# Cavitation and durable remission in a PD-L1–positive, TP53-mutant SMARCA4-deficient lung tumor following immunochemotherapy and radiotherapy: A case report

**Authors:** Kelan Deng, Guixia Liu, Yinping Li, Peiling Bao, Yue Zhang, Zhibin Xie

PMC · DOI: 10.1016/j.rmcr.2026.102390 · Respiratory Medicine Case Reports · 2026-02-26

## TL;DR

A rare lung tumor showed durable remission after immunochemotherapy and radiotherapy, suggesting potential biomarkers for treatment response.

## Contribution

This case report identifies PD-L1 expression and radiologic cavitation as potential biomarkers for treatment efficacy in SMARCA4-deficient tumors.

## Key findings

- The patient achieved partial remission and tumor cavitation after immunochemotherapy.
- Combination therapy with radiotherapy extended survival to 17 months.
- PD-L1 expression and cavitation may indicate treatment response in SMARCA4-deficient tumors.

## Abstract

SMARCA4-deficient undifferentiated tumors (SMARCA4-UTs) are rare, aggressive thoracic malignancies with dismal prognosis. Most cases are refractory to conventional therapy, a significant number of patients show no response to one or more chemotherapy regimens, exhibiting an overall survival (OS) of less than six months. We report a case of a 52-year-old male heavy smoker with a right lower lobe SMARCA4-UTs harboring TP53 mutation and PD-L1 expression (tumor proportion score [TPS] 30%, combined positive score [CPS] 30%). The tumor showed loss of SMARCA4 (also known as BRG1), high Ki-67 (∼50%), and rapid growth. After six cycles of tislelizumab + paclitaxel/cisplatin, the lesion demonstrated partial remission and progressive cavitation on CT imaging. Consolidative radiotherapy (60 Gy/30 fractions) further reduced the tumor burden. The survival period of this patient was 17 months long. This case highlights that PD-L1 expression and radiologic cavitation may serve as potential efficacy biomarkers in SMARCA4-UTs, even in tumors with TP53 mutations and a high proliferative index. Combined immunotherapy with chemotherapy and radiotherapy may confer durable disease control in this aggressive lung cancer subtype.

•In SMARCA4-UT, PD-L1 expression & cavitation may predict immunochemotherapy efficacy, even with TP53 mutation. Combo therapy offers durable control.

In SMARCA4-UT, PD-L1 expression & cavitation may predict immunochemotherapy efficacy, even with TP53 mutation. Combo therapy offers durable control.

## Linked entities

- **Genes:** SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597], TP53 (tumor protein p53) [NCBI Gene 7157], SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597]
- **Proteins:** CD274 (CD274 molecule), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Chemicals:** paclitaxel (PubChem CID 36314), cisplatin (PubChem CID 5460033)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** KRT19 (keratin 19) [NCBI Gene 3880] {aka CK19, K19, K1CS}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, STK11 (serine/threonine kinase 11) [NCBI Gene 6794] {aka LKB1, PJS, hLKB1}, CD44 (CD44 molecule (IN blood group)) [NCBI Gene 960] {aka CDW44, CSPG8, ECM-III, ECMR-III, H-CAM, HCELL}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, ENO2 (enolase 2) [NCBI Gene 2026] {aka HEL-S-279, NSE}, DNAH8 (dynein axonemal heavy chain 8) [NCBI Gene 1769] {aka ATPase, SPGF46, hdhc9}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, KEAP1 (kelch like ECH associated protein 1) [NCBI Gene 9817] {aka INrf2, KLHL19}, BANF1 (barrier to autointegration nuclear assembly factor 1) [NCBI Gene 8815] {aka BAF, BCRP1, D14S1460, NGPS}, SMARCA4 (SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4) [NCBI Gene 6597] {aka BAF190, BAF190A, BRG1, CSS4, MRD16, OTSC12}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, MIR215 (microRNA 215) [NCBI Gene 406997] {aka MIRN215, miRNA215, mir-215}
- **Diseases:** lung lesion (MESH:D008171), cancer (MESH:D009369), lung cancer (MESH:D008175), epithelial tumors (MESH:D002277), sarcoma (MESH:D012509), SCCA (MESH:D002294), non-small cell lung cancer (MESH:D002289), malignant rhabdomyosarcoma (MESH:D012208), lymphadenopathy (MESH:D008206), Hemoptysis (MESH:D006469), obstructive pneumonia (MESH:D011014), metastasis (MESH:D009362), necrosis (MESH:D009336)
- **Chemicals:** paclitaxel (MESH:D017239), platinum (MESH:D010984), tislelizumab (MESH:C000707970), cisplatin (MESH:D002945)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12966867/full.md

## References

12 references — full list in the complete paper: https://tomesphere.com/paper/PMC12966867/full.md

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Source: https://tomesphere.com/paper/PMC12966867