Recent multi-agent frameworks have shown promise for oncology decision support, yet most assume centralized data access and rely on prompt-based assignment, limiting their applicability in privacy-sensitive clinical settings. We propose Contribution-Aware Medical Multi-Agents (CoMMa), a decentralized LLM-agent framework where specialists operate on partitioned clinical data streams. Unlike prior approaches that share inputs across agents, CoMMa enforces data decentralization to include stronger role specialization and further enhances this via agent-specific finetuning. To enable reliable and interpretable coordination, we introduce a contribution-aware aggregation mechanism that replaces stochastic, narrative-based reasoning with deterministic embedding projections to approximate each agent's marginal utility. This yields explicit credit assignment over agents, providing a stable and interpretable decision pathway aligned with clinical requirements. We evaluate CoMMa on multiple oncology benchmarks, including real-world multidisciplinary tumor board datasets from large academic hospitals in North America and East Asia, as well as public datasets, demonstrating strong performance and generalization across heterogeneous clinical settings.
Figures & tables
Figure 1: Comparison of medical decision-making frameworks. (a) Single-agent and (b) role-based multi-agent systems rely on shared inputs and narrative reasoning. (c) CoMMa introduces decentralized data streams, agent-specific specialization, and contribution-aware aggregation for interpretable and stable clinical decision-making. (d) Summary table comparing key design elements across the three decision-making frameworks under a unified formulation.
Figure 2: Architectural overview of CoMMa for decentralized multi-agent oncology decision support. Patient evidence is partitioned into distinct clinical streams and processed by specialist agents with separate observation spaces. Agent-specific representations are refined through cross-agent collaborative reasoning and aggregated by a sample-specific contribution gate regularized with Shapley-based attribution during model training.
Methods
HCC Tumorboard
Lung Cure
MTBBench
Treatment Recommendation
TNM Stage Prediction
Progression
Recurrence
AUC
Acc
AUC
Acc
AUC
Acc
AUC
Acc
GPT 4.1
In-context learning
N/A
0.784 ± 0.007
N/A
0.798 ± 0.070
N/A
0.485 ± 0.113
N/A
0.425 ± 0.086
Llama3.1-70B Grattafiori et al. (2024)
Single-Agent
0.590 ± 0.066
0.690 ± 0.064
0.782 ± 0.061
0.735 ± 0.044
0.503 ± 0.001
0.519 ± 0.004
0.526 ± 0.018
0.491 ± 0.011
Table 1: Performance comparison on three oncology benchmarks: HCC Tumorboard, Lung Cure, and MTBBench. CoMMa consistently improves predictive performance over single-agent and existing multi-agent baselines across multiple open-source LLM backbones.
Eqn. (2)
Lpg
Lshap
Llama3.1-70B
Qwen2.5-72B
AUC
Acc
AUC
Acc
✓
✓
0.706±0.007
0.688±0.068
0.682±0.015
0.738±0.004
✓
✓
0.691±0.015
0.659±0.042
0.691±0.031
0.728±0.015
✓
✓
0.692±0.012
0.741±0.056
0.681±0.024
0.722±0.046
✓
✓
✓
0.711 ± 0.011
0.795 ± 0.010
0.700 ± 0.014
0.750 ± 0.032
1. Replace learned weights with uniform dist.
0.693±0.008
0.683±0.072
0.625±0.023
0.661±0.055
Table 2: Ablation study on HCC Tumorboard treatment recommendation.
Figure 3: Comparison of AUC/Acc across different methods using the medical-related Meditron-70B backbone Chen et al. (2023) on multiple clinical evaluation tasks.
HCC Tumorboard
Llama
Qwen
Gemma
AUC
Acc
AUC
Acc
AUC
Acc
AI-Hospital-FT
0.676
0.753
0.684
0.738
0.607
0.751
CoMMa
0.711
0.795
0.700
0.750
0.680
0.758
Table 3: Fine-tuned baselines (mean of 3 seeds).
Figure 4: Performance and representative case analysis on TumorBoardRank using Gemma4-31B. Left: overall comparison. Right: normalized option-ranking scores for a representative case, with physician consensus as the reference distribution.
Figure 5: View-weight and pairwise-alignment analysis for a representative TumorBoardRank case using Gemma4-31B. (a) View-level confidence and learned CoMMa weights across evidence streams. (b) Pairwise alignment with physician-consensus option ordering, where sign indicates agreement and magnitude indicates confidence.
Appendix figures & tables10 assets
Supplementary material from the paper’s appendix.
Appendix
Decentralized Data
x1
x2
x3
x4
MRI imaging features
OPTN † information
Performance score
Laboratory data
Context example
Number of tumors: 4.0 Size of largest tumor (cm): 2.6 Location largest (segment): 8 Vascular invasion: 0 Extrahepatic spread: 0 Thrombus (portal vein): 0 ⋮
Number of OPTN 5A tumors: 0 Number of OPTN 5B tumors: 2 Number of OPTN 5X tumors: 0 Number of OPTN 5T tumors: 0
Table 8: Computational Complexity and cost Comparison on HCC Tumorboard Dataset.
