International single-arm phase II trial of pazopanib in advanced extraskeletal myxoid chondrosarcoma: A Collaborative Spanish (GEIS), Italian (ISG) and French (FSG) Sarcoma Groups study.

Authors

Silvia Stacchiotti

Silvia Stacchiotti

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy

Silvia Stacchiotti , Stefano Ferrari , Andres Redondo , Emanuela Palmerini , Nadia Hindi , M. Angeles Vaz , Anna Maria Frezza , Antonio Gutierrez , Antonio Lopez-Pousa , Giovanni Grignani , Antoine Italiano , Sarah Dumont , Jean-Yves Blay , Nicolas Penel , Daniel Bernabeu , Enrique de Alava , Dominique Ranchère-Vince , Paola Collini , Josefina Cruz , Javier Martin Broto

Organizations

Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy, Istituto Ortopedico Rizzoli, Bologna, Italy, Hospital Universitario La Paz, Madrid, Spain, Hospital Ramón y Cajal, Madrid, Spain, Hospital Universitario Son Espases, Palma de Mallorca, Spain, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, IRCCS C. Andiolo, Candiolo, Italy, Institut Bergonié, Bordeaux, France, Gustave Roussy Cancer Campus, Villejuif, France, Centre Léon-Bérard, Lyon, France, Centre Oscar Lambret, Lille, France, Centro de Investigación del Cáncer, CSIC-Universidad de Salamanca, Salamanca, Spain, Hospital Universitario de Canarias, Santa Cruz de Tenerife, Spain, Virgen del Rocio University Hospital, Institute of Biomedicine Research (IBIS), Seville, Spain

Research Funding

Pharmaceutical/Biotech Company

Background: Extraskeletal myxoid chondrosarcoma (EMC) is an exceedingly rare sarcoma, marked by a specific translocation involving the gene NR4A3 that can be rearranged with different partners. Preliminary retrospective data suggest that sunitinib is active, but no formal prospective studies are available. We report on a multicentric European prospective, investigator-driven, Phase 2 study on pazopanib (P) in NR4A3+ advanced EMC patients (pts), carried out by the Spanish, Italian and French Sarcoma groups. Methods: From June 2014 to November 2016, 24 advanced EMC pts entered this study (median age: 64 yrs - disease extent: metastatic 77%, locally advanced 23% - prior medical treatment: 18 (86%) naive; 2 (9%) 1 line, 1 (5%) > 1 line). Path diagnosis and NR4A3 rearrangement (FISH and/or real-time PCR analysis) were centrally confirmed. Pts received P 800 mg/day (relative dose intensity = 0,82%, 658 mg/day), until progression or toxicity. The primary study end-point was response rate as per RECIST 1.1. Secondary end-points were overall survival, progression-free survival (PFS), clinical benefit rate (CBR) (RECIST CR+PR+SD≥6mos). An exploratory evaluation of the correlation between the rearrangement subtype and the outcome is ongoing. Results: 20/24 pts were evaluable for response (1 early death; 3 too early). One patient (5%) had a partial response, 17 (75%) stable disease, 2 (10%) progression as their best RECIST responses. At the time of this analysis, 12 pts were still under treatment, while 12 interrupted P (10 progression, 1 toxicity, 1 other). At a 13-month median follow-up, the median PFS was 13 months (range 1.6-25.1), with 29% pts progression-free at 18 months and a 65% CBR. Median OS was not reached. Conclusions: This Phase 2 study is formally negative since the target of at least 3/21 RECIST responses was not reached. However, looking at PFS, P was associated with a prolonged disease stabilization in a significant proportion of pts. This suggests to further explore the use of P in EMC. Clinical trial information: NCT02066285

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Abstract Details

Meeting

2017 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Sarcoma

Track

Sarcoma

Sub Track

Soft Tissue Tumors

Clinical Trial Registration Number

NCT02066285

Citation

J Clin Oncol 35, 2017 (suppl; abstr 11062)

DOI

10.1200/JCO.2017.35.15_suppl.11062

Abstract #

11062

Poster Bd #

385

Abstract Disclosures