2014
DOI: 10.1182/blood-2014-04-567909
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Multiparameter flow cytometry for staging of solitary bone plasmacytoma: new criteria for risk of progression to myeloma

Abstract: Key Points MFC is a valuable biomarker to discriminate “true” SBP patients from those with “occult” BM clonal PCs and high-risk of progression to MM.

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Cited by 66 publications
(55 citation statements)
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“…Thus, we believe dose escalation is only potentially beneficial, requiring for evidence from well-designed studies. On the other hand, risk factors for MM are: serum β2 microglobulin≥3.5 mg/L (Guo et al, 2013), bone invasion (Ozsahin et al, 2006), involvement of axial bone (Bataille et al, 1981), age (Tournier-Rangeard et al, 2006), monoclonal urinary light chains (Hill et al, 2014) and positive multiparameter flow cytometry (Paiva et al, 2014). Reported by Huang et al, in patients with SP of cervical spine, adjunctive RT following excision obviously decreased MM progression (Huang et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…Thus, we believe dose escalation is only potentially beneficial, requiring for evidence from well-designed studies. On the other hand, risk factors for MM are: serum β2 microglobulin≥3.5 mg/L (Guo et al, 2013), bone invasion (Ozsahin et al, 2006), involvement of axial bone (Bataille et al, 1981), age (Tournier-Rangeard et al, 2006), monoclonal urinary light chains (Hill et al, 2014) and positive multiparameter flow cytometry (Paiva et al, 2014). Reported by Huang et al, in patients with SP of cervical spine, adjunctive RT following excision obviously decreased MM progression (Huang et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…The prognosis of solitary plasmacytoma varies depending on presence of clonal plasma cells in the bone marrow. [12][13][14][15][16] It therefore consists of two distinct entities: solitary plasmacytoma (no clonal BMPCs) and solitary plasmacytoma with low marrow involvement (<10% clonal BMPCs). By contrast, patients with solitary plasmacytoma and 10% or more of clonal plasma cells are classifi ed as multiple myeloma.…”
Section: Other Specifi C Disease Statesmentioning
confidence: 99%
“…[5][6][7][8][9] The diagnosis of MGUS requires the absence of hypercalcaemia, renal failure, anaemia, and bone lesions (referred to as CRAB features) that can be attributed to the underlying plasma cell disorder (all features must be absent; table 1). [10][11][12][13][14][15][16][17][18][19][20] About 80% of multiple myeloma originates from non-IgM immunoglobulin MGUS (nonIgM MGUS), and 20% from light-chain immunoglobulin MGUS (LC-MGUS). In the event of progression, IgM immunoglobulin MGUS (IgM MGUS) usually evolves into Waldenström macroglobulinaemia, but in rare instances IgM MGUS can progress to multiple myeloma (IgM myeloma).…”
Section: Introductionmentioning
confidence: 99%
“…In the second study of 663 consecutive patients who underwent stem cell transplantation for PCM, 55 (8Á3%) cases had EMD, comprising 8 (14Á5%) for whom EMD was present at diagnosis and 42 (76%) patients who developed EMD at the time of relapse (Weinstock et al, 2015). The inherent fallibility of BM-based MRD assessment of PCM in the setting of patchy disease was exemplified by two separate groups, expert in FC, who demonstrated occult marrow disease by FC in 49% and 68% of patients with solitary plasmacytoma of bone respectively (Hill et al, 2014;Paiva et al, 2014), and 38% of patients with EMD , thus confirming the absence of detectable BM disease in the substantial remainder.…”
Section: á3-8á0 (Median 0á9) Disease Duration (Years) 1á2-7á1 (Mediamentioning
confidence: 99%