# A Study of Age and Sex Bias in Multiple Instance Learning based Classification of Acute Myeloid Leukemia Subtypes

arXiv: https://arxiv.org/abs/2308.12675 · HTML: https://mlsanity.com/paper/2308.12675/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Builds on 9 of its 25 references that are in the map.
- First posted on arXiv 24 Aug 2023.

## Builds on (most cited first, 9 of 9)

- [Deep Residual Learning for Image Recognition](https://mlsanity.com/paper/1512.03385/) (2015)
- [ImageNet Large Scale Visual Recognition Challenge](https://mlsanity.com/paper/1409.0575/) (2014)
- [Attention-based Deep Multiple Instance Learning](https://mlsanity.com/paper/1802.04712/) (2018)
- [Attention based Multiple Instance Learning for Classification of Blood Cell Disorders](https://mlsanity.com/paper/2007.11641/) (2020)
- [A Study of Demographic Bias in CNN-based Brain MR Segmentation](https://mlsanity.com/paper/2208.06613/) (2022)
- [Unsupervised Cross-Domain Feature Extraction for Single Blood Cell Image Classification](https://mlsanity.com/paper/2207.00501/) (2022)
- [A systematic study of race and sex bias in CNN-based cardiac MR segmentation](https://mlsanity.com/paper/2209.01627/) (2022)
- [Pixel-Level Explanation of Multiple Instance Learning Models in Biomedical Single Cell Images](https://mlsanity.com/paper/2303.08632/) (2023)
- [Towards unraveling calibration biases in medical image analysis](https://mlsanity.com/paper/2305.05101/) (2023)

## Abstract (arXiv)

Accurate classification of Acute Myeloid Leukemia (AML) subtypes is crucial for clinical decision-making and patient care. In this study, we investigate the potential presence of age and sex bias in AML subtype classification using Multiple Instance Learning (MIL) architectures. To that end, we train multiple MIL models using different levels of sex imbalance in the training set and excluding certain age groups. To assess the sex bias, we evaluate the performance of the models on male and female test sets. For age bias, models are tested against underrepresented age groups in the training data. We find a significant effect of sex and age bias on the performance of the model for AML subtype classification. Specifically, we observe that females are more likely to be affected by sex imbalance dataset and certain age groups, such as patients with 72 to 86 years of age with the RUNX1::RUNX1T1 genetic subtype, are significantly affected by an age bias present in the training data. Ensuring inclusivity in the training data is thus essential for generating reliable and equitable outcomes in AML genetic subtype classification, ultimately benefiting diverse patient populations.
