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Combination therapy with Olaratumab/doxorubicin in advanced or metastatic soft tissue sarcoma -a single-Centre experience.

Authors :
Striefler, Jana Käthe
Brandes, Franziska
Baur, Alexander
Pfitzner, Berit Maria
Kaul, David
Rau, Daniel
Dörr, Anne
Schmiester, Maren
Koulaxouzidis, Georgios
Bullinger, Lars
Märdian, Sven
Flörcken, Anne
Source :
BMC Cancer. 1/29/2020, Vol. 20 Issue 1, p1-8. 8p. 3 Diagrams, 4 Charts.
Publication Year :
2020

Abstract

<bold>Background: </bold>The antibody targeting platelet-derived growth factor receptor alpha (PDGFRA), olaratumab, was approved in 2016 for metastatic soft tissue sarcoma (STS) in combination with doxorubicin based on promising results of a phase Ib/II trial by the Food and Drug Administration (FDA). However, recently the phase III ANNOUNCE trial could not confirm the additional value of olaratumab in this context.<bold>Methods: </bold>Here, in a retrospective analysis we share our single-centre experience with olaratumab/doxorubicin in STS by including n = 32 patients treated with olaratumab/doxorubicin between 2016 and 2019.<bold>Results: </bold>Median progression-free survival (PFS) in the overall cohort was 3.1 months (range 0.6-16.2). A response [complete remission (CR), partial remission (PR) or stable disease (SD)] was seen in n = 11 (34%) cases, whereas n = 21 (66%) patients showed progressive disease (PD). In n = 9 patients surgery was performed subsequently in an individual therapeutic approach. Out of n = 5 patients receiving additional regional hyperthermia, n = 3 achieved PR or SD.<bold>Conclusions: </bold>This single-centre experience does also not support the promising phase Ib/II results for olaratumab/doxorubicin in STS. However, our findings do not preclude that olaratumab combination therapy could be valuable in a neoadjuvant setting. This warrants further exploration also taking into account the heterogeneous nature of STS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14712407
Volume :
20
Issue :
1
Database :
Academic Search Index
Journal :
BMC Cancer
Publication Type :
Academic Journal
Accession number :
141452248
Full Text :
https://doi.org/10.1186/s12885-020-6551-y