Rationale: a number of recent phase III randomized trials have shown a survival benefit of a treatment with subcutaneous low-molecular weight heparin in patients with advanced solid malignancies. The survival advantages observed in the studies persist for months after the active treatment with LMWHs. Therefore these survival advantages are thought to be due to effects of LMWHs on tumor cell biology. First line treatment of advanced NSCLC patients with the Cisplatin + Docetaxel combination has been widely studied, and is amongst the most active treatments currently available. The occurrence of grade 3/4 thrombopenia in several phase III trials was in the 0-3% range, making it an ideal chemotherapy regimen to combine with LMWHs in the treatment of advanced NSCLC.
Purpose: the aim of this study is to evaluate the potential beneficial antitumoral effect of LMWH enoxaparin in patients with locally advanced or metastatic NSCLC determined by the time to progression, the overall survival and the symptom control. LMWH will be added to a first line cisplatin-based chemotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
104
docetaxel 75 mg/m2 d1 and cisplatin 75mg/m2 d1 (q 3wks for 4 cycles)
cisplatin 75 mg/m2 d1 and docetaxel 75 mg/m2 d1 (q 3 wks for 4 cycles) + daily enoxaparin 1mg/kg/d sc
University Hospital Antwerp
Edegem, Antwerp, Belgium
Centre Hospitalier Universitaire Sart Tilman
Liège, Liège, Belgium
Progression Free Survival
Time frame: during chemotherapy and follow-up
Symptom control evaluated with the Lung Cancer Symptoms Scale (LCSS)
Time frame: during chemotherapy and follow-up
Overall Survival
Time frame: during chemotherapy and follow-up
Best Overall Response
Time frame: during chemotherapy and follow-up
Incidence of total documented thromboembolic and hemorrhagic events
Time frame: during chemotherapy and follow-up
Overall safety and tolerability
Time frame: during chemotherapy and follow-up
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