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Clinical calculator summary

Original 2017 Bigot Gustave Roussy Immune Score

A three-factor additive baseline prognostic score using albumin, LDH relative to local ULN, and NLR.

Evidence-based context for fast calculator use

Purpose:
Reproduce the original low- versus high-score phase-I cohort grouping and show its historical discovery-cohort observation.
Population:
Adults with mixed advanced solid tumors entering phase-I immune-checkpoint-therapy trials at baseline.
Factors:
Albumin <35 g/L, LDH above local laboratory ULN, NLR >6
Reference:
Bigot et al. Eur J Cancer. 2017;84:212-218.
HomeGRIm Score
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GRIm Score

g/L
U/L
U/L

Clinical Context & Background

This calculator reproduces the original 2017 Gustave Roussy Immune Score (GRIm-Score). It assigns one point each for baseline albumin below 35 g/L, LDH above the local laboratory upper limit of normal, and neutrophil-to-lymphocyte ratio above 6. All comparisons use unrounded raw values.
The original discovery and validation cohorts included adults with mixed advanced solid tumors entering phase-I immune-checkpoint-therapy trials; the model was not lung-cancer-specific. GRIm is a prognostic grouping, not an individualized survival estimate, immunotherapy-benefit prediction, candidate-selection rule, or treatment recommendation. It is not intended for screening, diagnosis, early-stage disease, treatment-response assessment, or post-treatment reassessment.
Formula Logic
Original 2017 GRIm score = 1 point each for albumin <35 g/L, LDH above the local laboratory upper limit of normal, and NLR >6.

Reference Data

ScoreOriginal groupDiscovery-cohort median OS
0-1Low group68.9 weeks
2-3High group20.4 weeks

Clinical Workflow

Use, Interpret, And Continue The Patient Pathway

Expand for workflow guidance, limitations, examples, and related next steps.

When To Use

  • Use baseline pretreatment values for adults with advanced solid tumors entering phase-I immune-checkpoint-therapy trials resembling the original cohorts.
  • Enter LDH and its local laboratory ULN in identical units; use the unrounded NLR.

How To Interpret

  • Scores 0-1 form the original Low group; scores 2-3 form the High group.
  • Albumin exactly 35 g/L, LDH exactly at ULN, and NLR exactly 6 each score zero.

What To Do Next

  • Integrate the result with protocol criteria, performance status, disease status, organ function, comorbidity, patient goals, and specialist assessment.
  • Do not select, withhold, or recommend immunotherapy because of GRIm alone.

Limitations

  • The original cohorts contained mixed advanced solid tumors and were not lung-cancer-specific.
  • Not validated for screening, diagnosis, early-stage disease, treatment response, or post-treatment reassessment.
  • GRIm is prognostic and is not a validated prediction of immunotherapy benefit or a treatment-selection rule.
  • No unsupported upper limits are imposed on the laboratory inputs.

Validated Population

Baseline adults with mixed advanced solid tumors entering the original phase-I immune-checkpoint-therapy trials.

Equality example

Albumin 35 g/L, LDH equal to its local ULN, and NLR 6 each score zero, producing a total score of 0.

Calculation verification history

Verified
  1. : Production browser revalidation

    • Three source-backed cases passed through visible production controls at GRIm scores 0, 1, and 3.
    • Raw albumin, LDH/ULN, and NLR thresholds produced the expected Low and High groups.
    • No unexpected N/A, literal undefined value, stale control, unsupported gauge, or browser-console error was observed.
    Download latest production check (Excel)

    Case-level evidence is retained in validation/browser-revalidation/grim-immunotherapy-lung-cancer-score-2026-08-03.json.

  2. : Production browser validation

    • Ten source-backed cases were exercised on the public production route through visible browser controls; 10/10 case records passed their expected-versus-observed assertions across 11 visible submissions.
    • Overall browser status: failed-console. medium: Production emitted minified React error #418 during route loads/reloads used by this run.
    • Case-level inputs, expected and observed results, reset/repeat behavior, failure reproductions, and console evidence are retained in the production-browser evidence record.

    Case-level production evidence is retained in validation/browser-production/grim-immunotherapy-lung-cancer-score.json.

  3. : Browser input adapter corrected and reverified

    • Accepted finite number values already normalized by the shared calculator form while retaining strict malformed-input rejection.
    • No equation, cutoff, unit, classification, or applicability rule changed; calculator-specific verification and the calculator-wide browser-input audit passed.
  4. : Full validation test

    • 320/320 independent model, exact-boundary, invalid-input, UI/integration, outcome, trace, wording, and immutability checks passed.
    • No registered master panel calculates GRIm; no panel receives inherited GRIm verification.
  5. : Calculation and input-contract correction

    • Replaced favorable pre-scored defaults with required raw albumin, LDH, local LDH ULN, and NLR; missing, extra, coercive, nonfinite, and out-of-domain values are rejected.
    • Restored exact equality behavior, complete contribution trace, original discovery-cohort median-survival rows, and mixed-solid-tumor prognostic scope without claiming individualized survival, immunotherapy benefit, or treatment selection.

Verification confirms the calculator implementation against the cited model; it is not independent clinical validation, regulatory approval, or medical advice.

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Frequently Asked Questions

Does albumin exactly 35 g/L score a point?

No. The original adverse criterion is strictly below 35 g/L.

Do LDH exactly at ULN or NLR exactly 6 score points?

No. Both original adverse criteria are strict greater-than comparisons.

Does GRIm predict immunotherapy benefit?

No. It is a historical prognostic grouping and must not be used as a stand-alone treatment-selection or immunotherapy-benefit tool.

Evidence-based oncology decision support. Verify with clinical guidelines.