Usage of granulocyte colony-stimulating factor every 2 days is clinically useful and cost-effective for febrile neutropenia during early courses of chemotherapy
Background In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated. Methods Thirty patients with newly d...
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Published in | International journal of clinical oncology Vol. 16; no. 2; pp. 118 - 124 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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Japan
Springer Japan
01.04.2011
Springer Nature B.V |
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Abstract | Background
In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated.
Methods
Thirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10
9
/L) and/or neutropenia (<0.5 × 10
9
/L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed.
Results
No significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF.
Conclusion
We concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy. |
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AbstractList | In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated.BACKGROUNDIn order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated.Thirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10(9)/L) and/or neutropenia (<0.5 × 10(9)/L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed.METHODSThirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10(9)/L) and/or neutropenia (<0.5 × 10(9)/L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed.No significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF.RESULTSNo significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF.We concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy.CONCLUSIONWe concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy. In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated. Thirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10(9)/L) and/or neutropenia (<0.5 × 10(9)/L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed. No significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF. We concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy. Background In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated. Methods Thirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10 9 /L) and/or neutropenia (<0.5 × 10 9 /L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed. Results No significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF. Conclusion We concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy. In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients treated with a single chemotherapy regimen during early courses was prospectively evaluated. Thirty patients with newly diagnosed non-Hodgkin lymphoma (NHL) treated with the first course of an R-CHOP regimen were enrolled randomly. After treatment with the first course of chemotherapy, a daily dose of G-CSF (lenograstim, 100 μg) was administered to half (15 cases) of the patients, and a dose of G-CSF (100 μg) was administered every other day to the other half of the patients when leukocytopenia (<1.5 × 10^sup 9^/L) and/or neutropenia (<0.5 × 10^sup 9^/L) occurred. Changes in leukocyte and neutrophil counts, prophylaxis, febrile neutropenia (FN) events, and cost performance between the two groups were analyzed. No significant difference between the two groups was observed in recoveries of leukocyte and neutrophil counts and evidence of FN. The only difference was the total cost of G-CSF. We concluded that every-other-day use of G-CSF was as clinically effective for the prophylaxis of FN as the daily use of G-CSF, and economically speaking, the administration of G-CSF every other day should be more beneficial for patients with NHL during early courses of R-CHOP chemotherapy.[PUBLICATION ABSTRACT] |
Author | TAKAOKA Ikue YAKUSHIJIN Yoshihiro AZUMA Taichi SHIKATA Hisaharu HATO Takaaki YAMANOUCHI Jun YASUKAWA Masaki HORIKAWA Tamami TAKEUCHI Kazuhito NARUMI Hiroshi |
Author_xml | – sequence: 1 givenname: Yoshihiro surname: Yakushijin fullname: Yakushijin, Yoshihiro email: yoshiyak@m.ehime-u.ac.jp organization: Cancer Center of Ehime University Hospital, Ehime University Graduate School of Medicine – sequence: 2 givenname: Hisaharu surname: Shikata fullname: Shikata, Hisaharu organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 3 givenname: Ikue surname: Takaoka fullname: Takaoka, Ikue organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 4 givenname: Tamami surname: Horikawa fullname: Horikawa, Tamami organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 5 givenname: Kazuhito surname: Takeuchi fullname: Takeuchi, Kazuhito organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 6 givenname: Jun surname: Yamanouchi fullname: Yamanouchi, Jun organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 7 givenname: Taichi surname: Azuma fullname: Azuma, Taichi organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 8 givenname: Hiroshi surname: Narumi fullname: Narumi, Hiroshi organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine – sequence: 9 givenname: Takaaki surname: Hato fullname: Hato, Takaaki organization: Division of Blood Transfusion and Cell Therapy, Ehime University Graduate School of Medicine – sequence: 10 givenname: Masaki surname: Yasukawa fullname: Yasukawa, Masaki organization: Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine |
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CitedBy_id | crossref_primary_10_1016_j_clinthera_2014_06_034 crossref_primary_10_1016_j_transci_2013_05_026 crossref_primary_10_1007_s10147_013_0523_z crossref_primary_10_1111_jep_12597 crossref_primary_10_4103_ijh_ijh_37_21 crossref_primary_10_1038_s41598_017_04495_x |
Cites_doi | 10.1046/j.1365-2141.1997.2393053.x 10.1093/infdis/163.3.579 10.2165/00003495-200059030-00017 10.1056/NEJM199207023270106 10.1002/ajh.21206 10.1200/JCO.2006.06.4451 10.1016/j.clinthera.2009.05.003 10.1200/JCO.20.3.727 10.1185/030079903125002531 10.1016/0161-5890(90)90060-D 10.1634/theoncologist.12-12-1416 10.1200/JCO.2004.03.213 10.1185/030079907X219599 10.1182/blood.V82.11.3265.3265 10.1182/blood.V88.6.1907.bloodjournal8861907 10.2165/00044011-200929080-00001 10.1093/annonc/mdg019 |
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Keywords | Granulocyte colony-stimulating factors (G-CSF) Cost-benefit R-CHOP Non-Hodgkin lymphoma (NHL) Febrile neutropenia (FN) |
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In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF... In order to analyze the clinical activity and cost-effectiveness of granulocyte colony-stimulating factors (G-CSF), the prophylactic usage of G-CSF in patients... |
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Title | Usage of granulocyte colony-stimulating factor every 2 days is clinically useful and cost-effective for febrile neutropenia during early courses of chemotherapy |
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