# Autofluorescence bronchoscopy findings of pseudoprogression after neoadjuvant chemo-immunotherapy in squamous cell lung cancer: A case report

**Authors:** Himeko Mori, Yasuharu Sekine, Keisuke Kuroda, Sho Ueda, Yusuke Saeki, Naohiro Kobayashi, Hideo Ichimura, Noriko Takemura-Kobayashi, Daisuke Matsubara, Yukio Sato

PMC · DOI: 10.1016/j.rmcr.2026.102388 · Respiratory Medicine Case Reports · 2026-02-20

## TL;DR

A case report shows that autofluorescence bronchoscopy can help distinguish pseudoprogression from residual cancer after immunotherapy in lung cancer.

## Contribution

This case demonstrates how autofluorescence bronchoscopy can identify pseudoprogression in lung cancer following chemo-immunotherapy.

## Key findings

- Autofluorescence attenuation after treatment was linked to pseudoprogression, not residual cancer.
- Histopathology showed immune cell infiltration without cancer cells, confirming pseudoprogression.
- Re-biopsy is recommended before surgery to avoid misdiagnosis in post-immunotherapy cases.

## Abstract

In recent years, multiple clinical trials have demonstrated the efficacy of neoadjuvant chemotherapy (NAC) combined with immune checkpoint inhibitors (ICI) for stage II–III non-small cell lung cancer (NSCLC). Pseudoprogression, a phenomenon in which activated lymphocytes infiltrate tumors and cause transient enlargement, can complicate post-treatment assessment. We report a case of stage III squamous cell carcinoma in the right lower lobe with endobronchial spread treated with NAC plus ICI. Autofluorescence imaging (AFI) bronchoscopy after treatment showed further autofluorescence attenuation despite no residual malignancy, consistent with pseudoprogression. Histopathology revealed infiltration of CD4+, CD8+ lymphocytes, and CD68+ macrophages without cancer cells. This case highlights that autofluorescence attenuation after immunotherapy may reflect pseudoprogression rather than residual tumor, emphasizing the importance of re-biopsy before surgical decision-making.

## Linked entities

- **Proteins:** CD4 (CD4 molecule), CD8A (CD8 subunit alpha), CD68 (CD68 molecule)
- **Diseases:** non-small cell lung cancer (MONDO:0005233), squamous cell carcinoma (MONDO:0005096)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, ELN (elastin) [NCBI Gene 2006] {aka ADCL1, SVAS, WBS, WS}, TENM1 (teneurin transmembrane protein 1) [NCBI Gene 10178] {aka ODZ1, ODZ3, TEN-M1, TEN1, TNM, TNM1}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** diabetes (MESH:D003920), S6 tumor (MESH:D009369), lung cancer (MESH:D008175), edema (MESH:D004487), tracheobronchial amyloidosis (MESH:C566362), cough (MESH:D003371), inflammation (MESH:D007249), hypertension (MESH:D006973), III (MESH:C537189), bronchial ulcers (MESH:D001982), squamous cell lung cancer (MESH:D018307), stage II (MESH:D062706), dysplastic (MESH:D004416), squamous cell carcinoma (MESH:D002294), NSCLC (MESH:D002289), endobronchial lesion (MESH:D009059), bleeding (MESH:D006470), hemoptysis (MESH:D006469), tuberculosis (MESH:D014376), obstructive pneumonia (MESH:D011014), chronic obstructive pulmonary disease (MESH:D029424)
- **Chemicals:** paclitaxel (MESH:D017239), FDG (MESH:D019788), carboplatin (MESH:D016190), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12945578/full.md

## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12945578/full.md

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Source: https://tomesphere.com/paper/PMC12945578