate by sex and age.

  • Fig. 5. Kaplan-Meier curve of overall survival. STS, soft tissue sarcoma.

  • Fig. 6. Kaplan-Meier curve of overall survival by treatment modalities in advanced soft tissue sarcoma (STS). The cases of CD (clinical deterioration < 1 year) were included in the relevant groups according to the modalities. ‘With surgery’ (n=1,789)=‘Pre-Tx’ (n=1,396)+‘Post-Tx’ (n= 60)+‘CD-Pre/Post-OP’ (n=333). ‘Without surgery’ (n=956) =‘CTx/CCRT’ (n=657)+‘CD-CTx/CCRT’ (n=299). OP, only surgery; CTx/CCRT, chemotherapy±radiotherapy; PreTx, patients who received surgery with preoperative treatment followed by any treatment for cancer (chemotherapy, radiotherapy, or surgery) 1 year after the initial surgery; Post-Tx, patients who received surgery with postoperative treatment followed by any treatment for cancer (chemotherapy, radiotherapy, or surgery) 1 year after the initial surgery; CTx/CCRT, patients who received only chemotherapy with or without radiotherapy.


Reference

References

1. Wibmer C, Leithner A, Zielonke N, Sperl M, Windhager R. Increasing incidence rates of soft tissue sarcomas? A population-based epidemiologic study and literature review. Ann Oncol. 2010; 21:1106–11.
Article
2. Burningham Z, Hashibe M, Spector L, Schiffman JD. The epidemiology of sarcoma. Clin Sarcoma Res. 2012; 2:14.
Article
3. Casali PG, Blay JY; ESMO/CONTICANET/EUROBONET Consensus Panel of experts. Soft tissue sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and followup. Ann Oncol. 2010; 21 Suppl 5:v198–203.
Article
4. Schoffski P, Cornillie J, Wozniak A, Li H, Hompes D. Soft tissue sarcoma: an update on systemic treatment options for patients with advanced disease. Oncol Res Treat. 2014; 37:355–62.
Article
5. Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin. 2016; 66:7–30.
Article
6. Stiller CA, Trama A, Serraino D, Rossi S, Navarro C, Chirlaque MD, et al. Descriptive epidemiology of sarcomas in Europe: report from the RARECARE project. Eur J Cancer. 2013; 49:684–95.
Article
7. Statistics Korea. Estimates of future population 2010-2060 [Internet]. Daejeon: Statistics Korea;2011. [cited 2018 Dec 10]. Available from: http://kosis.kr./eng/.
8. Kang S, Kim HS, Choi ES, Han I. Incidence and treatment pattern of extremity soft tissue sarcoma in Korea, 2009-2011: a nationwide study based on the Health Insurance Review and Assessment Service database. Cancer Res Treat. 2015; 47:575–82.
Article
9. Fletcher CD, Unni KK, Mertens F. World Health Organization classification of tumours pathology and genetics of tumours of soft tissue and bone. Lyon: IARC Press;2002.
10. Corless CL, Schroeder A, Griffith D, Town A, McGreevey L, Harrell P, et al. PDGFRA mutations in gastrointestinal stromal tumors: frequency, spectrum and in vitro sensitivity to imatinib. J Clin Oncol. 2005; 23:5357–64.
Article
11. Italiano A, Mathoulin-Pelissier S, Cesne AL, Terrier P, Bonvalot S, Collin F, et al. Trends in survival for patients with metastatic soft-tissue sarcoma. Cancer. 2011; 117:1049–54.
Article
12. Sheng JY, Movva S. Systemic therapy for advanced soft tissue sarcoma. Surg Clin North Am. 2016; 96:1141–56.
Article
13. Krikelis D, Judson I. Role of chemotherapy in the management of soft tissue sarcomas. Expert Rev Anticancer Ther. 2010; 10:249–60.
Article
14. Seong SC, Kim YY, Khang YH, Heon Park J, Kang HJ, Lee H, et al. Data resource profile: the National Health Information Database of the National Health Insurance Service in South Korea. Int J Epidemiol. 2017; 46:799–800.
15. Ogura K, Higashi T, Kawai A. Statistics of soft-tissue sarcoma in Japan: report from the Bone and Soft Tissue Tumor Registry in Japan. J Orthop Sci. 2017; 22:755–64.
