TY - JOUR
T1 - Diagnostic and clinical relevance of the number of circulating CD34+ cells in myelofibrosis with myeloid metaplasia
AU - Barosi, Giovanni
AU - Viarengo, Gianluca
AU - Pecci, Alessandro
AU - Rosti, Vittorio
AU - Piaggio, Giovanna
AU - Marchetti, Monia
AU - Frassoni, Francesco
PY - 2001/12/1
Y1 - 2001/12/1
N2 - The absolute content of CD34+ cells in the peripheral blood of 84 patients with myelofibrosis with myeloid metaplasia (MMM) and 23 patients with other Philadelphia-negative (Ph-) chronic myeloproliferative disorders (CMDs) was investigated. In MMM, the median absolute number of circulating CD34+ cells was consistently high (91.6 × 106/L; range, 0-2460 × 106/L). Receiver operating characteristic curve analysis showed that 15 × 106/L as a decision criterion for CD34+ cells produced an almost complete discrimination between MMM patients out of therapy and other Ph- CMDs (positive predictive value, 98.4%; negative predictive value, 85.0%). MMM patients with higher numbers of CD34+ cells had a significantly longer disease duration (P = .019) and higher spleen volume index (P = .014), liver volume (P = .000), percentage of circulating immature myeloid cells (P = .020), and percentage of myeloid blasts (P = .000). When CD34+ cells were correlated with the use of Dupriez risk stratification, CD34+ cells increased significantly from low-risk (median, 68.1 × 106/L) to intermediate-risk (median, 112.8 × 106/L) and high-risk patients (median 666.1 × 106/L) (F = 4.95; P = .009). When CD34+ cells were correlated with a severity score on the basis of both myeloproliferative and myelodepletive characteristics of the disease, only the myeloproliferation index was significantly associated with CD34+ cell level (F = 5.7; P= .000). Overall survival and interval to blast transformation from the time of CD34+ cell analysis were significantly shorter in patients with more than 300 × 106/L CD34+ cells (P= .005 and .0005, respectively). In conclusion, the absolute number of CD34+ circulating cells allows MMM to be distinguished from other Ph-CMDs; it is strongly associated with the extent of myeloproliferation and predicts evolution toward blast transformation.
AB - The absolute content of CD34+ cells in the peripheral blood of 84 patients with myelofibrosis with myeloid metaplasia (MMM) and 23 patients with other Philadelphia-negative (Ph-) chronic myeloproliferative disorders (CMDs) was investigated. In MMM, the median absolute number of circulating CD34+ cells was consistently high (91.6 × 106/L; range, 0-2460 × 106/L). Receiver operating characteristic curve analysis showed that 15 × 106/L as a decision criterion for CD34+ cells produced an almost complete discrimination between MMM patients out of therapy and other Ph- CMDs (positive predictive value, 98.4%; negative predictive value, 85.0%). MMM patients with higher numbers of CD34+ cells had a significantly longer disease duration (P = .019) and higher spleen volume index (P = .014), liver volume (P = .000), percentage of circulating immature myeloid cells (P = .020), and percentage of myeloid blasts (P = .000). When CD34+ cells were correlated with the use of Dupriez risk stratification, CD34+ cells increased significantly from low-risk (median, 68.1 × 106/L) to intermediate-risk (median, 112.8 × 106/L) and high-risk patients (median 666.1 × 106/L) (F = 4.95; P = .009). When CD34+ cells were correlated with a severity score on the basis of both myeloproliferative and myelodepletive characteristics of the disease, only the myeloproliferation index was significantly associated with CD34+ cell level (F = 5.7; P= .000). Overall survival and interval to blast transformation from the time of CD34+ cell analysis were significantly shorter in patients with more than 300 × 106/L CD34+ cells (P= .005 and .0005, respectively). In conclusion, the absolute number of CD34+ circulating cells allows MMM to be distinguished from other Ph-CMDs; it is strongly associated with the extent of myeloproliferation and predicts evolution toward blast transformation.
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U2 - 10.1182/blood.V98.12.3249
DO - 10.1182/blood.V98.12.3249
M3 - Article
C2 - 11719361
AN - SCOPUS:0035760303
VL - 98
SP - 3249
EP - 3255
JO - Blood
JF - Blood
SN - 0006-4971
IS - 12
ER -