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Why is Pancreatic Cancer so Thrombogenic?

Why is Pancreatic Cancer so Thrombogenic?. M. DICATO M.D., FRCP Hematology- Oncology Centre Hospitalier L- 1210 Luxembourg. Total VTE Mortality per Year. (Extrapolated to 25 EU Countries). Deaths due to VTE : 543,454 1 More than double the combined deaths due to:

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Why is Pancreatic Cancer so Thrombogenic?

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  1. Why is Pancreatic Cancer so Thrombogenic? M. DICATO M.D., FRCP Hematology- Oncology Centre Hospitalier L- 1210 Luxembourg

  2. Total VTE Mortality per Year. (Extrapolated to 25 EU Countries) • Deaths due to VTE : 543,4541 • More than double the combined deaths due to: • AIDS 5,8602 • breast cancer 86,8312 • prostate cancer 63,6362 • transport accidents 53,5992 1Cohen AT. Presented at the 5th Annual Congress of the European Federation of Internal Medicine; 2005. 2Eurostat statistics on health and safety 2001. Available from: http://epp.eurostat.cec.eu.int. Adapted from Dr A.T. Cohen’s presentation at the ISTH July 7,2007

  3. Risk of DVT in Hospitalized Patients • No prophylaxis + routine objective screening for DVT Patient group DVT incidence Medical patients 10 - 20 % Major gyne/urol/gen surgery 15 - 40 % Neurosurgery 15 - 40 % Stroke 20 - 50 % Hip/knee surgery 40 - 60 % Major trauma 40 - 80 % Spinal cord injury 60 - 80 % Critical care patients 15 - 80 %

  4. Risk Factors for VTE • Previous venous thromboembolism • Increased age • Surgery • Trauma - major, local leg • Immobilization - bedrest, stroke, paralysis • Malignancy and its treatment (CTX, hormonal..) • Heart or respiratory failure • Estrogen use, pregnancy, postpartum, SERMs • Central venous lines • Thrombophilic abnormalities

  5. Risk Factors for VTE • Previous venous thromboembolism • Increased age • Surgery • Trauma - major, local leg • Immobilization - bedrest, stroke, paralysis • Malignancy and its treatment (CTX, hormonal..) • Heart or respiratory failure • Estrogen use, pregnancy, postpartum, SERMs • Central venous lines • Thrombophilic abnormalities Most hospitalized patients have at least one risk factor for VTE

  6. Thrombophilia Mutations In cancer patients with VTE, testing for mutations [ VLeiden, PT, (MTHFR )] is only useful if there is a previous personal or family history of VTE (M. Dicato et al. :Blood 2001,S1: 3984)

  7. Relative Risk of VTE in Cancer Patients Stein, Am J Med, 2006

  8. VTE Risk and Cancer • Rate of growth and spread • Sites: pancreas (rate 8.1%), kidneys & ovaries (5.6%), stomach (4.9%).. • Therapy: thalidomide, lenalidomide (?), bevacizumab (2 fold arterial thrombosis p= 0.031, VTE none, posthoc analysis, Scapatacci; meta-analysis: VTE RR 1.33, p< 0.001, Nalluri) • ESA: RR 1.7 • RBC Transfusions vs none: 7.2 vs 3%

  9. Risk factors for VTE in patients with cancer (2) G. Lyman, Cancer 2011, 117: 1334- 49

  10. MM SHAH JOP, 2010,11:331

  11. Patient- disease- treatmentrelatedriskfactors Is there are Biomarker? • ?Biomarkers: Recentriskfactors - Platelet count > 350.000 - WBC >11.000 • CRP • TF expression • D-dimers Khorana et al.: ASCO Ed. Book, 2008

  12. L. Plawny, M. Dicato: Thrombosis in Cancer in Mellar & Davis, p275-283

  13. Physiopathology VIIA Xa TF, CP Tumour cells TNF-IL-1 TF VIIa monocytes endothelial cells Thrombin Platelet aggregation Pathways of activation of coagulation in cancer : TF (tissue factor) and CP (cancer procoagulant) activate factors VIIa and Xa. TNF (tumour necrosis factor), IL-1 (interleukin-1) induce TF expression on monocytes and on endothelial cells.

  14. Possible roles of TF activity in cancer initiation of a hypercoagulable state and thrombosis primary tumor growth – angiogenesis secondary tumor spread - metastasis

  15. ASCO 2010: JCO 2010,28(suppl 15):4126

  16. GWAS in VTE (www.genome.gov/gwastudies/) • aPTT: decrease is risk of VTE: GWAS: Ile582Thr (in KNG1gene encoding HMWK) KNG1 Knock out mice have an increase aPTT and arterial thrombosis • PS: any SNP contributing to plasma variability, C’ and others; role of inflammation in VTE • vWF increase • Other GWAS data: Prot C level interference Plasminogen activator inhibitor-1 (PAI-1), MPV: SNPs variability on ABO: VTE, lipids, inflammatory markers, DM type 2 and CHD. • Overall these risk are 1- 1.5. Multiple SNPs with modest effect and rare variants with stronger impact; add DNA methylation modif, histone modifications…

  17. Physiopathology VIIA Xa TF, CP Tumour cells TNF-IL-1 TF VIIa monocytes endothelial cells Thrombin Platelet aggregation Pathways of activation of coagulation in cancer : TF (tissue factor) and CP (cancer procoagulant) activate factors VIIa and Xa. TNF (tumour necrosis factor), IL-1 (interleukin-1) induce TF expression on monocytes and on endothelial cells.

