Postoperative Morbidity After Resection of Recurrent Retroperitoneal Sarcoma: A Report from the Transatlantic Australasian RPS Working Group (TARPSWG).


Journal

Annals of surgical oncology
ISSN: 1534-4681
Titre abrégé: Ann Surg Oncol
Pays: United States
ID NLM: 9420840

Informations de publication

Date de publication:
May 2021
Historique:
received: 13 06 2020
accepted: 13 10 2020
pubmed: 4 1 2021
medline: 15 5 2021
entrez: 3 1 2021
Statut: ppublish

Résumé

This study aimed to evaluate perioperative morbidity after surgery for first locally recurrent (LR1) retroperitoneal sarcoma (RPS). Data concerning the safety of resecting recurrent RPS are lacking. Data were collected on all patients undergoing resection of RPS-LR1 at 22 Trans-Atlantic Australasian Retroperitoneal Sarcoma Working Group (TARPSWG) centers from 2002 to 2011. Uni- and multivariable logistic models were fitted to study the association between major (Clavien-Dindo grade ≥ 3) complications and patient/surgery characteristics as well as outcome. The resected organ score, a method of standardizing the number of organs resected, as previously described by the TARPSWG, was used. The 681 patients in this study had a median age of 59 years, and 51.8% were female. The most common histologic subtype was de-differentiated liposarcoma (43%), the median resected organ score was 1, and 83.3% of the patients achieved an R0 or R1 resection. Major complications occurred for 16% of the patients, and the 90-day mortality rate was 0.4%. In the multivariable analysis, a transfusion requirement was found to be a significant predictor of major complications (p < 0.001) and worse overall survival (OS) (p = 0.010). However, having a major complication was not associated with a worse OS or a higher incidence of local recurrence or distant metastasis. A surgical approach to recurrent RPS is relatively safe and comparable with primary RPS in terms of complications and postoperative mortality when performed at specialized sarcoma centers. Because alternative effective therapies still are lacking, when indicated, resection of a recurrent RPS is a reasonable option. Every effort should be made to minimize the need for blood transfusions.

Sections du résumé

BACKGROUND BACKGROUND
This study aimed to evaluate perioperative morbidity after surgery for first locally recurrent (LR1) retroperitoneal sarcoma (RPS). Data concerning the safety of resecting recurrent RPS are lacking.
METHODS METHODS
Data were collected on all patients undergoing resection of RPS-LR1 at 22 Trans-Atlantic Australasian Retroperitoneal Sarcoma Working Group (TARPSWG) centers from 2002 to 2011. Uni- and multivariable logistic models were fitted to study the association between major (Clavien-Dindo grade ≥ 3) complications and patient/surgery characteristics as well as outcome. The resected organ score, a method of standardizing the number of organs resected, as previously described by the TARPSWG, was used.
RESULTS RESULTS
The 681 patients in this study had a median age of 59 years, and 51.8% were female. The most common histologic subtype was de-differentiated liposarcoma (43%), the median resected organ score was 1, and 83.3% of the patients achieved an R0 or R1 resection. Major complications occurred for 16% of the patients, and the 90-day mortality rate was 0.4%. In the multivariable analysis, a transfusion requirement was found to be a significant predictor of major complications (p < 0.001) and worse overall survival (OS) (p = 0.010). However, having a major complication was not associated with a worse OS or a higher incidence of local recurrence or distant metastasis.
CONCLUSIONS CONCLUSIONS
A surgical approach to recurrent RPS is relatively safe and comparable with primary RPS in terms of complications and postoperative mortality when performed at specialized sarcoma centers. Because alternative effective therapies still are lacking, when indicated, resection of a recurrent RPS is a reasonable option. Every effort should be made to minimize the need for blood transfusions.

Identifiants

pubmed: 33389288
doi: 10.1245/s10434-020-09445-y
pii: 10.1245/s10434-020-09445-y
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2705-2714