HCC
Llama
Qwen
Gemma
AUC
Acc
AUC
Acc
AUC
Acc
MAC
0.656
0.780
0.690
0.738
0.650
0.739
MDAgents
0.676
0.776
0.685
0.741
0.626
0.731
AI-Hospital
0.676
0.753
0.684
0.738
0.607
0.751
CoMMa
0.711
0.795
0.700
0.750
0.680
0.758
Appendix
Table 9: Comparison with fine-tuned multi-agent baselines on HCC Tumorboard. Results are averaged over 3 random seeds.
Figure 6: Additional agentic framework response comparison on HCC Tumorboard dataset - #1. (a) Single-agent in-context learning (GPT-4.1), (b) Role-based multi-agent framework (MDAgents-Advanced), and (c) CoMMa. For the role-based multi-agent, intermediate discussions are omitted, and only the final consensus is visualized. For CoMMa, class-wise logits and cutoff thresholds are transformed into percentiles.
Figure 7: Additional agentic framework response comparison on HCC Tumorboard dataset - #2.(a) Single-agent in-context learning (GPT-4.1), (b) Role-based multi-agent framework (MDAgents-Advanced), and (c) CoMMa. For the role-based multi-agent, intermediate discussions are omitted, and only the final consensus is visualized. For CoMMa, class-wise logits and cutoff thresholds are transformed into percentiles.
Figure 8: Additional agentic framework response comparison on MTBBench - tumor progress question. (a) Single-agent in-context learning (GPT-4.1), (b) Role-based multi-agent framework (MDAgents-Advanced), and (c) CoMMa. For the role-based multi-agent, intermediate discussions are omitted, and only the final consensus is visualized. For CoMMa, class-wise logits and cutoff thresholds are transformed into percentiles.
Figure 9: Additional agentic framework response comparison on MTBBench - tumor recurrence question. (a) Single-agent in-context learning (GPT-4.1), (b) Role-based multi-agent framework (MDAgents-Advanced), and (c) CoMMa. For the role-based multi-agent, intermediate discussions are omitted, and only the final consensus is visualized. For CoMMa, class-wise logits and cutoff thresholds are transformed into percentiles.
Large language models (LLMs) have revolutionized medical reasoning tasks, yet single-agent systems often falter on complex, interdisciplinary problems requiring robust handling of uncertainty and conflicting evidence. Multi-agent systems (MAS) leveraging LLMs enable collaborative intelligence, but prevailing centralized architectures suffer from scalability bottlenecks, single points of failure, and role confusion in resource-constrained environments. Decentralized MAS (D-MAS) promise enhanced autonomy and resilience via peer-to-peer interactions, but their application to high-stakes healthcare domains remains underexplored. We introduce MediHive, a novel decentralized multi-agent framework for medical question answering that integrates a shared memory pool with iterative fusion mechanisms. MediHive deploys LLM-based agents that autonomously self-assign specialized roles, conduct initial analyses, detect divergences through conditional evidence-based debates, and locally fuse peer insights over multiple rounds to achieve consensus. Empirically, MediHive outperforms single-LLM and centralized baselines on MedQA and PubMedQA datasets, attaining accuracies of 84.3% and 78.4%, respectively. Our work advances scalable, fault-tolerant D-MAS for medical AI, addressing key limitations of centralized designs while demonstrating superior performance in reasoning-intensive tasks.
Xiaoyang Wang, Christopher C. Yang
College of Computing and Informatics, Drexel University, Philadelphia, PA 19104, USA
Large language models applied to clinical prediction exhibit case-level heterogeneity: simple cases yield consistent outputs, while complex cases produce divergent predictions under minor prompt changes. Existing single-agent strategies sample from one role-conditioned distribution, and multi-agent frameworks use fixed roles with flat majority voting, discarding the diagnostic signal in disagreement. We propose CAMP (Case-Adaptive Multi-agent Panel), where an attending-physician agent dynamically assembles a specialist panel tailored to each case's diagnostic uncertainty. Each specialist evaluates candidates via three-valued voting (KEEP/REFUSE/NEUTRAL), enabling principled abstention outside one's expertise. A hybrid router directs each diagnosis through strong consensus, fallback to the attending physician's judgment, or evidence-based arbitration that weighs argument quality over vote counts. On diagnostic prediction and brief hospital course generation from MIMIC-IV across four LLM backbones, CAMP consistently outperforms strong baselines while consuming fewer tokens than most competing multi-agent methods, with voting records and arbitration traces offering transparent decision audits.
Yuxing Lu, Yushuhong Lin, Jason Zhang
Georgia Institute of Technology · Peking University
Large Language Models (LLMs) are increasingly applied to clinical prediction tasks such as in-hospital mortality and readmission from electronic health records (EHRs). Privacy and compliance constraints motivate systems that can be deployed locally, which has increased interest in open-weight multi-agent designs. However, most medical multi-agent systems are evaluated as a single block, leaving unclear which agent role contributes to prediction and whether retrieval drives observed gains. We study a role-specialized Mixture-of-Agents (MoA) that combines medical knowledge retrieval with contrastive similar-patient reasoning. By varying the role design while holding the retrieval setup fixed, we localize the main effect to the final integrator. Pairing large open-weight analysts with a small open-weight integrator matches closed-model prompting on F1 for mortality prediction while flagging substantially more true high-risk patients. Mechanism analysis shows the role assignment directly yields a high-recall operating point without threshold tuning. The effect is task-dependent, with smaller gains for readmission because the available records correlate weakly with this longer-horizon outcome. These results position role design as a key factor in privacy-constrained, training-free clinical LLM prediction.