# Reframing tumor bed evaluation in non-small cell lung cancer: histopathological challenges and future directions in the era of neoadjuvant immunotherapy

**Authors:** Federica Pezzuto, Eleonora Faccioli, Omar El Mnif, Giuseppe Maggioni, Francesca Lunardi, Francesco Fortarezza, Chiara Giraudo, Marco Schiavon, Laura Bonanno, Giulia Pasello, Andrea Dell’Amore, Fiorella Calabrese

PMC · DOI: 10.3389/fonc.2026.1716992 · Frontiers in Oncology · 2026-02-04

## TL;DR

This paper discusses how traditional methods for evaluating lung cancer treatment responses are inadequate with immunotherapy and suggests new approaches using digital tools and AI.

## Contribution

The paper introduces the need for immune-adapted criteria and multidimensional assessment tools in evaluating NSCLC responses to immunotherapy.

## Key findings

- Traditional endpoints like MPR and pCR may not capture immune-mediated tumor changes.
- Digital pathology and AI can provide objective quantification of histologic features.
- Combining digital, radiologic, and molecular data improves response assessment and clinical trial consistency.

## Abstract

The introduction of neoadjuvant immunotherapy in non-small cell lung cancer (NSCLC) has led to complex tumor responses that challenge conventional pathological assessment. Thus, traditional endpoints such as major pathological response (MPR) and pathological complete response (pCR) may become insufficient to capture the full spectrum of immune-mediated changes. Indeed, these parameters were originally developed in the context of cytotoxic chemotherapy and may not reflect immune-mediated phenomena and stromal remodeling which can significantly alter the appearance of the tumor bed. As a result, MPR and pCR may underrepresent the true extent of biological response in patients treated with immunotherapy. This review outlines current limitations in morphologic evaluation and highlights the need for immune-adapted criteria. Furthermore, it explores the additional value of digital pathology and AI that offer objective and reproducible quantification of histologic features. Integrating these tools with radiologic and molecular data supports a multidimensional approach to response assessment, aiming to refine prognostication, guide adjuvant therapy, and ensure consistency in clinical trial designs.

## Linked entities

- **Diseases:** non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Genes:** NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, IL9 (interleukin 9) [NCBI Gene 3578] {aka HP40, IL-9, P40}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, GZMB (granzyme B) [NCBI Gene 3002] {aka C11, CCPI, CGL-1, CGL1, CSP-B, CSPB}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, TRBV20OR9-2 (T cell receptor beta variable 20/OR9-2 (non-functional)) [NCBI Gene 6962] {aka CDR3, TCRBV20S2, TCRBV2O, TCRBV2S2O}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** cytotoxic (MESH:D064420), death (MESH:D003643), necrosis (MESH:D009336), TLS (MESH:D000072717), Lung Cancer (MESH:D008175), adenocarcinoma (MESH:D000230), Solid Tumors (MESH:D009369), Stable Disease (MESH:D060050), SD (MESH:D012735), granulomatous (MESH:D013968), PD (MESH:D010300), inflammation (MESH:D007249), fibrosis (MESH:D005355), NSCLC (MESH:D002289), pulmonary mass (MESH:C536030), squamous cell carcinoma (MESH:D002294)
- **Chemicals:** etoposide (MESH:D005047), FDG (MESH:D019788), hematoxylin (MESH:D006416), [18F] FDG-FDG (-), cisplatin (MESH:D002945), docetaxel (MESH:D000077143), eosin (MESH:D004801), lipid (MESH:D008055), platinum (MESH:D010984), cholesterol (MESH:D002784), [18F (MESH:C000615276)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12913143/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913143/full.md

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Source: https://tomesphere.com/paper/PMC12913143