본문 바로가기
KERD
논문KCI 등재

Radiation-Induced Sarcoma: A 15-Year Experience in a Single Large Tertiary Referral Center

1

조회

0

다운로드

0

인용

0

참고문헌

키워드

주제분류의학일반

초록

Purpose The purpose of this study is to report on the incidence and the experience in management of radiation-induced sarcoma (RIS) at a large single center in Korea for 15 years. Materials and Methods We retrospectively reviewed the sarcoma registry of a large institution from January 2000 to April 2014. Results Out of the 3,674 patients listed in the registry, 33 patients (0.9%) diagnosed with RIS were identified. The median latency of RIS was 12.1 years. The number of cases of RIS increased from four cases in the years 2000-2003 to 14 cases in the years 2012-2014. The most common histology was osteosarcoma (36.4%). The median follow-up period was 23.1 months, the median overall survival (OS) of all patients was 2.9 years, and their 5-year survival rate was 44.7%. Univariate and multivariate analyses showed association of the age at diagnosis (p=0.01) and the treatment aim (p=0.001) with the OS. The median OS and the 5-year survival rate of patients treated with curative surgery (n=19) were 9.6 years and 65%, respectively, and of the conservatively treated patients, 0.7 years and 0% (n=14). Re-irradiation was delivered to nine patients, and radiation toxicity was observed in five patients. Conclusion In this study, RIS accounted for 0.9% of the cases of sarcoma, with increasing incidence. Despite the association of curative resection with increased survival, it could be applied to only 58% of the patients. Considering the limited treatment options for RIS, conduct of a genetic study to identify the underlying mechanism of RIS is needed.

Abstract

Purpose The purpose of this study is to report on the incidence and the experience in management of radiation-induced sarcoma (RIS) at a large single center in Korea for 15 years. Materials and Methods We retrospectively reviewed the sarcoma registry of a large institution from January 2000 to April 2014. Results Out of the 3,674 patients listed in the registry, 33 patients (0.9%) diagnosed with RIS were identified. The median latency of RIS was 12.1 years. The number of cases of RIS increased from four cases in the years 2000-2003 to 14 cases in the years 2012-2014. The most common histology was osteosarcoma (36.4%). The median follow-up period was 23.1 months, the median overall survival (OS) of all patients was 2.9 years, and their 5-year survival rate was 44.7%. Univariate and multivariate analyses showed association of the age at diagnosis (p=0.01) and the treatment aim (p=0.001) with the OS. The median OS and the 5-year survival rate of patients treated with curative surgery (n=19) were 9.6 years and 65%, respectively, and of the conservatively treated patients, 0.7 years and 0% (n=14). Re-irradiation was delivered to nine patients, and radiation toxicity was observed in five patients. Conclusion In this study, RIS accounted for 0.9% of the cases of sarcoma, with increasing incidence. Despite the association of curative resection with increased survival, it could be applied to only 58% of the patients. Considering the limited treatment options for RIS, conduct of a genetic study to identify the underlying mechanism of RIS is needed.

참고문헌 (24)

