Training-Free Medical Image Segmentation vs Trained Networks
A multi-domain data-efficiency study — frozen LLM polygon traces + a numpy genome + a gated SAM decoder, with zero gradient training.
4 modalitiesmeasured, from scratchGT-free at inferenceLLM-agnostic skillsupdated 2026-07-02
Results — best trained NN across N vs the LLM pipeline
Strongest trained NN per cell — max of SegFormer (mit_b2), pretrained U-Net (resnet34), and nnU-Net, 2-seed means — at matched budgets N = 10 / 25 / 50 / 100, against the LLM pipeline (re-measured from scratch via eval_all_domains.py). The LLM's only label-fit module is a ~5–8-param genome; localization and SAM are GT-free/frozen — so the LLM number is ~flat in N while the NN climbs. Bold = LLM ahead of the best NN at that budget.
Domain
best NN N=10
N=25
N=50
N=100
LLM pipeline
ISIC 2018 (derm)
0.815
0.829
0.832
0.868
0.880
MSD Spleen (CT)
0.633
0.802
0.859
0.907
0.875
Kvasir-SEG (endo)
0.756
0.824
0.833
0.889
0.332
ChestXray (X-ray)
0.938
0.948
0.952
0.953
0.825
The LLM pipeline wins the scarce-label regime where it has a cue — ISIC through N=100 (best NN needs N=189 to reach 0.887), Spleen through N=50 (crossover ~N=70, via a GT-free cross-slice prior) — and loses at every budget on the no-cue ceilings: Kvasir polyp (structural — no GT-free cue localizes it) and Chest X-ray (box-prompted SAM caps at a GT-box 0.943 < 0.953). SegFormer is the strongest NN in 10 of 12 sweep cells.
Data-efficiency
LLM pipeline (dashed — genome re-fit per N; ~flat) vs trained NN (solid — matched N). Spleen is capped at N=25 (30 training draws) and Kvasir at N=50 (91 draws).
Qualitative examples — 3 best / 3 worst per dataset
Green = ground truth, red = prediction. Top row = 3 highest-Dice cases, bottom row = 3 lowest.
ISIC 2018 — skin lesion (pigment cue, LLM's best domain)
MSD Spleen — CT (localizer + within-volume prior)
The worst cases are localizer failures (prediction lands on stomach/liver, Dice≈0). A GT-free cross-slice prior (centroid trajectory + sibling-mask seed) plus a selective multi-prototype re-decode recovers them from confident sibling slices, lifting the spleen pipeline to 0.875 (0.786→0.840→0.868→0.875 this session, zero regressions).
Kvasir-SEG — polyp (no GT-free cue: structural ceiling)
Even "best" cases are modest — polyps share color/texture with mucosa, so the coordinate draws mislocalize and SAM segments the wrong region. No GT-free signal fixes this (a redness-box lever was tested and rejected).
ChestXray — bilateral lungs (box-prompted SAM)
The worst cases miss the costophrenic recesses / a full lung field; a perfect GT box caps SAM at 0.943, below the trained U-Net's 0.953.
What we learned
ISIC: the LLM pipeline beats nnU-Net at every budget (+0.116 at N=10 → +0.025 at N=100) — genuinely more label-efficient for dermoscopy.
Spleen: a GT-free within-volume prior (re-decode mislocalized/over-seg CT slices from confident sibling slices) lifts 0.786 → 0.840, beating U-Net through N=50.
Kvasir: honest 100-image Dice is 0.332 — no GT-free cue localizes the polyp (the 0.86 sometimes cited used GT-hand-redrawn images).
Chest X-ray: box-prompted frozen SAM is architecturally capped — even a perfect GT box reaches only 0.943 < the trained U-Net's 0.953.
Honest-reporting note: earlier drafts carried optimistic hardcoded values (ISIC 0.885, Kvasir 0.860, CXR 0.855). This report uses numbers re-measured from scratch with the current pipeline: ISIC 0.880, Kvasir 0.332, CXR 0.825.