Article
16. SEER cancer statistics review, 1975-2008 [Internet]. Bethesda, MD: National Cancer Institute;2011. [cited 2018 Dec 10]. Available from: http://seer.cancer.gov/csr/1975_20.
17. Ray-Coquard I, Collard O, Ducimetiere F, Laramas M, Mercier F, Ladarre N, et al. Treatment patterns and survival in an exhaustive French cohort of pazopanib-eligible patients with metastatic soft tissue sarcoma (STS). BMC Cancer. 2017; 17:111.
Article
18. Maretty-Nielsen K, Aggerholm-Pedersen N, Safwat A, Baerentzen S, Pedersen AB, Keller J. Prevalence and prognostic impact of comorbidity in soft tissue sarcoma: a population-based cohort study. Acta Oncol. 2014; 53:1188–96.
Article
19. Toro JR, Travis LB, Wu HJ, Zhu K, Fletcher CD, Devesa SS. 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. 2006; 119:2922–30.
Article
20. Bhatt N, Deady S, Gillis A, Bertuzzi A, Fabre A, Heffernan E, et al. Epidemiological study of soft-tissue sarcomas in Ireland. Cancer Med. 2016; 5:129–35.
Article
21. Francis M, Dennis N, Charman J, Lawrence G, Grimer R. Bone and soft tissue sarcomas: UK incidence and survival: 1996 to 2010. London: National Cancer Intelligence Network;2013.
22. Gustafson P. Soft tissue sarcoma. Epidemiology and prognosis in 508 patients. Acta Orthop Scand Suppl. 1994; 259:1–31.
23. Yang L, Fang ZW, Fan ZF, Wang N, Yuan YN, Li HC, et al. An analysis of incidence trends and characteristics of soft tissue sarcoma in Beijing, 1999-2013. Zhonghua Zhong Liu Za Zhi. 2017; 39:471–6.
24. Forman D, Bray F, Brewster DH, Gombe Mbalawa C, Kohler B, Pineros M, et al. Cancer incidence in five continents. Vol. X. Lyon: International Agency for Research on Cancer;2014.
25. Surveillance, Epidemiology, and End Results Program [Internet]. Bethesda, MD: National Cancer Institute;2016. [cited 2018 Dec 20]. Available from: http://www.seer.cancer.gov.
26. Mytelka DS, Lorenzo M, Stafkey-Mailey D, D'Yachkova Y, Nagar SP, Candrilli SD, et al. Advanced soft tissue sarcoma: systemic treatment patterns and survival in Germany. Value Health. 2016; 19:A76.
Article
27. Mytelka DS, Lorenzo M, Stafkey-Mailey D, D'Yachkova Y, Nagar SP, Candrilli SD, et al. Real-world treatment patterns and outcomes for patients with advanced soft tissue sarcoma receiving systemic therapy in the United Kingdom. Value Health. 2016; 19:A751.
Article
28. Bae S, Crowe P, Gowda R, Joubert W, Carey-Smith R, Stalley P, et al. Patterns of care for patients with advanced soft tissue sarcoma: experience from Australian sarcoma services. Clin Sarcoma Res. 2016; 6:11.
Article
29. Judson I, Verweij J, Gelderblom H, Hartmann JT, Schoffski P, Blay JY, et al. Doxorubicin alone versus intensified doxorubicin plus ifosfamide for first-line treatment of advanced or metastatic soft-tissue sarcoma: a randomised controlled phase 3 trial. Lancet Oncol. 2014; 15:415–23.
Article
30. Tap WD, Jones RL, Van Tine BA, Chmielowski B, Elias AD, Adkins D, et al. Olaratumab and doxorubicin versus doxorubicin alone for treatment of soft-tissue sarcoma: an open-label phase 1b and randomised phase 2 trial. Lancet. 2016; 388:488–97.
Article
31. Hoang HL, Ensor K, Rosen G, Leon Pachter H, Raccuia JS. Prognostic factors and survival in patients treated surgically for recurrent metastatic uterine leiomyosarcoma. Int J Surg Oncol. 2014; 2014:919323.
Article
32. Potter DA, Glenn J, Kinsella T, Glatstein E, Lack EE, Restrepo C, et al. Patterns of recurrence in patients with high-grade softtissue sarcomas. J Clin Oncol. 1985; 3:353–66.
Article
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