The prophylactic effects of long-acting granulocyte colony-stimulating factor for febrile neutropenia in newly diagnosed patients with epithelial ovarian cancer: a randomised controlled study

被引:6
作者
Li, Lei [1 ]
Ma, Shuiqing [1 ]
Wu, Ming [1 ]
Tan, Xianjie [1 ]
Zhong, Sen [1 ]
Lang, Jinghe [1 ]
机构
[1] Peking Union Med Coll Hosp, Dept Obstet & Gynecol, Beijing, Peoples R China
关键词
Granulocyte colony-stimulating factor; febrile neutropenia; myelosuppression; ovarian cancer; adverse events; CHEMOTHERAPY-INDUCED NEUTROPENIA; CELL LUNG-CANCER; SINGLE-ADMINISTRATION PEGFILGRASTIM; MULTICENTER PHASE-III; BREAST-CANCER; DAILY FILGRASTIM; DOUBLE-BLIND; RECEIVING CHEMOTHERAPY; CLINICAL-PRACTICE; OPEN-LABEL;
D O I
10.1136/bmjspcare-2019-001862
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Objective This study explored the prophylactic effects of long-acting granulocyte colony-stimulating factor (G-CSF) for febrile neutropenia (FN) in newly diagnosed patients with epithelial ovarian cancer (EOC). Methods Patients were randomised into a study group (long-acting G-CSF for all chemotherapy cycles) and a control group (short-acting G-CSF for first cycle and treatment per physician discretion for subsequent cycles) at a ratio of 1:2. The incidences of FN and myelosuppression and the number of clinical visits, medication doses, complete blood count (CBC) tests and adverse events were compared between the two groups. A regression model was used to determine the risk factors for FN. Results From 30 November 2018 to 1 April 2019, 84 cases were included in the final analysis; there were 24 (28.6%) and 60 (71.4%) patients in the study and control groups, respectively, and 605 chemotherapy cycles. The study group or chemotherapy cycles utilising long-acting G-CSF had significantly fewer utilisations and doses of short-acting G-CSF; clinical visits; CBC tests; and incidences of FN and myelosuppression; and less G-CSF-associated pain. The utilisation of G-CSF was the only independent factor for FN in a binary regression model. Conclusion Long-acting G-CSF could effectively reduce the incidences of FN and myelosuppression and had mild adverse effects in newly diagnosed patients with EOC receiving chemotherapy. Trial registration number NCT03740464.
引用
收藏
页码:373 / 380
页数:8
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