Prediction of venous thromboembolism in patients with multiple myeloma treated with lenalidomide, bortezomib, dexamethasone, and transplantation: Lessons from the substudy of IFM/DFCI 2009 cohort.


Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
08 2022
Historique:
revised: 23 03 2022
received: 10 12 2021
accepted: 08 05 2022
pubmed: 14 5 2022
medline: 23 7 2022
entrez: 13 5 2022
Statut: ppublish

Résumé

Venous thromboembolism (VTE) is a concern for patients with newly diagnosed multiple myeloma. We aimed to evaluate VTE incidence, risk factors, and risk score. We performed a substudy of the "Intergroupe Francophone du Myelome 2009" randomized controlled trial. We assessed 700 patients receiving lenalidomide/bortezomib/dexamethasone, followed or not by autologous hematopoietic stem cell transplantation. VTE incidence at 6 months was 4.8% (95% confidence interval [CI]: 3.3-6.9%) and 1.5% (95% CI: 0.8-2.9%) from 6 to 12 months. Using multivariate analysis we confirmed history of VTE (odds ratio 5.1 [1.6-16.7], P = .007) as a strong VTE-related risk factor, invalidated erythropoietin exposure (0.6 [0.2-1.7], P = .3) as risk factor, and added two new risk factors: fracture at diagnosis (2.6 [1.3-5.5], P = .01), and serum gamma globulin level > 27 g/L (2.8 [1.2-6.8,] P = .02). Moreover, we noticed that VTE occurred earlier in patients with gamma globulin levels >27 g/L, suggesting a need to revisit the thromboprophylaxis timeframe. Heparin administration was associated with a decreased risk (0.3 [0.1-0.7], P = .005) but failed to erase the risk regardless of dose. The area under the receiver operating characteristic curve of the IMPEDE VTE score was 0.67, as previously reported, confirming our cohort was well representative. Prospective studies are warranted in light of these results to improve VTE risk stratification and to design adapted thromboprophylaxis in terms of timing and dose.

Sections du résumé

BACKGROUND
Venous thromboembolism (VTE) is a concern for patients with newly diagnosed multiple myeloma.
OBJECTIVES
We aimed to evaluate VTE incidence, risk factors, and risk score.
PATIENTS/METHODS
We performed a substudy of the "Intergroupe Francophone du Myelome 2009" randomized controlled trial.
RESULTS
We assessed 700 patients receiving lenalidomide/bortezomib/dexamethasone, followed or not by autologous hematopoietic stem cell transplantation. VTE incidence at 6 months was 4.8% (95% confidence interval [CI]: 3.3-6.9%) and 1.5% (95% CI: 0.8-2.9%) from 6 to 12 months. Using multivariate analysis we confirmed history of VTE (odds ratio 5.1 [1.6-16.7], P = .007) as a strong VTE-related risk factor, invalidated erythropoietin exposure (0.6 [0.2-1.7], P = .3) as risk factor, and added two new risk factors: fracture at diagnosis (2.6 [1.3-5.5], P = .01), and serum gamma globulin level > 27 g/L (2.8 [1.2-6.8,] P = .02). Moreover, we noticed that VTE occurred earlier in patients with gamma globulin levels >27 g/L, suggesting a need to revisit the thromboprophylaxis timeframe. Heparin administration was associated with a decreased risk (0.3 [0.1-0.7], P = .005) but failed to erase the risk regardless of dose. The area under the receiver operating characteristic curve of the IMPEDE VTE score was 0.67, as previously reported, confirming our cohort was well representative.
CONCLUSIONS
Prospective studies are warranted in light of these results to improve VTE risk stratification and to design adapted thromboprophylaxis in terms of timing and dose.

Identifiants

pubmed: 35557490
doi: 10.1111/jth.15758
pii: S1538-7836(22)02072-4
doi:

Substances chimiques

Anticoagulants 0
gamma-Globulins 0
Bortezomib 69G8BD63PP
Dexamethasone 7S5I7G3JQL
Lenalidomide F0P408N6V4

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

1859-1867

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2022 International Society on Thrombosis and Haemostasis.

