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Essential thrombocythaemia (ET): lines of therapy

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5 standard-of-care settings across 4 lines and 2 biomarker subgroups. Rows come from the cancer page's standard of care; the grid places each on its line and subgroup.

LineAll comersRisk group
Screening, prevention and diagnosis1·
Early / localised·2
Second line1·
Other settings1·

Screening, prevention and diagnosis

SubgroupSettingApproachProducts and trialsEvidence
All comersDiagnosisFull blood count, JAK2, CALR and MPL testing, bone marrow biopsy to confirm ET and exclude prefibrotic myelofibrosis, and exclusion of reactive causes (iron deficiency, inflammation, infection, splenectomy).52

Early / localised

SubgroupSettingApproachProducts and trialsEvidence
Risk groupVery low and low riskObservation alone in very low risk (under 60, no clot, JAK2-negative); low-dose aspirin for low risk and for anyone with microvascular symptoms, once acquired von Willebrand deficiency is excluded at very high platelet counts.28
Risk groupHigh risk (over 60 with JAK2 or prior clot)Cytoreduction to a platelet count under 400 x 10^9/L: hydroxyurea first line (PT-1), pegylated or ropeginterferon alfa-2b preferred under 60 and in pregnancy, anagrelide second line.75

Second line

SubgroupSettingApproachProducts and trialsEvidence
All comersProgression to myelofibrosisManaged as myelofibrosis: JAK inhibitors for spleen and symptoms, transplant for fit higher-risk patients.87

Other settings

SubgroupSettingApproachProducts and trialsEvidence
All comersHydroxyurea resistance or intoleranceSwitch to interferon or anagrelide; ruxolitinib did not beat best available therapy in MAJIC-ET but relieves symptoms.87

Lines and subgroups are parsed from the setting text of each standard-of-care row and can misclassify an unusual phrasing; the row’s own setting is always shown. Guideline chips reflect the NCCN category and ESMO-MCBS grade recorded on the cancer page, checked on its stated date. Not medical advice.