JAK2 detection accuracy
Hello, my 22 year old son had a DVST about five months ago and following with all the testing his blood test showed less than 1% JAK2 was repeated and showed a 1% JAK2 He just had a bone marrow biopsy done, and it showed no detection of JAK2. This has all been very confusing and conflicting. His blood counts are in normal range. RBC has been slightly high at one blood draw. Before the bone marrow biopsy was done, he was told he had PV and now with the bone marrow biopsy results they are saying no evidence of an MPN. Just don’t know what to believe. Anyone have any input?
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Hi Everyone,
https://www.nccn.org/patientresources/patient-resources/guidelines-for-patients/guidelines-for-patients-details?patientGuidelineId=27
Here is a great resource for you.
@meghan213, what are the next steps for your husband?
Wow That’s a bit crazy especially being that that particular blood test is very expensive! Mine came back positive the first time and all my other labs confirmed Polycythemia Vera so I opted out for the bone marrow test. Most oncologists say some just want/need final confirmation but the treatment is the same. I would proceed being the tests are contradicting. What is the potential diagnosis?
The bmb can detect level of fibrosis in the bone marrow as well as offering a firm diagnosis. Does anybody know if bmb also indicates allele burden?
From my understanding, both the bone marrow biopsy and a peripheral blood test can be used in detection of the JAK2 mutation and measurement of its allele burden in patients with myeloproliferative syndromes (myeloproliferative neoplasms). Though the peripheral blood test is generally sufficient in detecting the mutation.