arXiv:2604.04894v1 Announce Type: cross Abstract: Reinforcement learning with verifiable rewards (RLVR) has significantly advanced the reasoning capabilities of large language models (LLMs). However, it faces a fundamental limitation termed \textit{restricted exploration}, where the policy rapidly converges to a narrow set of solutions. While entropy regularization is a popular approach used to sustain exploration, it often proves unreliable for LLMs, suffering from high hyperparameter sensitivity and yielding only marginal performance gains. Motivated by these inefficiencies, we propose to rethink the relationship between policy entropy and exploration. By deriving a parametric formulation of group-relative advantage estimation and analyzing entropy dynamics, we conceptually decompose policy entropy into \textit{informative entropy}, which preserves diverse solution paths, and \textit{spurious entropy}, which erodes reasoning patterns. Our analysis reveals that, in contrast to blind maximization, effective exploration requires \textit{entropy refinement}-a mechanism implicitly embedded in group-relative advantage estimation that sustains informative entropy on positive rollouts while suppressing spurious entropy on negative ones. Guided by this insight, we propose \textbf{AsymGRPO}, an exploratory framework that explicitly decouples the modulation of positive and negative rollouts. This allows for independent control over the preservation of informative entropy and the suppression of spurious noise. Extensive experiments demonstrate that AsymGRPO achieves superior performance compared to strong baselines and exhibits the potential to synergize with existing entropy regularization methods.

arXiv:2602.14010v1 Announce Type: cross Abstract: Pathology foundation models (PFMs) have enabled robust generalization in computational pathology through large-scale datasets and expansive architectures, but their substantial computational cost, particularly for gigapixel whole slide images, limits clinical accessibility and scalability. Here, we present LitePath, a deployment-friendly foundational framework designed to mitigate model over-parameterization and patch level redundancy. LitePath integrates LiteFM, a compact model distilled from three large PFMs (Virchow2, H-Optimus-1 and UNI2) using 190 million patches, and the Adaptive Patch Selector (APS), a lightweight component for task-specific patch selection. The framework reduces model parameters by 28x and lowers FLOPs by 403.5x relative to Virchow2, enabling deployment on low-power edge hardware such as the NVIDIA Jetson Orin Nano Super. On this device, LitePath processes 208 slides per hour, 104.5x faster than Virchow2, and consumes 0.36 kWh per 3,000 slides, 171x lower than Virchow2 on an RTX3090 GPU. We validated accuracy using 37 cohorts across four organs and 26 tasks (26 internal, 9 external, and 2 prospective), comprising 15,672 slides from 9,808 patients disjoint from the pretraining data. LitePath ranks second among 19 evaluated models and outperforms larger models including H-Optimus-1, mSTAR, UNI2 and GPFM, while retaining 99.71% of the AUC of Virchow2 on average. To quantify the balance between accuracy and efficiency, we propose the Deployability Score (D-Score), defined as the weighted geometric mean of normalized AUC and normalized FLOP, where LitePath achieves the highest value, surpassing Virchow2 by 10.64%. These results demonstrate that LitePath enables rapid, cost-effective and energy-efficient pathology image analysis on accessible hardware while maintaining accuracy comparable to state-of-the-art PFMs and reducing the carbon footprint of AI deployment.