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Neutropenia Prediction Based on First-Cycle Blood Counts Using a FOS-3NN Classifier.
Elize A Shirdel1, Michael J Korenberg, Yolanda Madarnas
1Department of Electrical and Computer Engineering, Queen's University, Kingston, ON, Canada K7L 3N6.
Advances in Bioinformatics
|March 29, 2012
Summary
A new model accurately predicts neutropenic events in breast cancer patients receiving adjuvant chemotherapy. This tool helps classify patients into low- and high-risk groups, enabling timely treatment and optimal outcomes.
Area of Science:
- Oncology
- Hematology
- Biostatistics
Background:
- Adjuvant chemotherapy delivery is crucial for breast cancer treatment success.
- Neutropenia, a common chemotherapy complication, often leads to treatment delays or dose reductions.
- Predicting neutropenic risk in breast cancer patients remains challenging.
Purpose of the Study:
- To develop and validate a predictive model for neutropenic events in early-stage breast cancer patients undergoing adjuvant chemotherapy.
- To stratify patients into low- and high-risk groups for neutropenia based on early treatment response.
Main Methods:
- A cohort of 35 early-stage breast cancer patients receiving adjuvant chemotherapy was analyzed.
- The FOS-3NN model was developed to stratify patient risk using complete blood count data after the first chemotherapy cycle.
- Risk classification was independent of breast cancer subtype and clinical markers, focusing on blood count kinetics.
Main Results:
- The FOS-3NN model demonstrated high accuracy in an independent test set.
- 19 out of 21 unseen patients were correctly classified (P < 0.00023, Matthews' correlation coefficient +0.83).
- The model effectively predicted neutropenic events based on early chemotherapy response.
Conclusions:
- A novel model, FOS-3NN, accurately predicts neutropenic events in breast cancer patients during adjuvant chemotherapy.
- This predictive capability aids in managing treatment schedules and optimizing patient outcomes.
- The model offers a reliable method for classifying neutropenic risk early in the treatment course.
