Clinical utility of investigations in triple-negative thrombocytosis: A real-world, multicentre evaluation of UK practice
- PMID: 39004100
- DOI: 10.1111/bjh.19643
Clinical utility of investigations in triple-negative thrombocytosis: A real-world, multicentre evaluation of UK practice
Abstract
Diagnosis of essential thrombocythaemia (ET) is challenging in patients lacking JAK2/CALR/MPL mutations. In a retrospective evaluation of 320 patients with 'triple-negative thrombocytosis', we assessed utility of bone marrow histology (90.9% of patients) and myeloid gene panel (MGP, 55.6%). Supportive histology ('myeloproliferative neoplasm-definite/probable', 36.8%) was associated with higher platelet counts and varied between centres. 14.6% MGP revealed significant variants: 3.4% JAK2/CALR/MPL and 11.2% other myeloid genes. Final clinical diagnosis was strongly predicted by histology, not MGP. 23.7% received cytoreduction (17.6% under 60 years). Real-world 'triple-negative' ET diagnosis currently depends heavily on histology; we advocate caution in MGP-negative cases and that specific guidelines are needed.
Keywords: diagnosis; molecular; myeloproliferative; thrombocytosis; triple‐negative.
© 2024 British Society for Haematology and John Wiley & Sons Ltd.
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