Literature DB >> 30262574

Anti-tumour effect of low molecular weight heparin in localised lung cancer: a phase III clinical trial.

Guy Meyer1,2,3,4, Benjamin Besse5,6, Hélène Doubre7, Anaïs Charles-Nelson1, Sandro Aquilanti8, Armine Izadifar9, Reza Azarian10, Isabelle Monnet11, Corinne Lamour12,13, Renaud Descourt14, Gérard Oliviero15, Laurent Taillade16, Christos Chouaid11, Frederique Giraud17, Pierre-Emmanuel Falcoz18, Marie-Pierre Revel2,17, Virginie Westeel19, Adrien Dixmier20, Jean Tredaniel2,21, Stéphanie Dehette22, Chantal Decroisette23, Alain Prevost24, Eric Pichon25, Elizabeth Fabre1, Jean-Charles Soria5,6, Sylvie Friard7, Jean-Baptiste Stern26, Laurence Jabot11, Georges Dennewald9, Gérard Pavy8, Patrick Petitpretz10, Jean-Marc Tourani12,13, Marco Alifano2,17, Gilles Chatellier1,2,3, Philippe Girard26.   

Abstract

The anti-tumour and anti-metastatic properties of heparins have not been tested in patients with early stage cancer. Whether adjuvant low molecular weight heparin (LMWH) tinzaparin impacts the survival of patients with resected non-small cell lung cancer (NSCLC) was investigated.Patients with completely resected stage I, II or IIIA NSCLC were randomly allocated to receive subcutaneous tinzaparin 100 IU·kg-1 once a day for 12 weeks or no treatment in addition to standard of care. The trial was open-label with blinded central adjudication of study outcomes. The primary outcome was overall survival.In 549 patients randomised to tinzaparin (n=269) or control (n=280), mean±sd age was 61.6±8.9 years, 190 (34.6%) patients had stage II-III disease, and 220 (40.1%) patients received adjuvant chemotherapy. Median follow-up was 5.7 years. There was no significant difference in overall survival between groups (hazard ratio (HR) 1.24, 95% CI 0.92-1.68; p=0.17). There was no difference in the cumulative incidence of recurrence between groups (subdistribution HR 0.94, 95% CI 0.68-1.30; p=0.70).Adjuvant tinzaparin had no detectable impact on overall and recurrence-free survival of patients with completely resected stage I-IIIA NSCLC. These results do not support further clinical evaluation of LMWHs as anti-tumour agents.
Copyright ©ERS 2018.

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Year:  2018        PMID: 30262574     DOI: 10.1183/13993003.01220-2018

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


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