Febrile Neutropenia | Multi-level Evaluation of Chemotherapy-induced Febrile Neutropenia Prophylaxis, Outcomes, and Determinants With Granulocyte-colony Stimulating Factor
Febrile Neutropenia research study
What is the primary objective of this study?
This international, prospective, observational, open-label, pharmaco-epidemiologic study observes cancer patients at risk for chemotherapy-induced febrile neutropenia (FN) who are receiving filgrastim biosimilar (EP2006) for primary or secondary FN prophylaxis to better describe the patient population at risk for FN and treated prophylactically in physician's best clinical judgement with filgrastim biosimilar (EP2006), to describe prophylaxis patterns involving filgrastim biosimilar (EP2006), and to evaluate hematology levels and variability in hematological outcomes, impact on chemotherapy delivery, radiotherapy, surgery, and mortality. Additionally the study aims to identify patient cohorts who are vulnerable to poor response to FN prophylaxis and experience break-through episodes of FN, understand the differences between prophylaxis responders and non-responders, and describe the degree to which prophylaxis of FN is in congruence with guideline recommendations.
Who is eligible to participate?
Inclusion Criteria: - Male or female adults (age > / = 18 years) - Diagnosed with one of the following types and stages of tumors: stage III or IV breast cancer; stage III or IV ovarian cancer; stage III or IV bladder cancer; stage III or IV lung cancer; metastatic prostate cancer; stage III or IV diffuse large B-cell lymphoma; multiple myeloma. - Planned to receive primary prophylaxis with filgrastim biosimilar (EP2006) at the first cycle of chemotherapy (regardless of line of chemotherapy); or receiving secondary prophylaxis with filgrastim biosimilar (EP2006) irrespective of chemotherapy cycle. - Treated with commercially available filgrastim biosimilar per physician's best clinical judgment and per current European filgrastim biosimilar (EP2006) label. - Female patients must be either post-menopausal for one year or surgically sterile or using effective contraceptive methods such as barrier method with spermicide or an intra-uterine device. Oral contraceptive use is allowed. - Informed written consent to participate in the study by patients or their legal guardian. Exclusion Criteria: - Patients with myeloid malignancies, with the exception of multiple myeloma. - Sensitivity to filgrastim biosimilar or any other CSF. - Hypersensitivity to E. coli-derived proteins. - Radiotherapy to ≥ 20% of total body bone. - Infection within two weeks of starting current line of chemotherapy. - Patients with several medical condition(s) that in view of the investigator prohibits participation in the study. - Patients with willfully negligent nonadherence to their cancer treatment. - Use of any investigational agent in the 30 days prior to enrollment. - Women of childbearing potential not using the contraception method(s) described above. - Women who are breastfeeding.
Which medical condition, disease, disorder, syndrome, illness, or injury is researched?
Interventions can include giving participants drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available or noninvasive approaches such as surveys, education, and interviews.
Research studies and clinical trials typically have two or more research arms. An arm is a group of people who receive the same treatment in the study.
Only 1 groupCancer patients treated with chemotherapy and who are prescribed commercially available filgrastim biosimilar for primary or secondary prophylaxis for FN.
Start Date: March 2010
Completed Date: August 2013
Primary Outcome: Chemotherapy Toxicity (%FN Risk)
Secondary Outcome: Cohort Identification
Study sponsors, principal investigator, and references
Principal Investigator: Sandoz GmBH
Lead Sponsor: Sandoz