Essential thrombocythemia (ET): When to start hydroxyurea (HU)?
I was just diagnosed with ET. I am 61 years old. My platelet count is 640k right now.
Doctor suggested I take a baby aspirin everyday and HU. I am hesitant about taking HU. I have heard of doctors waiting till the platelet count is higher to take HU.
Any insight? How bad is HU for your body, I was reading it can cause cancer too.
Thank you
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So sorry to hear about your hip and ankle injury. That has the be so painful and frustrating. Praying all goes well with the CBC check. I was on Hydroxyurea for one month before the first check..... don't be discouraged if the numbers have not changed ...they will!
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3 Reactions@rivieramaya2009 Thank you! Yes, I am lucky it is recognized today and there is an answer to the problem. And good luck with your on-going health. What is MF? I'm new to all this.
@diannerk MF is the abbreviation for Myelofibrosis. It is one of three diseases that are MPN’s (myeloproliferative Neoplasms. MF being the most serious. Take care!
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1 Reaction@janemc I was diagnosed with ET in November 2025. A blood test in July showed that my platelets were 600. Having had a more diagnostic blood test by a heamotologist in 2 months my platelets had risen to over 800 in just 2 months. I was diagnosed to have the JAX2 mutation.
This diagnosis came out of the blue as I have had no major illnesses during my life - Ive had 2 hip replacements during my sixties . I am 87 years old live alone and generally manage very well domestically.
I have been taking 500mg a day for 5 days and 2x 500 on Sat and Sundays plus small aspirin every day.
I'm being monitored. My white cells have been dropping so its worrying .
My side effects are heart burn, frequency and Ive had a UTI recently. Also whether associated or not my weight has increased which Im trying to keep under control.
While I hate having to take Udrea I am aware there is no other option. Best wishes to all fellow sufferers.
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1 Reaction@sorrento10
By taking your meds and being closely monitored by your oncologist, you're doing everything right.
My best wishes to YOU! Please keep us posted on your blood counts.
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1 ReactionIn early 2025 I started to have night sweats and fatigue. I was diagnosed with ET in Aug of 2025 and started on HU at 500mg twice daily. Platlets went down and stayed within acceptable range. No more night sweats. Then in Oct of 2025 I was hospitalized after I woke up one morning and was unable to sit up in bed with a 102 deg temp. Diagnosis was "fever of unknown origin". Drs tested me for all kinds of diseases but tests were all negative. Ended up receiving two types of antibiotics which took care of the fever. Disharged and continued with HU and was fatigued but otherwise ok.
Earlier this month I had a recurrence of the fever/weakness and was hospitalized again. New oncologist stopped the HU and is recommending Besremi injections which I will start next week. I am now also having stability problems. Get dizzy easily and must use a cane to get around. Am curious about others' transitions from HU to Besremi. Abrupt halt or did you first reduce HU when you started Besremi?
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