Literature DB >> 34207591

The Impact of Thromboprophylaxis on the Survival of Patients with Advanced Pancreatic Cancer. The Pancreatic Cancer and Tinzaparin (PaCT) Study.

Michalis V Karamouzis1, Ilias Athanasiadis2, Georgios Samelis3, Christos Vallilas1, Alexandros Bokas4, Adamantia Nikolaidi2, Areti Dimitriadou3, Panagiotis Sarantis1, Nikolaos Pistamaltzian2, Dimitrios Schizas5, Alexandros Papalampros5, Evangelos Felekouras5, Dimitrios Dimitroulis6, Eustathios Antoniou6, Georgios Sotiropoulos6, Pavlos Papakotoulas4.   

Abstract

Pancreatic cancer (PaC) induces a prothrombotic and hypercoagulable state. The aim of this study was to investigate the effect of tinzaparin in combination with chemotherapy. The PaCT (pancreatic cancer and tinzaparin) study was a retrospective observational study that collected data regarding progression free survival (PFS) in advanced or metastatic PaC patients who received thromboprophylaxis with tinzaparin during chemotherapy with nab-paclitaxel (N) and gemcitabine (G). The primary end point was to compare, from already published data, the PFS of patients receiving thromboprophylaxis with tinzaparin with the PFS of patients receiving chemotherapy with N-G but no thromboprophylaxis. Secondary end points were efficacy and safety of anticoagulation. In total, 110 PaC patients, 93% with advanced or metastatic disease, treated with N-G and tinzaparin (10,291 ± 1176 Anti-Xa IU, OD, median duration 8.7, IQR: 5.6-11.9 months) were enrolled. Of these, 52% were males and; the median age was 68 (40-86 years). The tumor was located to in the pancreatic head at in 45% of the patients. The median PFS was 7.9 months (IQR: 5.0-11.8 months). Out of 14 similar studies (involving 2994 patients) identified via systematic search, it was determined that the weighted PFS of patients receiving N-G but no anticoagulation was 5.6 months. Therefore, patients receiving tinzaparin had 39.54% higher PFS than patients without thromboprophylaxis (p < 0.05). During the follow-up period of 18.3 ± 11.7 months, three (2.7%) thrombotic events were recorded while two clinically relevant non-major bleeding events occurred (1.9%). In conclusion, PFS in advanced PaC patients undergoing chemotherapy is positively impacted by anticoagulation. Thromboprophylaxis with tinzaparin in treatment dose is efficient and safe.

Entities:  

Keywords:  LMWHs; chemotherapy; pancreatic cancer; survival; thromboprophylaxis; tinzaparin

Year:  2021        PMID: 34207591     DOI: 10.3390/cancers13122884

Source DB:  PubMed          Journal:  Cancers (Basel)        ISSN: 2072-6694            Impact factor:   6.639


  3 in total

Review 1.  Cancer-Associated Thrombosis: Not All Low-Molecular-Weight Heparins Are the Same, Focus on Tinzaparin, A Narrative Review.

Authors:  Agnese Maria Fioretti; Tiziana Leopizzi; Agata Puzzovivo; Francesco Giotta; Vito Lorusso; Giovanni Luzzi; Stefano Oliva
Journal:  Int J Clin Pract       Date:  2022-07-19       Impact factor: 3.149

Review 2.  Tinzaparin-a review of its molecular profile, pharmacology, special properties, and clinical uses.

Authors:  Marina Amerali; Marianna Politou
Journal:  Eur J Clin Pharmacol       Date:  2022-07-23       Impact factor: 3.064

3.  Tumour cell-activated platelets modulate the immunological activity of CD4+, CD8+, and NK cells, which is efficiently antagonized by heparin.

Authors:  Lukas M Gockel; Katrin Nekipelov; Vito Ferro; Gerd Bendas; Martin Schlesinger
Journal:  Cancer Immunol Immunother       Date:  2022-03-14       Impact factor: 6.630

  3 in total

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