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Références

Erzen D, Sencar M, Novak J. Retroperitoneal sarcoma: 25 years of experience with aggressive surgical treatment at the Institute of Oncology, Ljubljana. J Surg Oncol. 2005;91:1–9.
doi: 10.1002/jso.20265
Lewis JJ, LeungD, Woodruff JM, et al. Retroperitoneal sarcoma: analysis of 500 patients treated and followed at a single institution. Ann Surg. 1998;228:355.
doi: 10.1097/00000658-199809000-00008
Gronchi A, Strauss DC, Miceli R, et al. Variability in patterns of recurrence after resection of primary retroperitoneal sarcoma (RPS): a report on 1007 patients from the Multi-Institutional Collaborative RPS Working Group. Ann Surg. 2016;263:1002–9.
doi: 10.1097/SLA.0000000000001447
TARPSWG. Management of recurrent retroperitoneal sarcoma (RPS): a consensus approach from the Trans-Atlantic RPS Working Group. Ann Surg Oncol. 2016;23:3531–40.
doi: 10.1245/s10434-016-5336-7
MacNeill AJ, Gronchi A, Micelli R, et al. Postoperative morbidity after radical resection of primary retroperitoneal sarcoma a report from the Transatlantic RPS Working Group. Ann Surg Oncol. 2017;24:688–9.
doi: 10.1245/s10434-017-5889-0
Gronchi A, Miceli R, Allard MA, et al. Personalizing the approach to retroperitoneal soft tissue sarcoma: histology-specific patterns of failure and post-relapse outcome after primary extended resection. Ann Surg Oncol. 2015;22:1447–54.
doi: 10.1245/s10434-014-4130-7
Tan MC, Brennan MF, Kuk D, et al. Histology-based classification predicts pattern of recurrence and improves risk stratification in primary retroperitoneal sarcoma. Ann Surg. 2016;263:593–600.
doi: 10.1097/SLA.0000000000001149
Singer S, Anotnescu CR, Riedel E, Brennan MF. Histologic subtype and margin of resection predict pattern of recurrence and survival for retroperitoneal liposarcoma. Ann Surg. 2003;238:358–70.
doi: 10.1097/01.sla.0000086542.11899.38
Gyorki DE, Brennan MF. Management of recurrent retroperitoneal sarcoma. J Surg Oncol. 2014;109:53–9.
doi: 10.1002/jso.23463
Raut CP, Callegro D, Miceli R, et al. Predicting survival in patients undergoing resection for locally recurrent retroperitoneal sarcoma: a study and novel nomogram from TARPSWG. Clin Cancer Res. 2019;25:2664–71.
doi: 10.1158/1078-0432.CCR-18-2700
Durrleman S, Simon R. Flexible regression models with cubic splines. Stat Med. 1989;8:551–61.
doi: 10.1002/sim.4780080504
Peacock O, Patel S, Simpson JA, et al. A systematic review of population-based studies examining outcomes in primary retroperitoneal sarcoma surgery. Surg Oncol. 2019;29:53–63.
doi: 10.1016/j.suronc.2019.03.002
Judge SJ, Lata-Arias K, Yanagisawa M, et al. Morbidity, mortality, and temporal trends in the surgical management of retroperitoneal sarcoma: an ACS-NSQIP follow-up analysis. J Surg Oncol. 2019;120:753–60.
pubmed: 31355444 pmcid: 31355444
MacNeill AJ, Miceli R, Strauss D, et al. Post-relapse outcomes after primary extended resection of retroperitoneal sarcoma: a report from the Trans‐Atlantic RPS Working Group. Cancer 2017;123:1971–8.
doi: 10.1002/cncr.30572
Nizri E, Fiore M, Colombo CS, et al. Completion surgery of residual disease after primary inadequate surgery of retroperitoneal sarcomas achieves comparable oncological outcomes: a propensity score analysis. J Surg Oncol. 2019;119:318–23.
pubmed: 30554403 pmcid: 30554403
Weingart SN, Nelson J, Koethe B, et al. Developing a cancer-specific trigger tool to identify treatment-related adverse events using administrative data. Cancer Med. 2020. https://doi.org/10.1002/cam4.2812 .
doi: 10.1002/cam4.2812 pubmed: 32285614 pmcid: 32285614
Fisher OM, Alzahrani NA, Kozman MA, et al. Intraoperative packed red blood cell transfusion (iPRBT) and PCI-normalised iPRBT rates (iPRBT/PCI ratio) negatively affect short- and long-term outcomes of patients undergoing cytoreductive surgery and intraperitoneal chemotherapy: an analysis of 880 patients. Euro J Surg Oncol. 2019;45:2412–23.
doi: 10.1016/j.ejso.2019.07.031
Kwon HY, Kim BR, Kim YW. Association of preoperative anemia and perioperative allogenic red blood cell transfusion with oncologic outcomes in patients with nonmetastatic colorectal cancer. Curr Oncol. 2019;26:e357–66.
doi: 10.3747/co.26.4983
Iwata T, Kimura S, Foerster B, et al. Perioperative blood transfusion affects oncologic outcomes after nephrectomy for renal cell carcinoma: a systematic review and meta-analysis. Urol Oncol. 2019;37:273–81.
doi: 10.1016/j.urolonc.2019.01.018
Liu X, Ma M, et al. Effect of perioperative blood transfusion on prognosis of patients with gastric cancer: a retrospective analysis of a single center database. BMC Cancer. 2018;18:649.
doi: 10.1186/s12885-018-4574-4
Mavros MN, Xu L, Masgood H, et al. Perioperative blood transfusion and the prognosis of pancreatic cancer surgery: systematic review and meta-analysis. Ann Surg Oncol. 2015;22:4382–91.
doi: 10.1245/s10434-015-4823-6
Wada H, Eguchi H, Nagano H, et al. Perioperative allogenic blood transfusion is a poor prognostic factor after hepatocellular carcinoma surgery: a multi-center analysis. Surg Today. 2018;48:73–9.
doi: 10.1007/s00595-017-1553-3
Schack A, Berkfors AA, Ekeloef S, et al. The effect of perioperative iron therapy in acute major noncardiac surgery on allogenic blood transfusion and postoperative haemoglobin levels: a systematic review and meta-analysis. World J Surg. 2019;43:1677–91.
doi: 10.1007/s00268-019-04971-7
Portuondo JI, Shah SR, Signh H, et al. Failure to rescue as a surgical quality indicator: current concepts and future directions for improving surgical outcomes. Anesthesiology. 2019;131:426–37.
doi: 10.1097/ALN.0000000000002602