  18. Why is Pancreatic Cancer so Thrombogenic? • Location: retroperitoneal, bedridden.. • Thrombophilic state:TF, Thrombin, GWAS… • Decrease in inhibitors: AT, Prot C&S, thrombomodulin.. • Platelet aggregation increase..Mucin • Inflammation: TGF, TNF,… • KRAS- mdm2/p53

  19. ASCO 2010, Riess H. et al.: Prospective randomised trial of simultaneous pancreatic cancer treatment with enoxaparin and chemotherapy: Final results of the CONKO-004 trial, JCO 2010, 28( Suppl.15): 4033

  20. Limitations of vitamin K antagonists (VKAs) Warfarin thrombosis • Unpredictable pharmacology • Narrow therapeutic window • Difficult to keep within therapeutic range • Multiple drug–drug and food–drug interactions • Dosing problems in the initial phase of therapy • Increased risk of major and minor bleeding Warfarin bleeding Narrow therapeutic window Thrombosis Bleeding Dose Ansell et al., Chest 2004; Hirsh et al., Chest 2004

  21. What is New? Clinic: • Prevention of VTE: Semuloparin • Real life VTE Research: • Genome wide association studies

  22. Oral Anticoagulants: • Coumarinics: Pharmacogenetics: CYP2C9 VKORC1 • Antithrombins: Ximelagatran: hepatotoxicity, off market EMEA 2008 Dabigatran • Anti Xa: Rivaroxaban (Xarelto) marketed 2008/2009; VTE med. 2011 Dabigatran (Pradaxa) Apixaban

  23. Thank You

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  27. Back- up slides

  28. ASCO Guideline: Recommendations for Venous Thromboembolism Prophylaxis and Treatment in Patients with CancerG.H. Lyman et al.: JCO 2007, 25:5490 - 5505

  29. 1. Should hospitalized patients with cancer receive anticoagulation for VTE prophylaxis? • Recommendation: hospitalized patients with cancer should be considered candidates for VTE prophylaxis in the absence of bleeding or other anticoagulant contraindications JCO 2007

  30. 2. Should ambulatory patients with cancer receive anticoagulation for VTE prophylaxis during systemic chemotherapy? • Routine prophylaxis not recommended • Thalidomide or lenalidomide with chemotherpy or dexamethasone is a high risk and warrants prophylaxis • Randomised controlled studies needed • Research identifying better risk markers needed JCO 2007

  31. 3. Should patients with cancer undergoing surgery receive perioperative VTE prophylaxis? • All patients should be considered for prophylaxis • Laparotomy, laparoscopy or thoracotomy of >30’ should receive prophylaxis unless contraindicated • Prophylaxis should be started preoperatively or as soon as possible postoperatively • Mechanical methods may be added • Prophylaxis to be continued for at least 7-10 days, up to 4 weeks to be considered in major abdominal or pelvic surgery for cancer with high-risk (residual malignant disease, obesity) and with a history of previous VTE JCO 2007

  32. 4.What is the best treatment for patients with cancer with established VTE to prevent recurrent VTE? • LMWH for initial 5-10 days • LMWH for at least 6 months is preferred. VKA with a target INR of 2-3 is acceptable, when LMWH not available • After 6 months consider indefinite anticoagulation for selected patients with active cancer • Vena cava filter is only indicated for patients with contraindications to anticoagulant therapy and recurrence needing long term treatment • For patients with CNS malignancies anticoagulation is recommended as for other cancer patients. To be avoided in active intracranial bleeding, recent surgery, bleeding diathesis • For elderly patients as for other patients with close monitoring JCO 2007

  33. 5. Should patients with cancer receive anticoagulants in the absence of established VTE to improve survival • Anticoagulants are not recommended to improve survival in patients with cancer without VTE • Patients with cancer should be encouraged to participate in clinical trials designed to evaluate anticoagulant therapy as an adjunct to standard anticancer therapy

  34. G. Lyman, Cancer 2011, 117: 1334

  35. Acquired APC Resistance (1/2) ASCO 2006:  8563 : adriamycin and epirubicin downregulate endothelial Protein C receptor and impair the APC (activated protein C) pathway. The conversion of Protein C to APC is hampered. After the treatment with these anthracyclins 25 % of patients had a low APC. Conclusion : This might be one of the contributing factors of chemotherapy induced thrombophilia.

  36. Acquired APC Resistance (2/2) -62 patients with MM (Blood Coag. Fibrinolys.:2002,13: 187) 23% APC resistance at baseline: 50% developed VTE. Increase of VTE with thalidomide, ++ Dexa & ADR -1178 patients (Br. J. Haem. 2006, 134: 399) 109 patients APC resistance, 36 V Leiden 30/31 acquired APC resistance normalised after Rp

  37. G. Lyman, Cancer 2011, 117: 1334

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