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Extremity Soft Tissue Sarcoma: A Multi-Institutional Validation of Prognostic Nomograms.
Squires, Malcolm Hart; Ethun, Cecilia G; Donahue, Erin E; Benbow, Jennifer H; Anderson, Colin J; Jagosky, Megan H; Manandhar, Munsa; Patt, Joshua C; Kneisl, Jeffrey S; Salo, Jonathan C; Hill, Joshua S; Ahrens, William; Prabhu, Roshan S; Livingston, Michael B; Gower, Nicole L; Needham, McKenzie; Trufan, Sally J; Fields, Ryan C; Krasnick, Bradley A; Bedi, Meena; Votanopoulos, Konstantinos; Chouliaras, Konstantinos; Grignol, Valerie; Roggin, Kevin K; Tseng, Jennifer; Poultsides, George; Tran, Thuy B; Cardona, Kenneth; Howard, J Harrison.
Affiliation
  • Squires MH; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA. Malcolm.Squires@atriumhealth.org.
  • Ethun CG; Emory University, Atlanta, GA, USA.
  • Donahue EE; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Benbow JH; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Anderson CJ; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Jagosky MH; Musculoskeletal Institute, Atrium Health, Charlotte, NC, USA.
  • Manandhar M; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Patt JC; University of South Alabama, Mobile, AL, USA.
  • Kneisl JS; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Salo JC; Musculoskeletal Institute, Atrium Health, Charlotte, NC, USA.
  • Hill JS; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Ahrens W; Musculoskeletal Institute, Atrium Health, Charlotte, NC, USA.
  • Prabhu RS; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Livingston MB; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Gower NL; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Needham M; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Trufan SJ; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Fields RC; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Krasnick BA; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Bedi M; Levine Cancer Institute, Atrium Health, Charlotte, NC, USA.
  • Votanopoulos K; Washington University School of Medicine, St. Louis, MO, USA.
  • Chouliaras K; Washington University School of Medicine, St. Louis, MO, USA.
  • Grignol V; Medical College of Wisconsin, Milwaukee, WI, USA.
  • Roggin KK; Wake Forest University, Winston Salem, NC, USA.
  • Tseng J; Wake Forest University, Winston Salem, NC, USA.
  • Poultsides G; The Ohio State University, Columbus, OH, USA.
  • Tran TB; University of Chicago, Chicago, IL, USA.
  • Cardona K; University of Chicago, Chicago, IL, USA.
  • Howard JH; Stanford University, Stanford, CA, USA.
Ann Surg Oncol ; 29(5): 3291-3301, 2022 May.
Article in En | MEDLINE | ID: mdl-35015183
ABSTRACT

BACKGROUND:

Prognostic nomograms for patients with resected extremity soft tissue sarcoma (STS) include the Sarculator and Memorial Sloan Kettering (MSKCC) nomograms. We sought to validate these two nomograms within a large, modern, multi-institutional cohort of resected primary extremity STS patients.

METHODS:

Resected primary extremity STS patients from 2000 to 2017 were identified across nine high-volume U.S. institutions. Predicted 5- and 10-year overall survival (OS) and distant metastases cumulative incidence (DMCI), and 4-, 8-, and 12-year disease-specific survival (DSS) were calculated with Sarculator and MSKCC nomograms, respectively. Predicted survival probabilities stratified in quintiles were compared in calibration plots to observed survival assessed by Kaplan-Meier estimates. Cumulative incidence was estimated for DMCI. Harrell's concordance index (C-index) assessed discriminative ability of nomograms.

RESULTS:

A total of 1326 patients underwent resection of primary extremity STS. Common histologies included undifferentiated pleomorphic sarcoma (35%), fibrosarcoma (13%), and leiomyosarcoma (9%). Median tumor size was 8.0 cm (IQR 4.5-13.0). Tumor grade distribution was Grade 1 (13%), Grade 2 (9%), Grade 3 (78%). Median OS was 172 months, with estimated 5- and 10-year OS of 70% and 58%. C-indices for 5- and 10-year OS (Sarculator) were 0.72 (95% CI 0.70-0.75) and 0.73 (95% CI 0.70-0.75), and 0.72 (95% CI 0.69-0.75) for 5- and 10-year DMCI. C-indices for 4-, 8-, and 12-year DSS (MSKCC) were 0.71 (95% CI 0.68-0.75). Calibration plots showed good prognostication across all outcomes.

CONCLUSIONS:

Sarculator and MSKCC nomograms demonstrated good prognostic ability for survival and recurrence outcomes in a modern, multi-institutional validation cohort of resected primary extremity STS patients. External validation of these nomograms supports their ongoing incorporation into clinical practice.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Soft Tissue Neoplasms Type of study: Clinical_trials / Prognostic_studies Limits: Humans Language: En Journal: Ann Surg Oncol Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sarcoma / Soft Tissue Neoplasms Type of study: Clinical_trials / Prognostic_studies Limits: Humans Language: En Journal: Ann Surg Oncol Journal subject: NEOPLASIAS Year: 2022 Document type: Article Affiliation country: