Copyright: ©Author(s) 2026.
World J Gastrointest Oncol. Sep 15, 2026; 18(9): 121975
Published online Sep 15, 2026. doi: 10.4251/wjgo.121975
Published online Sep 15, 2026. doi: 10.4251/wjgo.121975
Table 1 Overview of multitask learning models in hepatocellular carcinoma
| Ref. | Year | Task(s) | Architecture | Imaging | Key finding |
| Zhao et al[55] | 2025 | CK19 positivity + MVI prediction | Expert sharing network with spatial transformation and relation reasoning | Gd-EOB-DTPA-enhanced MRI: Hepatobiliary phase | CK19 AUC = 0.87 internal CV, 0.80 external; MVI AUC: 0.88 internal CV, 0.85 external |
| You et al[30] | 2026 | HCC segmentation + histological grading | Integrated MTL framework; segmentation models + radiomics classification; transformer-RFE-fused model | MRI: Arterial-phase T1WI, portal-venous-phase T1WI, wavelet-fused arterial/portal-venous T1WI | Fused MRI test DSC 0.92; training ACC 93.2%, testing ACC 92.5%; testing AUC up to 0.960 in fused modality |
| Wang et al[52] | 2024 | OS prediction/survival risk stratification | DeepSurv, NMTLR, RSF, Cox-PH comparison | Structured SEER registry data; no imaging | NMTLR test C-index 0.7353; 1 year, 3 years, 5 years AUC = 0.824, AUC = 0.813, AUC = 0.803 |
| Wang et al[51] | 2024 | MVI prediction + RFS prediction + PA-TACE benefit analysis | Transformer-based multitask deep learning model | MRI: Fat-saturated T2WI, DWI, arterial-phase T1WI, portal-venous-phase T1WI | MVI AUCs were 0.918 training, 0.800 internal, and 0.837/0.815/0.800 external; RFS C-index was 0.763 training, 0.716 internal, and 0.628/0.675/0.728 external; PA-TACE benefit was observed only in the predicted high-MVI-risk/Low-survival-score subgroup |
| Song et al[16] | 2024 | Early recurrence prediction + FLL classification | Multitask self-supervised pre-training with phase-shuffle prediction and case discrimination; ResNet18 backbone | Multi-phase CT: NC, ART, PV | ER prediction ACC 74.65%, AUC = 0.739; FLL classification ACC 88.06%, AUC = 0.791; outperformed ImageNet transfer learning, single-task self-supervised pre-training, and DINOv2 |
| Wen et al[36] | 2023 | HCC segmentation + pathological differentiation prediction | MTL model with segmentation subnet and classification subnet; boundary-aware attention; multi-scale feature fusion; dynamic weight averaging | Contrast-enhanced MRI: Arterial, portal venous, delayed phases | The model outperformed comparator multitasks methods; Dice 83.90%; classification ACC 80.67%, AUC = 0.791, recall 86.08%, and F1 score 80.05% |
| Xie et al[37] | 2023 | MVI prediction + 3D tumor segmentation | Triplet-uncertainty MTL; 3D U-Net/VGG-based branches | Contrast-enhanced MRI: NR phase/sequence; 3D tumor ROI | TU-MTL achieved the best joint performance, with MVI ACC 80.96%, SEN 74.03%, SPE 88.94%, AUC = 0.8208, segmentation Dice 82.07%, and JC 82.13% |
| He et al[18] | 2023 | MTM subtype prediction + OS prediction after HAIC | Multitask deep learning radiomics model; 3D MobileNetV1 + radiomics + clinical integration | Dual-phase contrast-enhanced CT: Arterial + venous phases | MTM AUCs were 0.968/0.912/0.773; MDLR prognostic AUCs were 0.855/0.805/0.792 across cohorts |
| Xiao et al[54] | 2022 | HCC detection + size grading + multi-index quantification | TrdAL: CNN encoder + modality-aware Transformer + radiomics-guided discriminator + task-interaction loss | Multi-modality MRI: In-phase, out-phase, T2FS, DWI | Detection ACC 93.33%, SEN 93.15%, SPE 93.71%, IoU 82.93%; size-grading ACC 77.78%-96.87%; center-point MAE 2.74 mm; max-diameter MAE 3.17 mm; area MAE 144.51 mm2 |
| Li et al[10] | 2022 | Objective response prediction after TACE + tumor segmentation | Tumor-aware multitask deep learning network with shared encoder, OR prediction pathway, and segmentation pathway | Contrast-enhanced CT: Arterial phase + portal venous phase | Multi-DL achieved AUC 0.871, ACC 83.9%, SEN 85.7%, SPE 82.9%, and Dice 73.6%; also stratified survival risk |
| Li et al[40] | 2022 | MVI prediction + auxiliary tumor segmentation | Split-attention ResNeSt encoder + U-Net decoder MTL | Gd-EOB-DTPA-enhanced MRI: NR phase/sequence | For HCC MVI prediction, internal ACC 74.2%, SEN 80.0%, SPC 70.7%, AUC 0.803; external ACC 89.4%, SEN 83.3%, SPC 82.3%, AUC 0.885 |
| Chu et al[49] | 2022 | MVI + VETC prediction; prognostic stratification | 3D CNN-based multitask learning | Multiphase Gd-EOB-DTPA-enhanced MRI: Late arterial, portal venous, hepatobiliary phases | MTL improved MVI prediction from AUC 0.896 to 0.917 with ACC 90.0%; VETC was predicted with AUC = 0.8604 and ACC 82.5%; MVI/VETC-based stratification was associated with OS/RFS |
| Wang et al[53] | 2021 | HCC segmentation + auxiliary patch classification | Hybrid MTL network: Shared SE-ResNeXt-101 encoder + two pixel-wise segmentation branches + auxiliary patch-level classification branch + SKM/scSEM ensemble | H&E-stained whole-slide images | The ensemble model achieved PAIP Jaccard index 79.7%, CRAG Dice 92.3%, and UHCMC&CWRU Dice 76.5% |
| Fu et al[7] | 2021 | Future macrovascular invasion prediction + OS stratification | MTnet with segmentation subnet + clinical/radiological/radiomic fusion | Portal venous phase CT | Combined model CR-DR achieved AUC 0.877 in training and 0.836 in external validation; model-defined risk groups stratified time to macrovascular invasion and OS |
| Liu et al[50] | 2020 | MVI prediction + Edmondson-Steiner grading + survival prediction after TACE | Hybrid ML/DL framework; RF + SVM histologic scores + DL-score + Cox-PH model | Contrast-enhanced CT: Late arterial + portal venous phases | Test AUCs were 0.79 for MVI and 0.72 for Edmondson-Steiner grade; OS C-index was 0.73, with 3 years, 5 years, and 10 years AUCs of 0.85, 0.90, and 0.89 |
| Huang et al[56] | 2022 | IVIM parameter fitting + MVI prediction | Transformer-based multitask deep learning (CCT-inspired) | IVIM-DWI MRI: 9 b-value images | Joint learning improved both IVIM fitting and MVI prediction; AUC = 0.855, outperforming single-task and other MTL models |
Table 2 Study design, validation, and limitations of included multitask learning studies
| Ref. | Primary task category | Sample size | Study design | Ext valid | Key study-level limitations |
| Zhao et al[55] | Diagnostic/biologic aggressiveness prediction | 145 | Retrospective multicenter study; 10-fold CV in center 1 + external independent test set from centers 2 and 3 | Yes | Limited sample size; single-center training with potential inter-center domain bias; HBP-only model; no clinical-variable integration; no prospective validation |
| You et al[30] | Structural + diagnostic grading | 1673 | Retrospective single-center study; 80/10/10 train-validation-test split + five-fold CV | No | Single-center retrospective design; no external or prospective validation; arterial/portal-venous MRI only; clinical/genomic variables not integrated; sequential pipeline without demonstrated joint multitask optimization or shared-representation learning |
| Wang et al[52] | Prognostic survival prediction | 2197 | Retrospective SEER database study; 7:3 train/test split + five-fold CV | No | Registry-based design; no imaging data; no independent external validation; limited clinical granularity; black-box interpretability remains limited |
| Wang et al[51] | Biologic + prognostic + treatment-benefit prediction | 725 | Retrospective multicenter study; training/internal test split + three external test sets | Yes | Retrospective design; predominantly HBV-related Chinese cohort; moderate RFS performance in some external sets; nonrandomized PA-TACE benefit analysis; no prospective validation |
| Song et al[16] | Prognostic recurrence prediction | 167 patients/765 CT slices; FLL classification: 85 CT volumes/489 slices | Retrospective single-center study; 10-fold CV for ER prediction + 5-fold CV for FLL classification | No | Small single-center HCC cohort; no external or prospective validation; ROI-based 2D slice analysis; multitask component limited to pre-training; method restricted to multi-phase CT images |
