COLLECTION OF PERIPHERAL-BLOOD PROGENITOR CELLS AFTER THE ADMINISTRATION OF CYCLOPHOSPHAMIDE, ETOPOSIDE, AND GRANULOCYTE-COLONY-STIMULATINGFACTOR - AN ANALYSIS OF 497 PATIENTS
Ch. Weaver et al., COLLECTION OF PERIPHERAL-BLOOD PROGENITOR CELLS AFTER THE ADMINISTRATION OF CYCLOPHOSPHAMIDE, ETOPOSIDE, AND GRANULOCYTE-COLONY-STIMULATINGFACTOR - AN ANALYSIS OF 497 PATIENTS, Transfusion, 37(9), 1997, pp. 896-903
BACKGROUND: There is great interpatient variability in the number of p
eripheral blood stem cells collected, as measured by CD34+ cell conten
t, alter the administration of chemotherapy and a growth factor. The a
bility to predict patients who fail to yield adequate quantities of CD
34+ cells would be of value. However, very few reports include large n
umbers of patients treated in an identical fashion. STUDY DESIGN AND M
ETHODS: Between 1991 and 1995, 497 consecutive patients with a variety
of malignant diseases received cyclophosphamide (4 g/m(2)), etoposide
(600 mg/m(2)), and granulocyte-colony-stimulating factor (6 mu g/kg/d
ay) for mobilization and collection of a target dose greater than or e
qual to 2.5 x 10(6) CD34+ cells per kg. Multivariate analyses were per
formed to determine the factors associated with failure to achieve thi
s target harvest. RESULTS: A median of 14.71 x 10(6) CD34+ cells per k
g (range, 0.08-137.55) was harvested with a median of 2 (range, 1-11)
apheresis procedures. Ninety-one percent of patients yielded greater t
han or equal to 2.5 x 10(6) CD34+ cells per kg. Patients with Stage II
-III breast cancer, who had pretreatment platelet counts greater than
or equal to 150 x 10(9) per L and patients who underwent II prior chem
otherapy regimen had improved CD34+ cell yields. However, most patient
s with adverse risk factors yielded greater than or equal to 2.5 x 10(
6) CD34+ cells per kg. CONCLUSION: A regimen of cyclophosphamide, etop
oside, and granulocyte-colony-stimulating factor led to the successful
collection of adequate numbers of CD34+ cells in most patients withou
t excessive toxicity. These observations confirm previous reports that
intense prior therapy adversely affects the quantity of CD34+ cells h
arvested. Pretreatment and posttreatment variables did not predict wit
h any certainty the small fraction of patients who fail to yield great
er than or equal to 2.5 x 10(6) CD34+ cells per kg via multiple aphere
sis procedures.