M. Boccadoro et al., Multiple myeloma: the number of reinfused plasma cells does not influence outcome of patients treated with intensified chemotherapy and PBPC support, BONE MAR TR, 25(1), 2000, pp. 25-29
Citations number
29
Categorie Soggetti
Hematology,"Medical Research Diagnosis & Treatment
Multiple myeloma (MM) is characterized by the expansion of tumor plasma cel
ls in bone marrow (BM), but neoplastic cells have been consistently detecte
d in peripheral blood (PB), Peripheral blood progenitor cell (PBPC) collect
ions have been widely used to support high-dose therapy for MM patients. A
flow cytometric technique has been used to detect plasma cells in PB and PB
PC harvests. High CD38 expression identified these cells, and their nature
was confirmed by the coexpression of specific antigens, such as CD138 and c
ytoplasmic immunoglobulins. Malignant plasma cell reinfusion could negative
ly affect response rate and survival, as demonstrated in other hematologica
l malignancies. To address this issue, the relationship between the number
of reinfused plasma cells, response to chemotherapy and event-free survival
(EFS) have been analyzed. Sixty-four MM patients were treated with intensi
fied chemotherapy at diagnosis. They were mobilized with cyclophosphamide a
nd G-CSF, and then treated with melphalan 100 mg/m(2) (MEL100) followed by
PBPC support. A second course was given after 2 months, and a third to pati
ents not in complete remission. There was no correlation between the number
of reinfused plasma cells and response rate after this intensified chemoth
erapy: patients attaining complete remission received 3.6 x 10(6)/kg CD38() cells, while those with a partial or no response received 5.6 and 2.9 x 1
0(6)/kg CD38(+) cells. Similarly, there was no correlation between the numb
er of reinfused plasma cells and EFS, Patients receiving less than 4.85 x 1
0(6)/kg CD38(+) cells experienced a median EFS of 34.2 months as opposed to
36.4 months for those receiving more than 4.85 x 10(6)/kg CD38(+) cells (P
= 0.7). Recurrence of the disease is consistently observed in MM: our data
suggest that in vivo residual tumor cells, rather than reinfused plasma ce
lls are more likely to be responsible for relapse.