| Wen et al[36] | Structural + pathological differentiation prediction | 295 patients/885 CE-MRI | Retrospective single-center study; train-test split + five-fold CV within the training set | No | Single-center design; no external or prospective validation; modest cohort size; simplified pathological differentiation categories |
| Xie et al[37] | Structural + biologic aggressiveness prediction | 137 | Single-institution study; random train/validation-test split | No | Small cohort; no external or prospective validation; limited MRI phase/sequence reporting; internal split only |
| He et al[18] | Biologic subtype + prognostic prediction | MTM cohort: 159; HAIC cohort: 752 | Retrospective multi-institutional study; training/internal test cohorts from one institution + external test cohort from four centers | Yes | Retrospective design; MTM cohort mainly surgical; HAIC-only prognostic cohort; limited generalizability to other treatment contexts; no prospective validation; whole-liver ROI approach not compared with tumor-specific ROI; complications during and after HAIC or TKI treatment were not analyzed |
| Xiao et al[54] | Structural detection + quantitative assessment | 135 subjects/10800 MRI slices | Single-dataset experimental study; five-fold CV | No | Small dataset; no external or prospective validation; single-source MRI dataset; protocol-specific multimodality inputs |
| Li et al[10] | Treatment response prediction + segmentation | 248 | Retrospective two-center study; training/internal validation cohort + external testing cohort | Yes | Retrospective design; two-center dataset; 2D-only network with limited spatial-context utilization; small DEB-TACE subgroup; no prospective validation |
| Li et al[40] | Biologic aggressiveness prediction + segmentation | 85 | Two-center study; internal CV in center 1 + external validation in center 2 | Yes | Small HCC cohort; limited external cohort size; MRI phase/sequence reporting incomplete; no prospective validation |
| Chu et al[49] | Biologic aggressiveness prediction + prognostic stratification | 133 | Single-center retrospective cohort; 7:3 train/internal validation split | No | Limited sample size; single-center design; strict exclusion criteria; no external validation |
| Wang et al[53] | Pathology-based structural segmentation | PAIP: 100 HCC WSIs; CRAG: 213 images; UHCMC & CWRU: 110 images | Public benchmark-based experimental study; PAIP train/validation/test split + CRAG and UHCMC&CWRU train/test splits | No | HCC validation limited to PAIP; external benchmark datasets were non-HCC pathology images; pathology-only input; no prospective clinical validation |
| Fu et al[7] | Future macrovascular invasion prediction + survival stratification | 366 | Retrospective multicenter study; training dataset from four hospitals + external validation dataset from one hospital | Yes | Retrospective design; strict inclusion criteria; HBV-predominant Chinese cohort; no prospective validation; black-box interpretability remains limited |
| Liu et al[50] | Histologic surrogate prediction + post-TACE survival prediction | 494 surgical cohort; 243 TACE cohort | Retrospective single-center study; surgical cohort for histologic-score development + TACE cohort for survival modeling | No | Survival model limited to TACE-treated patients; retrospective design; no external validation; complex multi-stage pipeline introduces risk of compounding overfitting; label reliability for histological surrogates not formally assessed |
| Huang et al[56] | Structural + biologic aggressiveness prediction | 114 HCC samples | Single-center study; 4-fold CV repeated five times | No | Small single-center cohort; no external validation; slice-based analysis; IVIM parameter fitting evaluated indirectly using reconstructed b-value images |
- Citation: Akbulut S, Colak C. Multitask learning in hepatocellular carcinoma: Integrating diagnosis, prognosis, and clinical decision support. World J Gastrointest Oncol 2026; 18(9): 121975
- URL: https://www.wjgnet.com/1948-5204/full/v18/i9/121975.htm
- DOI: https://dx.doi.org/10.4251/wjgo.121975