  1. Kadouri L, "Genetic predisposition to radiation induced sarcoma : possible role for BRCA and p53 mutations", Breast Cancer Res Treat, 140, pp.207~211 (2013)
  2. Mark RJ, "Postirradiation sarcomas : a single-institution study and review of the literature", Cancer, 73, pp.2653~2662 (1994)
  3. Gladdy RA, "Do radiation-associated soft tissue sarcomas have the same prognosis as sporadic soft tissue sarcomas?", J Clin Oncol, 28, pp.2064~2069 (2010)
  4. Lagrange JL, "Sarcoma after radiation therapy: retrospective multiinstitutional study of 80 histologically confirmed cases. Radiation Therapist and Pathologist Groups of the Federation Nationale des Centres de Lutte Contre le Cancer", Radiology, 216, pp.197~205 (2000)
  5. Bjerkehagen B, "Why do patients with radiation-induced sarcomas have a poor sarcoma-related survival?", Br J Cancer, 106, pp.297~306 (2012)
  6. Dineen SP, "Radiation-associated undifferentiated pleomorphic sarcoma is associated with worse clinical outcomes than sporadic lesions", Ann Surg Oncol, 22, pp.3913~3920 (2015)
  7. Thijssens KM, "Radiation-induced sarcoma : a challenge for the surgeon", Ann Surg Oncol, 12, pp.237~245 (2005)
  8. Neuhaus SJ, "Treatment and outcome of radiation-induced softtissue sarcomas at a specialist institution", Eur J Surg Oncol, 35, pp.654~659 (2009)
  9. Cahan WG, "Sarcoma arising in irradiated bone : report of 11cases", Cancer, 1, pp.3~29 (1948)
  10. Cho KH, "The challenges faced by the Korean Society for Radiation Oncology in the national healthcare system in Korea", Int J Radiat Oncol Biol Phys, 90, pp.725~728 (2014)
  11. Cha C, "Longterm results with resection of radiation-induced soft tissue sarcomas", Ann Surg, 239, pp.903~910 (2004)
  12. Pisters PW, "Long-term results of a prospective randomized trial of adjuvant brachytherapy in soft tissue sarcoma", J Clin Oncol, 14, pp.859~868 (1996)
  13. Yang JC, "Randomized prospective study of the benefit of adjuvant radiation therapy in the treatment of soft tissue sarcomas of the extremity", J Clin Oncol, 16, pp.197~203 (1998)
  14. Berrington de Gonzalez A, "Sarcoma risk after radiation exposure", Clin Sarcoma Res, 2, pp.18~ (2012)
  15. Rubino C, "Radiation dose and risk of soft tissue and bone sarcoma after breast cancer treatment", Breast Cancer Res Treat, 89, pp.277~288 (2005)
  16. Hall EJ, "Radiation-induced second cancers : the impact of 3D-CRT and IMRT", Int J Radiat Oncol Biol Phys, 56, pp.83~88 (2003)
  17. Schneider U, "Second cancers in children treated with modern radiotherapy techniques", Radiother Oncol, 89, pp.135~140 (2008)
  18. Tucker MA, "Bone sarcomas linked to radiotherapy and chemotherapy in children", N Engl J Med, 317, pp.588~593 (1987)
  19. Hawkins MM, "Radiotherapy, alkylating agents, and risk of bone cancer after childhood cancer", J Natl Cancer Inst, 88, pp.270~278 (1996)
  20. Le Vu B, "Radiation dose, chemotherapy and risk of osteosarcoma after solid tumours during childhood", Int J Cancer, 77, pp.370~377 (1998)
  21. Menu-Branthomme A, "Radiation dose, chemotherapy and risk of soft tissue sarcoma after solid tumours during childhood", Int J Cancer, 110, pp.87~93 (2004)
  22. Kacker C, "High frequency of MYC gene amplification is a common feature of radiation-induced sarcomas. Further results from EORTC STBSG TL 01", 01, 2013, pp.52, 93~98
  23. Kansara M, "Immune response to RB1-regulated senescence limits radiation-induced osteosarcoma formation", J Clin Invest, 123, pp.5351~5360 (2013)
  24. Hadj-Hamou NS, "A transcriptome signature distinguished sporadic from postradiotherapy radiation-induced sarcomas", Carcinogenesis, 32, pp.929~934 (2011)

관련 논문AI추천

Efficacy of Postoperative Radiotherapy Using Modern Techniques in Patients with Retroperitoneal Soft Tissue Sarcoma금웅섭, 김현주, 김효송, 서창옥, 조재호연세대학교의과대학 · Yonsei Medical Journal2018 · 제59권 제9호유방암치료 후 흉골에 발생한 방사선속발성 골육종 1예손장신, 염윤식, 윤대성, 임현우, 전현정, 정원규, 조도연대한내과학회 · 대한내과학회지2010 · 제78권 제4호Characteristics and Treatment Patterns of Patients with Advanced Soft Tissue Sarcoma in Korea김선민, 김효송, 남정모, 라선영, 장석용, 최선규, 한민경, Diego Novick, Jae Min Cho, Maria Victoria Moneta, Sae Young Lee대한암학회 · Cancer Research and Treatment2019 · 제51권 제4호Incidence and Treatment Pattern of Extremity Soft Tissue Sarcoma in Korea, 2009-2011: A Nationwide Study Based on the Health Insurance Review and Assessment Service Database강승철, 김한수, 최은석, 한일규대한암학회 · Cancer Research and Treatment2015 · 제47권 제4호Role of Radiotherapy in the Multimodal Treatment of Ewing Sarcoma Family Tumors서창옥, 유철주, 이수현, 이윤한, 임도훈, 임정호, 최윤선대한암학회 · Cancer Research and Treatment2015 · 제47권 제4호Type and Incidence of Soft Tissue Sarcomas in Korea: 2001-2007강혜윤, 구혜수, 권미선, 김동훈, 김미정, 김수진, 김영실, 김철환, 박용구, 박혜림, 백승삼, 유진영, 이안희, 이재혁, 이혜경, 장규윤, 주영채, 최경운, 최준혁대한병리학회 · Journal of Pathology and Translational Medicine2011 · 제45권 제6호

이 간행물의 다른 논문 (50건)