Références

Dimopoulos MA, Moreau P, Terpos E, et al. Multiple myeloma: EHA-ESMO clinical practice guidelines for diagnosis, treatment and follow-up†. Ann Oncol. 2021;32:309-322.
Carrier M, Le Gal G, Tay J, Wu C, Lee AY. Rates of venous thromboembolism in multiple myeloma patients undergoing immunomodulatory therapy with thalidomide or lenalidomide: a systematic review and meta-analysis. J Thromb Haemost. 2011;9:653-663.
Covut F, Ahmed R, Chawla S, et al. Validation of the IMPEDE VTE score for prediction of venous thromboembolism in multiple myeloma: a retrospective cohort study. Br J Haematol. 2021;193:1213-1219.
Hatswell AJ, Burns D, Baio G, Wadelin F. Frequentist and Bayesian meta-regression of health state utilities for multiple myeloma incorporating systematic review and analysis of individual patient data. Health Econ. 2019;28:653-665.
Chalayer E, Bourmaud A, Tinquaut F, Chauvin F, Tardy B. Cost-effectiveness analysis of low-molecular-weight heparin versus aspirin thromboprophylaxis in patients newly diagnosed with multiple myeloma. Thromb Res. 2016;145:119-125.
Leleu X, Rodon P, Hulin C, et al. MELISSE, a large multicentric observational study to determine risk factors of venous thromboembolism in patients with multiple myeloma treated with immunomodulatory drugs. Thromb Haemost. 2013;110:844-851.
Annibali O, Napolitano M, Avvisati G, Siragusa S. Incidence of venous thromboembolism and use of anticoagulation in hematological malignancies: critical review of the literature. Crit Rev Oncol Hematol. 2018;124:41-50.
Palumbo A, Cavo M, Bringhen S, et al. Aspirin, warfarin, or enoxaparin thromboprophylaxis in patients with multiple myeloma treated with thalidomide: a phase III, open-label, randomized trial. J Clin Oncol. 2011;29:986-993.
Larocca A, Cavallo F, Bringhen S, et al. Aspirin or enoxaparin thromboprophylaxis for patients with newly diagnosed multiple myeloma treated with lenalidomide. Blood. 2012;119:933-939. quiz 1093.
imwg. IMWG guidelines for the prevention of thalidomide- and lenalidomide-associated thrombosis in myeloma. Int Myeloma Working Group. 2015. https://www.myeloma.org/resource-library/imwg-guidelines-prevention-thalidomide-lenalidomide-associated-thrombosis-myeloma
Palumbo A, Rajkumar SV, Dimopoulos MA, et al. Prevention of thalidomide- and lenalidomide-associated thrombosis in myeloma. Leukemia. 2008;22:414-423.
Bradbury CA, Jenner MW, Striha A, et al. Thrombotic events in patients with myeloma treated with immunomodulatory drugs; results of the myeloma XI study. Blood. Am Soc Hematol. 2017;130(suppl 1):553.
Chalayer E, Chapelle C, Leleu X, Elalamy I, Laporte S, Tardy B. Does the choice of thrombotic prophylactic drug depend on the known risk factors of patients with multiple myeloma in clinical practice? Thromb Res. 2016;143:101-102.
Sanfilippo KM, Luo S, Wang T-F, et al. Predicting venous thromboembolism in multiple myeloma: development and validation of the IMPEDE VTE score. Am J Hematol. 2019;94:1176-1184.
Attal M, Lauwers-Cances V, Hulin C, et al. Lenalidomide, bortezomib, and dexamethasone with transplantation for myeloma. N Engl J Med. 2017;376:1311-1320.
Steyerberg EW, Eijkemans MJC, Harrell FE, Habbema JDF. Prognostic modeling with logistic regression analysis: in search of a sensible strategy in small data sets. Med Decis Making. 2001;21:45-56.
Zangari M, Fink L, Zhan F, Tricot G. Low venous thromboembolic risk with bortezomib in multiple myeloma and potential protective effect with thalidomide/lenalidomide-based therapy: review of data from phase 3 trials and studies of novel combination regimens. Clin Lymphoma Myeloma Leuk. 2011;11:228-236.
Chalayer E, Tardy-Poncet B, Karlin L, et al. Thrombin generation in newly diagnosed multiple myeloma during the first three cycles of treatment: an observational cohort study. RTPH. 2019;3:89-98.
Chakraborty R, Bin Riaz I, Malik SU, et al. Venous thromboembolism risk with contemporary lenalidomide-based regimens despite thromboprophylaxis in multiple myeloma: a systematic review and meta-analysis. Cancer. 2020;126:1640-1650.
Ghansah H, Debreceni IB, Fejes Z, Nagy B, Kappelmayer J. The proteasome inhibitor bortezomib induces apoptosis and activation in gel-filtered human platelets. Int J Mol Sci. 2021;22:8955.
Libourel EJ, Sonneveld P, van der Holt B, de Maat MPM, Leebeek FWG. High incidence of arterial thrombosis in young patients treated for multiple myeloma: results of a prospective cohort study. Blood. 2010;116:22-26.
Bravo-Perez C, Fernández-Caballero M, Soler-Espejo E, et al. Heparin versus aspirin thromboprophylaxis adds independent value to IMPEDE-VTE score for venous thrombosis prediction in multiple myeloma. J Thromb Thrombolysis. 2021;52:848-853.
