2020
DOI: 10.1111/bjh.16533
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Anti‐myeloma potential of ruxolitinib in co‐existing JAK2V617F‐positive smouldering myeloma and polycythaemia vera

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Cited by 4 publications
(6 citation statements)
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“…A recent study analyzed two different patients both diagnosed with JAK2 mutation positive PCV and each later developed smoldering myeloma. Interestingly, the JAK2 V617F mutation was detected in the bone marrow plasma cells of these two patients as well, suggesting a single driver mutation for both the plasma cell and erythrocyte proliferations in these cases [ 11 ]. It is possible that patients with concurrent PCV and MM have a common pluripotent hematopoietic stem cell dysfunction causing proliferative diseases in both myeloid and lymphoid cell lines [ 10 , 12 ].…”
Section: Discussionmentioning
confidence: 99%
“…A recent study analyzed two different patients both diagnosed with JAK2 mutation positive PCV and each later developed smoldering myeloma. Interestingly, the JAK2 V617F mutation was detected in the bone marrow plasma cells of these two patients as well, suggesting a single driver mutation for both the plasma cell and erythrocyte proliferations in these cases [ 11 ]. It is possible that patients with concurrent PCV and MM have a common pluripotent hematopoietic stem cell dysfunction causing proliferative diseases in both myeloid and lymphoid cell lines [ 10 , 12 ].…”
Section: Discussionmentioning
confidence: 99%
“…The coexistence of MM and PV is rare, 1 , 2 , 3 , 4 , 5 , 6 and the treatment of MM under these conditions has not been described in detail. MM was previously considered an incurable hematologic neoplasm, with patients rarely achieving complete remission with alkylating reagents and steroids.…”
Section: Discussionmentioning
confidence: 99%
“… 21 Recently, MM and MPN clones were directly analyzed in patients with JAK2 mutations, a characteristic acquired mutation found in patients with MPN. 22 Lee et al 6 demonstrated JAK2 mutations in both myeloid and CD138‐sorted plasma cells of two patients with smoldering MM associated with JAK2 mutation‐positive PV, suggesting shared stem cell progenitors of MM and PV. Conversely, Kuroda et al 23 reported that the plasma cell fraction was negative for JAK2 mutations in a patient with MM associated with JAK2‐positive essential thrombocythemia, another type of MPN, suggesting different origins in their patient.…”
Section: Discussionmentioning
confidence: 99%
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