# Effects of Sarcopenia on the Outcomes and Safety of Chemoradiotherapy Followed by Durvalumab for the Treatment of Patients With Locally Advanced Non‐Small Cell Lung Cancer

**Authors:** Kentaro Tamura, Hidehito Horinouchi, Mototaka Miyake, Ken Masuda, Yuki Shinno, Yusuke Okuma, Tatsuya Yoshida, Noboru Yamamoto, Yasushi Goto

PMC · DOI: 10.1111/1759-7714.70145 · 2025-08-15

## TL;DR

This study found that muscle loss during chemoradiotherapy in lung cancer patients does not affect the effectiveness or safety of durvalumab treatment.

## Contribution

The study is the first to clarify that sarcopenia during chemoradiotherapy does not impact durvalumab outcomes in locally advanced non-small cell lung cancer.

## Key findings

- Skeletal muscle index significantly decreased during chemoradiation therapy.
- No significant differences in treatment response, survival, or adverse events were observed between patients with and without skeletal muscle loss.

## Abstract

Sarcopenia is associated with poor outcomes of various cancers treated with immune checkpoint inhibitors. Durvalumab is the standard of care for patients with locally advanced (LA) non‐small cell lung cancer (NSCLC) after chemoradiation therapy (CRT). However, the effect of sarcopenia on the efficacy and safety of durvalumab in patients with LA‐NSCLC remains unclear.

This single‐center retrospective study was conducted between 2018 and 2021. Body composition indices were measured using computed tomography scans taken at the third lumbar vertebra before and after CRT. The cutoff values were set based on the change ratios for each index before and after CRT. Tumor response, survival, and the efficacy and safety of durvalumab were compared between patients who showed skeletal muscle loss and those who did not.

Among 153 eligible patients (median age: 65 years; 74.5% men), skeletal muscle index (SMI) significantly decreased during CRT. With the threshold set at a −10% change in SMI, no significant difference in objective response rate (ΔSMI ≤ −10% vs. ΔSMI > −10%: 76.6% vs. 75.7%, p = 1.000), progression‐free survival (hazard ratio [HR], 0.99, p = 0.983), overall survival (HR 1.04, p = 0.909), or the frequency of immune‐related adverse events (44.9% vs. 44.2%, p = 1.000) was observed between the two groups.

Although muscle loss during CRT is common, it does not compromise the efficacy or safety of subsequent durvalumab therapy in patients with LA‐NSCLC. Future studies are needed to delineate sarcopenia criteria specific to LA‐NSCLC and assess interventions, including rehabilitation and pharmacotherapy.

Muscle loss during chemoradiotherapy is common in patients with locally advanced non‐small cell lung cancer. However, our retrospective study showed that this muscle loss does not negatively affect the efficacy or safety of subsequent durvalumab treatment.

## Linked entities

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

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, GHSR (growth hormone secretagogue receptor) [NCBI Gene 2693] {aka GHDP, GHS-R1a, GHSR-1a}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}
- **Diseases:** Muscle loss (MESH:D009135), weight loss (MESH:D015431), Cancer (MESH:D009369), muscle (MESH:D019042), skeletal (MESH:C564967), obese (MESH:D009765), nausea (MESH:D009325), squamous cell carcinoma (MESH:D002294), LA (MESH:D020178), Comorbidity (MESH:D004194), overdose (MESH:D062787), lung cancer (MESH:D008175), Cachexia (MESH:D002100), falls (MESH:C537863), NSCLC (MESH:D002289), muscle mass (MESH:C536030), stage III disease (MESH:D007676), adenocarcinoma (MESH:D000230), SMI (MESH:D005207), Sarcopenia (MESH:D055948), Chronic inflammation (MESH:D007249), anorexia (MESH:D000855), muscle damage (MESH:D009133), death (MESH:D003643), fractures (MESH:D050723)
- **Chemicals:** Durvalumab (MESH:C000613593), steroids (MESH:D013256), platinum (MESH:D010984), AbbVie (-), cisplatin (MESH:D002945), CBDCA (MESH:D016190), Anamorelin (MESH:C000593861)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** L858R, 19del

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12355038/full.md

---
Source: https://tomesphere.com/paper/PMC12355038