A closer look at the natural history and recurrence patterns of high-grade truncal/extremity leiomyosarcomas: A multi-institutional analysis from the US Sarcoma Collaborative.


Journal

Surgical oncology
ISSN: 1879-3320
Titre abrégé: Surg Oncol
Pays: Netherlands
ID NLM: 9208188

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 16 12 2019
revised: 27 04 2020
accepted: 18 06 2020
entrez: 6 9 2020
pubmed: 7 9 2020
medline: 9 7 2021
Statut: ppublish

Résumé

Natural history and outcomes for truncal/extremity (TE) soft tissue sarcoma (STS) is derived primarily from studies investigating all histiotypes as one homogenous cohort. We aimed to define the recurrence rate (RR), recurrence patterns, and response to radiation of TE leiomyosarcomas (LMS). Patients from the US Sarcoma Collaborative database with primary, high-grade TE STS were identified. Patients were grouped into LMS or other histology (non-LMS). Primary endpoints were locoregional recurrence-free survival (LR-RFS), distant-RFS (D-RFS), and disease specific survival (DSS). Of 1215 patients, 93 had LMS and 1122 non-LMS. In LMS patients, median age was 63 and median tumor size was 6 cm. In non-LMS patients, median age was 58 and median tumor size was 8 cm. In LMS patients, overall RR was 42% with 15% LR-RR and 29% D-RR. The 3yr LR-RFS, D-RFS, and DSS were 84%, 65%, and 76%, respectively. When considering high-risk (>5 cm and high-grade, n = 49) LMS patients, the overall RR was 45% with 12% LR-RR and 35% D-RR. 61% received radiation. The 3yr LR-RFS (78vs93%, p = 0.39), D-RFS (53vs63%, p = 0.27), and DSS (67vs91%, p = 0.17) were similar in those who did and did not receive radiation. High-risk, non-LMS patients had a similar overall RR of 42% with 15% LR-RR and 30% D-RR. 60% of non-LMS patients received radiation. There was an improved 3yr LR-RFS (82vs75%, p = 0.030) and DSS (77vs65%,p = 0.007) in non-LMS patients who received radiation. In our cohort, patients with LMS have a low local recurrence rate (12-15%) and modest distant recurrence rate (29-35%). However, LMS patients had no improvement in local control or long-term outcomes with radiation. The value of radiation in these patients merits further investigation.

Sections du résumé

BACKGROUND/OBJECTIVE OBJECTIVE
Natural history and outcomes for truncal/extremity (TE) soft tissue sarcoma (STS) is derived primarily from studies investigating all histiotypes as one homogenous cohort. We aimed to define the recurrence rate (RR), recurrence patterns, and response to radiation of TE leiomyosarcomas (LMS).
METHODS METHODS
Patients from the US Sarcoma Collaborative database with primary, high-grade TE STS were identified. Patients were grouped into LMS or other histology (non-LMS). Primary endpoints were locoregional recurrence-free survival (LR-RFS), distant-RFS (D-RFS), and disease specific survival (DSS).
RESULTS RESULTS
Of 1215 patients, 93 had LMS and 1122 non-LMS. In LMS patients, median age was 63 and median tumor size was 6 cm. In non-LMS patients, median age was 58 and median tumor size was 8 cm. In LMS patients, overall RR was 42% with 15% LR-RR and 29% D-RR. The 3yr LR-RFS, D-RFS, and DSS were 84%, 65%, and 76%, respectively. When considering high-risk (>5 cm and high-grade, n = 49) LMS patients, the overall RR was 45% with 12% LR-RR and 35% D-RR. 61% received radiation. The 3yr LR-RFS (78vs93%, p = 0.39), D-RFS (53vs63%, p = 0.27), and DSS (67vs91%, p = 0.17) were similar in those who did and did not receive radiation. High-risk, non-LMS patients had a similar overall RR of 42% with 15% LR-RR and 30% D-RR. 60% of non-LMS patients received radiation. There was an improved 3yr LR-RFS (82vs75%, p = 0.030) and DSS (77vs65%,p = 0.007) in non-LMS patients who received radiation.
CONCLUSIONS CONCLUSIONS
In our cohort, patients with LMS have a low local recurrence rate (12-15%) and modest distant recurrence rate (29-35%). However, LMS patients had no improvement in local control or long-term outcomes with radiation. The value of radiation in these patients merits further investigation.

Identifiants

pubmed: 32891345
pii: S0960-7404(20)30330-3
doi: 10.1016/j.suronc.2020.06.003
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

292-297

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Rachel M Lee (RM)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Cecilia G Ethun (CG)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Mohammad Y Zaidi (MY)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Thuy B Tran (TB)

Department of Surgery, Stanford University Medical Center, Palo Alto, CA, USA.

George A Poultsides (GA)

Department of Surgery, Stanford University Medical Center, Palo Alto, CA, USA.

Valerie P Grignol (VP)

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

John H Howard (JH)

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

Meena Bedi (M)

Department of Radiation Oncology, Medical College of Wisconsin, Milwaukee, WI, USA.

T Clark Gamblin (TC)

Division of Surgical Oncology, Department of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.

Jennifer Tseng (J)

Department of Surgery, University of Chicago Medicine, Chicago, IL, USA.

Kevin K Roggin (KK)

Department of Surgery, University of Chicago Medicine, Chicago, IL, USA.

Konstantinos Chouliaras (K)

Department of Surgery, Wake Forest University, Winston-Salem, NC, USA.

Konstantinos Votanopoulos (K)

Department of Surgery, Wake Forest University, Winston-Salem, NC, USA.

Bradley A Krasnick (BA)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.

Ryan C Fields (RC)

Department of Surgery, Washington University School of Medicine, St Louis, MO, USA.

Shervin V Oskouei (SV)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

David K Monson (DK)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Nickolas B Reimer (NB)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Shishir K Maithel (SK)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA.

Kenneth Cardona (K)

Division of Surgical Oncology, Department of Surgery, Winship Cancer Institute, Emory University, Atlanta, GA, USA. Electronic address: ken.cardona@emory.edu.

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Classifications MeSH