Completed Cancer NIHR-supported project Digestion, Kidneys & Other Organs

Multicentre Assessment of G-CSF and dose Intensity of Chemotherapy - Non-interventional Study (MAGIC)

In plain English

AI plain-English summary

Chemotherapy patients often have their doses reduced or delayed because their infection-fighting white blood cells drop to dangerously low levels—a condition called neutropenia that can be fatal. This study examines whether giving a drug called G-CSF as a preventive measure helps breast cancer patients receive their full, planned chemotherapy doses on schedule. The problem is real and measurable. When neutropenia forces doctors to cut back chemotherapy, patients may have lower chances of survival. G-CSF is known to shorten the duration of neutropenia and reduce febrile neutropenia—a severe infection-related complication—but its real-world impact on maintaining full chemotherapy dose intensity in breast cancer patients is not well documented. The researchers will retrospectively extract data from routine clinical practice across multiple UK hospitals, without direct patient contact. They will analyse how often patients who received G-CSF as primary prophylaxis completed their planned chemotherapy at full dose intensity. If the results show that G-CSF consistently helps patients maintain full chemotherapy doses, this could change standard practice. More patients might receive G-CSF preventively, potentially improving survival rates for breast cancer by ensuring they get the chemotherapy their doctors originally intended.

View original technical description
Neutropenia(defined as an absolute neutrophil count [ANC] of <1.0 x109/L) is a potentially serious complication of chemotherapy, which can cause significant morbidity and mortality, result in dose delays and reductions, and can ultimately lead to reduced cancer survival.Granulocyte-colony stimulating factor (G-CSF) is indicated for the reduction in the duration of neutropenia and the incidence of febrile neutropenia (FN)Th in patients treated with established cytotoxic chemotherapy for malignancy (with the exception of chronic myeloid leukaemia and myelodysplastic syndromes).Hence, the primary objective of this study is to provide real-world evidence on the use of granulocyte-colony stimulating factor (G-CSF) as primary prophylaxis for (neo)adjuvant chemotherapy in patients with primary breast cancer and its impact on relative dose intensity (RDI). This is a non-interventional study, designed to retrospectively extract data of patients with breast cancer who received G-CSF as primary prophylaxis for (neo)adjuvant chemotherapy as part of routine clinical practice within each participating hospital.There will be no direct patient contact with the study team throughout the research. However, the care team of patients meeting the inclusion criteria will contact patients to collect informed consent.

Researchers

Daniel Rea (Principal Investigator)

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