Factors associated with disease-free and abdominal recurrence-free survival in abdominopelvic and retroperitoneal sarcomas.


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 2022
Historique:
received: 07 02 2022
accepted: 14 02 2022
pubmed: 4 3 2022
medline: 17 5 2022
entrez: 3 3 2022
Statut: ppublish

Résumé

Retroperitoneal and abdominopelvic sarcomas are rare heterogeneous malignancies. The only therapy proven to improve disease-free survival (DFS) is R0/R1 surgical resection. We sought to analyze whether additional factors such as radiation and systemic therapy were associated with DFS and abdominal recurrence-free survival (RFS). Retrospective review of adults (≥18) with resectable abdominopelvic and retroperitoneal sarcomas who underwent intent-to-cure surgery at a high-volume tertiary referral center between 1998 and 2015. The main outcome measures were DFS and abdominal RFS. Overall, 159 patients met the criteria for inclusion. Median follow-up was 4.8 years (range 0.1-18.9 years). The most common histology was liposarcoma (49%). Systemic therapy was administered to 48% of patients and was not associated with improved outcomes. The neoadjuvant radiotherapy group (11%) had improved adjusted DFS (5.46 years, 95% CI [3.68, 7.24] vs. 3.1 years, 95% CI [2.48, 3.73]) and abdominal RFS (6.14 years, 95% CI [4.38, 7.89] vs. 3.22 years, 95% CI [2.61, 3.84]). The adjuvant radiotherapy group (19%) had no improvement. In a cohort of patients undergoing resection for retroperitoneal or abdominopelvic sarcoma, neoadjuvant radiation improved DFS and abdominal RFS. A follow-up of over three years was needed to appreciate a difference in outcomes.

Sections du résumé

BACKGROUND AND OBJECTIVES OBJECTIVE
Retroperitoneal and abdominopelvic sarcomas are rare heterogeneous malignancies. The only therapy proven to improve disease-free survival (DFS) is R0/R1 surgical resection. We sought to analyze whether additional factors such as radiation and systemic therapy were associated with DFS and abdominal recurrence-free survival (RFS).
METHODS METHODS
Retrospective review of adults (≥18) with resectable abdominopelvic and retroperitoneal sarcomas who underwent intent-to-cure surgery at a high-volume tertiary referral center between 1998 and 2015. The main outcome measures were DFS and abdominal RFS.
RESULTS RESULTS
Overall, 159 patients met the criteria for inclusion. Median follow-up was 4.8 years (range 0.1-18.9 years). The most common histology was liposarcoma (49%). Systemic therapy was administered to 48% of patients and was not associated with improved outcomes. The neoadjuvant radiotherapy group (11%) had improved adjusted DFS (5.46 years, 95% CI [3.68, 7.24] vs. 3.1 years, 95% CI [2.48, 3.73]) and abdominal RFS (6.14 years, 95% CI [4.38, 7.89] vs. 3.22 years, 95% CI [2.61, 3.84]). The adjuvant radiotherapy group (19%) had no improvement.
CONCLUSIONS CONCLUSIONS
In a cohort of patients undergoing resection for retroperitoneal or abdominopelvic sarcoma, neoadjuvant radiation improved DFS and abdominal RFS. A follow-up of over three years was needed to appreciate a difference in outcomes.

Identifiants

pubmed: 35239187
doi: 10.1002/jso.26828
pmc: PMC9313796
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1292-1300

Informations de copyright

© 2022 The Authors. Journal of Surgical Oncology published by Wiley Periodicals LLC.

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Auteurs

Brooke C Bredbeck (BC)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.

Lia D Delaney (LD)

University of Michigan Medical School, Ann Arbor, Michigan, USA.

Varun G Kathawate (VG)

University of Michigan Medical School, Ann Arbor, Michigan, USA.

Cameron A Harter (CA)

University of Michigan Medical School, Ann Arbor, Michigan, USA.

Jodi Wilkowski (J)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.

Rashmi Chugh (R)

Department of Medicine, University of Michigan , Ann Arbor, Michigan, USA.
Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.

Kyle C Cuneo (KC)

Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.
Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.

Lesly A Dossett (LA)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.

Michael S Sabel (MS)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.

Christina V Angeles (CV)

Department of Surgery, University of Michigan, Ann Arbor, Michigan, USA.
Rogel Cancer Center, University of Michigan, Ann Arbor, Michigan, USA.

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