Neoadjuvant Chemotherapy in High-Grade Myxoid Liposarcoma: Results of the Expanded Cohort of a Randomized Trial From Italian (ISG), Spanish (GEIS), French (FSG), and Polish Sarcoma Groups (PSG)

Author:

Gronchi Alessandro1ORCID,Palmerini Emanuela2ORCID,Quagliuolo Vittorio3,Martin Broto Javier456ORCID,Lopez Pousa Antonio7,Grignani Giovanni8ORCID,Brunello Antonella9ORCID,Blay Jean-Yves10ORCID,Tendero Oscar11,Diaz Beveridge Robert12,Ferraresi Virginia13,Lugowska Iwona14,Pizzamiglio Sara15,Verderio Paolo15ORCID,Fontana Valeria16,Donati Davide Maria17ORCID,Palassini Elena18,Sanfilippo Roberta18ORCID,Bianchi Giuseppe17ORCID,Bertuzzi Alexia19,Morosi Carlo20,Pasquali Sandro1ORCID,Stacchiotti Silvia18,Bagué Silvia21,Coindre Jean Michel22,Miceli Rosalba23ORCID,Dei Tos Angelo Paolo24,Casali Paolo Giovanni1825ORCID

Affiliation:

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

2. Osteoncologia, Sarcomi dell'osso e dei tessuti molli, e Terapie Innovative, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy

3. Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Italy

4. Medical Oncology Department, Fundación Jimenez Diaz University Hospital, Madrid, Spain

5. University Hospital General de Villalba, Madrid, Spain

6. Instituto de Investigacion Sanitaria Fundacion Jimenez Diaz (IIS/FJD, UAM), Madrid, Spain

7. Department of Cancer Medicine, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

8. Department of Cancer Medicine, Ospedale Città della Scienza e della Salute, Torino, Italy

9. Department of Oncology, Medical Oncology 1 Unit, Istituto Oncologico Veneto IOV, IRCCS, Padova, Italy

10. Department of Cancer Medicine, Centre Léon Bérard Cancer Center, UNICANCER & Université Claude Bernard, Lyon, France

11. Department of Surgery, Hospital Universitari Son Espases, Palma de Mallorca, Spain

12. Department of Cancer Medicine, Hospital Universitari i Politècnic La Fe, Valencia, Spain

13. Department of Cancer Medicine, Istituto Regina Elena, Rome, Italy

14. Department of Soft Tissue/Bone Sarcoma and Melanoma, Centrum Onkologii, Instytutim, Marii Sklodowskiej-Curie, Warszawa, Poland

15. Unit of Bioinformatics and Biostatistics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

16. Department of Epidemiology, Clinical Trial Center, IRCCS Ospedale Policlinico San Martino, IST Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy

17. Orthopaedic Oncology Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy

18. Department of Cancer Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

19. Department of Cancer Medicine, IRCCS Humanitas Research Hospital, Rozzano, Italy

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

21. Department of Pathology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain

22. Department of Pathology, Institut Bergonié, Bordeaux, France

23. Unit of Biostatistics for Clinical Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

24. Department of Pathology, University of Padua, Padova, Italy

25. Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy

Abstract

PURPOSE A randomized trial was conducted to compare neoadjuvant standard (S) anthracycline + ifosfamide (AI) regimen with histology-tailored (HT) regimen in selected localized high-risk soft tissue sarcoma (STS). The results of the trial demonstrated the superiority of S in all STS histologies except for high-grade myxoid liposarcoma (HG-MLPS) where S and HT appeared to be equivalent. To further evaluate the noninferiority of HT compared with S, the HG-MLPS cohort was expanded. PATIENTS AND METHODS Patients had localized high-grade (cellular component >5%; size ≥5 cm; deeply seated) MLPS of extremities or trunk wall. The primary end point was disease-free survival (DFS). The secondary end point was overall survival (OS). The trial used a noninferiority Bayesian design, wherein HT would be considered not inferior to S if the posterior probability of the true hazard ratio (HR) being >1.25 was <5%. RESULTS From May 2011 to June 2020, 101 patients with HG-MLPS were randomly assigned, 45 to the HT arm and 56 to the S arm. The median follow-up was 66 months (IQR, 37-89). Median size was 107 mm (IQR, 84-143), 106 mm (IQR, 75-135) in the HT arm and 108 mm (IQR, 86-150) in the S arm. At 60 months, the DFS and OS probabilities were 0.86 and 0.73 (HR, 0.60 [95% CI, 0.24 to 1.46]; log-rank P = .26 for DFS) and 0.88 and 0.90 (HR, 1.20 [95% CI, 0.37 to 3.93]; log-rank P = .77 for OS) in the HT and S arms, respectively. The posterior probability of HR being >1.25 for DFS met the Bayesian monitoring cutoff of <5% (4.93%). This result confirmed the noninferiority of trabectedin to AI suggested in the original study cohort. CONCLUSION Trabectedin may be an alternative to standard AI in HG-MLPS of the extremities or trunk when neoadjuvant treatment is a consideration.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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