# Multidisciplinary international expert consensus recommendations on tissue acquisition in non-small cell lung cancer

**Authors:** Pyng Lee, Karim Abdelhamid, Rachel Butler, Wendy Cooper, Misako Nagasaka, Solange Peters, Luis Seijo, Gerard Silvestri, Bernard Wee, Kazuhiro Yasufuku, Neal Navani

PMC · DOI: 10.1016/j.ebiom.2026.106223 · 2026-03-19

## TL;DR

This paper provides expert consensus recommendations on how to best obtain and handle tissue samples for non-small cell lung cancer patients to improve precision medicine outcomes.

## Contribution

The paper offers a multidisciplinary international consensus on tissue acquisition practices for non-small cell lung cancer.

## Key findings

- The most advanced disease site should be selected for biopsy.
- Biopsy techniques should be chosen based on the tissue location and patient factors.
- A patient-centered approach is emphasized for optimal tissue acquisition.

## Abstract

The practice of precision medicine has transformed outcomes for patients with advanced non-small cell lung cancer (NSCLC). Precision medicine is increasingly applied to the therapeutic algorithms of early-stage NSCLC both in the neoadjuvant and adjuvant space. Procuring sufficient tumour specimens safely and preparing tissue are key components. Whilst there are guidelines on how to optimise tissue acquisition and handling, real-world practice identifies wide variation in diagnostic yields and procedural complication rates, which underscores the need for a consensus-driven multidisciplinary approach.

This article reflects the collective consensus of an international expert panel of different specialities from the United States, Europe, and Asia–Pacific regions. Consensus recommendations were developed following a structured virtual working group discussion, during which the group shared recommendations for tissue acquisition and initial handling. The manuscript was finalised through successive rounds of offline review until consensus was achieved.

The site of involvement that denotes the most advanced stage should be chosen for biopsy. The choice of technique should depend on where the tissue is acquired from, e.g., pulmonary nodules, intra-thoracic lymph nodes, tissue in advanced stage disease, or pleural disease.

The optimal biopsy technique should support simultaneous diagnosis and staging and be selected based on the patient's clinical presentation, the expected diagnostic yield, the required sample type, and the degree of invasiveness, while maintaining a patient-centred approach.

10.13039/100004325AstraZeneca.

## Linked entities

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

## Full-text entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, SLTM (SAFB like transcription modulator) [NCBI Gene 79811] {aka Met}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098] {aka MCF3, ROS, c-ros-1}
- **Diseases:** bleeding (MESH:D006470), lung nodules (MESH:D003074), pleural malignancy (MESH:D016066), tuberculous effusions (MESH:D000080324), metastases (MESH:D009362), pleural disease (MESH:D010995), bone lesion (MESH:D001847), lung cancer (MESH:D008175), NSCLC (MESH:D002289), pneumothorax (MESH:D011030), pulmonary nodules (MESH:D055613), lung disease (MESH:D008171), atelectasis (MESH:D001261), mesothelioma (MESH:D008654), adrenal gland lesions (MESH:D000307), malignant mesothelioma (MESH:D000086002), Cancer (MESH:D009369), liver lesions (MESH:D008107), emphysema (MESH:D004646), pleural effusions (MESH:D010996), pulmonary fibrosis (MESH:D011658)
- **Chemicals:** formalin (MESH:D005557), osimertinib (MESH:C000596361)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13015214/full.md

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Source: https://tomesphere.com/paper/PMC13015214