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/L-may be too stringent. We reviewed outcomes of 176 multiple myeloma (MM) patients diagnosed between 1971 and 2016, and who had CPCs detectable at diagnosis, to determine whether a lower threshold could be used to diagnose PCL. Median overall survival (mOS) was 1.1 years (95% CI 0.8-1.4) and was similar between patients with < 5% (n = 54, mOS = 1.4 years 0.7-2.0), 5-19% (n = 63, mOS = 1.1 years 0.7-1.4), and ≥ 20% CPCs (n = 59, mOS = 1.1 years 0.7-1.5, p = 0.349). As survival was similar between those with 5-19% and ≥ 20% CPCs, we stratified patients by < 5% (mOS = 1.4 years 0.7-2.0) and ≥ 5% CPCs (mOS = 1.1 years 0.8-1.4, p = 0.154). Outcomes of those with ≥ 5% CPCs were much poorer when compared with a cohort of MM patients diagnosed between 1971 and 2016, who did not have CPCs at diagnosis (n = 9724, mOS = 4.4 yrs 4.3-4.5, p < 0.001); survival was also lower in patients diagnosed after 2001 with ≥ 5% CPCs (n = 62, mOS = 1.4 years 0.8-2.5) compared with patients with standard risk (n = 1326, mOS = 7.5 years 7.0-8.7) and high-risk MM (n = 381, mOS = 4.3 years 3.5-4.9, p < 0.001). We therefore propose that the definition of PCL be revised to patients with ≥ 5% CPCs on peripheral blood smear, who otherwise meet diagnostic criteria for MM.
Ravi et al. (Thu,) studied this question.
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