Chalayer E, Teste A, Guyotat D, Elalamy I, Leleu X, Tardy B. Predicting the risk of venous thromboembolism in newly diagnosed myeloma with immunomodulatory drugs: external validation of the IMPEDE VTE score. Am J Hematol. 2020;95:E18-E20.
Li A, Wu Q, Luo S, et al. Derivation and validation of a risk assessment model for immunomodulatory drug-associated thrombosis among patients with multiple myeloma. J Natl Compr Canc Netw. 2019;17:840-847.
Teste AH, Thollot FT, Sotton S, et al. IMPEDE VTE vs SAVED scores to predict the risk of venous thromboembolism in newly diagnosed multiple myeloma with immunomodulatory drugs: how to choose? Int Conf Thromb Hemost Issues Can. 2021;200(Suppl 1):S61-S62.
Chalayer E, Chapelle C, Leleu X, Elalamy I, Laporte S, Tardy B. Usual risk factors do not predict venous thromboembolism in newly diagnosed myeloma treated with immunomodulatory drugs. Am J Hematol. 2016;91:E455-E456.
Singh AK, Szczech L, Tang KL, et al. Correction of anemia with epoetin alfa in chronic kidney disease. NEJM. 2006;355:2085-2098.
Anaissie EJ, Coleman EA, Goodwin JA, et al. Prophylactic recombinant erythropoietin therapy and thalidomide are predictors of venous thromboembolism in patients with multiple myeloma: limited effectiveness of thromboprophylaxis. Cancer. 2012;118:549-557.
Liu C, Song Y, Zhao J, et al. Elevated D-dimer and fibrinogen levels in serum of preoperative bone fracture patients. SpringerPlus. 2016;5:161.
Charles SA, Chaudier TF, Daguenet E, et al. D-dimers cut off level to predict the risk of venous thromboembolism in newly diagnosed multiple myeloma. Int Conf Thromb Hemost Issues Can. 2022;213:S13.
Chakraborty R. Abnormal metaphase cytogenetics adds to currently known risk-factors for venous thromboembolism in multiple myeloma: derivation of the PRISM score. ASH. 2020;136:29-30.
Khorana AA, Francis CW, Culakova E, Kuderer NM, Lyman GH. Frequency, risk factors, and trends for venous thromboembolism among hospitalized cancer patients. Cancer. 2007;110:2339-2346.
Mehta J, Singhal S. Hyperviscosity syndrome in plasma cell dyscrasias. Semin Thromb Hemost. 2003;29:467-472.
Hinterleitner C, Pecher A-C, Kreißelmeier K-P, et al. Disease progression and defects in primary hemostasis as major cause of bleeding in multiple myeloma. Eur J Haematol. 2020;104:26-35.
Pollreisz A, Assinger A, Hacker S, et al. Intravenous immunoglobulins induce CD32-mediated platelet aggregation in vitro. Br J Dermatol. 2008;159:578-584.
Carr ME, Zekert SL. Abnormal clot retraction, altered fibrin structure, and normal platelet function in multiple myeloma. Am J Physiol Heart Circ Physiol. 1994;266:H1195-H1201.
Rutjes AW, Porreca E, Candeloro M, Valeriani E, Di Nisio M. Primary prophylaxis for venous thromboembolism in ambulatory cancer patients receiving chemotherapy. Cochrane Database Syst Rev. 2020;2020:CD008500.
Swan D, Rocci A, Bradbury C, Thachil J. Venous thromboembolism in multiple myeloma - choice of prophylaxis, role of direct oral anticoagulants and special considerations. Br J Haematol. 2018;183:538-556.
Li A, Garcia DA, Lyman GH, Carrier M. Direct oral anticoagulant (DOAC) versus low-molecular-weight heparin (LMWH) for treatment of cancer associated thrombosis (CAT): a systematic review and meta-analysis. Thromb Res. 2019;173:158-163.
Sorigue M, Cañamero E, Siguenza P, Nomdedeu M, López-Núñez JJ. Recent developments and persisting challenges in the prevention and treatment of venous thromboembolism in patients with hematological malignancies. Leuk Lymphoma. 2020;61:1277-1291.

Auteurs

Emilie Chalayer (E)

Department of Haematology and Cell Therapy, Centre Hospitalo-Universtiaire de Saint Etienne, Saint Etienne, France.
U1059 INSERM, Team SAINBIOSE DVH, Université Jean Monnet Saint-Etienne, Saint-Etienne, France.

Alexis Talbot (A)

Hopital Saint Louis, Department of Haematology, Paris, France.

Laurent Frenzel (L)

Department of Haematology, Institut Necker, Paris, France.

Lionel Karlin (L)

Department of Haematology, Hospices Civils de Lyon, Lyon, France.

Philippe Collet (P)

Department of Haematology and Cell Therapy, Institut de Cancerologie Lucien Neuwirth, St Priest en Jarez, France.

Denis Guyotat (D)

Department of Haematology and Cell Therapy, Institut de Cancerologie Lucien Neuwirth, St Priest en Jarez, France.

Michel Attal (M)

Department of Haematology, Institut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.

Xavier Leleu (X)

Department of Haematology, Centre Hospitalier et Universitaire la Miletrie, Poitiers, France.

Bernard Tardy (B)

Centre d'investigation Clinique INSERM CIC 1408, CHU Saint Etienne, France.

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