Outcomes of palliative-intent surgery in retroperitoneal sarcoma-Results from the US Sarcoma Collaborative.


Journal

Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 30 08 2019
accepted: 16 02 2020
pubmed: 14 3 2020
medline: 29 5 2020
entrez: 14 3 2020
Statut: ppublish

Résumé

Outcomes of palliative-intent surgery in retroperitoneal sarcomas (RPS) are not well understood. This study aims to define indications for and outcomes after palliative-intent RPS resection. Using a retrospective 8-institution database, patients undergoing resection of primary/recurrent RPS with palliative intent were identified. Logistic regression and Cox-proportional hazards models were constructed to analyze factors associated with postoperative complications and overall survival (OS). Of 3088 patients, 70 underwent 87 palliative-intent procedures. Most common indications were pain (26%) and bowel obstruction (21%). Dedifferentiated liposarcoma (n = 17, 24%), leiomyosarcoma (n = 13, 19%) were predominant subtypes. Median OS was 10.69 months (IQR, 3.91-23.23). R2 resection (OR, 8.60; CI, 1.42-52.15; P = .019), larger tumors (OR, 10.87; CI, 1.44-82.11; P = .021) and low preoperative albumin (OR, 0.14; CI, 0.04-0.57; P = .006) were associated with postoperative complications. Postoperative complications (HR, 1.95; CI, 1.02-3.71; P = .043) and high-grade histology (HR, 6.56; CI, 1.72-25.05; P = .006) rather than resection status were associated with reduced OS. However, in R2-resected patients, development of postoperative complications significantly reduced survival (P = .042). Postoperative complications and high-grade histology rather than resection status impacts survival in palliative-intent RPS resections. Given the higher incidence of postoperative complications which may diminish survival, palliative-intent R2 resection should be offered only after cautious consideration.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Outcomes of palliative-intent surgery in retroperitoneal sarcomas (RPS) are not well understood. This study aims to define indications for and outcomes after palliative-intent RPS resection.
METHODS METHODS
Using a retrospective 8-institution database, patients undergoing resection of primary/recurrent RPS with palliative intent were identified. Logistic regression and Cox-proportional hazards models were constructed to analyze factors associated with postoperative complications and overall survival (OS).
RESULTS RESULTS
Of 3088 patients, 70 underwent 87 palliative-intent procedures. Most common indications were pain (26%) and bowel obstruction (21%). Dedifferentiated liposarcoma (n = 17, 24%), leiomyosarcoma (n = 13, 19%) were predominant subtypes. Median OS was 10.69 months (IQR, 3.91-23.23). R2 resection (OR, 8.60; CI, 1.42-52.15; P = .019), larger tumors (OR, 10.87; CI, 1.44-82.11; P = .021) and low preoperative albumin (OR, 0.14; CI, 0.04-0.57; P = .006) were associated with postoperative complications. Postoperative complications (HR, 1.95; CI, 1.02-3.71; P = .043) and high-grade histology (HR, 6.56; CI, 1.72-25.05; P = .006) rather than resection status were associated with reduced OS. However, in R2-resected patients, development of postoperative complications significantly reduced survival (P = .042).
CONCLUSIONS CONCLUSIONS
Postoperative complications and high-grade histology rather than resection status impacts survival in palliative-intent RPS resections. Given the higher incidence of postoperative complications which may diminish survival, palliative-intent R2 resection should be offered only after cautious consideration.

Identifiants

pubmed: 32167587
doi: 10.1002/jso.25890
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1140-1147

Informations de copyright

© 2020 Wiley Periodicals, Inc.

Références

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Auteurs

Sam Z Thalji (SZ)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

Susan Tsai (S)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

T Clark Gamblin (TC)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

Callisia Clarke (C)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

Kathleen Christians (K)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

John Charlson (J)

Department of Medical Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin.

Cecilia G Ethun (CG)

Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.

George Poultsides (G)

Department of Surgery, Stanford University Medical Center, Palo Alto, California.

Valerie P Grignol (VP)

Division of Surgical Oncology, Department of Surgery, The Ohio State University, Columbus, Ohio.

Kevin K Roggin (KK)

Department of Surgery, University of Chicago Medicine, Chicago, Illinois.

Konstantinos Votanopoulos (K)

Department of Surgery, Wake Forest University, Winston-Salem, North Carolina.

Ryan C Fields (RC)

Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.

Daniel E Abbott (DE)

Department of Surgery, University of Wisconsin, Madison, Wisconsin.

Kenneth Cardona (K)

Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, Georgia.

Harveshp Mogal (H)

Department of Surgery, Medical College of Wisconsin, Milwaukee, Wisconsin.

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