Multivisceral resection for retroperitoneal liposarcoma-is it worth it? A 20-year single-center experience

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Citações na Scopus
0
Tipo de produção
article
Data de publicação
2023
Título da Revista
ISSN da Revista
Título do Volume
Editora
SPRINGER
Citação
SURGERY TODAY, v.53, n.10, p.1181-1187, 2023
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
PurposeSoft tissue sarcomas are rare malignant tumors. Liposarcoma constitutes the most frequent histological subtype of retroperitoneal sarcoma. The prognosis of soft tissue sarcomas depends on clinical and histologic characteristics.ObjectiveEvaluate variables that may be related to the overall and local recurrence-free survival in patients with retroperitoneal liposarcoma and discuss the need for visceral resection en-bloc for tumors.MethodsA retrospective analysis was conducted of the medical records of 60 patients seen between 1997 and 2017 who underwent surgical resection of retroperitoneal liposarcoma.ResultsThe overall survival rate at 5 years of follow-up was 75.22% (95% confidence interval [CI] 0.58-0.86). The probability of a local recurrence-free survival at 5 years of follow-up was 26.04% (95% CI 0.11-0.44). The multivariate analysis showed that dedifferentiated or pleomorphic tumors and R2/fragmented resection were associated with a shorter time to recurrence. No other characteristics markedly influenced the overall survival (P > 0.05).ConclusionPatients with dedifferentiated or pleomorphic tumors and incomplete resection were associated with higher local recurrence rates than others. This study reinforces the need for complete and en-bloc resection with organs when there is clear involvement or technical surgical difficulty to maintain the tumor integrity.
Palavras-chave
Liposarcoma, Retroperitoneal space, Survival analysis, Surgical oncology, Retrospective study
Referências
  1. de Vreeze R, 2010, J MOL DIAGN, V12, P238, DOI 10.2353/jmoldx.2010.090117
  2. Diamantis A, 2020, RADIOL ONCOL, V54, P14, DOI 10.2478/raon-2020-0012
  3. Dickson MA, 2016, JAMA ONCOL, V2, P937, DOI 10.1001/jamaoncol.2016.0264
  4. Ewing J, 1919, NEOPLASTIC DIS TXB T
  5. Fabre-Guillevin E, 2006, CANCER-AM CANCER SOC, V106, P2725, DOI 10.1002/cncr.21933
  6. Fletcher C, 2002, WHO CLASSIFICATION T, V4
  7. Ikoma N, 2019, MD ANDERSON SURG ONC, V5, P233
  8. Keung EZ, 2014, J AM COLL SURGEONS, V218, P206, DOI 10.1016/j.jamcollsurg.2013.10.009
  9. Neuhaus SJ, 2005, BRIT J SURG, V92, P246, DOI 10.1002/bjs.4802
  10. Park JO, 2009, ANN SURG, V250, P977, DOI 10.1097/SLA.0b013e3181b2468b
  11. Russo P, 1997, ANN SURG ONCOL, V4, P421, DOI 10.1007/BF02305556
  12. Singer S, 2003, ANN SURG, V238, P358, DOI 10.1097/01.sla.0000086542.11899.38
  13. Wibmer C, 2010, ANN ONCOL, V21, P1106, DOI 10.1093/annonc/mdp415