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. 2020 Aug 1;1(1):113–121. doi: 10.1002/jha2.69

TABLE 1.

Bone marrow specimen description

Specimen ID Age/Sex Disease * Subtype Prior Lines of Therapy Latest line of treatment Cytogenetic Risk
PCD1020 66/F MM IgG‐K 3 Velcade maintenance High Risk
PCD1201 66/F MM IgG‐L 3 RV maintenance(off therapy for 40mo) High Risk
PCD1218 52/M MM IgG‐L 5 Elo‐Rd High Risk
PCD1300 57/M MM/PCL IgA‐K 3 KRd followed by Mel200‐ASCT(off therapy for 13mo) High Risk
PCD1421 59/M MM KLC 3 Velcade Maintenance(off therapy for 7mo) High Risk
PCD1427 65/F MM IgG‐L 3 KRd‐Elo Standard
PCD1441 71/M MM LLC 4 KRd‐Elo Standard
PCD1447 68/F MM IgG‐K 4 CarCy(off therapy for 12mo) High Risk
PCD1527 54/F MM KLC 3 Dara‐Vd High Risk
PCD1542 53/M MM IgG‐K 6 Pom‐Dex Standard

Abbreviations: MM: multiple myeloma Myeloma, PCL: plasma cell leukemia. Bor/V: Bortezomib, Car/K: Carlfilzomib, Dara: daratumumab, Dex/d: dexamethasone, Elo Elotuzimab, Mel200‐AST: high‐dose Melphalan and autologous stem cell transplant, Pom: pomalidamide R: Revlimid,

*

All patients were relapsing at the time of bone marrow aspirate collection.

[As per IWMG criteria] Standard Risk: normal cytogenetics, hyperdiploidy, or t(11;14); Intermediate Risk: [t(6;14), del 13, or others not in good or high risk; High Risk: del 17p, t(4;14), t(14;16), t(14;20), amplification 1q21, complex cytogenetics, or hypodiploidy.

Plasma cells from this BMMC specimen were CD38 negative.