Auteurs

Carolyn Nessim (C)

Department of Surgery, The Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada. cnessim@toh.ca.

Chandrajit P Raut (CP)

Department of Surgery, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, USA.

Dario Callegaro (D)

Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Francesco Barretta (F)

Unit of Clinical Epidemiology and Trial Organization, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Rosalba Miceli (R)

Unit of Clinical Epidemiology and Trial Organization, Department of Applied Research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Mark Fairweather (M)

Department of Surgery, Brigham and Women's Hospital and Dana-Farber Cancer Institute, Boston, MA, USA.

Piotr Rutkowski (P)

Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

Jean-Yves Blay (JY)

Department of Medical Oncology, Center Léon Bérard Cancer Center, Lyon, France.

Dirk Strauss (D)

Department of Surgery, Royal Marsden Hospital NHS Foundation Trust, London, UK.

Ricardo Gonzalez (R)

Department of Surgery, Moffitt Cancer Center, Tampa, FL, USA.

Nita Ahuja (N)

Department of Surgery, Yale School of Medicine, New Haven, CT, USA.

Giovanni Grignani (G)

Division of Medical Oncology, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, TO, Italy.

Vittorio Quagliuolo (V)

Department of Surgery, Istituto Clinico Humanitas IRCCS, Milan, Italy.

Eberhard Stoeckle (E)

Department of Surgery, Institut Bergonié, Bordeaux, France.

Antonino De Paoli (A)

Department of Radiation Oncology, Centro di Riferimento Oncologico, Aviano, Italy.

Venu G Pillarisetty (VG)

Department of Surgery, University of Washington School of Medicine, Seattle, WA, USA.

Carol J Swallow (CJ)

Department of Surgery, Mount Sinai Hospital and Princess Margaret Cancer Center, Toronto, Canada.

Sanjay P Bagaria (SP)

Department of Surgery, Mayo Clinic, Jacksonville, FL, USA.

Robert J Canter (RJ)

Department of Surgery, UC Davis Health, Sacramento, CA, USA.

John T Mullen (JT)

Department of Surgery, Massachusetts General Hospital, Boston, MA, USA.

Yvonne Schrage (Y)

Department of Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Department of Surgery, Netherlands Cancer Institute, Amsterdam, The Netherlands.

Elisabetta Pennacchioli (E)

Division of Melanoma, Sarcomas and Rare Tumors, IEO, European Institute of Oncology, IRCCS, Milan, Italy.

Winan van Houdt (W)

Department of Surgery, Istituto Europeo di Oncologia, Milan, Italy.

Kenneth Cardona (K)

Department of Surgery, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.

Marco Fiore (M)

Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Alessandro Gronchi (A)

Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Guy Lahat (G)

Department of Surgery, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH