1995
DOI: 10.1159/000227449
|View full text |Cite
|
Sign up to set email alerts
|

Usefulness of Granulocyte Colony-Stimulating Factor on Neutropenia in Patients of Invasive Mole and Choriocarcinoma

Abstract: The effect of human granulocyte colony stimulating factor (hG-CSF) was investigated on the proliferation of choriocarcinoma cells in vitro. No growth-stimulating effect was observed. Then, 22 patients with invasive mole and 9 patients with choriocarcinoma who received combination chemotherapy were treated with hG-CSF when white blood cell counts decreased below 2,000/ mm3. The duration of neutropenia was reduced significantly by 3-4 days with the use of hG-CSF. No side effects were observed. These r… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

1997
1997
2006
2006

Publication Types

Select...
4
1

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(1 citation statement)
references
References 5 publications
0
1
0
Order By: Relevance
“…To decrease the incidence of severe neutropenia, which occurs almost universally with these protocols, and to avoid treatment delays, G-CSF is administered on days 6-14 of each treatment cycle, and a complete blood count is obtained on days 8 and 15. 80 Another approach to improving response to secondary therapy for high-risk disease is to administer chemotherapy agents with known activity at doses much higher than usual. Collins et al 81 treated a patient with refractory disease in the lung and brain after both EMA-CO and PVB chemotherapy with very high dose etoposide, 4,200 mg/m 2 at 60 hours IV infusion and cyclophosphamide 50 mg/kg IV daily, for 4 days without bone marrow support.…”
Section: Resistant High-risk Diseasementioning
confidence: 99%
“…To decrease the incidence of severe neutropenia, which occurs almost universally with these protocols, and to avoid treatment delays, G-CSF is administered on days 6-14 of each treatment cycle, and a complete blood count is obtained on days 8 and 15. 80 Another approach to improving response to secondary therapy for high-risk disease is to administer chemotherapy agents with known activity at doses much higher than usual. Collins et al 81 treated a patient with refractory disease in the lung and brain after both EMA-CO and PVB chemotherapy with very high dose etoposide, 4,200 mg/m 2 at 60 hours IV infusion and cyclophosphamide 50 mg/kg IV daily, for 4 days without bone marrow support.…”
Section: Resistant High-risk Diseasementioning
confidence: 99%