Last updated on August 2020

S1415CD Trial Assessing CSF Prescribing Effectiveness and Risk (TrACER)

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Stage IVA Colorectal Cancer | Febrile Neutropenia | Stage IIIC Breast Cancer | Stage IIA Breast Cancer | Stage IV Breast Cancer | Stage 0 Breast Cancer | Stage IIA Non-Small Cell Lung Carcinoma | Stage IA Breast Cancer | Stage 0 Colorectal Cancer | Stage IB Non-Small Cell Lung Carcinoma | Stage IVB Colorectal Cancer | Stage I Colorectal Cancer | Stage IV Non-Small Cell Lung Cancer | Stage 0 Non-Small Cell Lung Cancer | Stage IIB Colorectal Cancer | Stage IA Non-Small Cell Lung Carcinoma | Stage IIIC Colorectal Cancer | Stage IIIA Non-Small Cell Lung Cancer | Stage IIB Non-Small Cell Lung Carcinoma | Stage IIIB Non-Small Cell Lung Cancer | Stage IIIB Breast Cancer | Stage IIIA Colorectal Cancer | Stage IIIB Colorectal Cancer | Stage IB Breast Cancer | Stage IIIA Breast Cancer | Stage IIA Colorectal Cancer | Stage IIB Breast Cancer | Stage IIC Colorectal Cancer
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  • Patients must have a current diagnosis of breast cancer, non-small cell lung cancer, or colorectal cancer; the current diagnosis may be an initial diagnosis or recurrence and/or progression of previously diagnosed disease; cancer may be metastatic or non-metastatic
  • Patients must be registered prior to or on the same day as their first cycle of chemotherapy for their current disease and stage 9or disease setting).
  • Patients must not have had any systemic therapy (chemotherapy or combination regimens) in the 180 days just prior to registration. Prior biologic therapy, immunotherapy, tyrosine kinase inhibitors, and hormonal therapy are allowed.
  • Patients must be planning to receive one of the study-allowed regimens as their initial treatment for their current disease; myelosuppressive therapy must follow the standard regimen, although a dose reduction of up to 10% is permitted. This treatment may be neoadjuvant or adjuvant chemotherapy.
  • Patients must not be receiving or planning to receive concurrent radiation during systemic treatment.
  • Patients must not have any known contraindication to CSFs prior to registration, including prior hypersensitivity to Escherichia coli-derived proteins, filgrastim, pegfilgrastim, or tbo-filgrastim
  • Patients must be able to understand and provide information for the patient-completed study forms in either English or Spanish
  • Patients may have had a prior malignancy
  • Patients must not be participating or plan to participate in other clinical trials that involve investigational systemic cancer treatments or investigational uses of CSF during their first 6 months after registration
  • Patients must be informed of the investigational nature of this study and must sign and give written informed consent in accordance with institutional and federal guidelines
  • As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

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