Predicting Live Birth After Fresh Embryo Transfer in IVF/ICSI: Differential ICM/Trophectoderm Morphology Encoding and a Hybrid Attention--Logistic Regression Ensemble
Organizations: School of Computer Science, Wuhan University, Wuhan, China · Department of Obstetrics and Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China · Reproductive Medical Center, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, P.R. China, and also with the Clinical Medicine Research Center of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, Hubei, P.R. China
Abstract
Predicting live birth before fresh embryo transfer could support shared decision-making in IVF/ICSI, but routine clinical data are small, heterogeneous, and contain pathway-dependent variables prone to outcome leakage. We aimed to construct a curated single-centre IVF/ICSI dataset and develop a prediction model suited to small tabular clinical data. Materials and Methods: We assembled 616 fresh embryo-transfer cycles (251 live birth, 365 non-live birth) with clinical, laboratory, and embryological predictors, and embryo morphology encoded with a novel differential weighting of the inner cell mass and trophectoderm. After KNN imputation, robust scaling, and selection of 50 features, we developed a Hybrid Attention Network (HAN), a learnable feature-attention gate followed by a compact multilayer perceptron, and a HAN + logistic-regression (LR) ensemble with a validation-tuned weight. Models were benchmarked against classical machine learning, TabPFN, and text-serialized language models on a held-out test set; AUC-ROC was the primary metric. Results: The HAN + LR ensemble achieved the highest test AUC-ROC (0.710; accuracy 0.710, F1 0.630), ahead of the HAN backbone alone (0.700), logistic regression (0.667), the TabPFN + LR hybrid (0.666), and TabPFN (0.650). Text-serialized language models performed near chance (AUC 0.61). The differentially weighted trophectoderm feature ranked highest by consensus importance across models. Discussion: A compact attention network combined with a linear model outperformed both components and strong foundation-model baselines on a small clinical cohort. Conclusion: The curated dataset and HAN + LR ensemble offer a transparent, reproducible basis for IVF/ICSI live-birth prediction; external validation is the next step.
Figures & tables
| Variable | Live birth (n = 251) | Non-live birth (n = 365) | SMD | Selected | |
|---|---|---|---|---|---|
| Female factors | |||||
| Female age (years) | 31.8 3.7 | 33.1 4.0 | 0.001 | 0.34 | |
| Female smoking history, n (%) | 0.722 | – | – | ||
| Have | 4 (1.6%) | 4 (1.1%) | |||
| None | 247 (98.4%) | 361 (98.9%) | |||
| Female height (cm) | 160.8 4.9 | 161.2 4.5 | 0.269 | 0.09 | |
| Variable | Live birth (n = 251) | Non-live birth (n = 365) | SMD | Selected | |
|---|---|---|---|---|---|
| Stimulation and laboratory | |||||
| Ovarian stimulation protocol, n (%) | 0.795 | – | |||
| Antagonist regimen | 199 (79.3%) | 296 (81.1%) | |||
| Extra Long Plan | 3 (1.2%) | 7 (1.9%) | |||
| Long protocol for early follicular phase | 21 (8.4%) | 29 (7.9%) | |||
| Luteal phase extension protocol | 26 (10.4%) | 29 (7.9%) | |||
| Component | Setting |
|---|---|
| Feature Attention Module | Learnable per-feature gate, sigmoid, element-wise multiplicative |
| MLP layers | (LayerNorm, ReLU, dropout 0.25); (ReLU, dropout 0.15); (sigmoid) |
| HAN ensemble | 3 seeds (42, 123, 456), probabilities averaged |
| Parameters | 1,635 per HAN instance; 4,957 total |
| Ensemble rule | ; by validation grid search |
| Optimizer / loss | AdamW (lr 0.002, weight decay 0.001); binary cross-entropy |
| Model | AUC | Acc | Prec | Rec | F1 |
|---|---|---|---|---|---|
| HAN + LR (proposed) | 0.710 | 0.710 | 0.657 | 0.605 | 0.630 |
| HAN backbone (alone) | 0.700 | 0.667 | 0.590 | 0.605 | 0.597 |
| Logistic regression | 0.667 | 0.645 | 0.558 | 0.632 | 0.593 |
| TabPFN + LR | 0.666 | 0.656 | 0.615 | 0.421 | 0.500 |
| TabPFN | 0.650 | 0.613 | 0.545 | 0.316 | 0.400 |
| Support-vector machine | 0.632 | 0.624 | 0.588 | 0.263 | 0.364 |
| Feature | Domain | Consensus (%) | RF | GB | XGB | LR | HAN |
|---|---|---|---|---|---|---|---|
| Blastocyst 1 TE (weighted) | Oocyte retrieval and embryo development | 4.53 | 0.008 | 0.019 | 0.014 | 1.208 | 0.537 |
| Ovarian stimulation protocol (Extra Long Plan) | Stimulation and laboratory | 3.35 | 0.001 | 0.000 | 0.000 | 0.759 | 0.560 |
| Method of fertilization (IVF+RICSI) | Stimulation and laboratory | 2.93 | 0.001 | 0.000 | 0.000 | 0.599 | 0.555 |
| Cleavage embryo 1 grade | Oocyte retrieval and embryo development | 2.66 | 0.003 | 0.000 | 0.001 | 0.523 | 0.520 |
| Number of follicles punctured | Oocyte retrieval and embryo development | 2.61 | 0.024 | 0.007 | 0.009 | 0.464 | 0.522 |
| Number of oocytes retrieved | Oocyte retrieval and embryo development | 2.57 | 0.020 | 0.019 | 0.015 | 0.427 | 0.532 |
Clinical Outcome Prediction
Clinical outcome prediction uses patient records, imaging, signals, and biomarkers to estimate risks, disease trajectories, treatment response, and survival.
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