COLLECTION OF PERIPHERAL-BLOOD PROGENITOR CELLS AFTER THE ADMINISTRATION OF CYCLOPHOSPHAMIDE, ETOPOSIDE, AND GRANULOCYTE-COLONY-STIMULATINGFACTOR - AN ANALYSIS OF 497 PATIENTS

Citation
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
Citations number
27
Categorie Soggetti
Hematology
Journal title
ISSN journal
00411132
Volume
37
Issue
9
Year of publication
1997
Pages
896 - 903
Database
ISI
SICI code
0041-1132(1997)37:9<896:COPPCA>2.0.ZU;2-Q
Abstract
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.