EditorialHypercoagulability and the clinical manifestation of VTE are shared by most cancers and the use of chemotherapy canfurther increase this risk. VTE in cancer patients results in increased morbidity and mortality [1]. Patients with advanced pancreatic cancer (APC) have one of the worst prognoses of all malignancies and the highest incidence of disease provoked venous thromboembolism (VTE) [2]. Given the prominence of VTE in APC, it is not surprising that data on VTE prevention for APC have been generated from subgroup analysis of non-APC targeted placebo-controlled randomized trials of cancer patients treated with chemotherapy. Further data is derived from trials dedicated to evaluate VTE prophylaxis in APC patients. These studies have been rather homogeneous in that only low molecular weight heparins (LMWH) have been investigated for anticoagulation. The choice of LMWH was partly industry driven (e.g. study of new agent such as the semi-synthetic LMWH semuloparin) and partly due to the established superiority of LMWH over vitamin K analogues in terms of safety and efficacy both in VTE prophylaxis when given in nononcologic settings and in the therapeutic (treatment) settings of malignancy associated established VTE [3]. SAVE-ONCO and PROTECHT are the largest trials that enrolled between them more than 4000 patients with non-selected solid cancers using LMWH for the variable length of palliative chemotherapy. Both studies showed similar reduction in the symptomatic venous thrombosis (DVT) and non-fatal pulmonary embolism (PE) and in the case of SAVE-ONO, arterial thromboemoblic events were also decreased. There was a subgroup of around 300 APC patients in both of these trials but benefit in APC subgroup was only seen in SAVE-ONCO study. While the VTE reduction for the whole patient population (primary aim of the study) was from 3.9% to 2%, it went from 10.9% in the placebo arm to 2.4% in the LMWH arm for the APC subgroup [4,5]. Two trials evaluated VTE prevention by enrolling APC patients only who were receiving gemcitabine based first line palliative chemotherapies. These studies randomized over 400 APC patients equally into LMWH or placebo. CONKO 004 showed that the use of enoxaparin at an unconventionally (high) primary prophylaxis dose of 1 mg/kg reduced the incidence of symptomatic (DVT and PE combined) from 9.87 to 1.25% [6]. FRAGEM had a broader primary endpoint of all-type VTE (i.e.DVT/PE but also incidental PE and arterial and splanchnic VTE), [2] and an "even higher" dose of LMWH (dalteparin at 150-200 u/kg) was used. It showed a significant 85% risk reduction in all-type VTE in the dalteparin arm as compared to placebo (3.4% vs. 23%) over the 3 months of thromboprophylaxis [7]. None of these studies increased risk of major bleeding significantly and no fatalities were noted in APC due to haemorrhage in either of these RCTs. Subsequent meta-analysis of these trials have verified the significant impact of thromboprophylaxis on APC related VTE [1].Up to a quarter of APC patients die within the fir...