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E-Poster Display

1554P - Can thromboprophylaxis impact PFS in patients with advanced pancreatic cancer? Intermediate results of PaCT study

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Pancreatic Adenocarcinoma

Presenters

Michail Karamouzis

Citation

Annals of Oncology (2020) 31 (suppl_4): S881-S897. 10.1016/annonc/annonc285

Authors

M.V. Karamouzis1, I. Athanasiadis2, G.F. Samelis3, C. Vallilas1, A. Bokas4, A. Nikolaidi2, A. Dimitriadou3, Z. Kakosaiou1, N.F. Pistamaltzian5, D. Schizas6, A. Papalampros6, E. Felekouras6, D. Dimitroulis7, E. Antoniou7, G. Sotiropoulos7, P. Papakotoulas8

Author affiliations

  • 1 Department Of Biological Chemistry, School of Medicine, University of Athens, 106 76 - Kolonaki (Athens)/GR
  • 2 Oncology Dept., Mitera Hospital, 151 23 - Marousi/GR
  • 3 Oncology Unit, Hippokration General Hospital, 115 27 - Athens/GR
  • 4 1st Clinical Oncology Dept, Theagenio Cancer Hospital, 546 39 - Thessaloniki/GR
  • 5 Oncology Clinic Department, Mitera Hospital, 151 23 - Marousi/GR
  • 6 First Department Of Surgery, School of Medicine, University of Athens, 11527 - Athens/GR
  • 7 Second Department Of Surgery, School of Medicine, University of Athens, 11527 - Athens/GR
  • 8 Department Of Medical Oncology, Theagenio Cancer Hospital, 546 39 - Thessaloniki/GR

Resources

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Abstract 1554P

Background

PaC is one of the most fatal cancers and cancer associated thrombosis (CAT) is a leading cause of death in these pts. 5-year survival rate for PaC is estimated around 8%. PaC induces a prothrombotic and hypercoagulable state. LMWHs are attributed to various non anticoagulant effects and could enhance the anti-tumor effect of therapy.

Methods

PaCT (Pancreatic Cancer & Tinzaparin) is a retrospective observational study aiming to collect data regarding progression free survival (PFS) in active advanced PaC pts who received thromboprophylaxis with tinzaparin, as suggested by SCC ISTH guidance, during chemotherapy. Primary end point is the impact of LMWHs in PFS compared to PFS with chemotherapy only; secondary are efficacy and safety of anticoagulation.

Results

We report intermediate results. 127 PaC pts, 87% with advanced or metastatic disease, treated with highly thrombogenic agents and receiving thromboprophylaxis were enrolled. 54% males, median age 66.1±9.9 years, BMI 25.3±4.0 Kg/m2. A sub-cohort of 68 pts, all with advanced or metastatic disease at 1st line treatment with nab-paclitaxel + gemcitabine who received tinzaparin [10,348±1,418 Anti-Xa IU, OD, median duration 7.8, IQR: 5.4-11.8mo] had median PFS 7.8 months (mo) (IQR: 5.4-11.8mo). PFS in 2 studies in pts with same characteristics, apart use of thromboprophylaxis, was [patients/median PFS]: 431/5.5mo, 75/5.2 and in a recent meta-analysis of 21 studies median PFS was 5.4 mo. Comparing[FC1] in our sub-cohort. PFS of pts receiving tinzaparin was 44% higher than in patients without such protection (p<0.05). During follow up period of 16.7±9.9 mo of 68 pts, no thrombotic events were recorded while 2 clinically relevant non major bleeding events occurred.

Conclusions

PFS in advanced PaC pts undergoing chemotherapy seems to positively impacted by anticoagulation. Thromboprophylaxis with tinzaparin in treatment doses is an efficient and safe approach.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Karamouzis Michalis.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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