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Arterial thrombosis in Philadelphia-negative myeloproliferative neoplasms predicts second cancer: A case-control study

De Stefano, V.; Ghirardi, A.; Masciulli, A.; Carobbio, A.; Palandri, F.; Vianelli, N.; Rossi, E.; Betti, S.; Di Veroli, A.; Iurlo, A.; Cattaneo, D.; Finazzi, G.; Bonifacio, M.; Scaffidi, L.; Patriarca, A.; Rumi, E.; Casetti, I.C.; Stephenson, C.; Guglielmelli, P.; Elli, E.M.; Palova, M.; Rapezzi, D.; Erez, D.; Gomez, M.; Wille, K.; Pérez Encinas, Manuel Mateo; Lunghi, F.; Angona, A.; Fox, M.L.; Beggiato, E.; Benevolo, G.; Carli, G.; Cacciola, R.; McMullin, M.F.; Tieghi, A.; Recasens, V.; Isfort, S.; Marchetti, M.; Griesshammer, M.; Alvarez-Larran, A.; Vannucchi, A.M.; Rambaldi, A.; Barbui, T
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URI: http://hdl.handle.net/20.500.11940/20397
DOI: 10.1182/BLOOD.2019002614
ISSN: 1528-0020
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Blood. 2020;135(5):381-6. (321.2Kb)
Date issued
2020
Journal title
Blood
Type of content
Article
Abstract
Patients with Philadelphia-negative myeloproliferative neoplasm (MPN) are prone to the development of second cancers, but the factors associated with these events have been poorly explored. In an international nested case-control study, we recruited 647 patients with carcinoma, nonmelanoma skin cancer, hematological second cancer, and melanoma diagnosed concurrently or after MPN diagnosis. Up to 3 control patients without a history of cancer and matched with each case for center, sex, age at MPN diagnosis, date of diagnosis, and MPN disease duration were included (n 5 1234). Cases were comparable to controls for MPN type, driver mutations and cardiovascular risk factors. The frequency of thrombosis preceding MPN was similar for cases and controls (P 5 .462). Thrombotic events after MPN and before second cancer were higher in cases than in controls (11.6% vs 8.1%; P 5 .013), because of a higher proportion of arterial thromboses (6.2% vs 3.7%; P 5 .015). After adjustment for confounders, the occurrence of arterial thrombosis remained independently associated with the risk of carcinoma (odds ratio, 1.97; 95% confidence interval, 1.14-3.41), suggesting that MPN patients experiencing arterial events after MPN diagnosis deserve careful clinical surveillance for early detection of carcinoma.

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