Activity of Cabazitaxel in Metastatic or Inoperable Locally Advanced Dedifferentiated Liposarcoma

Author:

Sanfilippo Roberta1,Hayward Richard L.2,Musoro Jammbe3,Benson Charlotte4,Leahy Michael Gordon5,Brunello Antonella6,Blay Jean-Yves7,Steeghs Neeltje8,Desar Ingrid M. E.9,Ali Nasim10,Hervieu Alice11,Thway Khin12,Marreaud Sandrine3,Litiere Saskia3,Kasper Bernd13

Affiliation:

1. Medical Oncology Unit 2, Medical Oncology Dpt, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy

2. Edinburgh Western General Hospital, Edinburgh, United Kingdom

3. EORTC, Brussels, Belgium

4. The Royal Marsden Hospital, London, United Kingdom

5. Christie Hosp NHS Trust, Manchester, United Kingdom

6. Medical Oncology Unit 1, Department of Oncology, Istituto Oncologico Veneto IOV IRCCS, Padua, Italy

7. Centre Léon Bérard, & Univ Claude Bernard Lyon I, Unicancer, Lyon, France

8. Netherlands Cancer Institute, Amsterdam, the Netherlands

9. Radboud University Medical Center, Nijmegen, the Netherlands

10. Clatterbrige Cancer Centre, Wirral, United Kingdom

11. Centre Georges-François Leclerc, Dijon, France

12. The Royal Marsden NHS Foundation Trust, London, United Kingdom

13. Mannheim Cancer Center (MCC), University of Heidelberg, Mannheim University Medical Center, Mannheim, Germany

Abstract

ImportanceTreatment options for patients with unresectable and/or metastatic dedifferentiated liposarcoma (DDLPS) are limited. New drugs are required.ObjectiveTo assess whether cabazitaxel demonstrated sufficient antitumor activity in patients with metastatic or inoperable locally advanced DDLPS to justify further investigation in a phase 3 setting.Design, Setting, and ParticipantsThis international multicenter, open-label single-arm phase 2 trial was conducted at 10 institutions in 4 European countries from March 2015 to March 2019. Eligible patients had to have metastatic or locally advanced histologically proven DDLPS with evidence of disease progression within the past 6 months and had to have received no more than 1 previous line of chemotherapy.InterventionsAfter mandatory central review of tumor blocks, if the DDLPS diagnosis was confirmed, patients started treatment within 72 hours after registration. Cabazitaxel was administered at a dose of 25 mg/m2 IV infusion over 1 hour every 21 days until intolerance, progression, or withdrawal of consent.Main Outcomes and MeasuresThe primary end point was progression-free survival (PFS) rate at 12 weeks per RECIST 1.1. Based on a Simon 2-stage design, at least 4 of 17 (stage 1) and 11 of 37 (stage 2) eligible and evaluable patients who were progression free at 12 weeks were needed. The final analysis report was completed on November 17, 2021.ResultsForty patients were registered, with 2 patients being ineligible. The number of cycles ranged from 1 to 30, with a median of 5; 26 patients (65%) received at least 4 cycles of cabazitaxel. Progression-free survival at 12 weeks was 55%, achieving the primary study end point. At a median follow-up of 21.6 months, median PFS was 6 months and median OS 21 months. Response rate (RR) was 8% with 1 clinical response (CR) and 2 partial responses (PR). Twenty-three (60.5%) patients had a stable disease (SD). Disease control (PR+SD) was achieved in 26 patients (68%).Conclusions and RelevanceThis nonrandomized phase 2 clinical trial met its primary end point, with 21 of 38 patients (55%) being progression free at 12 weeks. These results suggest important activity of cabazitaxel in patients with metastatic or inoperable locally advanced DDLPS. The drug is worth being further studied in these tumors in a phase 3 setting.

Publisher

American Medical Association (AMA)

Subject

Oncology,Cancer Research

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