Literature DB >> 22954508

Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial.

Penella J Woll1, Peter Reichardt, Axel Le Cesne, Sylvie Bonvalot, Alberto Azzarelli, Harald J Hoekstra, Michael Leahy, Frits Van Coevorden, Jaap Verweij, Pancras C W Hogendoorn, Monia Ouali, Sandrine Marreaud, Vivien H C Bramwell, Peter Hohenberger.   

Abstract

BACKGROUND: The effect of adjuvant chemotherapy on survival for resected soft-tissue sarcoma remains unknown. We investigated the effect of intensive adjuvant chemotherapy on survival in patients after resection of high-risk soft-tissue sarcomas.
METHODS: In this multicentre randomised trial, patients with macroscopically resected, Trojani grade II-III soft-tissue sarcomas at any site, no metastases, performance status lower than 2 and aged between 16 and 70 years were eligible within 4 weeks of definitive surgery. Patients were randomly assigned to receive adjuvant chemotherapy or no chemotherapy (control group). Randomisation was done with a minimisation technique, stratified by hospital, site of primary tumour, tumour size, planned radiotherapy, and isolated limb perfusion therapy. Chemotherapy consisted of five cycles of doxorubicin 75 mg/m(2), ifosfamide 5 g/m(2), and lenograstim every 3 weeks. Patients in both groups received radiotherapy if the resection was marginal or the tumour recurrent. The primary endpoint was overall survival and analyses were done by intention to treat. The final results are presented. This trial is registered with ClinicalTrials.gov, NCT00002641.
FINDINGS: Between February, 1995, and December, 2003, 351 patients were randomly assigned to the adjuvant chemotherapy group (175 patients) or to the control group (176). 258 (73%) of 351 patients received radiotherapy, 129 in each group. Overall survival did not differ significantly between groups (hazard ratio [HR] 0·94 [95% CI 0·68-1·31], p=0·72) nor did relapse-free survival (HR 0·91 [0·67-1·22], p=0·51). 5-year overall survival rate was 66·5% (58·8-73·0) in the chemotherapy group and 67·8% (60·3-74·2) in the control group. Chemotherapy was well tolerated, with 130 (80%) of 163 patients who started it completing all five cycles. 16 (10%) patients had grade 3 or 4 fever or infection, but no deaths due to toxic effects were recorded.
INTERPRETATION: Adjuvant chemotherapy with doxorubicin and ifosfamide in resected soft-tissue sarcoma showed no benefit in relapse-free survival or overall survival. Future studies should focus on patients with larger, grade III, and extremity sarcomas.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22954508     DOI: 10.1016/S1470-2045(12)70346-7

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  119 in total

Review 1.  Principles in Management of Soft Tissue Sarcoma.

Authors:  Aimee M Crago; Murray F Brennan
Journal:  Adv Surg       Date:  2015-05-05

2.  Clinical Observations and Molecular Variables of Primary Vascular Leiomyosarcoma.

Authors:  Christina L Roland; Genevieve M Boland; Elizabeth G Demicco; Kristelle Lusby; Davis Ingram; Caitlin D May; Christine M Kivlin; Kelsey Watson; Ghadah A Al Sannaa; Wei-Lien Wang; Vinod Ravi; Raphael E Pollock; Dina Lev; Janice N Cormier; Kelly K Hunt; Barry W Feig; Alexander J Lazar; Keila E Torres
Journal:  JAMA Surg       Date:  2016-04       Impact factor: 14.766

3.  Relevance of Reference Centers in Sarcoma Care and Quality Item Evaluation: Results from the Prospective Registry of the Spanish Group for Research in Sarcoma (GEIS).

Authors:  Javier Martin-Broto; Nadia Hindi; Josefina Cruz; Javier Martinez-Trufero; Claudia Valverde; Luis M De Sande; Angeles Sala; Lorena Bellido; Ana De Juan; Jordi Rubió-Casadevall; Roberto Diaz-Beveridge; Ricardo Cubedo; Oscar Tendero; Diego Salinas; Isidro Gracia; Rafael Ramos; Silvia Baguè; Antonio Gutierrez; José Duran-Moreno; Antonio Lopez-Pousa
Journal:  Oncologist       Date:  2018-11-08

4.  [Soft tissue sarcomas and gastrointestinal stromal tumors].

Authors:  P Reichardt
Journal:  Internist (Berl)       Date:  2016-03       Impact factor: 0.743

5.  Sarcoma: Does histotype-tailored neoadjuvant therapy improve outcomes?

Authors:  Robin L Jones; Khin Thway
Journal:  Nat Rev Clin Oncol       Date:  2017-08-08       Impact factor: 66.675

6.  High-grade myxofibrosarcoma of the abdominal wall.

Authors:  Richard Antbring; Sam G Parker; Jeffrey T Lordan; Alastair Cj Windsor
Journal:  BMJ Case Rep       Date:  2017-06-02

Review 7.  Preoperative therapy for extremity soft tissue sarcomas.

Authors:  Lara E Davis; Christopher W Ryan
Journal:  Curr Treat Options Oncol       Date:  2015-06

Review 8.  [Multimodal treatment of sarcomas: standards and new aspects in pharmacological and radio-oncological treatment].

Authors:  L H Lindner
Journal:  Chirurg       Date:  2019-06       Impact factor: 0.955

Review 9.  Surgical management of retroperitoneal and pelvic sarcomas.

Authors:  Marcus C B Tan; Sam S Yoon
Journal:  J Surg Oncol       Date:  2014-12-05       Impact factor: 3.454

10.  Recombinant granulocyte colony-stimulating factor (rG-CSF) in the management of neutropenia induced by anthracyclines and ifosfamide in patients with soft tissue sarcomas (NEUSAR).

Authors:  Alberto Bongiovanni; Manuela Monti; Flavia Foca; Federica Recine; Nada Riva; Valentina Di Iorio; Chiara Liverani; Alessandro De Vita; Giacomo Miserocchi; Laura Mercatali; Dino Amadori; Toni Ibrahim
Journal:  Support Care Cancer       Date:  2016-08-27       Impact factor: 3.603

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