Secondary prophylactic C-CSF (filgrastim) administration in chemotherapy of stage I and II Hodgkin's lymphoma with ABVD

Citation
A. Rueda et al., Secondary prophylactic C-CSF (filgrastim) administration in chemotherapy of stage I and II Hodgkin's lymphoma with ABVD, LEUK LYMPH, 41(3-4), 2001, pp. 353-358
Citations number
21
Categorie Soggetti
Hematology,"Onconogenesis & Cancer Research
Journal title
LEUKEMIA & LYMPHOMA
ISSN journal
10428194 → ACNP
Volume
41
Issue
3-4
Year of publication
2001
Pages
353 - 358
Database
ISI
SICI code
1042-8194(200104)41:3-4<353:SPC(AI>2.0.ZU;2-Q
Abstract
The purpose of this study was to determine the effect of granulocyte colony -stimulating factor (filgrastim. G-CSF) for maintenance of chemotherapy dos e-intensity in patients with stage I or II Hodgkin`s lymphoma treated with six cycles of doxorubicin, bleomycin, vinblastine. and dacarbazine (ABVD). 7Fifty-six patients with stage I or II Hodgkin's lymphoma treated with ABVD were eligible For secondary prophylactic G-CSF administration because of n eutropenia (absolute neutrophil count < 1 x 10(9)/L) causing treatment dela y or febrile neutropenia. Patients received 300 mug (total dose) of G-CSF ( filgrastim) subcutaneously on days 3 to 7 and 17 to 21 of each cycle in ord er to prevent dose reduction or delay in subsequent cycles of treatment con tinuing the G-CSF until completion of chemotherapy. Results showed that 30 (54%) of the patients required the use of G-CSF, 26 (47%) during the first or second cycle. After G-CSF administration delay in chemotherapy did not o ccur in 25 patients, whereas: delays in the Fifth or sixth cycle occurred i n four patients, Despite treatment with G-CSF, one patient had febrile neut ropenia. Dose intensity greater than 90% of that planned was delivered to m ore the 85% of patients. In conclusion: Secondary prophylactic G-CSF administration was necessary in more than half of patients with stage I or II Hodgkin's lymphoma during ch emotherapy with 48VD. The use of G-CSF allowed maintenance of chemotherapy schedule and dose intensity in the majority of patients.