Neutrophil Recovery in Breast Cancer Patients Receiving Docetaxel-Containing Chemotherapy with and without Granulocyte Colony-Stimulating Factor Prophylaxis

Autor: E.M.G. Jacobs, Frank P. J. Peters, Vivianne C. G. Tjan-Heijnen, Agnes J. van de Wouw, Nelly Peer, Annette W.G. van der Velden, M. Wouter Dercksen, Jacqueline M. Stouthard, Birgit E.P.J. Vriens, Maureen J.B. Aarts, Caroline M.P.W. Mandigers, Jolien Tol, Tineke J. Smilde, Laurence J. C. van Warmerdam, Carin C.D. van der Rijt, Maaike de Boer
Přispěvatelé: Interne Geneeskunde, MUMC+: MA Medische Oncologie (9), RS: GROW - R3 - Innovative Cancer Diagnostics & Therapy, Medical Oncology
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Cancer Research
PHARMACOKINETICS
Neutrophils
medicine.medical_treatment
MULTICENTER
Docetaxel
Gastroenterology
PEGFILGRASTIM
0302 clinical medicine
Breast cancer
hemic and lymphatic diseases
Granulocyte Colony-Stimulating Factor
Randomized Controlled Trials as Topic
RISK
Neutrophil
General Medicine
Middle Aged
Granulocyte colony-stimulating factor
Women's cancers Radboud Institute for Health Sciences [Radboudumc 17]
medicine.anatomical_structure
Oncology
030220 oncology & carcinogenesis
Absolute neutrophil count
Female
Taxoids
Granulocyte colony-stimulating factor prophylaxis
Pegfilgrastim
medicine.drug
Adult
medicine.medical_specialty
INDUCED FEBRILE NEUTROPENIA
CELL LUNG-CANCER
Antineoplastic Agents
Breast Neoplasms
Neutropenia
1ST
03 medical and health sciences
All institutes and research themes of the Radboud University Medical Center
SDG 3 - Good Health and Well-being
White blood cell
Internal medicine
medicine
Humans
Chemotherapy
Aged
business.industry
medicine.disease
PHASE-III
PREVENTION
Surgery
Blood Cell Count
Clinical Trials
Phase III as Topic

business
Febrile neutropenia
030215 immunology
Zdroj: Oncology, 93(5), 323-328. Karger
Oncology (Basel), 93(5), 323-328. Karger
Oncology (Basel: 1948), 93, 323-328
Oncology (Basel: 1948), 93, 5, pp. 323-328
ISSN: 0030-2414
Popis: Objective: The primary outcome of the current study is, whether there is a protective effect of prior chemotherapy or of prior granulocyte colony-stimulating factor (G-CSF) on the next cycle blood cell counts. Methods: Hematologic toxicity was evaluated, based on a randomized phase III study in breast cancer patients (n = 167) with >20% risk of febrile neutropenia. The primary endpoint was the nadir blood cell counts for patients treated with G-CSF given during all 6 chemotherapy cycles or limited to the first 2 chemotherapy cycles only. Results: For the present analyses, 47 patients were eligible. In the G-CSF 1-6 arm, the median white blood cell count (WBC) and absolute neutrophil count (ANC) nadir slowly decreased from 10.8 × 109/L in cycle 1 to 7.5 × 109/L in cycle 6 and from 7.1 × 109/L to 5.5 × 109/L, respectively. The median WBC nadir in the G-CSF 1-2 arm decreased from 1.2 × 109/L in cycle 3 to 0.9 × 109/L in cycle 6 and the ANC nadir showed a grade 4 neutropenia of 0.1 × 109/L in cycles 3-6. All patients had ANC recovery to normal levels (≥1.5 × 109/L) without delay on day 1 of the next cycle. Conclusion: We conclude that there is no protective effect of prior G-CSF or prior chemotherapy use on nadir blood cell counts in subsequent cycles.
Databáze: OpenAIRE