A. Sureda et al., Mini-ICE regimen as mobilization therapy for chronic myelogenous leukaemiapatients at diagnosis, BONE MAR TR, 24(12), 1999, pp. 1285-1290
Citations number
27
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Between April 1996 and May 1998, 20 consecutive patients with Ph chromosome
-positive CML in first chronic phase without an HLA-identical sibling recei
ved the mini-ICE regimen shortly after diagnosis to mobilize progenitor cel
ls into the peripheral blood (PBPCs), The sex distribution was 12 males and
eight females and the median (range) age 48.5 (2262) years. The time inter
val between diagnosis and mobilization was a median (range) of 2 (0-5) mont
hs. Leukaphereses were initiated during recovery from chemotherapy-induced
aplasia, A median number of 3 (1-7) aphereses per patient were performed to
collect greater than or equal to 2.0 x 10(6) CD34(+) cells/kg, Cytogenetic
analysis was performed on the aphereses products of 18 patients. Complete
cytogenetic Ph chromosome negativity was observed in four patients, nine ha
d a partial negativity, three a minimal negativity and two no negative cell
s. Southern blot for bcr-abl was negative in the remaining two patients but
the polymerase chain reaction analysis was positive. Following reinfusion,
severe neutropenia was present for a median of 8.5 (3-19) days and severe
thrombocytopenia lasted a median of 8 (3-18) days. Ten patients did not dev
elop febrile neutropenia with four of them being treated on an outpatient b
asis. Treatment-related mortality was not observed. In conclusion, our expe
rience demonstrates the feasibility of mobilizing PBPCs shortly after the d
iagnosis of CML with a safe regimen. Of note, mini-ICE allowed the collecti
on of apheresis products with at least a major component of Ph-negative cel
ls in almost 75% of the patients.