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Trabectedin in combination with doxorubicin for first-line treatment of advanced uterine or soft-tissue leiomyosarcoma (LMS-02): a non-randomised, multicentre, phase 2 trial - 31/03/15

Doi : 10.1016/S1470-2045(15)70070-7 
Patricia Pautier, DrMD a, , Anne Floquet, MD c, Christine Chevreau, MD d, Nicolas Penel, MD e, Cécile Guillemet, MD f, Corinne Delcambre, MD g, Didier Cupissol, MD h, Frédéric Selle, MD i, Nicolas Isambert, MD j, Sophie Piperno-Neumann, MD k, Antoine Thyss, ProfMD l, François Bertucci, ProfMD m, Emmanuelle Bompas, MD n, Jerôme Alexandre, ProfMD o, Olivier Collard, MD p, Sandrine Lavau-Denes, MD q, Patrick Soulié, MD r, Maud Toulmonde, MD c, Axel Le Cesne, MD a, Benjamin Lacas, MSc b, Florence Duffaud, ProfMD s

for the French Sarcoma Group

a Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France 
b Department of Biostatistics, Institut Gustave Roussy, Villejuif, France 
c Department of Medical Oncology, Institut Bergonié, Bordeaux, France 
d Department of Medical Oncology, Institut Claudius-Regaud, Toulouse, France 
e Department of Medical Oncology, Centre Oscar-Lambret, Lille, France 
f Department of Medical Oncology, Centre Henri-Becquerel, Rouen, France 
g Department of Medical Oncology, Centre François-Baclesse, Caen, France 
h Department of Medical Oncology, Centre Val d’Aurelle, Montpellier, France 
i Department of Medical Oncology, Hôpital Tenon, Paris, France 
j Department of Medical Oncology, Centre GF Leclerc, Dijon, France 
k Department of Medical Oncology, Institut Curie, Paris, France 
l Department of Medical Oncology Centre Antoine Lacassagne, Nice, France 
m Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France 
n Department of Medical Oncology, Centre René Gauducheau, Saint Herblain, France 
o Department of Medical Oncology, Hôpital Cochin, Paris, France 
p Department of Medical Oncology, Institut de Cancérologie de la Loire, Saint Priest en Jarez, France 
q Department of Medical Oncology, Centre Hospitalo-Universitaire Dupuytren, Limoges, France 
r Department of Medical Oncology, Centre Paul Papin, Angers, France 
s Department of Medical Oncology, La Timone University Hospital, Marseille, France 

* Correspondence to: Dr Patricia Pautier, Department of Medical Oncology, Institut Gustave-Roussy, 94805 Villejuif Cedex, France

Summary

Background

Metastatic leiomyosarcomas of uterine or soft-tissue origin have poor prognosis and moderate chemosensitivity. Trabectedin has shown activity in pretreated leiomyosarcoma. We did a single-group, multicentre, phase 2 trial (LMS-02) to assess the effect of first-line doxorubicin and trabectedin combination on disease control and survival.

Methods

Adults (18 years to physiological age ≤70 years) with measurable metastatic or unresectable uterine leiomyosarcoma or soft-tissue leiomyosarcoma who had not received any previous chemotherapy were enrolled at 19 centres in France. Treatment consisted of 60 mg/m2 intravenous doxorubicin followed by 1·1 mg/m2 trabectedin in a 3 h intravenous infusion on day 1, both by the central venous route, and 6 mg subcutaneous pegfilgrastim on day 2, repeated every 3 weeks for up to six cycles. Surgery for residual disease was permitted. The primary endpoint was the proportion of patients achieving disease control, defined as complete or partial response or stable disease. Stratification was done by anatomical site and analyses were per protocol. This study is registered with ClinicalTrials.gov, number NCT02131480.

Findings

Between July 28, 2010, and May 10, 2013, 109 patients were enrolled and treated, of whom 108 were assessable for response: 47 in the uterine leiomyosarcoma group and 61 in the soft-tissue leiomyosarcoma group. 32 (68%) patients in the uterine leiomyosarcoma group and 45 (74%) in the soft-tissue leiomyosarcoma group received all six cycles of treatment. Of 47 patients with uterine leiomyosarcoma, 28 (59·6%, 95% CI 44·3–73·6) achieved a partial response and 13 (27·7%, 15·6–42·6) stable disease; 41 (87·2%, 74·3–95·2) patients achieved disease control. Of 61 patients with soft-tissue leiomyosarcoma, two (3·3%, 95% CI 0·4–11·7) achieved a complete response, 22 (36·1%, 25·0–50·8) had a partial response, and 32 (52·5%, 40·8–67·3) had stable disease; 56 (91·8%, 81·9–97·3) of patients achieved disease control. The most common grade 3–4 treatment-associated adverse events were neutropenia (84 [78%] of 108 patients), increased alanine aminotransferase concentration (42 [39%]), thrombocytopenia (40 [37%]), anaemia (29 [27%]), febrile neutropenia (26 [24%]), and fatigue (21 [19%]).

Interpretation

Despite expected but manageable toxic effects, these results support the activity of doxorubicin plus trabectedin as first-line treatment for uterine leiomyosarcoma and soft-tissue leiomyosarcoma. This combination should be developed further in a phase 3 trial against the present standard of care.

Funding

Pharmamar and Amgen.

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Vol 16 - N° 4

P. 457-464 - avril 2015 Retour au numéro
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