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AdaSurvMamba advances multimodal survival analysis by addressing the rigidity of standard state-space models in processing complex medical data like whole slide images and genomic profiles. The proposed framework dynamically adjusts cross-modal interaction strengths and reorganizes token scanning to preserve semantic continuity, yielding consistent improvements across five TCGA cohorts. This work highlights a significant step forward in applying adaptive sequence modeling architectures to critical healthcare diagnostics.
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AdaSurvMamba: Dynamic Fusion and Semantic Scanning for Multimodal Survival Analysis

arXiv3 min read

arXiv:2607.16260v1 Announce Type: cross Abstract: Multimodal survival analysis utilizing whole slide images (WSIs) and genomic profiles is fundamental for cancer prognosis. Recently, state-space models like Mamba have emerged as powerful tools for sequence modeling. However, translating this success to complex multimodal tasks is hindered by two critical limitations. First, conventional fusion strategies assume a static multimodal interaction strength, ignoring the fluctuating diagnostic importance of each modality across different patients and local regions. Second, the standard Mamba architecture processes tokens along predefined physical paths. This rigid scanning disrupts the semantic continuity of spatially scattered medical features and exacerbates long-range decay. To address these challenges, we introduce AdaSurvMamba as a novel adaptive framework for multimodal survival analysis. The framework features a Dual-Scale Importance-Aware Reconstruction (DSIR) module to dynamically modulate cross-modal interaction strength. It evaluates diagnostic importance at both the sequence and token levels to reconstruct the input representations. Furthermore, we propose a Semantic Aggregation Scanning (SAS) module to overcome contextual fragmentation. The SAS module dynamically reorganizes discrete tokens into semantically continuous sequences via a shared prototype pool. It explicitly modulates the state transition step size using global modality context and semantic priors to adaptively control the information absorption rate. Experiments across five TCGA cohorts demonstrate consistent gains over existing methods. Code is available at https://github.com/zjlGO/AdaSurvMamba.

Abstract:Multimodal survival analysis utilizing whole slide images (WSIs) and genomic profiles is fundamental for cancer prognosis. Recently, state-space models like Mamba have emerged as powerful tools for sequence modeling. However, translating this success to complex multimodal tasks is hindered by two critical limitations. First, conventional fusion strategies assume a static multimodal interaction strength, ignoring the fluctuating diagnostic importance of each modality across different patients and local regions. Second, the standard Mamba architecture processes tokens along predefined physical paths. This rigid scanning disrupts the semantic continuity of spatially scattered medical features and exacerbates long-range decay. To address these challenges, we introduce AdaSurvMamba as a novel adaptive framework for multimodal survival analysis. The framework features a Dual-Scale Importance-Aware Reconstruction (DSIR) module to dynamically modulate cross-modal interaction strength. It evaluates diagnostic importance at both the sequence and token levels to reconstruct the input representations. Furthermore, we propose a Semantic Aggregation Scanning (SAS) module to overcome contextual fragmentation. The SAS module dynamically reorganizes discrete tokens into semantically continuous sequences via a shared prototype pool. It explicitly modulates the state transition step size using global modality context and semantic priors to adaptively control the information absorption rate. Experiments across five TCGA cohorts demonstrate consistent gains over existing methods. Code is available at this https URL.

Machine Learning (cs.LG); Artificial Intelligence (cs.AI); Computer Vision and Pattern Recognition (cs.CV)

arXiv:2607.16260 [cs.LG]

(or arXiv:2607.16260v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2607.16260 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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Full text under the publisher's open licence · 313 words

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