Randomized phase III trial of intravenous (IV) versus hepatic intra-arterial (HIA) fotemustine in patients with liver metastases from uveal melanoma: Final results of the EORTC 18021 study.

Authors

null

Serge Leyvraz

Centre Pluridisciplinaire d'Oncologie, Lausanne, Switzerland

Serge Leyvraz , Stefan Suciu , Sophie Piperno-Neumann , Jean-Francois Baurain , Marcin Zdzienicki , Alessandro Testori , Ernest Marshall , Max E. Scheulen , Thomas Jouary , Sylvie Negrier , Jan Baptist Vermorken , Eckhart Kaempgen , Xavier Durando , Dirk Schadendorf , Ravichandra Karra Gurunath , Larissa Polders , Gaetan De Schaetzen , Simon Vanderschaeghe , Marie-Pierre Gauthier , Ulrich Keilholz

Organizations

Centre Pluridisciplinaire d'Oncologie, Lausanne, Switzerland, EORTC Headquarters, Brussels, Belgium, Institut Curie, Paris, France, Centre du Cancer, Cliniques Universitaires Saint-Luc, Brussels, Belgium, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland, European Institute of Oncology, Milan, Italy, Clatterbridge Centre for Oncology, Wirral, United Kingdom, Innere Klinik (Tumorforschung), West German Cancer Center, University of Essen Medical School, Essen, Germany, University Hospital Bordeaux Saint André, Bordeaux, France, Léon-Bérard Cancer Centre, Lyon, France, Antwerp University Hospital, Edegem, Belgium, Universitätsklinik Erlangen, Erlangen, Germany, Centre Jean Perrin, Clermont-Ferrand, France, University Hospital Essen, Essen, Germany, Department of Hematology and Medical Oncology, Charité, CBF, Berlin, Germany

Research Funding

Other
Background: HIA fotemustine has shown promising results in Phase II studies that led to the EORTC randomized phase III trial (18021) in unpretreated patients (pts) with liver metastases from uveal melanoma. Methods: The treatment consisted in an induction cycle of either HIA (fotemustine 100 mg/m² over 4 hours, day 1, 8, 15, 22) vs IV control arm (fotemustine 100 mg/m² over 1 hour, day 1, 8, 15). After a 5-week break, maintenance cycles were given every 3 weeks. Randomization was stratified by PS (0 vs 1), LDH (normal vs abnormal) and center. Main endpoint was overall survival (OS). Required accrual per protocol was set to 262 pts, with final analysis planned after 220 deaths (hazard ratio (HR) =0.67, power=85%, 1-sided α=2.5%). Due to poor accrual an interim analysis was done after 134 deaths, in order to test futility (power=79%). Results: Between Feb-2005- Feb-2011, 171 pts were randomized (HIA: 86, IV: 85). Characteristics: PS 1: 20%, abnormal LDH: 42%, male: 50%, median age: 59 y.; balanced between arms. In the HIA arm 20 (23%) pts never started treatment mainly due to catheter problems and 2 pts in the IV arm. In those who started the treatment, leucopenia grade 3-4 was 18% and thrombopenia grade 3-4: 21% in the HIA arm compared to 32% and 42% in the IV arm. Non-hematological grade 3-4 toxicities were minimal (GI toxicity, catheter complications). In May 2011, as the OS HR=1.097 was > critical value 0.87, the IDMC recommended stopping accrual for futility. The final results from Jan-2012 are presented in the table below. Treatment comparison adjusted by PS and LDH provided similar results. Conclusions: Even if HIA fotemustine administration could not start in 23% of pts, it led to a higher ORR and longer PFS compared to IV administration. HIA did not translate into an improvement in OS.
All pts
(N=171)
Treatment started
(N=149)
Endpoint HIA (N=86) IV (N=85) HIA (N=66) IV (N=83)
Response
CR+PR=ORR, N (%) 9 (10.5) 2 (2.4) 9 (13.6) 2 (2.4)
PFS
Events, N 84 85 64 83
Median (months) 4.5 3.7 5.4 3.7
HR (95% CI), p value 0.62 (0.45 , 0.84), 0.002 0.53 (0.38 , 0.75), 0.0002
OS
Deaths, N 79 76 59 74
Median (months) 14.6 13.0 14.6 13.7
HR (95% CI), p value 1.09 (0.79 , 1.50), 0.59 1.00 (0.71 , 1.42), 0.98

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Abstract Details

Meeting

2012 ASCO Annual Meeting

Session Type

Poster Discussion Session

Session Title

Melanoma/Skin Cancers

Track

Melanoma/Skin Cancers

Sub Track

Melanoma

Clinical Trial Registration Number

NCT00110123

Citation

J Clin Oncol 30, 2012 (suppl; abstr 8532)

DOI

10.1200/jco.2012.30.15_suppl.8532

Abstract #

8532

Poster Bd #

21

Abstract Disclosures

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