dc.description.abstract |
ABSTRACT
Background:
Breast cancer is the second most common female cancer following cancer of the cervix in
Tanzania (1). Chemotherapy plays a role in curative and palliative treatment; however, it may
lead to life threatening complications if rigorous preventive and management measures are not
taken. Neutropenic fever is an oncologic emergency among other common side effects. It is
critical to recognize neutropenia early and to initiate empiric antibacterial therapy promptly in
order to avoid progression to sepsis syndrome and possibly death. This study was aimed at
showing the prevalence of chemotherapy-associated febrile neutropenia for cancer patients
treated at Ocean Road Cancer Institute.
Aim:
To determine the prevalence of chemotherapy associated febrile neutropenia and associated
factors in breast cancer patients treated with chemotherapy at ORCI
Material and Methods:
A retrospective cohort study was conducted from March 2019 to April 2019. Breast cancer
patients who had received at least one drug of chemotherapy that is known to cause
neutropenia were eligible. Data collected included details on patient demographics and,
hematological and clinical characteristics pre and post chemotherapy administration.
Categorization was done into mild, moderate and severe neutropenia as follows:
1.1-2x109
/L, (mild), 0.5-1x109
/L (moderate) and less than 0.5 x109
/L (severe). Data were
collected over three consecutive cycles. SPSS version 20 was used to analyze data using t-tests
and linear regression analysis.
Results
This study involved 241 patients whose clinical data were abstracted from medical records.
All patients were female, with mean age of 51 years and standard deviation of 13.7. The
majority of patients were from coastal regions. Most (97.5%) had locally advanced breast
cancer. Seventy-five percent of the study participants were prescribed chemotherapy as
adjuvant treatment. Combination regimens including doxorubicin, cyclophosphamide,
Fluorouracil were the most commonly administered chemotherapy regimens. Administered
doses for this regimen were respectively as follows: 60:600:50 mg/m2
.
The proportion of patients with neutropenia during the course of treatment was 27.4%. The
pretreatment neutrophil count versus treatment neutrophil count for 3 cycles did not show
significant association (2%). Among patients who had neutropenia before treatment (N=241),
16.6% were of advanced age, 51 years old and above. Pretreatment neutropenia was associated
with having a neutropenia episode during the treatment with a p-value of 0.02. The average
neutrophil count of each of three cycles were respectively 4.2%, 33.4%, and 62.2% meaning
moderate and mild neutropenia respectively then normal neutrophil count. Pretreatment
anemia was found to be associated with neutropenia during chemotherapy (p-value 0.06).
Conclusion
This study found that the prevalence of chemotherapy-associated neutropenia among breast
cancer patients receiving chemotherapy at ORCI is high as compared to what is observed in
developed countries in prospective studies; 37% versus 11.6% (2). Neutropenia in these
patients is associated with low pretreatment hemoglobin, advanced age, and stage. Though
strong clinical and treatment factors have been shown to be associated with neutropenia,
specific chemotherapy drugs like taxanes, methotrexate and cyclophosphamide are the drugs
most associated with neutropenia. Early identification of risk factors associated with
neutropenia in history and physical exam before initiation of chemotherapy is necessary for
better outcome |
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