Literature DB >> 27220538

Prognosis of T1 synovial sarcoma depends upon surgery by oncologic surgeons.

Marc El Beaino1, Dejka M Araujo2, Vancheswaran Gopalakrishnan3, Alexander J Lazar4, Patrick P Lin1.   

Abstract

BACKGROUND: The prognosis of early stage synovial sarcomas is not well-defined since long-term follow-up is lacking in most studies. The optimal use of surgery, radiation, and chemotherapy needs to be clarified for this group.
METHODS: From 1994 to 2012, 63 patients were treated for localized synovial sarcoma with T1 (<5 cm) tumors. There were 27 males and 36 females. Mean follow-up was 85 months (range 13-210).
RESULTS: At 10 years, local recurrence-free survival was 82% (95% confidence interval [CI] 67-97%), and distant recurrence-free survival was 95% (95%CI 89-100%). Two patients developed metastases after 10 years. Local recurrence was associated with lack of re-excision and treatment by non-oncologic surgeons. Microscopic residual tumor was found in 43% of re-excised specimens. Metastasis was associated with local recurrence, tumor size ≥3 cm, and treatment by non-oncologic surgeons. Radiation and chemotherapy treatment did not have a significant effect in this patient cohort.
CONCLUSIONS: Early stage synovial sarcomas with T1 tumors have a relatively favorable prognosis but the potential for late relapse, and long-term follow-up beyond 10 years is recommended. Re-excision of the tumor bed and definitive treatment by trained oncologic surgeons may decrease the risk of local recurrence and metastasis. J. Surg. Oncol. 2016;114:490-494.
© 2016 Wiley Periodicals, Inc. © 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  metastasis; prognosis; survival; synovial sarcoma

Mesh:

Year:  2016        PMID: 27220538     DOI: 10.1002/jso.24306

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  4 in total

1.  Surgery alone is sufficient therapy for children and adolescents with low-risk synovial sarcoma: A joint analysis from the European paediatric soft tissue sarcoma Study Group and the Children's Oncology Group.

Authors:  Andrea Ferrari; Yueh-Yun Chi; Gian Luca De Salvo; Daniel Orbach; Bernadette Brennan; R Lor Randall; M Beth McCarville; Jennifer O Black; Rita Alaggio; Douglas S Hawkins; Gianni Bisogno; Sheri L Spunt
Journal:  Eur J Cancer       Date:  2017-04-07       Impact factor: 9.162

2.  Clinical comparison of tenosynovial giant cell tumors, synovial chondromatosis, and synovial sarcoma: analysis and report of 53 cases.

Authors:  Wei Wang; Man-Mei Long; Cheng-Jiang Wei; Xi-Wei Cui; Jie-Yi Ren; Yi-Hui Gu; Qing-Feng Li; Shun-Dong Dai; Bin Gu; Zhi-Chao Wang
Journal:  Ann Transl Med       Date:  2021-07

3.  Beclin1 overexpression suppresses tumor cell proliferation and survival via an autophagy‑dependent pathway in human synovial sarcoma cells.

Authors:  Jialin Zhu; Yongsong Cai; Ke Xu; Xiaoyu Ren; Jian Sun; Shemin Lu; Jinghong Chen; Peng Xu
Journal:  Oncol Rep       Date:  2018-07-25       Impact factor: 3.906

Review 4.  Systemic Anti-Cancer Therapy in Synovial Sarcoma: A Systematic Review.

Authors:  Richard F Riedel; Robin L Jones; Antoine Italiano; Chet Bohac; Juliette C Thompson; Kerstin Mueller; Zaeem Khan; Seth M Pollack; Brian A Van Tine
Journal:  Cancers (Basel)       Date:  2018-11-01       Impact factor: 6.639

  4 in total

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