Predicting Survival in Patients Undergoing Resection for Locally Recurrent Retroperitoneal Sarcoma: A Study and Novel Nomogram from TARPSWG.


Journal

Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500

Informations de publication

Date de publication:
15 04 2019
Historique:
received: 22 08 2018
revised: 21 11 2018
accepted: 24 01 2019
pubmed: 7 2 2019
medline: 30 5 2020
entrez: 7 2 2019
Statut: ppublish

Résumé

The role of surgery for first relapse locally recurrent retroperitoneal sarcoma (RPS-LR1) is uncertain. We report outcomes of the largest RPS-LR1 series and propose a new prognostic nomogram. Patients with consecutive RPS-LR1 without distant metastases who underwent resection at 22 centers (2002-2011) were included. Endpoints were disease-free and overall survival (DFS, OS) and crude-cumulative-incidence (CCI) of local/distant recurrence from second surgery. Nomograms predicting DFS and OS from second surgery were developed and validated (calibration plots); discrimination was assessed (Harrell C index). Of 684 patients identified, full prognostic variable data were available for 602. Initial surgery for primary RPS was performed at our institutions in 188 patients (31%) and elsewhere in 414 (69%). At a median follow-up of 119 months [Interquartile range (IQR), 80-169] from initial surgery and 75 months (IQR 50-105) from second surgery, 6-year DFS and OS were 19.2% [95% confidence interval (CI), 16.0-23.0%] and 54.1% (95% CI, 49.8-58.8%), respectively. Recurrence patterns and survival probability were histology-specific, with liposarcoma subtypes having the highest 6-year CCI of second local recurrence (LR, 60.2%-70.9%) and leiomyosarcoma (LMS) having higher 6-year CCI of distant metastasis (DM, 36.3%). Nomograms included age at second surgery, multifocality, grade, completeness of second surgery, histology, chemotherapy/radiotherapy at first surgery, and number of organs resected at first surgery. OS and DFS nomograms showed good calibration and discriminative ability (C index 0.70 and 0.67, respectively). We developed nomograms to predict DFS and OS for patients undergoing RPS-LR1 resection. Nomograms provide individualized, disease-relevant estimations of survival for RPS-LR1 patients and assist in clinical decisions.

Identifiants

pubmed: 30723141
pii: 1078-0432.CCR-18-2700
doi: 10.1158/1078-0432.CCR-18-2700
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2664-2671

Informations de copyright

©2019 American Association for Cancer Research.

Auteurs

Chandrajit P Raut (CP)

Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts. craut@bwh.harvard.edu.

Dario Callegaro (D)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Rosalba Miceli (R)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Francesco Barretta (F)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Piotr Rutkowski (P)

Maria Sklodowska-Curie Memorial Cancer Center, Institute of Oncology, Warsaw, Poland.

Jean-Yves Blay (JY)

Centre Leon Berard, Lyon, France.

Guy Lahat (G)

Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

Dirk C Strauss (DC)

Royal Marsden Hospital, London, United Kingdom.

Ricardo Gonzalez (R)

Moffitt Cancer Center, Tampa, Florida.

Nita Ahuja (N)

Johns Hopkins University School of Medicine, Baltimore, Maryland.

Giovanni Grignani (G)

Candiolo Cancer Institute - FPO, IRCCS, Torino, Italy.

Vittorio Quagliuolo (V)

Istituto Clinico Humanitas IRCCS, Milan, Italy.

Eberhard Stoeckle (E)

Institut Bergonié, Regional Cancer Centre, Bordeaux Cedex, France.

Antonino De Paoli (A)

Centro di Riferimento Oncologico, Aviano, Italy.

Venu G Pillarisetty (VG)

Seattle Cancer Care Alliance, University of Washington School of Medicine, Seattle, Washington.

Carolyn Nessim (C)

The Ottawa Hospital, University of Ottawa, Ottawa, Canada.

Carol J Swallow (CJ)

Mount Sinai Hospital, Princess Margaret Hospital, University of Toronto, Toronto, Canada.

Sanjay Bagaria (S)

Mayo Clinic Jacksonville, Jacksonville, Florida.

Robert Canter (R)

University of California-Davis School of Medicine, Davis, California.

John Mullen (J)

Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.

Hans J Gelderblom (HJ)

Leiden University Medical Center, Leiden, the Netherlands.

Elisabetta Pennacchioli (E)

Istituto Europeo di Oncologia, Milano, Italy.

Frits van Coevorden (F)

Netherlands Cancer Institute, Amsterdam, the Netherlands.

Kenneth Cardona (K)

Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia.

Marco Fiore (M)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Mark Fairweather (M)

Brigham and Women's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.

Alessandro Gronchi (A)

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

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